생체재료학회지 (Biomaterials Research)

  • 제19권1호
  • /
  • Pages.15-20
  • /
  • 2015
  • /
  • 1226-4601(pISSN)
  • /
  • 2055-7124(eISSN)
한국생체재료학회 (Korean Society for Biomaterials)
권호 표지
DOI QR코드

DOI QR Code

Behaviors of stem cells on carbon nanotube

  • Lee, Ju-Ro (School of Chemical and Biological Engineering, Seoul National University) ;
  • Ryu, Seungmi (Interdisciplinary Program for Bioengineering, Seoul National University) ;
  • Kim, Soojin (Department of Biomedical Engineering, University of Alabama at Birmingham) ;
  • Kim, Byung-Soo (School of Chemical and Biological Engineering, Seoul National University)
  • 투고 : 2014.07.30
  • 심사 : 2014.12.11
  • 발행 : 2015.03.31
⟨ 이전 논문 다음 논문 ⟩

초록

Regulating stem cell microenvironment is one of the essential elements in stem cell culture. Recently, carbon nanotube (CNT) has come into the spotlight as a biomaterial that retains unique properties. Based on its high chemical stability, elasticity, mechanical strength, and electrical conductivity, CNT shows great potential as an application for biomedical substrate. Also, properties of CNT could be further regulated by appropriate chemical modifications of CNT. Recent studies reported that modulating the cellular microenvironment through the use of CNT and chemically modified CNT as cell culture substrates can affect proliferation and differentiation of various types of stem cells. This review summarizes the unique biological effects of CNT on stem cells.

키워드

과제정보

연구 과제 주관 기관 : Korea Health Industry Development Institute (KHIDI)

