참고문헌
- Mankin HJ. The response of articular cartilage to mechanical injury. J Bone Joint Surg Am. 1982;64:460-6. https://doi.org/10.2106/00004623-198264030-00022
- Pearle AD, Warren RF, Rodeo SA. Basic science of articular cartilage and osteoarthritis. Clin Sports Med. 2005;24:1-12. https://doi.org/10.1016/j.csm.2004.08.007
- Hunziker EB. Articular cartilage repair: basic science and clinical progress. A review of the current status and prospects. Osteoarthritis Cartilage. 2002;10:432-63. https://doi.org/10.1053/joca.2002.0801
- O'Driscoll SW. The healing and regeneration of articular cartilage. J Bone Joint Surg Am. 1998;80:1795-812. https://doi.org/10.2106/00004623-199812000-00011
- Camp CL, Stuart MJ, Krych AJ. Current concepts of articular cartilage restoration techniques in the knee. Sports Health. 2014;6:265-73. https://doi.org/10.1177/1941738113508917
- Armiento AR, Stoddart MJ, Alini M, Eglin D. Biomaterials for articular cartilage tissue engineering: learning from biology. Acta Biomater. 2018;65:1-20. https://doi.org/10.1016/j.actbio.2017.11.021
- Huang BJ, Hu JC, Athanasiou KA. Cell-based tissue engineering strategies used in the clinical repair of articular cartilage. Biomaterials. 2016;98:1-22. https://doi.org/10.1016/j.biomaterials.2016.04.018
- Cole BJ, D'Amato M. Autologous chondrocyte implantation. Oper Tech Orthop. 2001;11:115-31. https://doi.org/10.1016/S1048-6666(01)80021-5
- Brittberg M. Autologous chondrocyte implantation-technique and long-term follow-up. Injury. 2008;39 Suppl 1:S40-9.
- Benya PD, Shaffer JD. Dedifferentiated chondrocytes reexpress the differentiated collagen phenotype when cultured in agarose gels. Cell. 1982;30:215-24. https://doi.org/10.1016/0092-8674(82)90027-7
- Higuchi A, Kumar SS, Benelli G, Alarfaj AA, Munusamy MA, Umezawa A, et al. Stem cell therapies for reversing vision loss. Trends Biotechnol. 2017;35:1102-17. https://doi.org/10.1016/j.tibtech.2017.06.016
- Higuchi A, Ling QD, Ko YA, Chang Y, Umezawa A. Biomaterials for the feeder-free culture of human embryonic stem cells and induced pluripotent stem cells. Chem Rev. 2011;111:3021-35. https://doi.org/10.1021/cr1003612
- Somoza RA, Welter JF, Correa D, Caplan AI. Chondrogenic differentiation of mesenchymal stem cells: challenges and unfulfilled expectations. Tissue Eng Part B Rev. 2014;20:596-608. https://doi.org/10.1089/ten.teb.2013.0771
- Nehrer S, Breinan HA, Ramappa A, Shortkroff S, Young G, Minas T, et al. Canine chondrocytes seeded in type I and type II collagen implants investigated in vitro. J Biomed Mater Res. 1997;38:95-104. https://doi.org/10.1002/(SICI)1097-4636(199722)38:2<95::AID-JBM3>3.0.CO;2-B
- Shakibaei M, De Souza P, Merker HJ. Integrin expression and collagen type II implicated in maintenance of chondrocyte shape in monolayer culture: an immunomorphological study. Cell Biol Int. 1997;21:115-25. https://doi.org/10.1006/cbir.1996.0118
- van Susante JL, Buma P, van Osch GJ, Versleyen D, van der Kraan PM, van der Berg WB, et al. Culture of chondrocytes in alginate and collagen carrier gels. Acta Orthop Scand. 1995;66:549-56. https://doi.org/10.3109/17453679509002314
- Lu Z, Doulabi BZ, Huang C, Bank RA, Helder MN. Collagen type II enhances chondrogenesis in adipose tissue-derived stem cells by affecting cell shape. Tissue Eng Part A. 2010;16:81-90.
- Takahashi T, Ogasawara T, Asawa Y, Mori Y, Uchinuma E, Takato T, et al. Three-dimensional microenvironments retain chondrocyte phenotypes during proliferation culture. Tissue Eng. 2007;13:1583-92. https://doi.org/10.1089/ten.2006.0322
- Pieper JS, van der Kraan PM, Hafmans T, Kamp J, Buma P, van Susante JL, et al. Crosslinked type II collagen matrices: preparation, characterization, and potential for cartilage engineering. Biomaterials. 2002;23:3183-92. https://doi.org/10.1016/S0142-9612(02)00067-4
- Galois L, Hutasse S, Cortial D, Rousseau CF, Grossin L, Ronziere MC, et al. Bovine chondrocyte behaviour in three-dimensional type I collagen gel in terms of gel contraction, proliferation and gene expression. Biomaterials. 2006;27:79-90. https://doi.org/10.1016/j.biomaterials.2005.05.098
- Li WJ, Jiang YJ, Tuan RS. Chondrocyte phenotype in engineered fibrous matrix is regulated by fiber size. Tissue Eng. 2006;12:1775-85. https://doi.org/10.1089/ten.2006.12.1775
- Noriega SE, Hasanova GI, Schneider MJ, Larsen GF, Subramanian A. Effect of fiber diameter on the spreading, proliferation and differentiation of chondrocytes on electrospun chitosan matrices. Cells Tissues Organs. 2012;195:207-21. https://doi.org/10.1159/000325144
- Nehrer S, Breinan HA, Ramappa A, Young G, Shortkroff S, Louie LK, et al. Matrix collagen type and pore size influence behaviour of seeded canine chondrocytes. Biomaterials. 1997;18:769-76. https://doi.org/10.1016/S0142-9612(97)00001-X
- Freyria AM, Ronziere MC, Cortial D, Galois L, Hartmann D, Herbage D, et al. Comparative phenotypic analysis of articular chondrocytes cultured within type I or type II collagen scaffolds. Tissue Eng Part A. 2009;15:1233-45. https://doi.org/10.1089/ten.tea.2008.0114
- Camper L, Hellman U, Lundgren-Akerlund E. Isolation, cloning, and sequence analysis of the integrin subunit alpha10, a beta1-associated collagen binding integrin expressed on chondrocytes. J Biol Chem. 1998;273:20383-9. https://doi.org/10.1074/jbc.273.32.20383
- Schuh E, Kramer J, Rohwedel J, Notbohm H, Muller R, Gutsmann T, et al. Effect of matrix elasticity on the maintenance of the chondrogenic phenotype. Tissue Eng Part A. 2010;16:1281-90. https://doi.org/10.1089/ten.tea.2009.0614
- Li X, Chen S, Li J, Wang X, Zhang J, Kawazoe N, et al. 3D culture of chondrocytes in gelatin hydrogels with different stiffness. Polymers (Basel). 2016;8:269. https://doi.org/10.3390/polym8080269
- Bates GP, Schor SL, Grant ME. A comparison of the effects of different substrata on chondrocyte morphology and the synthesis of collagen types IX and X. In Vitro Cell Dev Biol. 1987;23:374-80. https://doi.org/10.1007/BF02620995
- Duval E, Leclercq S, Elissalde JM, Demoor M, Galera P, Boumediene K. Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia not only induces type II collagen and aggrecan, but it also inhibits type I and type III collagen in the hypoxia-inducible factor 1alpha-dependent redifferentiation of chondrocytes. Arthritis Rheum. 2009;60:3038-48. https://doi.org/10.1002/art.24851
