References
- Taylor, D. R. and N. M. Hooper. 2006. The prion protein and lipid rafts. Mol. Membr. Biol. 23: 89-99. https://doi.org/10.1080/09687860500449994
- Jackson, G. S., I. Murray, L. L. Hosszu, N. Gibbs, J. P. Waltho, A. R. Clarke, and J. Collinge. 2001. Location and properties of metal-binding sites on the human prion protein. Proc. Natl. Acad. Sci. U. S. A. 98: 8531-8535. https://doi.org/10.1073/pnas.151038498
- Riek, R., S. Hornemann, G. Wider, M. Billeter, R. Glockshuber, and K. Wüthrich. 1996. NMR structure of the mouse prion protein domain PrP(121-231). Nature 382: 180-182. https://doi.org/10.1038/382180a0
- Ermonval, M., S. Mouillet-Richard, P. Codogno, O. Kellermann, and J. Botti. 2003. Evolving views in prion glycosylation: functional and pathological implications. Biochimie. 85: 33-45. https://doi.org/10.1016/S0300-9084(03)00040-3
- Collinge, J. 2001. Prion diseases of humans and animals: their causes and molecular basis. Annu. Rev. Neurosci. 24: 519-550 https://doi.org/10.1146/annurev.neuro.24.1.519
- Prusiner, S. B. 1998. Prions. Proc. Natl. Acad. Sci. U. S. A. 95: 13363-13383. https://doi.org/10.1073/pnas.95.23.13363
- Kretzschmar, H. A., S. B. Prusiner, L. E. Stowring, and S. J. DeArmond. 1986. Scrapie prion proteins are synthesized in neurons. Am. J. Pathol. 122: 1-5.
- Zhang, C. C., A. D. Steele, S. Lindquist, and H. F. Lodish. 2006. Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their selfrenewal. Proc. Natl. Acad. Sci. U. S. A. 103: 2184-2189. https://doi.org/10.1073/pnas.0510577103
- Durig, J., A. Giese, W. Schulz-Schaeffer, C. Rosenthal, U. Schmucker, J. Bieschke, U. Duhrsen, and H. A. Kretzschmar. 2000. Differential constitutive and activation-dependent expression of prion protein in human peripheral blood leucocytes. Br. J. Haematol. 108: 488-495. https://doi.org/10.1046/j.1365-2141.2000.01881.x
- Dodelet, V. C. and N. R. Cashman. 1998. Prion protein expression in human leukocyte differentiation. Blood 91: 1556-1561.
- Burthem, J., B. Urban, A. Pain, and D. J. Roberts. 2001. The normal cellular prion protein is strongly expressed by myeloid dendritic cells. Blood 98: 3733-3738. https://doi.org/10.1182/blood.V98.13.3733
- Thielen, C., N. Antoine, F. Melot, J. Y. Cesbron, E. Heinen, and R. Tsunoda. 2001. Human FDC express PrPc in vivo and in vitro. Dev. Immunol. 8: 259-266. https://doi.org/10.1155/2001/45454
- Taylor, D. R., E. T. Parkin, S. L. Cocklin, J. R. Ault, A. E. Ashcroft, A. J. Turner, and N. M. Hooper. 2009. Role of ADAMs in the ectodomain shedding and conformational conversion of the prion protein. J. Biol. Chem. 284: 22590-22600. https://doi.org/10.1074/jbc.M109.032599
- Endres, K., G. Mitteregger, E. Kojro, H. Kretzschmar, and F. Fahrenholz. 2009. Influence of ADAM10 on prion protein processing and scrapie infectiosity in vivo. Neurobiol. Dis. 36: 233-241. https://doi.org/10.1016/j.nbd.2009.07.015
- Parizek, P., C. Roeckl, J. Weber, E. Flechsig, A. Aguzzi, and A. J. Raeber. 2001. Similar turnover and shedding of the cellular prion protein in primary lymphoid and neuronal cells. J. Biol. Chem. 276: 44627-44632. https://doi.org/10.1074/jbc.M107458200
- Isaacs, J. D., G. S. Jackson, and D. M. Altmann. 2006. The role of the cellular prion protein in the immune system. Clin. Exp. Immunol. 146: 1-8. https://doi.org/10.1111/j.1365-2249.2006.03194.x
- Hu, W., R. N. Rosenberg, and O. Stuve. 2007. Prion proteins: a biological role beyond prion diseases. Acta. Neurol. Scand. 116: 75-82. https://doi.org/10.1111/j.1600-0404.2007.00868.x
- de Almeida, C. J., L. B. Chiarini, J. P. da Silva, P. M. R. e Silva, M. A. Martins, and R. Linden. 2005. The cellular prion protein modulates phagocytosis and inflammatory response. J. Leukoc. Biol. 77: 238-246. https://doi.org/10.1189/jlb.1103531
- Nitta, K., A. Sakudo, J. Masuyama, G. Xue, K. Sugiura, and T. Onodera. 2009. Role of cellular prion proteins in the function of macrophages and dendritic cells. Protein. Pept. Lett. 16: 239-246. https://doi.org/10.2174/092986609787601705
