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Integrin-linked kinase is required for laminin-2–induced oligodendrocyte cell spreading and CNS myelination
Open accessAbstract
Early steps in myelination in the central nervous system (CNS) include a specialized and extreme form of cell spreading in which oligodendrocytes extend large lamellae that spiral around axons to form myelin. Recent studies have demonstrated that laminin-2 (LN-2; α2β1γ1) stimulates oligodendrocytes to extend elaborate membrane sheets in vitro (cell spreading), mediated by integrin α6β1. Although a congenital LN-2 deficiency in humans is associated with CNS white matter changes, LN-2–deficient (dy/dy) mice have shown abnormalities primarily within the peripheral nervous system. Here, we demonstrate a critical role for LN-2 in CNS myelination by showing that dy/dy mice have quantitative and morphologic defects in CNS myelin. We have defined the molecular pathway through which LN-2 signals oligodendrocyte cell spreading by demonstrating requirements for phosphoinositide 3-kinase activity and integrin-linked kinase (ILK). Interaction of oligodendrocytes with LN-2 stimulates ILK activity. A dominant negative ILK inhibits LN-2–induced myelinlike membrane formation. A critical component of the myelination signaling cascade includes LN-2 and integrin signals through ILK.
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“There are many examples of regional differences in dysmyelination caused by genetic manipulation of mice between areas such as the optic nerve, spinal cord, cerebellum and corpus callosum.”
From SJL Mice Exposed to Cuprizone Intoxication Reveal Strain and Gender Pattern Differences in Demyelination (2009) · cites this paper as [11]
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“For example, laminin‐deficient dystrophia muscularis mice exhibit hypomyelination in the corpus callosum and optic nerve, but not the spinal cord (11)”
From SJL Mice Exposed to Cuprizone Intoxication Reveal Strain and Gender Pattern Differences in Demyelination (2009) · cites this paper as [11]
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Delcommenne, M., Tan, C., Gray, V., Rue, L., Woodgett, J. R., & Dedhar, S. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.19.11211 · Cited by 1,102
Paxillin and focal adhesion signalling
Turner, C. E. (2000) · Nature Cell Biology · doi:10.1038/35046659 · Cited by 839
Integrin-linked kinase (ILK) and its interactors
Wu, C., & Dedhar, S. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200108077 · Cited by 449
Persad, S., Attwell, S., Gray, V., Delcommenne, M., Troussard, A. A., Sanghera, J. S., & Dedhar, S. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.7.3207 · Cited by 428
Myelinated nerve fibres in the CNS
Hildebrand, C., Remahl, S., Persson, H., & Bjartmar, C. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90015-k · Cited by 395
Initial events of myelination involve Fyn tyrosine kinase signalling
Umemori, H., Satot, S., Yagi, T., Aizawal, S., & Yamamoto, T. S. (1994) · Nature · doi:10.1038/367572a0 · Cited by 387
Sakai, T., Li, S., Docheva, D., Grashoff, C., Sakai, K., Kostka, G., Braun, A., Pfeifer, A., Yurchenco, P. D., & Fässler, R. (2003) · Genes & Development · doi:10.1101/gad.255603 · Cited by 378
Kitamura, T., Ogawa, W., Sakaue, H., Hino, Y., Kuroda, S., Takata, M., Matsumoto, M., Maeda, T., Konishi, H., Kikkawa, U., et al. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.7.3708 · Cited by 328
Dependence of nodal sodium channel clustering on paranodal axoglial contact in the developing CNS
Rasband, M. N., Peles, E., Trimmer, J. S., Levinson, S. R., Lux, S. E., & Shrager, P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-17-07516.1999 · Cited by 325
Self-citationConditional disruption of β1 integrin in Schwann cells impedes interactions with axons