- Bosnakovski D, Mizuno M, Kim G, Takagi S, Okumura M, Fujinaga T. Chondrogenic differentiation of bovine bone marrow mesenchymal stem cells (MSCs) in different hydrogels: influence of collagen type II extracellular matrix on MSC chondrogenesis. Biotechnol Bioeng. 2006;93:1152-63. https://doi.org/10.1002/bit.20828
- Murphy CM, Matsiko A, Haugh MG, Gleeson JP, O'Brien FJ. Mesenchymal stem cell fate is regulated by the composition and mechanical properties of collagen-glycosaminoglycan scaffolds. J Mech Behav Biomed Mater. 2012;11:53-62. https://doi.org/10.1016/j.jmbbm.2011.11.009
- Higuchi A, Ling QD, Kumar SS, Chang Y, Alarfaj AA, Munusamy MA, et al. Physical cues of cell culture materials lead the direction of differentiation lineages of pluripotent stem cells. J Mater Chem B. 2015;3:8032-58. https://doi.org/10.1039/C5TB01276G
- Matsiko A, Gleeson JP, O'Brien FJ. Scaffold mean pore size influences mesenchymal stem cell chondrogenic differentiation and matrix deposition. Tissue Eng Part A. 2015;21:486-97. https://doi.org/10.1089/ten.tea.2013.0545
- Tamaddon M, Burrows M, Ferreira SA, Dazzi F, Apperley JF, Bradshaw A, et al. Monomeric, porous type II collagen scaffolds promote chondrogenic differentiation of human bone marrow mesenchymal stem cells in vitro. Sci Rep. 2017;7:43519. https://doi.org/10.1038/srep43519
- Matsiko A, Levingstone TJ, O'Brien FJ, Gleeson JP. Addition of hyaluronic acid improves cellular infiltration and promotes early-stage chondrogenesis in a collagen-based scaffold for cartilage tissue engineering. J Mech Behav Biomed Mater. 2012;11:41-52. https://doi.org/10.1016/j.jmbbm.2011.11.012
- Choi B, Kim S, Lin B, Wu BM, Lee M. Cartilaginous extracellular matrix-modified chitosan hydrogels for cartilage tissue engineering. ACS Appl Mater Interfaces. 2014;6:20110-21. https://doi.org/10.1021/am505723k
- Bian L, Hou C, Tous E, Rai R, Mauck RL, Burdick JA. The influence of hyaluronic acid hydrogel crosslinking density and macromolecular diffusivity on human MSC chondrogenesis and hypertrophy. Biomaterials. 2013;34:413-21. https://doi.org/10.1016/j.biomaterials.2012.09.052
- Varghese S, Hwang NS, Canver AC, Theprungsirikul P, Lin DW, Elisseeff J. Chondroitin sulfate based niches for chondrogenic differentiation of mesenchymal stem cells. Matrix Biol. 2008;27:12-21.
- Chen WC, Yao CL, Chu IM, Wei YH. Compare the effects of chondrogenesis by culture of human mesenchymal stem cells with various type of the chondroitin sulfate C. J Biosci Bioeng. 2011;111:226-31. https://doi.org/10.1016/j.jbiosc.2010.10.002
- Higuchi A, Ling QD, Hsu ST, Umezawa A. Biomimetic cell culture proteins as extracellular matrices for stem cell differentiation. Chem Rev. 2012;112:4507-40. https://doi.org/10.1021/cr3000169
- Albrecht C, Tichy B, Nurnberger S, Hosiner S, Zak L, Aldrian S, et al. Gene expression and cell differentiation in matrix-associated chondrocyte transplantation grafts: a comparative study. Osteoarthritis Cartilage. 2011;19:1219-27. https://doi.org/10.1016/j.joca.2011.07.004
- Zak L, Albrecht C, Wondrasch B, Widhalm H, Vekszler G, Trattnig S, et al. Results 2 years after matrix-associated autologous chondrocyte transplantation using the Novocart 3D scaffold. Am J Sports Med. 2014;42:1618-27. https://doi.org/10.1177/0363546514532337
- Saris D, Price A, Widuchowski W, Bertrand-Marchand M, Caron J, Drogset JO, et al. Matrix-applied characterized autologous cultured chondrocytes versus microfracture two-year follow-up of a prospective randomized trial. Am J Sports Med. 2014;42:1384-94. https://doi.org/10.1177/0363546514528093
- Petri M, Broese M, Simon A, Liodakis E, Ettinger M, Guenther D, et al. CaReS(MACT) versus microfracture in treating symptomatic patellofemoral cartilage defects: a retrospective matched-pair analysis. J Orthop Sci. 2013;18:38-44. https://doi.org/10.1007/s00776-012-0305-x
- Crawford DC, DeBerardino TM, Williams RJ 3rd. NeoCart, an autologous cartilage tissue implant, compared with microfracture for treatment of distal femoral cartilage lesions: an FDA phase-II prospective, randomized clinical trial after two years.. J Bone Joint Surg Am. 2012;94:979-89. https://doi.org/10.2106/JBJS.K.00533
- Ochi M, Uchio Y, Kawasaki K, Wakitani S, Iwasa J. Transplantation of cartilage-like tissue made by tissue engineering in the treatment of cartilage defects of the knee. J Bone Joint Surg Am. 2002;84:571-8. https://doi.org/10.1302/0301-620X.84B4.0840571
- Keselowsky BG, Collard DM, Garcia AJ. Surface chemistry modulates focal adhesion composition and signaling through changes in integrin binding. Biomaterials. 2004;25:5947-54. https://doi.org/10.1016/j.biomaterials.2004.01.062
- Salasznyk RM, Klees RF, Hughlock MK, Plopper GE. ERK signaling pathways regulate the osteogenic differentiation of human mesenchymal stem cells on collagen I and vitronectin. Cell Commun Adhes. 2004;11:137-53. https://doi.org/10.1080/15419060500242836
- Franceschi RT. The developmental control of osteoblast-specific gene expression: role of specific transcription factors and the extracellular matrix environment. Crit Rev Oral Biol Med. 1999;10:40-57. https://doi.org/10.1177/10454411990100010201
- Wallace DG, Rosenblatt J. Collagen gel systems for sustained delivery and tissue engineering. Adv Drug Deliv Rev. 2003;55:1631-49. https://doi.org/10.1016/j.addr.2003.08.004
- Gelse K, Poschl E, Aigner T. Collagens-structure, function, and biosynthesis. Adv Drug Deliv Rev. 2003;55:1531-46. https://doi.org/10.1016/j.addr.2003.08.002
-
Tulla M, Pentikainen OT, Viitasalo T, Kapyla J, Impola U, Nykvist P, et al. Selective binding of collagen subtypes by integrin
${\alpha}1I$ ,${\alpha}2I$ , and a10I domains. J Biol Chem. 2001;276:48206-12. https://doi.org/10.1074/jbc.M104058200 -
Hamaia SW, Luff D, Hunter EJ, Malcor JD, Bihan D, Gullberg D, et al. Unique charge-dependent constraint on collagen recognition by integrin
${\alpha}10{\beta}1$ . Matrix Biol. 2017;59:80-94. https://doi.org/10.1016/j.matbio.2016.08.010 - Kino-Oka M, Yashiki S, Ota Y, Mushiaki Y, Sugawara K, Yamamoto T, et al. Subculture of chondrocytes on a collagen type I-coated substrate with suppressed cellular dedifferentiation. Tissue Eng. 2005;11:597-608. https://doi.org/10.1089/ten.2005.11.597
- Farjanel J, Schurmann G, Bruckner P. Contacts with fibrils containing collagen I, but not collagens II, IX, and XI, can destabilize the cartilage phenotype of chondrocytes. Osteoarthritis Cartilage. 2001;9:S55-63.