참고문헌

  1. Hazeltine LB, Selekman JA, Palecek SP: Engineering the human pluripotent stem cell microenvironment to direct cell fate. Biotechnol Adv 2013, 31:1002-1019. https://doi.org/10.1016/j.biotechadv.2013.03.002
  2. Iijima S, Ajayan PM, Ichihashi T: Growth model for carbon nanotubes. Phys Rev Lett 1992, 69:3100-3103. https://doi.org/10.1103/PhysRevLett.69.3100
  3. Hummer G, Rasaiah JC, Noworyta JP: Water conduction through the hydrophobic channel of a carbon nanotube. Nature 2001, 414:188-190. https://doi.org/10.1038/35102535
  4. Zhang Q, Huang JQ, Zhao MQ, Qian WZ, Wei F: Carbon nanotube mass production: principles and processes. ChemSusChem 2011, 4:864-889. https://doi.org/10.1002/cssc.201100177
  5. Fischer JE: Chemical doping of single-wall carbon nanotubes. Accounts Chem Res 2002, 35:1079-1086. https://doi.org/10.1021/ar0101638
  6. Tasis D, Tagmatarchis N, Bianco A, Prato M: Chemistry of carbon nanotubes. Chem Rev 2006, 106:1105-1136. https://doi.org/10.1021/cr050569o
  7. Moore VC, Strano MS, Haroz EH, Hauge RH, Smalley RE, Schmidt J, Talmon Y: Individually suspended single-walled carbon nanotubes in various surfactants. Nano Lett 2003, 3:1379-1382. https://doi.org/10.1021/nl034524j
  8. Dieckmann GR, Dalton AB, Johnson PA, Razal J, Chen J, Giordano GM, Munoz E, Musselman IH, Baughman RH, Draper RK: Controlled assembly of carbon nanotubes by designed amphiphilic peptide helices. J Am Chem Soc 2003, 125:1770-1777. https://doi.org/10.1021/ja029084x
  9. Zheng M, Jagota A, Semke ED, Diner BA, Mclean RS, Lustig SR, Richardson RE, Tassi NG: DNA-assisted dispersion and separation of carbon nanotubes. Nat Mater 2003, 2:338-342. https://doi.org/10.1038/nmat877
  10. MacDonald RA, Laurenzi BF, Viswanathan G, Ajayan PM, Stegemann JP: Collagen-carbon nanotube composite materials as scaffolds in tissue engineering. J Biomed Mater Res A 2005, 74:489-496.
  11. Cheng HKF, Basu T, Sahoo NG, Li L, Chans SH: Current advances in the carbon nanotube/thermotropic main-chain liquid crystalline polymer nanocomposites and their blends. Polymers 2012, 4:889-912. https://doi.org/10.3390/polym4020889
  12. Fabbro A, Prato M, Ballerini L: Carbon nanotubes in neuroregeneration and repair. Adv Drug Deliv Rev 2013, 65:2034-2044. https://doi.org/10.1016/j.addr.2013.07.002
  13. Bates K, Kostarelos K: Carbon nanotubes as vectors for gene therapy: past achievements, present challenges and future goals. Adv Drug Dliv Rev 2013, 65:2023-2033. https://doi.org/10.1016/j.addr.2013.10.003
  14. Meredith JR, Jin C, Narayan RJ, Aggarwal R: Biomedical applications of carbon-nanotube composites. Front Biosci 2012, 5:610-621.
  15. Namgung S, Kim T, Baik KY, Lee M, Nam JM, Hong S: Fibronectin-Carbon-Nanotube Hybrid Nanostructures for Controlled Cell Growth. Small 2011, 7:56-61. https://doi.org/10.1002/smll.201001513
  16. Mazzatenta A, Giugliano M, Campidelli S, Gambazzi L, Businaro L, Markram H, Prato M, Ballerini L: Interfacing neurons with carbon nanotubes: Electrical signal transfer and synaptic stimulation in cultured brain circuits. J Neurosci 2007, 27:6931-6936. https://doi.org/10.1523/JNEUROSCI.1051-07.2007
  17. Jan E, Kotov NA: Successful differentiation of mouse neural stem cells on layer-by-layer assembled single-walled carbon nanotube composite. Nano Lett 2007, 7:1123-1128. https://doi.org/10.1021/nl0620132
  18. Dowell-Mesfin NM, Abdul-Karim MA, Turner AMP, Schanz S, Craighead HG, Roysam B, Turner JN, Shain W: Topographically modified surfaces affect orientation and growth of hippocampal neurons. J Neural Eng 2004, 1:78-90. https://doi.org/10.1088/1741-2560/1/2/003
  19. Hu H, Ni Y, Montana V, Haddon RC, Parpura V: Chemically functionalized carbon nanotubes as substrates for neuronal growth. Nano Lett 2004, 4:507-511. https://doi.org/10.1021/nl035193d
  20. Kam NW, Jan E, Kotov NA: Electrical stimulation of neural stem cells mediated by humanized carbon nanotube composite made with extracellular matrix protein. Nano Lett 2009, 9:273-278. https://doi.org/10.1021/nl802859a
  21. Park SY, Choi DS, Jin HJ, Park J, Byun KE, Lee KB, Hong S: Polarization-Controlled Differentiation of Human Neural Stem Cells Using Synergistic Cues from the Patterns of Carbon Nanotube Monolayer Coating. Acs Nano 2011, 5:4704-4711. https://doi.org/10.1021/nn2006128
  22. Chao TI, Xiang SH, Chen CS, Chin WC, Nelson AJ, Wang CC, Lu J: Carbon nanotubes promote neuron differentiation from human embryonic stem cells. Biochem Bioph Res Co 2009, 384:426-430. https://doi.org/10.1016/j.bbrc.2009.04.157
  23. Sridharan I, Kim T, Wang R: Adapting collagen/CNT matrix in directing hESC differentiation. Biochem Bioph Res Co 2009, 381:508-512. https://doi.org/10.1016/j.bbrc.2009.02.072
  24. Zimmerman L, Parr B, Lendahl U, Cunningham M, McKay R, Gavin B, Mann J, Vassileva G, McMahon A: Independent regulatory elements in the nestin gene direct transgene expression to neural stem cells or muscle precursors. Neuron 1994, 12:11-24. https://doi.org/10.1016/0896-6273(94)90148-1
  25. Chao TI, Xiang S, Lipstate JF, Wang C, Lu J: Poly(methacrylic acid)-grafted carbon nanotube scaffolds enhance differentiation of hESCs into neuronal cells. Adv Mater 2010, 22:3542-3547. https://doi.org/10.1002/adma.201000262
  26. Tay CY, Gu HG, Leong WS, Yu HY, Li HQ, Heng BC, Tantang H, Loo SCJ, Li LJ, Tan LP: Cellular behavior of human mesenchymal stem cells cultured on single-walled carbon nanotube film. Carbon 2010, 48:1095-1104. https://doi.org/10.1016/j.carbon.2009.11.031
  27. Johnson GVW, Jope RS: The Role of Microtubule-Associated Protein-2 (Map-2) in Neuronal Growth, Plasticity, and Degeneration. J Neurosci Res 1992, 33:505-512. https://doi.org/10.1002/jnr.490330402
  28. Namgung S, Baik KY, Park J, Hong S: Controlling the growth and differentiation of human mesenchymal stem cells by the arrangement of individual carbon nanotubes. Acs Nano 2011, 5:7383-7390. https://doi.org/10.1021/nn2023057
  29. Baik KY, Park SY, Heo K, Lee KB, Hong S: Carbon Nanotube Monolayer Cues for Osteogenesis of Mesenchymal Stem Cells. Small 2011, 7:741-745. https://doi.org/10.1002/smll.201001930
  30. Mooney E, Mackle JN, Blond DJ, O'Cearbhaill E, Shaw G, Blau WJ, Barry FP, Barron V, Murphy JM: The electrical stimulation of carbon nanotubes to provide a cardiomimetic cue to MSCs. Biomaterials 2012, 33:6132-6139. https://doi.org/10.1016/j.biomaterials.2012.05.032
  31. Zhu L, Chang DW, Dai LM, Hong YL: DNA damage induced by multiwalled carbon nanotubes in mouse embryonic stem cells. Nano Lett 2007, 7:3592-3597. https://doi.org/10.1021/nl071303v