Feltri, M. L., Porta, D. G., Previtali, S. C., Nodari, A., Migliavacca, B., Cassetti, A., Littlewood-Evans, A., Reichardt, L. F., Messing, A., Quattrini, A., et al. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200109021 · Cited by 325
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Miner, J. H., & Yurchenco, P. D. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.094555 · Cited by 756
ILK, PINCH and parvin: the tIPP of integrin signalling
Legate, K. R., Montañez, E., Kudlacek, O., & Füssler, R. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1789 · Cited by 678
Integrin-linked kinase: a cancer therapeutic target unique among its ILK
Hannigan, G. E., Troussard, A. A., & Dedhar, S. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1524 · Cited by 589
Pathophysiology of the brain extracellular matrix: a new target for remyelination
Lau, L. W., Cua, R., Keough, M. B., Haylock-Jacobs, S., & Yong, V. W. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3550 · Cited by 549
Extracellular Matrix: Functions in the Nervous System
Barros, C. S., Franco, S. J., & Muller, U. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005108 · Cited by 506
CNS Myelin Sheath Lengths Are an Intrinsic Property of Oligodendrocytes
Bechler, M. E., Byrne, L. M., & ffrench‐Constant, C. (2015) · Current Biology · doi:10.1016/j.cub.2015.07.056 · Cited by 372
Signals to promote myelin formation and repair
Taveggia, C., Feltri, M. L., & Wrabetz, L. G. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2010.37 · Cited by 285
Tyler, W. A., Gangoli, N., Gokina, P., Kim, H. A., Covey, M., Levison, S. W., & Wood, T. L. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0234-09.2009 · Cited by 263
Mechanisms regulating the development of oligodendrocytes and central nervous system myelin
Mitew, S., Hay, C. M., Peckham, H., Xiao, J., Koenning, M., & Emery, B. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.11.029 · Cited by 268
Iron in multiple sclerosis: roles in neurodegeneration and repair
Stephenson, E. L., Nathoo, N., Mahjoub, Y., Dunn, J. F., & Yong, V. W. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2014.118 · Cited by 253
Neuron-glia communication in the control of oligodendrocyte function and myelin biogenesis
Simons, M., & Trajković, K. (2006) · Journal of Cell Science · doi:10.1242/jcs.03242 · Cited by 233
The repair of brain lesion by implantation of hyaluronic acid hydrogels modified with laminin
Hou, S., Xu, Q., Tian, W., Cui, F., Cai, Q., Ma, J., & Lee, I.-S. (2005) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2005.04.016 · Cited by 218
Type III neuregulin‐1 promotes oligodendrocyte myelination
Taveggia, C., Thaker, P., Petrylak, A., Caporaso, G. L., Toews, A. D., Falls, D. L., Einheber, S., & Salzer, J. L. (2007) · Glia · doi:10.1002/glia.20612 · Cited by 201
Laminins and their roles in mammals
Miner, J. H. (2008) · Microscopy Research and Technique · doi:10.1002/jemt.20563 · Cited by 187
The extracellular matrix as modifier of neuroinflammation and remyelination in multiple sclerosis
Ghorbani, S., & Yong, V. W. (2021) · Brain · doi:10.1093/brain/awab059 · Cited by 191
Integrins direct Src family kinases to regulate distinct phases of oligodendrocyte development
Colognato, H., Ramachandrappa, S., Olsen, I. M. L., & ffrench‐Constant, C. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200404076 · Cited by 182
Role of the oligodendroglial cytoskeleton in differentiation and myelination
Bauer, N. G., Richter‐Landsberg, C., & ffrench‐Constant, C. (2009) · Glia · doi:10.1002/glia.20885 · Cited by 184
How factors secreted from astrocytes impact myelin repair
Moore, C. S., Abdullah, S. L., Brown, A. D., Arulpragasam, A. R., & Crocker, S. J. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22482 · Cited by 172
Laminin isoforms in development and disease
Schéele, S., Nyström, A., Durbeej, M., Talts, J. F., Ekblom, M., & Ekblom, P. (2007) · Journal of Molecular Medicine · doi:10.1007/s00109-007-0182-5 · Cited by 155
Myelin Recovery in Multiple Sclerosis: The Challenge of Remyelination