- Jin GZ, Kim HW. Effects of type I collagen concentration in hydrogel on the growth and phenotypic expression of rat chondrocytes. Tissue Eng Regen Med. 2017;14:383-91. https://doi.org/10.1007/s13770-017-0060-3
- Fertala A, Han WB, Ko FK. Mapping critical sites in collagen II for rational design of gene-engineered proteins for cell-supporting materials. J Biomed Mater Res. 2001;57:48-58. https://doi.org/10.1002/1097-4636(200110)57:1<48::AID-JBM1140>3.0.CO;2-S
- Lucic D, Mollenhauer J, Kilpatrick KE, Cole AA. N-telopeptide of type II collagen interacts with annexin V on human chondrocytes. Connect Tissue Res. 2003;44:225-39. https://doi.org/10.1080/03008200390248632
- Leitinger B, Steplewski A, Fertala A. The D2 period of collagen II contains a specific binding site for the human discoidin domain receptor, DDR2. J Mol Biol. 2004;344:993-1003. https://doi.org/10.1016/j.jmb.2004.09.089
- Bengtsson T, Aszodi A, Nicolae C, Hunziker EB, Lundgren- Akerlund E, Fassler R. Loss of alpha10beta1 integrin expression leads to moderate dysfunction of growth plate chondrocytes. J Cell Sci. 2005;118:929-36. https://doi.org/10.1242/jcs.01678
- von der Mark K, Mollenhauer J. Annexin V interactions with collagen. Cell Mol Life Sci. 1997;53:539-45. https://doi.org/10.1007/s000180050069
- Klatt AR, Paul-Klausch B, Klinger C, Kuhn C, Renno JH, Banerjee M, et al. A critical role for collagen II in cartilage matrix degradation: collagen II induces pro-inflammatory cytokines and MMPs in primary human chondrocytes. J Orthop Res. 2009;27:65-70. https://doi.org/10.1002/jor.20716
- Goldring MB. Chondrogenesis, chondrocyte differentiation, and articular cartilage metabolism in health and osteoarthritis. Ther Adv Musculoskelet Dis. 2012;4:269-85. https://doi.org/10.1177/1759720X12448454
- Gigante A, Bevilacqua C, Cappella M, Manzotti S, Greco F. Engineered articular cartilage: influence of the scaffold on cell phenotype and proliferation. J Mater Sci Mater Med. 2003;14:713-6. https://doi.org/10.1023/A:1024915817061
- Brodkin KR, Garcia AJ, Levenston ME. Chondrocyte phenotypes on different extracellular matrix monolayers. Biomaterials. 2004;25:5929-38. https://doi.org/10.1016/j.biomaterials.2004.01.044
- Ohno T, Tanisaka K, Hiraoka Y, Ushida T, Tamaki T, Tateishi T. Effect of type I and type II collagen sponges as 3D scaffolds for hyaline cartilage-like tissue regeneration on phenotypic control of seeded chondrocytes in vitro. Mater Sci Eng C Mater Biol Appl. 2004;24:407-11. https://doi.org/10.1016/j.msec.2003.11.011
- Hubka KM, Dahlin RL, Meretoja VV, Kasper FK, Mikos AG. Enhancing chondrogenic phenotype for cartilage tissue engineering: monoculture and coculture of articular chondrocytes and mesenchymal stem cells. Tissue Eng Part B Rev. 2014;20:641-54.
-
Woltersdorf C, Bonk M, Leitinger B, Huhtala M, Kapyla J, Heino J, et al. The binding capacity of
${\alpha}1{\beta}1-$ ,${\alpha}2{\beta}1-$ and${\alpha}0{\beta}1-$ integrins depends on non-collagenous surface macromolecules rather than the collagens in cartilage fibrils. Matrix Biol. 2017;63:91-105. https://doi.org/10.1016/j.matbio.2017.02.001 - Noth U, Rackwitz L, Heymer A, Weber M, Baumann B, Steinert A, et al. Chondrogenic differentiation of human mesenchymal stem cells in collagen type I hydrogels. J Biomed Mater Res A. 2007;83:626-35.
- Rutgers M, Saris DB, Vonk LA, van Rijen MH, Akrum V, Langeveld D, et al. Effect of collagen type I or type II on chondrogenesis by cultured human articular chondrocytes. Tissue Eng Part A. 2013;19:59-65. https://doi.org/10.1089/ten.tea.2011.0416
- Schedel J, Distler O, Woenckhaus M, Gay RE, Simmen B, Michel BA, et al. Discrepancy between mRNA and protein expression of tumour suppressor maspin in synovial tissue may contribute to synovial hyperplasia in rheumatoid arthritis. Ann Rheum Dis. 2004;63:1205-11. https://doi.org/10.1136/ard.2003.006312
- Lu ZF, Doulabi BZ, Wuisman PI, Bank RA, Helder MN. Influence of collagen type II and nucleus pulposus cells on aggregation and differentiation of adipose tissue-derived stem cells. J Cell Mol Med. 2008;12:2812-22. https://doi.org/10.1111/j.1582-4934.2008.00278.x
- Vincent I, Tomomei S, Toshiyuki I. Magnetite/hydroxyapatite composite particles-assisted pore alignment of tilapia fish scale collagen-based scaffold. Key Eng Mater. 2016;696:121-8. https://doi.org/10.4028/www.scientific.net/KEM.696.121
- Zhang J, Yang Z, Li C, Dou Y, Li Y, Thote T, et al. Cells behave distinctly within sponges and hydrogels due to differences of internal structure. Tissue Eng Part A. 2013;19:2166-75. https://doi.org/10.1089/ten.tea.2012.0393
- Nuernberger S, Cyran N, Albrecht C, Redl H, Vecsei V, Marlovits S. The influence of scaffold architecture on chondrocyte distribution and behavior in matrix-associated chondrocyte transplantation grafts. Biomaterials. 2011;32:1032-40. https://doi.org/10.1016/j.biomaterials.2010.08.100
- Wise JK, Yarin AL, Megaridis CM, Cho M. Chondrogenic differentiation of human mesenchymal stem cells on oriented nanofibrous scaffolds: engineering the superficial zone of articular cartilage. Tissue Eng Part A. 2009;15:913-21. https://doi.org/10.1089/ten.tea.2008.0109
- Matthews JA, Wnek GE, Simpson DG, Bowlin GL. Electrospinning of collagen nanofibers. Biomacromolecules. 2002;3:232-8. https://doi.org/10.1021/bm015533u
- Matthews JA, Boland ED, Wnek GE, Simpson DG, Bowlin GL. Electrospinning of collagen type II: a feasibility study. J Bioact Compat Polym. 2003;18:125-34. https://doi.org/10.1177/0883911503018002003
- Yunoki S, Ikoma T, Monkawa A, Ohta K, Kikuchi M, Sotome S, et al. Control of pore structure and mechanical property in hydroxyapatite/collagen composite using unidirectional ice growth. Mater Lett. 2006;60:999-1002. https://doi.org/10.1016/j.matlet.2005.10.064
- Ikoma T, Kobayashi H, Tanaka J, Walsh D, Mann S. Physical properties of type I collagen extracted from fish scales of Pagrus major and Oreochromis niloticas. Int J Biol Macromol. 2003;32:199-204. https://doi.org/10.1016/S0141-8130(03)00054-0
- Kawamata H, Kuwaki S, Mishina T, Ikoma T, Tanaka J, Nozaki R. Hierarchical viscosity of aqueous solution of tilapia scale collagen investigated via dielectric spectroscopy between 500 MHz and 2.5 THz. Sci Rep. 2017;7:45398. https://doi.org/10.1038/srep45398
- Yang YL, Motte S, Kaufman LJ. Pore size variable type I collagen gels and their interaction with glioma cells. Biomaterials. 2010;31:5678-88. https://doi.org/10.1016/j.biomaterials.2010.03.039
- Lee CR, Grodzinsky AJ, Spector M. The effects of cross-linking of collagen-glycosaminoglycan scaffolds on compressive stiffness, chondrocyte-mediated contraction, proliferation and biosynthesis. Biomaterials. 2001;22:3145-54. https://doi.org/10.1016/S0142-9612(01)00067-9
- Vickers SM, Squitieri LS, Spector M. Effects of cross-linking type II collagen-GAG scaffolds on chondrogenesis in vitro: dynamic pore reduction promotes cartilage formation. Tissue Eng. 2006;12:1345-55. https://doi.org/10.1089/ten.2006.12.1345
- Zhang J, Wu Y, Thote T, Lee EH, Ge Z, Yang Z. The influence of scaffold microstructure on chondrogenic differentiation of mesenchymal stem cells. Biomed Mater. 2014;9:035011. https://doi.org/10.1088/1748-6041/9/3/035011
- Miot S, Woodfield T, Daniels AU, Suetterlin R, Peterschmitt I, Heberer M, et al. Effects of scaffold composition and architecture on human nasal chondrocyte redifferentiation and cartilaginous matrix deposition. Biomaterials. 2005;26:2479-89. https://doi.org/10.1016/j.biomaterials.2004.06.048
- Chao PG, Yodmuang S, Wang X, Sun L, Kaplan DL, Vunjak- Novakovic G. Silk hydrogel for cartilage tissue engineering. J Biomed Mater Res B Appl Biomater. 2010;95:84-90.
