Myelin-mediated inhibition of oligodendrocyte precursor differentiation can be overcome by pharmacological modulation of Fyn-RhoA and protein kinase C signalling

被引:169
作者
Baer, Alexandra S. [2 ]
Syed, Yasir A. [2 ]
Kang, Sung Ung [3 ]
Mitteregger, Dieter [2 ]
Vig, Raluca [3 ]
Ffrench-Constant, Charles [4 ]
Franklin, Robin J. M. [5 ,6 ]
Altmann, Friedrich [7 ]
Lubec, Gert [3 ]
Kotter, Mark R. [1 ,2 ]
机构
[1] Univ Gottingen, Max Planck Inst Expt Med, Dept Neurosurg, D-37075 Gottingen, Germany
[2] Med Univ Vienna, Dept Neurosurg, Vienna, Austria
[3] Med Univ Vienna, Dept Pediat, Vienna, Austria
[4] Univ Edinburgh, MS Society, Ctr Translat Res, Queens Med Res Inst,Ctr Inflammat Res, Edinburgh, Midlothian, Scotland
[5] Univ Cambridge, Cambridge Ctr Brain Repair, Cambridge, England
[6] Univ Cambridge, Dept Vet Med, Cambridge, England
[7] Univ Bodenkultur Wien, Vienna, Austria
关键词
adult stem; precursor cells; oligodendrocyte; differentiation; myelin inhibitors; intracellular signalling; multiple sclerosis; remyelination; TOXIN-INDUCED DEMYELINATION; MULTIPLE-SCLEROSIS LESIONS; MESSENGER-RNA EXPRESSION; INCREASING LOCAL-LEVELS; ADULT HUMAN BRAIN; PROGENITOR CELLS; CNS REMYELINATION; SPINAL-CORD; MASS-SPECTROMETRY; PLASMA-MEMBRANE;
D O I
10.1093/brain/awn334
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Failure of oligodendrocyte precursor cell (OPC) differentiation contributes significantly to failed myelin sheath regeneration (remyelination) in chronic demyelinating diseases. Although the reasons for this failure are not completely understood, several lines of evidence point to factors present following demyelination that specifically inhibit differentiation of cells capable of generating remyelinating oligodendrocytes. We have previously demonstrated that myelin debris generated by demyelination inhibits remyelination by inhibiting OPC differentiation and that the inhibitory effects are associated with myelin proteins. In the present study, we narrow down the spectrum of potential protein candidates by proteomic analysis of inhibitory protein fractions prepared by CM and HighQ column chromatography followed by BN/SDS/SDSPAGE gel separation using Nano-HPLC-ESI-Q-TOF mass spectrometry. We show that the inhibitory effects on OPC differentiation mediated by myelin are regulated by Fyn-RhoA-ROCK signalling as well as by modulation of protein kinase C (PKC) signalling. We demonstrate that pharmacological or siRNA-mediated inhibition of RhoA-ROCK-II and/or PKC signalling can induce OPC differentiation in the presence of myelin. Our results, which provide a mechanistic link between myelin, a mediator of OPC differentiation inhibition associated with demyelinating pathologies and specific signalling pathways amenable to pharmacological manipulation, are therefore of significant potential value for future strategies aimed at enhancing CNS remyelination.
引用
收藏
页码:465 / 481
页数:17
相关论文
共 91 条
[1]
Astrocyte stellation induced by Rho kinase inhibitors in culture [J].
Abe, K ;
Misawa, M .
DEVELOPMENTAL BRAIN RESEARCH, 2003, 143 (01) :99-104
[2]
PROTEIN-KINASE-C REGULATES MARCKS CYCLING BETWEEN THE PLASMA-MEMBRANE AND LYSOSOMES IN FIBROBLASTS [J].
ALLEN, LAH ;
ADEREM, A .
EMBO JOURNAL, 1995, 14 (06) :1109-1121
[3]
PROTEIN-KINASE-C STIMULATION ENHANCES THE PROCESS FORMATION OF ADULT OLIGODENDROCYTES AND INDUCES PROLIFERATION [J].
ALTHAUS, HH ;
SCHROTER, J ;
SPOERRI, P ;
SCHWARTZ, P ;
KLOPPNER, S ;
ROHMANN, A ;
NEUHOFF, V .
JOURNAL OF NEUROSCIENCE RESEARCH, 1991, 29 (04) :481-489
[4]
NEURONAL STEM-CELLS IN THE BRAIN OF ADULT VERTEBRATES [J].
ALVAREZBUYLLA, A ;
LOIS, C .
STEM CELLS, 1995, 13 (03) :263-272
[5]
Cross-talk unfolded:: MARCKS proteins [J].
Arbuzova, A ;
Schmitz, AAP ;
Vergères, G .
BIOCHEMICAL JOURNAL, 2002, 362 :1-12
[6]
PROTEIN-KINASE-C ACTIVITY MODULATES MYELIN GENE-EXPRESSION IN ENRICHED OLIGODENDROCYTES [J].
ASOTRA, K ;
MACKLIN, WB .
JOURNAL OF NEUROSCIENCE RESEARCH, 1993, 34 (05) :571-588
[7]
Hyaluronan accumulates in demyelinated lesions and inhibits oligodendrocyte progenitor maturation [J].
Back, SA ;
Tuohy, TMF ;
Chen, HQ ;
Wallingford, N ;
Craig, A ;
Struve, J ;
Luo, NL ;
Banine, F ;
Liu, Y ;
Chang, A ;
Trapp, BD ;
Bebo, BF ;
Rao, MS ;
Sherman, LS .
NATURE MEDICINE, 2005, 11 (09) :966-972
[8]
MULTIPLE AND NOVEL SPECIFICITIES OF MONOCLONAL-ANTIBODIES O1, O4, AND R-MAB USED IN THE ANALYSIS OF OLIGODENDROCYTE DEVELOPMENT [J].
BANSAL, R ;
WARRINGTON, AE ;
GARD, AL ;
RANSCHT, B ;
PFEIFFER, SE .
JOURNAL OF NEUROSCIENCE RESEARCH, 1989, 24 (04) :548-557
[9]
Baron W, 1998, GLIA, V22, P121, DOI 10.1002/(SICI)1098-1136(199802)22:2<121::AID-GLIA3>3.0.CO
[10]
2-A