Podbielska, M., Banik, N. L., Kurowska, E., & Hogan, E. (2013) · Brain Sciences · doi:10.3390/brainsci3031282 · Cited by 171
Giera, S., Deng, Y., Luo, R., Ackerman, S. D., Mogha, A., Monk, K. R., Ying, Y., Jeong, S., Makinodan, M., Bialas, A. R., et al. (2015) · Nature Communications · doi:10.1038/ncomms7121 · Cited by 139
Integrin-Linked Kinase Regulates Endothelial Cell Survival and Vascular Development
Friedrich, E. B., Liu, E. H., Sinha, S., Cook, S. A., Milstone, D. S., MacRae, C. A., Mariotti, M., Kuhlencordt, P. J., Force, T. L., Rosenzweig, A., et al. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.18.8134-8144.2004 · Cited by 136
An Integrin–Contactin Complex Regulates CNS Myelination by Differential Fyn Phosphorylation
Laursen, L. S., Chan, C. W., & ffrench‐Constant, C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5942-08.2009 · Cited by 133
Laminin 1 chain reduces muscular dystrophy in laminin 2 chain deficient mice
Gawlik, K. I. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh190 · Cited by 131
The neurobiology of the dystrophin-associated glycoprotein complex
Waite, A. J., Tinsley, C. L., Locke, M., & Blake, D. J. (2009) · Annals of Medicine · doi:10.1080/07853890802668522 · Cited by 135
Pericytes Stimulate Oligodendrocyte Progenitor Cell Differentiation during CNS Remyelination
de la Fuente, A. G., Lange, S., Silva, M. E., González, G. A., Tempfer, H., van Wijngaarden, P., Zhao, C., Canio, L. D., Trost, A., Bieler, L., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.007 · Cited by 135
Dulamea, A. O. (2017) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-319-47861-6_7 · Cited by 128
From axon–glial signalling to myelination: the integrating role of oligodendroglial Fyn kinase
Krämer‐Albers, E., & White, R. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0616-z · Cited by 125
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Rajasekharan, S., Baker, K. A., Horn, K. E., Jarjour, A. A., Antel, J. P., & Kennedy, T. E. (2009) · Development · doi:10.1242/dev.018234 · Cited by 129
Pereira, J. A., Benninger, Y., Baumann, R., Gonçalves, A. F., Özçelik, M., Buerki‐Thurnherr, T., Tricaud, N., Meijer, D., Fässler, R., Suter, U., et al. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200809008 · Cited by 122
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Roth, J. G., Huang, M. S., Li, T. L., Feig, V. R., Jiang, Y., Cui, B., Greely, H. T., Bao, Z., Pașca, S. P., & Heilshorn, S. C. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00496-y · Cited by 122
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Baron, W., Colognato, H., & ffrench‐Constant, C. (2004) · Glia · doi:10.1002/glia.20132 · Cited by 126
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies
Gawlik, K. I., & Durbeej, M. (2011) · Skeletal Muscle · doi:10.1186/2044-5040-1-9 · Cited by 119
Laursen, L. S., Chan, C. W., & ffrench‐Constant, C. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201007014 · Cited by 126
Filipenko, N. R., Attwell, S., Roskelley, C. D., & Dedhar, S. (2005) · Oncogene · doi:10.1038/sj.onc.1208737 · Cited by 118
The extracellular matrix compartment of neural stem and glial progenitor cells
Faissner, A., & Reinhard, J. (2015) · Glia · doi:10.1002/glia.22839 · Cited by 116
Niewmierzycka, A., Mills, J., St‐Arnaud, R., Dedhar, S., & Reichardt, L. F. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1695-05.2005 · Cited by 115
Benninger, Y., Colognato, H., Buerki‐Thurnherr, T., Franklin, R. J. M., Leone, D. P., Atanasoski, S., Nave, K., ffrench‐Constant, C., Suter, U., & Relvas, J. B. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0444-06.2006 · Cited by 117
Colognato, H., Galvin, J. W., Wang, Z., Relucio, J. L. V., Nguyen, T., Harrison, D., Yurchenco, P. D., & ffrench‐Constant, C. (2007) · Development · doi:10.1242/dev.02819 · Cited by 108
EphA1 interacts with integrin-linked kinase and regulates cell morphology and motility