- Lee P, Tran K, Chang W, Shelke NB, Kumbar SG, Yu X. Influence of chondroitin sulfate and hyaluronic acid presence in nanofibers and its alignment on the bone marrow stromal cells: cartilage regeneration. J Biomed Nanotechnol. 2014;10:1469-79. https://doi.org/10.1166/jbn.2014.1831
- Discher DE, Janmey P, Wang YL. Tissue cells feel and respond to the stiffness of their substrate. Science. 2005;310:1139-43. https://doi.org/10.1126/science.1116995
- Hutmacher DW. Scaffolds in tissue engineering bone and cartilage. Biomaterials. 2000;21:2529-43. https://doi.org/10.1016/S0142-9612(00)00121-6
- Lv H, Wang H, Zhang Z, Yang W, Liu W, Li Y, et al. Biomaterial stiffness determines stem cell fate. Life Sci. 2017;178:42-8. https://doi.org/10.1016/j.lfs.2017.04.014
- Koay EJ, Shieh AC, Athanasiou KA. Creep indentation of single cells. J Biomech Eng. 2003;125:334-41. https://doi.org/10.1115/1.1572517
- Freeman PM, Natarajan RN, Kimura JH, Andriacchi TP. Chondrocyte cells respond mechanically to compressive loads. J Orthop Res. 1994;12:311-20. https://doi.org/10.1002/jor.1100120303
- Sanz-Ramos P, Mora G, Vicente-Pascual M, Ochoa I, Alcaine C, Moreno R, et al. Response of sheep chondrocytes to changes in substrate stiffness from 2 to 20 Pa: effect of cell passaging. Connect Tissue Res. 2013;54:159-66. https://doi.org/10.3109/03008207.2012.762360
- Schuh E, Hofmann S, Stok K, Notbohm H, Mu ller R, Rotter N. Chondrocyte redifferentiation in 3D: the effect of adhesion site density and substrate elasticity. J Biomed Mater Res A. 2012;100:38-47.
- Skotak M, Noriega S, Larsen G, Subramanian A. Electrospun cross-linked gelatin fibers with controlled diameter: the effect of matrix stiffness on proliferative and biosynthetic activity of chondrocytes cultured in vitro. J Biomed Mater Res A. 2010;95:828-36.
- Li WJ, Cooper JA, Mauck RL, Tuan RS. Fabrication and characterization of six electrospun poly(a-hydroxy ester)-based fibrous scaffolds for tissue engineering applications. Acta Biomater. 2006;2:377-85. https://doi.org/10.1016/j.actbio.2006.02.005
-
Park JS, Chu JS, Tsou AD, Diop R, Tang Z, Wang A, et al. The effect of matrix stiffness on the differentiation of mesenchymal stem cells in response to TGF-
${\beta}$ . Biomaterials. 2011;32:3921-30. https://doi.org/10.1016/j.biomaterials.2011.02.019 - Woods A, Wang G, Beier F. RhoA/ROCK signaling regulates Sox9 expression and actin organization during chondrogenesis. J Biol Chem. 2005;280:11626-34. https://doi.org/10.1074/jbc.M409158200
- Li YY, Choy TH, Ho FC, Chan PB. Scaffold composition affects cytoskeleton organization, cell-matrix interaction and the cellular fate of human mesenchymal stem cells upon chondrogenic differentiation. Biomaterials. 2015;52:208-20. https://doi.org/10.1016/j.biomaterials.2015.02.037
- Liu SQ, Tian Q, Hedrick JL, Po Hui JH, Ee PL, Yang YY. Biomimetic hydrogels for chondrogenic differentiation of human mesenchymal stem cells to neocartilage. Biomaterials. 2010;31:7298-307. https://doi.org/10.1016/j.biomaterials.2010.06.001
- Nam J, Johnson J, Lannutti JJ, Agarwal S. Modulation of embryonic mesenchymal progenitor cell differentiation via control over pure mechanical modulus in electrospun nanofibers. Acta Biomater. 2011;7:1516-24. https://doi.org/10.1016/j.actbio.2010.11.022
- Toh WS, Lim TC, Kurisawa M, Spector M. Modulation of mesenchymal stem cell chondrogenesis in a tunable hyaluronic acid hydrogel microenvironment. Biomaterials. 2012;33:3835-45. https://doi.org/10.1016/j.biomaterials.2012.01.065
- Lv H, Li L, Sun M, Zhang Y, Chen L, Rong Y, et al. Mechanism of regulation of stem cell differentiation by matrix stiffness. Stem Cell Res Ther. 2015;6:103. https://doi.org/10.1186/s13287-015-0083-4
- Zhang Q, Lu H, Kawazoe N, Chen G. Pore size effect of collagen scaffolds on cartilage regeneration. Acta Biomater. 2014;10:2005-13. https://doi.org/10.1016/j.actbio.2013.12.042
- Griffon DJ, Sedighi MR, Schaeffer DV, Eurell JA, Johnson AL. Chitosan scaffolds: interconnective pore size and cartilage engineering. Acta Biomater. 2006;2:313-20. https://doi.org/10.1016/j.actbio.2005.12.007
- Nava MM, Draghi L, Giordano C, Pietrabissa R. The effect of scaffold pore size in cartilage tissue engineering. J Appl Biomater Funct Mater. 2016;14:e223-9.