피인용 문헌

  1. Surface functionalization of nanobiomaterials for application in stem cell culture, tissue engineering, and regenerative medicine vol.32, pp.3, 2015, https://doi.org/10.1002/btpr.2262
  2. Multiwall carbon nanotubes/polycaprolactone scaffolds seeded with human dental pulp stem cells for bone tissue regeneration vol.27, pp.2, 2015, https://doi.org/10.1007/s10856-015-5640-y
  3. Neural differentiation on aligned fullerene C60 nanowhiskers vol.53, pp.80, 2017, https://doi.org/10.1039/c7cc06395d
  4. Guiding osteogenesis of mesenchymal stem cells using carbon-based nanomaterials vol.4, pp.None, 2015, https://doi.org/10.1186/s40580-017-0096-z
  5. Differentiation of stem cells from apical papilla into neural lineage using graphene dispersion and single walled carbon nanotubes vol.106, pp.10, 2015, https://doi.org/10.1002/jbm.a.36461
  6. Two-dimensional material-based bionano platforms to control mesenchymal stem cell differentiation vol.22, pp.1, 2015, https://doi.org/10.1186/s40824-018-0120-3
  7. Optogenetic Modulation and Reprogramming of Bacteriorhodopsin-Transfected Human Fibroblasts on Self-Assembled Fullerene C60 Nanosheets vol.3, pp.2, 2015, https://doi.org/10.1002/adbi.201800254
  8. Preparation and characterization of PCL-coated porous hydroxyapatite scaffolds in the presence of MWCNTs and graphene for orthopedic applications vol.26, pp.1, 2015, https://doi.org/10.1007/s10934-018-0644-x
  9. The Advances in Biomedical Applications of Carbon Nanotubes vol.5, pp.2, 2015, https://doi.org/10.3390/c5020029
  10. Electrical stimulation as a novel tool for regulating cell behavior in tissue engineering vol.23, pp.1, 2019, https://doi.org/10.1186/s40824-019-0176-8
  11. Transparent carbon nanotube electrodes for electric cell-substrate impedance sensing vol.9, pp.4, 2019, https://doi.org/10.1557/mrc.2019.116
  12. Stem Cell Mechanobiology and the Role of Biomaterials in Governing Mechanotransduction and Matrix Production for Tissue Regeneration vol.8, pp.None, 2020, https://doi.org/10.3389/fbioe.2020.597661
  13. Engineering of functionalized carbon nano-onions reinforced nanocomposites: Fabrication, biocompatibility, and mechanical properties vol.35, pp.8, 2015, https://doi.org/10.1557/jmr.2020.23
  14. Properties of differentiated SH-SY5Y grown on carbon-based materials vol.10, pp.33, 2020, https://doi.org/10.1039/d0ra03383a
  15. Polymeric nanocomposites reinforced with nanowhiskers: Design, development, and emerging applications vol.36, pp.3, 2015, https://doi.org/10.1177/8756087919898731
  16. Carbon nanostructures as a scaffold for human embryonic stem cell differentiation toward photoreceptor precursors vol.12, pp.36, 2015, https://doi.org/10.1039/d0nr02256j
  17. Modern World Applications for Nano-Bio Materials: Tissue Engineering and COVID-19 vol.9, pp.None, 2015, https://doi.org/10.3389/fbioe.2021.597958
  18. Tunable Substrate Functionalities Direct Stem Cell Fate toward Electrophysiologically Distinguishable Neuron-like and Glial-like Cells vol.13, pp.1, 2015, https://doi.org/10.1021/acsami.0c17257
  19. Manufacture and mechanical properties of knee implants using SWCNTs/UHMWPE composites vol.120, pp.None, 2015, https://doi.org/10.1016/j.jmbbm.2021.104554