Yamazaki, T., Masuda, J., Omori, T., Usui, R., Akiyama, H., & Maru, Y. (2008) · Journal of Cell Science · doi:10.1242/jcs.036467 · Cited by 107
Um, M., & Lodish, H. F. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m510943200 · Cited by 104
Axon‐oligodendrocyte interactions during developmental myelination, demyelination and repair
Piaton, G., Gould, R. M., & Lubetzki, C. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06831.x · Cited by 107
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Kim, H.-J., DiBernardo, A. B., Sloane, J. A., Rasband, M. N., Solomon, D., Kosaras, B., Kwak, S. P., & Vartanian, T. K. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4921-05.2006 · Cited by 99
Self-citationLourenço, T., de Faria, J. P., Bippes, C. A., Maia, J., Lopes‐da‐Silva, J. A., Relvas, J. B., & Grãos, M. (2016) · Scientific Reports · doi:10.1038/srep21563 · Cited by 104
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Wallquist, W., Plantman, S., Thams, S., Thyboll, J., Kortesmaa, J., Lännergren, J., Domogatskaya, A., Ögren, S. O., Risling, M., Hammarberg, H., et al. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5225-04.2005 · Cited by 94
Cassoli, J. S., Guest, P. C., Malchow, B., Schmitt, A., Falkai, P., & Martins‐de‐Souza, D. (2015) · Schizophrenia · doi:10.1038/npjschz.2015.34 · Cited by 91
Bacon, C., Lakics, V., Machesky, L. M., & Rumsby, M. G. (2007) · Glia · doi:10.1002/glia.20505 · Cited by 87
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Relucio, J. L. V., Menezes, M. J., Miyagoe‐Suzuki, Y., Takeda, S., & Colognato, H. (2012) · Glia · doi:10.1002/glia.22365 · Cited by 91
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Taylor, L. C., Gilmore, W., & Matsushima, G. K. (2009) · Brain Pathology · doi:10.1111/j.1750-3639.2008.00230.x · Cited by 84
Niciu, M. J., Ma, X., Meskini, R. E., Ronnett, G. V., Mains, R. E., & Eipper, B. A. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.01.044 · Cited by 84
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Czopka, T., von Holst, A., ffrench‐Constant, C., & Faissner, A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4957-09.2010 · Cited by 77
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Psenicka, M. W., Smith, B. C., Tinkey, R. A., & Williams, J. L. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.654284 · Cited by 73
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O'Meara, R. W., Michalski, J.-P., & Kothary, R. (2010) · Journal of signal transduction · doi:10.1155/2011/354091 · Cited by 77
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Qin, L., & Zhang, M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.131045 · Cited by 64
Kippert, A., Trajković, K., Rajendran, L., Ries, J., & Simons, M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4926-06.2007 · Cited by 58
Xu, R., Chandrasekharan, K., Yoon, J. H., Camboni, M., & Martin, P. T. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.060927 · Cited by 59
Regulation of the neural stem cell compartment by extracellular matrix constituents
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Hyysalo, A., Ristola, M., Mäkinen, M., Häyrynen, S., Nykter, M., & Narkilahti, S. (2017) · Stem Cell Research · doi:10.1016/j.scr.2017.09.002 · Cited by 53
Liu, A., Stadelmann, C., Moscarello, M. A., Brück, W., Sobel, A., Mastronardi, F. G., & Casaccia‐Bonnefil, P. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4174-04.2005 · Cited by 52
Lee, K. K., De Repentigny, Y., Saulnier, R., Rippstein, P., Macklin, W. B., & Kothary, R. (2006) · Glia · doi:10.1002/glia.20343 · Cited by 59
Cho, A., Jin, Y., Kim, S., Kumar, S., Shin, H., Kang, H., & Cho, S. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b03242 · Cited by 51
Thomason, E. J., Escalante, M., Osterhout, D. J., & Fuss, B. (2019) · Glia · doi:10.1002/glia.23735 · Cited by 55
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Forrest, A. D., Beggs, H. E., Reichardt, L. F., Dupree, J. L., Colello, R. J., & Fuss, B. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22022 · Cited by 52