- Lin S, Sangaj N, Razafiarison T, Zhang C, Varghese S. Influence of physical properties of biomaterials on cellular behavior. Pharm Res. 2011;28:1422-30. https://doi.org/10.1007/s11095-011-0378-9
- Bryant SJ, Anseth KS. Hydrogel properties influence ECM production by chondrocytes photoencapsulated in poly(ethylene glycol) hydrogels. J Biomed Mater Res. 2002;59:63-72. https://doi.org/10.1002/jbm.1217
- Zhao Y, Tan K, Zhou Y, Ye Z, Tan WS. A combinatorial variation in surface chemistry and pore size of three-dimensional porous poly(e-caprolactone) scaffolds modulates the behaviors of mesenchymal stem cells. Mater Sci Eng C Mater Biol Appl. 2016;59:193-202. https://doi.org/10.1016/j.msec.2015.10.017
- Oh SH, Kim TH, Im GI, Lee JH. Investigation of pore size effect on chondrogenic differentiation of adipose stem cells using a pore size gradient scaffold. Biomacromolecules. 2010;11:1948-55. https://doi.org/10.1021/bm100199m
- Im GI, Ko JY, Lee JH. Chondrogenesis of adipose stem cells in a porous polymer scaffold: influence of the pore size. Cell Transplant. 2012;21:2397-405. https://doi.org/10.3727/096368912X638865
- Malladi P, Xu Y, Chiou M, Giaccia AJ, Longaker MT. Effect of reduced oxygen tension on chondrogenesis and osteogenesis in adipose-derived mesenchymal cells. Am J Physiol Cell Physiol. 2006;290:C1139-46. https://doi.org/10.1152/ajpcell.00415.2005
- Buxton AN, Zhu J, Marchant R, West JL, Yoo JU, Johnstone B. Design and characterization of poly(ethylene glycol) photopolymerizable semi-interpenetrating networks for chondrogenesis of human mesenchymal stem cells. Tissue Eng. 2007;13:2549-60. https://doi.org/10.1089/ten.2007.0075
- Shanmugasundaram S, Chaudhry H, Arinzeh TL. Microscale versus nanoscale scaffold architecture for mesenchymal stem cell chondrogenesis. Tissue Eng Part A. 2011;17:831-40. https://doi.org/10.1089/ten.tea.2010.0409
- Bean AC, Tuan RS. Fiber diameter and seeding density influence chondrogenic differentiation of mesenchymal stem cells seeded on electrospun poly(e-caprolactone) scaffolds. Biomed Mater. 2015;10:015018. https://doi.org/10.1088/1748-6041/10/1/015018
- Chen G, Ushida T, Tateishi T. Scaffold design for tissue engineering. Macromol Biosci. 2002;2:67-77. https://doi.org/10.1002/1616-5195(20020201)2:2<67::AID-MABI67>3.0.CO;2-F
- Chen CW, Tsai YH, Deng WP, Shih SN, Fang CL, Burch JG, et al. Type I and II collagen regulation of chondrogenic differentiation by mesenchymal progenitor cells. J Orthop Res. 2005;23:446-53. https://doi.org/10.1016/j.orthres.2004.09.002
- Bax DV, Davidenko N, Gullberg D, Hamaia SW, Farndale RW, Best SM, et al. Fundamental insight into the effect of carbodiimide crosslinking on cellular recognition of collagen-based scaffolds. Acta Biomater. 2017;49:218-34. https://doi.org/10.1016/j.actbio.2016.11.059
- Raghunath J, Rollo J, Sales KM, Butler PE, Seifalian AM. Biomaterials and scaffold design: key to tissue-engineering cartilage. Biotechnol Appl Biochem. 2007;46:73-84. https://doi.org/10.1042/BA20060134
- Hardy JG, Scheibel TR. Composite materials based on silk proteins. Prog Polym Sci. 2010;35:1093-115. https://doi.org/10.1016/j.progpolymsci.2010.04.005
- Altman GH, Diaz F, Jakuba C, Calabro T, Horan RL, Chen J, et al. Silk-based biomaterials. Biomaterials. 2003;24:401-16. https://doi.org/10.1016/S0142-9612(02)00353-8
- Yeo IS, Oh JE, Jeong L, Lee TS, Lee SJ, Park WH, et al. Collagen-based biomimetic nanofibrous scaffolds: preparation and characterization of collagen/silk fibroin bicomponent nanofibrous structures. Biomacromolecules. 2008;9:1106-16. https://doi.org/10.1021/bm700875a
- Meinel L, Hofmann S, Karageorgiou V, Zichner L, Langer R, Kaplan D, et al. Engineering cartilage-like tissue using human mesenchymal stem cells and silk protein scaffolds. Biotechnol Bioeng. 2004;88:379-91. https://doi.org/10.1002/bit.20252
- Wang J, Yang Q, Cheng N, Tao X, Zhang Z, Sun X, et al. Collagen/silk fibroin composite scaffold incorporated with PLGA microsphere for cartilage repair. Mater Sci Eng C Mater Biol Appl. 2016;61:705-11. https://doi.org/10.1016/j.msec.2015.12.097
- Wang J, Zhou W, Hu W, Zhou L, Wang S, Zhang S. Collagen/silk fibroin bi-template induced biomimetic bone-like substitutes. J Biomed Mater Res A. 2011;99:327-34.
- Chen L, Hu J, Ran J, Shen X, Tong H. Preparation and evaluation of collagen-silk fibroin/hydroxyapatite nanocomposites for bone tissue engineering. Int J Biol Macromol. 2014;65:1-7. https://doi.org/10.1016/j.ijbiomac.2014.01.003
- Lv Q, Feng Q, Hu K, Cui F. Three-dimensional fibroin/collagen scaffolds derived from aqueous solution and the use for HepG2 culture. Polymer (Guildf). 2005;46:12662-9. https://doi.org/10.1016/j.polymer.2005.10.137
- Chomchalao P, Pongcharoen S, Sutheerawattananonda M, Tiyaboonchai W. Fibroin and fibroin blended three-dimensional scaffolds for rat chondrocyte culture. Biomed Eng Online. 2013;12:28. https://doi.org/10.1186/1475-925X-12-28
- Sun K, Li H, Li R, Nian Z, Li D, Xu C. Silk fibroin/collagen and silk fibroin/chitosan blended three-dimensional scaffolds for tissue engineering. Eur J Orthop Surg Traumatol. 2015;25:243-9.
- Di Martino A, Sittinger M, Risbud MV. Chitosan: a versatile biopolymer for orthopaedic tissue-engineering. Biomaterials. 2005;26:5983-90. https://doi.org/10.1016/j.biomaterials.2005.03.016
- Suh JK, Matthew HW. Application of chitosan-based polysaccharide biomaterials in cartilage tissue engineering: a review. Biomaterials. 2000;21:2589-98. https://doi.org/10.1016/S0142-9612(00)00126-5
- Chicatun F, Pedraza CE, Muja N, Ghezzi CE, McKee MD, Nazhat SN. Effect of chitosan incorporation and scaffold geometry on chondrocyte function in dense collagen type I hydrogels. Tissue Eng Part A. 2013;19:2553-64. https://doi.org/10.1089/ten.tea.2013.0114
- Yan J, Li X, Liu L, Wang F, Zhu TW, Zhang Q. Potential use of collagen-chitosan-hyaluronan tri-copolymer scaffold for cartilage tissue engineering. Artif Cells Blood Substit Immobil Biotechnol. 2006;34:27-39. https://doi.org/10.1080/10731190500430024
- Tan W, Krishnaraj R, Desai TA. Evaluation of nanostructured composite collagen-chitosan matrices for tissue engineering. Tissue Eng. 2001;7:203-10. https://doi.org/10.1089/107632701300062831
- Chen Z, Mo X, He C, Wang H. Intermolecular interactions in electrospun collagen-chitosan complex nanofibers. Carbohydr Polym. 2008;72:410-8. https://doi.org/10.1016/j.carbpol.2007.09.018
- Yan LP, Wang YJ, Ren L, Wu G, Caridade SG, Fan JB, et al. Genipin-cross-linked collagen/chitosan biomimetic scaffolds for articular cartilage tissue engineering applications. J Biomed Mater Res A. 2010;95:465-75.