- Uraki, R., A. Sakudo, S. Ando, H. Kitani, and T. Onodera. 2010. Enhancement of phagocytotic activity by prion protein in PrP-deficient macrophage cells. Int. J. Mol. Med. 26: 527-532
- Krebs, B., C. Dorner-Ciossek, R. Schmalzbauer, N. Vassallo, J. Herms, and H. A. Kretzschmar. 2006. Prion protein induced signaling cascades in monocytes. Biochem. Biophys. Res. Commun. 340: 13-22. https://doi.org/10.1016/j.bbrc.2005.11.158
- Jeon, J. W., J. G. Jung, E. C. Shin, H. I. Choi, H. Y. Kim, M. L. Cho, S. W. Kim, Y. S. Jang, M. H. Sohn, J. H. Moon, Y. H. Cho, K. L. Hoe, Y. S. Seo, and Y. W. Park. 2010. Soluble CD93 induces differentiation of monocytes and enhances TLR responses. J. Immunol. 185: 4921-4927. https://doi.org/10.4049/jimmunol.0904011
- Guha, M. and N. Mackman. 2001. LPS induction of gene expression in human monocytes. Cell. Signal. 13: 85-94. https://doi.org/10.1016/S0898-6568(00)00149-2
- Schmitt-Ulms, G., G. Legname, M. A. Baldwin, H. L. Ball, N. Bradon, P. J. Bosque, K. L. Crossin, G. M. Edelman, S. J. DeArmond, F. E. Cohen, and S. B. Prusiner. 2001. Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein. J. Mol. Biol. 314: 1209-1225. https://doi.org/10.1006/jmbi.2000.5183
- Gauczynski, S., J. M. Peyrin, S. Haik, C. Leucht, C. Hundt, R. Rieger, S. Krasemann, J. P. Deslys, D. Dormont, C. I. Lasmezas, and S. Weiss. 2001. The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein. EMBO J. 20: 5863-5875. https://doi.org/10.1093/emboj/20.21.5863
- Hundt, C., J. M. Peyrin, S. Haik, S. Gauczynski, C. Leucht, R. Rieger, M. L. Riley, J. P. Deslys, D. Dormont, C. I. Lasmezas, and S. Weiss. 2001. Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor. EMBO J. 20: 5876-5886. https://doi.org/10.1093/emboj/20.21.5876
- Graner, E., A. F. Mercadante, S. M. Zanata, O. V. Forlenza, A. L. Cabral, S. S. Veiga, M. A. Juliano, R. Roesler, R. Walz, A. Minetti, I. Izquierdo, V. R. Martins, and R. R. Brentani. 2000. Cellular prion protein binds laminin and mediates neuritogenesis. Brain. Res. Mol. Brain. Res. 76: 85-92. https://doi.org/10.1016/S0169-328X(99)00334-4
Cited by
- Functional Roles of Syk in Macrophage-Mediated Inflammatory Responses vol.2014, pp.None, 2013, https://doi.org/10.1155/2014/270302
- IKK β -Targeted Anti-Inflammatory Activities of a Butanol Fraction of Artificially Cultivated Cordyceps pruinosa Fruit Bodies vol.2014, pp.None, 2014, https://doi.org/10.1155/2014/562467
- Prion Protein Signaling in the Nervous System-A Review and Perspective vol.3, pp.None, 2014, https://doi.org/10.4137/sti.s12319
- Expression of genes involved in the T cell signalling pathway in circulating immune cells of cattle 24 months following oral challenge with Bovine Amyloidotic Spongiform Encephalopathy (BASE) vol.11, pp.None, 2013, https://doi.org/10.1186/s12917-015-0412-y
- Plasma Soluble Prion Protein, a Potential Biomarker for Sport-Related Concussions: A Pilot Study vol.10, pp.2, 2013, https://doi.org/10.1371/journal.pone.0117286
- Lipopolysaccharide로 유도된 RAW 264.7 세포와 마우스모델에 대한 진두발 에탄올 추출물의 항염증 효과 vol.44, pp.3, 2013, https://doi.org/10.4014/mbl.1603.03004
- The Biological Function of the Prion Protein: A Cell Surface Scaffold of Signaling Modules vol.10, pp.None, 2013, https://doi.org/10.3389/fnmol.2017.00077
- The Role of Shed PrPc in the Neuropathogenesis of HIV Infection vol.199, pp.1, 2013, https://doi.org/10.4049/jimmunol.1601041
- Expression and functions of cellular prion proteins in immunocytes vol.91, pp.3, 2013, https://doi.org/10.1111/sji.12854
- LETMD1 Regulates Phagocytosis and Inflammatory Responses to Lipopolysaccharide via Reactive Oxygen Species Generation and NF-κB Activation in Macrophages vol.204, pp.5, 2020, https://doi.org/10.4049/jimmunol.1900551
- Microglia in Prion Diseases: Angels or Demons? vol.21, pp.20, 2013, https://doi.org/10.3390/ijms21207765
- PrPC as a Transducer of Physiological and Pathological Signals vol.14, pp.None, 2013, https://doi.org/10.3389/fnmol.2021.762918