Fibronectin attenuates process outgrowth in oligodendrocytes by mislocalizing MMP-9 activity
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Fox, M. A., Alexander, J. K., Afshari, F. S., Colello, R. J., & Fuss, B. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.06.002 · Cited by 49
Lafrenaye, A. D., & Fuss, B. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06926.x · Cited by 44
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Ozgen, H., Schrimpf, W., Hendrix, J., de Jonge, J. C., Lamb, D. C., Hoekstra, D., Kahya, N., & Baron, W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101834 · Cited by 44
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Olsen, I. M. L., & ffrench‐Constant, C. (2005) · BMC Biology · doi:10.1186/1741-7007-3-25 · Cited by 41
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Proctor, D. T., Stotz, S. C., Scott, L. O. M., de la Hoz, C. L. R., Poon, K. W. C., Stys, P. K., & Colicos, M. A. (2015) · Glia · doi:10.1002/glia.22875 · Cited by 42
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Galvin, J. W., Eyermann, C. E., & Colognato, H. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22484 · Cited by 38
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Masaki, T., & Matsumura, K. (2010) · BioMed Research International · doi:10.1155/2010/740403 · Cited by 36
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Kim, W. K., Kim, D., Cui, J., Jang, H. H., Kim, K. S., Lee, H. J., Kim, S. U., & Ahn, S.-M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084292 · Cited by 34
Belkadi, A., & LoPresti, P. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05600.x · Cited by 33
O’Meara, R. W., Michalski, J., Anderson, C., Bhanot, K., Rippstein, P. U., & Kothary, R. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5582-12.2013 · Cited by 33
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Leiton, C. V., Aranmolate, A., Eyermann, C. E., Menezes, M. J., Escobar‐Hoyos, L. F., Husain, S., Winder, S. J., & Colognato, H. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13241 · Cited by 32
Kianoush, F., Nematollahi, M., Waterfield, J. D., & Brunette, D. M. (2017) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36107 · Cited by 32
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Metadata
- Authors
- Chun, S. J., Rasband, M. N., Sidman, R. L., Habib, A. A., & Vartanian, T.
- Affiliations
- Beth Israel Deaconess Medical Center (US)
- UConn Health (US)
- Corresponding author
- Vartanian, Timothy
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2003-10-27
- Volume
- 163
- Issue
- 2
- Pages
- 397-408
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2173507
- OpenAlex
- W2120316837
- Cited by
- 170
- References
- 41
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 3 · 2023: 2 · 2022: 5 · 2021: 6 · 2020: 5 · 2019: 10 · 2018: 4 · 2017: 8 · 2016: 6 · 2015: 10 · 2014: 4 · 2013: 7 · 2012: 8
- FWCI
- 2.44
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc-sa
- Locations
- The Journal of Cell Biology (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5k02ns002028-04)
- National Institute of Neurological Disorders and Stroke (K02 NS02028, P01 NS 38475, R01NS044916, P01NS038475, R01NS042317, R01 NS42317)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Keywords
- integrin-linked kinase, laminin-2, CNS myelination, alpha6beta1 integrin, phosphatidylinositol 3-kinase, myelination, integrin signaling
- MeSH terms
- Scaffold Protein ILK, Adenoviridae, Animals, Axons, Cell Survival, Cells, Cultured, Central Nervous System, Cytoskeletal Proteins, Enzyme Activation, Homozygote, Laminin, Mice, Mutant Strains, Mutation, Myelin Sheath, Oligodendroglia, Optic Nerve, Phosphoproteins, Cell Adhesion Molecules, Rats, Sprague-Dawley, Protein Serine-Threonine Kinases, Phosphatidylinositol 3-Kinases, Mice, Rats, Paxillin
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