- Haaparanta AM, Jarvinen E, Cengiz IF, Ella V, Kokkonen HT, Kiviranta I, et al. Preparation and characterization of collagen/PLA, chitosan/PLA, and collagen/chitosan/PLA hybrid scaffolds for cartilage tissue engineering. J Mater Sci Mater Med. 2014;25:1129-36. https://doi.org/10.1007/s10856-013-5129-5
- Raftery RM, Woods B, Marques ALP, Moreira-Silva J, Silva TH, Cryan SA, et al. Multifunctional biomaterials from the sea: assessing the effects of chitosan incorporation into collagen scaffolds on mechanical and biological functionality. Acta Biomater. 2016;43:160-9. https://doi.org/10.1016/j.actbio.2016.07.009
- Dai W, Kawazoe N, Lin X, Dong J, Chen G. The influence of structural design of PLGA/collagen hybrid scaffolds in cartilage tissue engineering. Biomaterials. 2010;31:2141-52. https://doi.org/10.1016/j.biomaterials.2009.11.070
- Aspberg A. Cartilage proteoglycans. In: Grassel S, Aszodi A, editors. Cartilage. Springer; 2016. p. 1-22.
- Knudson W, Loeser RF. CD44 and integrin matrix receptors participate in cartilage homeostasis. Cell Mol Life Sci. 2002;59:36-44. https://doi.org/10.1007/s00018-002-8403-0
- Mahmood TA, Miot S, Frank O, Martin I, Riesle J, Langer R, et al. Modulation of chondrocyte phenotype for tissue engineering by designing the biologic-polymer carrier interface. Biomacromolecules. 2006;7:3012-8. https://doi.org/10.1021/bm060489+
- Kawasaki K, Ochi M, Uchio Y, Adachi N, Matsusaki M. Hyaluronic acid enhances proliferation and chondroitin sulfate synthesis in cultured chondrocytes embedded in collagen gels. J Cell Physiol. 1999;179:142-8. https://doi.org/10.1002/(SICI)1097-4652(199905)179:2<142::AID-JCP4>3.0.CO;2-Q
- Zhang L, Li K, Xiao W, Zheng L, Xiao Y, Fan H, et al. Preparation of collagen-chondroitin sulfate-hyaluronic acid hybrid hydrogel scaffolds and cell compatibility in vitro. Carbohydr Polym. 2011;84:118-25. https://doi.org/10.1016/j.carbpol.2010.11.009
- van Susante JLC, Pieper J, Buma P, van Kuppevelt TH, van Beuningen H, van Der Kraan PM, et al. Linkage of chondroitinsulfate to type I collagen scaffolds stimulates the bioactivity of seeded chondrocytes in vitro. Biomaterials. 2001;22:2359-69. https://doi.org/10.1016/S0142-9612(00)00423-3
- Ko CS, Huang JP, Huang CW, Chu IM. Type II collagen-chondroitin sulfate-hyaluronan scaffold cross-linked by genipin for cartilage tissue engineering. J Biosci Bioeng. 2009;107:177-82. https://doi.org/10.1016/j.jbiosc.2008.09.020
- Zhu H, Mitsuhashi N, Klein A, Barsky LW, Weinberg K, Barr ML, et al. The role of the hyaluronan receptor CD44 in mesenchymal stem cell migration in the extracellular matrix. Stem Cells. 2006;24:928-35. https://doi.org/10.1634/stemcells.2005-0186
- Allemann F, Mizuno S, Eid K, Yates KE, Zaleske D, Glowacki J. Effects of hyaluronan on engineered articular cartilage extracellular matrix gene expression in 3-dimensional collagen scaffolds. J Biomed Mater Res. 2001;55:13-9. https://doi.org/10.1002/1097-4636(200104)55:1<13::AID-JBM20>3.0.CO;2-G
- Taguchi T, Ikoma T, Tanaka J. An improved method to prepare hyaluronic acid and type II collagen composite matrices. J Biomed Mater Res. 2002;61:330-6. https://doi.org/10.1002/jbm.10147
- Liao E, Yaszemski M, Krebsbach P, Hollister S. Tissue-engineered cartilage constructs using composite hyaluronic acid/collagen I hydrogels and designed poly(propylene fumarate) scaffolds. Tissue Eng. 2007;13:537-50. https://doi.org/10.1089/ten.2006.0117
- Nishimoto S, Takagi M, Wakitani S, Nihira T, Yoshida T. Effect of chondroitin sulfate and hyaluronic acid on gene expression in a three-dimensional culture of chondrocytes. J Biosci Bioeng. 2005;100:123-6. https://doi.org/10.1263/jbb.100.123
- Vazquez-Portalatin N, Kilmer CE, Panitch A, Liu JC. Characterization of collagen type I and II blended hydrogels for articular cartilage tissue engineering. Biomacromolecules. 2016;17:3145-52. https://doi.org/10.1021/acs.biomac.6b00684
- Guo Y, Yuan T, Xiao Z, Tang P, Xiao Y, Fan Y, et al. Hydrogels of collagen/chondroitin sulfate/hyaluronan interpenetrating polymer network for cartilage tissue engineering. J Mater Sci Mater Med. 2012;23:2267-79. https://doi.org/10.1007/s10856-012-4684-5
- Li X, Teng Y, Liu J, Lin H, Fan Y, Zhang X. Chondrogenic differentiation of BMSCs encapsulated in chondroinductive polysaccharide/collagen hybrid hydrogels. J Mater Chem B. 2017;5:5109-19. https://doi.org/10.1039/C7TB01020F
- Sionkowska A. Current research on the blends of natural and synthetic polymers as new biomaterials: review. Prog Polym Sci. 2011;36:1254-76. https://doi.org/10.1016/j.progpolymsci.2011.05.003
- Mehrasa M, Anarkoli AO, Rafienia M, Ghasemi N, Davary N, Bonakdar S, et al. Incorporation of zeolite and silica nanoparticles into electrospun PVA/collagen nanofibrous scaffolds: the influence on the physical, chemical properties and cell behavior. Int J Polym Mater. 2016;65:457-65. https://doi.org/10.1080/00914037.2015.1129958
- Lin HY, Tsai WC, Chang SH. Collagen-PVA aligned nanofiber on collagen sponge as bi-layered scaffold for surface cartilage repair. J Biomater Sci Polym Ed. 2017;28:664-78. https://doi.org/10.1080/09205063.2017.1295507
- Mansur HS, Sadahira CM, Souza AN, Mansur AAP. FTIR spectroscopy characterization of poly (vinyl alcohol) hydrogel with different hydrolysis degree and chemically crosslinked with glutaraldehyde. Mater Sci Eng C Mater Biol Appl. 2008;28:539-48. https://doi.org/10.1016/j.msec.2007.10.088
- Wan WK, Campbell G, Zhang ZF, Hui AJ, Boughner DR. Optimizing the tensile properties of polyvinyl alcohol hydrogel for the construction of a bioprosthetic heart valve stent. J Biomed Mater Res. 2002;63:854-61. https://doi.org/10.1002/jbm.10333
- Yousefi AM, Hoque ME, Prasad RGSV, Uth N. Current strategies in multiphasic scaffold design for osteochondral tissue engineering: a review. J Biomed Mater Res A. 2015;103:2460-81. https://doi.org/10.1002/jbm.a.35356
- Ohyabu Y, Adegawa T, Yoshioka T, Ikoma T, Shinozaki K, Uemura T, et al. A collagen sponge incorporating a hydroxyapatite/chondroitinsulfate composite as a scaffold for cartilage tissue engineering. J Biomater Sci Polym Ed. 2009;20:1861-74. https://doi.org/10.1163/156856208X386462
- Ohyabu Y, Adegawa T, Yoshioka T, Ikoma T, Uemura T, Tanaka J. Cartilage regeneration using a porous scaffold, a collagen sponge incorporating a hydroxyapatite/chondroitinsulfate composite. Mater Sci Eng B Solid State Mater Adv Technol. 2010;173:204-7. https://doi.org/10.1016/j.mseb.2009.12.008
- Chen S, Zhang Q, Kawazoe N, Chen G. Effect of high molecular weight hyaluronic acid on chondrocytes cultured in collagen/hyaluronic acid porous scaffolds. RSC Adv. 2015;5:94405-10. https://doi.org/10.1039/C5RA18755A
- Kreger ST, Voytik-Harbin SL. Hyaluronan concentration within a 3D collagen matrix modulates matrix viscoelasticity, but not fibroblast response. Matrix Biol. 2009;28:336-46. https://doi.org/10.1016/j.matbio.2009.05.001
- Jia L, Duan Z, Fan D, Mi Y, Hui J, Chang L. Human-like collagen/nano-hydroxyapatite scaffolds for the culture of chondrocytes. Mater Sci Eng C Mater Biol Appl. 2013;33:727-34. https://doi.org/10.1016/j.msec.2012.10.025
- Szczesny SE, Aeppli C, David A, Mauck RL. Fatigue loading of tendon results in collagen kinking and denaturation but does not change local tissue mechanics. J Biomech. 2018;71:251-6. https://doi.org/10.1016/j.jbiomech.2018.02.014
- Nakada A, Shigeno K, Sato T, Hatayama T, Wakatsuki M, Nakamura T. Optimal dehydrothermal processing conditions to improve biocompatibility and durability of a weakly denatured collagen scaffold. J Biomed Mater Res B Appl Biomater. 2017;105:2301-7. https://doi.org/10.1002/jbm.b.33766
- Zeugolis DI, Khew ST, Yew ES, Ekaputra AK, Tong YW, Yung LY, et al. Electro-spinning of pure collagen nano-fibres-just an expensive way to make gelatin? Biomaterials. 2008;29:2293-305. https://doi.org/10.1016/j.biomaterials.2008.02.009
- Grover CN, Cameron RE, Best SM. Investigating the morphological, mechanical and degradation properties of scaffolds comprising collagen, gelatin and elastin for use in soft tissue engineering. J Mech Behav Biomed Mater. 2012;10:62-74. https://doi.org/10.1016/j.jmbbm.2012.02.028
- Tuckwell DS, Ayad S, Grant ME, Takigawa M, Humphries MJ. Conformation dependence of integrin-type II collagen binding. Inability of collagen peptides to support alpha 2 beta 1 binding, and mediation of adhesion to denatured collagen by a novel alpha 5 beta 1-fibronectin bridge. J Cell Sci. 1994;107:993-1005.
- Lv Q, Hu K, Feng Q, Cui F. Fibroin/collagen hybrid hydrogels with crosslinking method: preparation, properties, and cytocompatibility. J Biomed Mater Res A. 2008;84:198-207.
- Sensini A, Gualandi C, Cristofolini L, Tozzi G, Dicarlo M, Teti G, et al. Biofabrication of bundles of poly (lactic acid)-collagen blends mimicking the fascicles of the human Achille tendon. Biofabrication. 2017;9:015025. https://doi.org/10.1088/1758-5090/aa6204
- Maisani M, Ziane S, Ehret C, Levesque L, Siadous R, Le Meins JF, et al. A new composite hydrogel combining the biological properties of collagen with the mechanical properties of a supramolecular scaffold for bone tissue engineering. J Tissue Eng Regen Med. 2018;12:e1489-500. https://doi.org/10.1002/term.2569
- Klumpp D, Rudisile M, Kuhnle RI, Hess A, Bitto FF, Arkudas A, et al. Three-dimensional vascularization of electrospun PCL/collagen-blend nanofibrous scaffolds in vivo. J Biomed Mater Res A. 2012;100:2302-11.
- Prabhakaran MP, Venugopal J, Ramakrishna S. Electrospun nanostructured scaffolds for bone tissue engineering. Acta Biomater. 2009;5:2884-93. https://doi.org/10.1016/j.actbio.2009.05.007
- Chen G, Sato T, Ushida T, Hirochika R, Shirasaki Y, Ochiai N, et al. The use of a novel PLGA fiber/collagen composite web as a scaffold for engineering of articular cartilage tissue with adjustable thickness. J Biomed Mater Res A. 2003;67:1170-80.
- Yen HJ, Tseng CS, Hsu SH, Tsai CL. Evaluation of chondrocyte growth in the highly porous scaffolds made by fused deposition manufacturing (FDM) filled with type II collagen. Biomed Microdevices. 2009;11:615-24. https://doi.org/10.1007/s10544-008-9271-7
- Reboredo JW, Weigel T, Steinert A, Rackwitz L, Rudert M, Walles H. Investigation of migration and differentiation of human mesenchymal stem cells on five-layered collagenous electrospun scaffold mimicking native cartilage structure. Adv Healthc Mater. 2016;5:2191-8. https://doi.org/10.1002/adhm.201600134
- Chen G, Sato T, Ushida T, Hirochika R, Tateishi T. Redifferentiation of dedifferentiated bovine chondrocytes when cultured in vitro in a PLGA-collagen hybrid mesh. FEBS Lett. 2003;542:95-9. https://doi.org/10.1016/S0014-5793(03)00354-5
- Chen CH, Shyu VB, Chen JP, Lee MY. Selective laser sintered poly-e-caprolactone scaffold hybridized with collagen hydrogel for cartilage tissue engineering. Biofabrication. 2014;6:015004. https://doi.org/10.1088/1758-5082/6/1/015004
- Tanaka Y, Yamaoka H, Nishizawa S, Nagata S, Ogasawara T, Asawa Y, et al. The optimization of porous polymeric scaffolds for chondrocyte/atelocollagen based tissue-engineered cartilage. Biomaterials. 2010;31:4506-16. https://doi.org/10.1016/j.biomaterials.2010.02.028
- Deponti D, Di Giancamillo A, Gervaso F, Domenicucci M, Domeneghini C, Sannino A, et al. Collagen scaffold for cartilage tissue engineering: the benefit of fibrin glue and the proper culture time in an infant cartilage model. Tissue Eng Part A. 2014;20:1113-26. https://doi.org/10.1089/ten.tea.2013.0171
- Xu T, Binder KW, Albanna MZ, Dice D, Zhao W, Yoo JJ, et al. Hybrid printing of mechanically and biologically improved constructs for cartilage tissue engineering applications. Biofabrication. 2013;5:015001.
피인용 문헌
- Effect of hydrolyzed collagen on thermal, mechanical and biological properties of poly(lactic acid) bionanocomposites vol.28, pp.4, 2019, https://doi.org/10.1007/s13726-019-00694-7
- Optimization of TGF-β1-transduced chondrocytes for cartilage regeneration in a 3D printed knee joint model vol.14, pp.5, 2019, https://doi.org/10.1371/journal.pone.0217601
- Chondrocytes From Device-Minced Articular Cartilage Show Potent Outgrowth Into Fibrin and Collagen Hydrogels vol.7, pp.9, 2019, https://doi.org/10.1177/2325967119867618
- Protein-Polymer Matrices with Embedded Carbon Nanotubes for Tissue Engineering: Regularities of Formation and Features of Interaction with Cell Membranes vol.12, pp.19, 2018, https://doi.org/10.3390/ma12193083
- An injectable, click-crosslinked, cytomodulin-modified hyaluronic acid hydrogel for cartilage tissue engineering vol.11, pp.1, 2019, https://doi.org/10.1038/s41427-019-0130-1
- An overview of advanced biocompatible and biomimetic materials for creation of replacement structures in the musculoskeletal systems: focusing on cartilage tissue engineering vol.13, pp.1, 2018, https://doi.org/10.1186/s13036-019-0209-9
- Integrated Biophysical Characterization of Fibrillar Collagen-Based Hydrogels vol.6, pp.3, 2018, https://doi.org/10.1021/acsbiomaterials.9b01873
- Freeze‐dry processing of three‐dimensional cell constructs for bone graft materials vol.108, pp.3, 2018, https://doi.org/10.1002/jbm.b.34448
- Apatite Coating of Iron Oxide Nanoparticles by Alternate Addition of Calcium and Phosphate Solutions: A Calcium and Carboxylate (Ca-COO) Complex-Mediated Apatite Deposition vol.30, pp.4, 2018, https://doi.org/10.1007/s10904-019-01255-4
- Proteins and Peptides as Important Modifiers of the Polymer Scaffolds for Tissue Engineering Applications—A Review vol.12, pp.4, 2018, https://doi.org/10.3390/polym12040844
- A Synthetic Cell-Penetrating Heparin-Binding Peptide Derived from BMP4 with Anti-Inflammatory and Chondrogenic Functions for the Treatment of Arthritis vol.21, pp.12, 2018, https://doi.org/10.3390/ijms21124251
- Articular cartilage repair using autologous collagen-induced chondrogenesis (ACIC): a pragmatic and cost-effective enhancement of a traditional technique vol.28, pp.8, 2018, https://doi.org/10.1007/s00167-020-05884-y
- Different types of cartilage neotissue fabricated from collagen hydrogels and mesenchymal stromal cells via SOX9 , TGFB1 or BMP2 gene transfer vol.15, pp.8, 2018, https://doi.org/10.1371/journal.pone.0237479
- Collagen: quantification, biomechanics and role of minor subtypes in cartilage vol.5, pp.10, 2018, https://doi.org/10.1038/s41578-020-0213-1
- Physical, Biomechanical, and Optical Characterization of Collagen and Elastin Blend Hydrogels vol.48, pp.12, 2020, https://doi.org/10.1007/s10439-020-02605-x
- Inducible Tertiary Lymphoid Structures: Promise and Challenges for Translating a New Class of Immunotherapy vol.12, pp.None, 2018, https://doi.org/10.3389/fimmu.2021.675538
- Construction and Evaluation of Osteochondral-Like Tissue Using Chondrocyte Sheet and Cancellous Bone vol.27, pp.3, 2021, https://doi.org/10.1089/ten.tea.2020.0107
- Bioprinting of human nasoseptal chondrocytes‐laden collagen hydrogel for cartilage tissue engineering vol.35, pp.3, 2018, https://doi.org/10.1096/fj.202002081r
- Applications of Biomaterials in 3D Cell Culture and Contributions of 3D Cell Culture to Drug Development and Basic Biomedical Research vol.22, pp.5, 2018, https://doi.org/10.3390/ijms22052491
- Current Update of Collagen Nanomaterials-Fabrication, Characterisation and Its Applications: A Review vol.13, pp.3, 2021, https://doi.org/10.3390/pharmaceutics13030316
- A Comparative Review of Natural and Synthetic Biopolymer Composite Scaffolds vol.13, pp.7, 2018, https://doi.org/10.3390/polym13071105
- An Overview on Collagen and Gelatin-Based Cryogels: Fabrication, Classification, Properties and Biomedical Applications vol.13, pp.14, 2021, https://doi.org/10.3390/polym13142299
- Decellularized sturgeon cartilage extracellular matrix scaffold inhibits chondrocyte hypertrophy in vitro and in vivo vol.15, pp.8, 2018, https://doi.org/10.1002/term.3222
- Biomaterial-Assisted Regenerative Medicine vol.22, pp.16, 2021, https://doi.org/10.3390/ijms22168657
- A Comparison of the Capacity of Mesenchymal Stromal Cells for Cartilage Regeneration Depending on Collagen-Based Injectable Biomimetic Scaffold Type vol.11, pp.8, 2018, https://doi.org/10.3390/life11080756
- Current Insights into Collagen Type I vol.13, pp.16, 2021, https://doi.org/10.3390/polym13162642
- Layer-specific stem cell differentiation in tri-layered tissue engineering biomaterials: Towards development of a single-stage cell-based approach for osteochondral defect repair vol.12, pp.None, 2018, https://doi.org/10.1016/j.mtbio.2021.100173
- Mechanotransducive Biomimetic Systems for Chondrogenic Differentiation In Vitro vol.22, pp.18, 2018, https://doi.org/10.3390/ijms22189690
- Optimization of extracellular matrix production from human induced pluripotent stem cell‐derived fibroblasts for scaffold fabrication for application in wound healing vol.109, pp.10, 2018, https://doi.org/10.1002/jbm.a.37173
- Immunoengineering the next generation of arthritis therapies vol.133, pp.None, 2021, https://doi.org/10.1016/j.actbio.2021.03.062
- Decellularized and biological scaffolds in dental and craniofacial tissue engineering: a comprehensive overview vol.15, pp.None, 2021, https://doi.org/10.1016/j.jmrt.2021.08.083
- 3D bioprinted silk fibroin hydrogels for tissue engineering vol.16, pp.12, 2018, https://doi.org/10.1038/s41596-021-00622-1
- In vivo biocompatibility evaluation of in situ-forming polyethylene glycol-collagen hydrogels in corneal defects vol.11, pp.1, 2018, https://doi.org/10.1038/s41598-021-03270-3
- Controlled Differentiation of Mesenchymal Stem Cells into Hyaline Cartilage in miR-140-Activated Collagen Hydrogel vol.13, pp.2, 2021, https://doi.org/10.1177/19476035211047627
- Combinations of Hydrogels and Mesenchymal Stromal Cells (MSCs) for Cartilage Tissue Engineering-A Review of the Literature vol.7, pp.4, 2021, https://doi.org/10.3390/gels7040217
- Childhood Cartilage ECM Enhances the Chondrogenesis of Endogenous Cells and Subchondral Bone Repair of the Unidirectional Collagen-dECM Scaffolds in Combination with Microfracture vol.13, pp.48, 2018, https://doi.org/10.1021/acsami.1c19447
- Biomaterial-mediated presentation of wnt5a mimetic ligands enhances chondrogenesis and metabolism of stem cells by activating non-canonical Wnt signaling vol.281, pp.None, 2022, https://doi.org/10.1016/j.biomaterials.2021.121316