Gene profiling and bioinformatic analysis of Schwann cell embryonic development and myelination

被引:68
作者
D'Antonio, M
Michalovich, D
Paterson, M
Droggiti, A
Woodhoo, A
Mirsky, R
Jessen, KR
机构
[1] UCL, Dept Anat & Dev Biol, London WC1E 6BT, England
[2] Inpharmatica Ltd, London, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
myelin; microarray; collagen type II; synuclein;
D O I
10.1002/glia.20309
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To elucidate the molecular mechanisms involved in Schwann cell development, we profiled gene expression in the developing and injured rat sciatic nerve. The genes that showed significant changes in expression in developing and dedifferentiated nerve were validated with RT-PCR, in situ hybridisation, Western blot and immunofluorescence. A comprehensive approach to annotating micro-array probes and their associated transcripts was performed using Biopendium(TM), a database of sequence and structural annotation. This approach significantly increased the number of genes for which a functional insight could be found. The analysis implicates agrin and two members of the collapsin response-mediated protein (CRMP) family in the switch from precursors to Schwann cells, and synuclein-1 and alpha B-crystallin in peripheral nerve myelination. We also identified a group of genes typically related to chondrogenesis and cartilage/bone development, including type II collagen, that were expressed in a manner similar to that of myelin-associated genes. The comprehensive function annotation also identified, among the genes regulated during nerve development or after nerve injury, proteins belonging to high-interest families, such as cytokines and kinases, and should therefore provide a uniquely valuable resource for future research. (C) 2005 Wiley-Liss, Inc.
引用
收藏
页码:501 / 515
页数:15
相关论文
共 97 条
[71]   Krox-20 inhibits Jun-NH2-terminal kinase/c-Jun to control Schwann cell proliferation and death [J].
Parkinson, DB ;
Bhaskaran, A ;
Droggiti, A ;
Dickinson, S ;
D'Antonio, M ;
Mirsky, R ;
Jessen, KR .
JOURNAL OF CELL BIOLOGY, 2004, 164 (03) :385-394
[72]   Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells [J].
Poliak, S ;
Matlis, S ;
Ullmer, C ;
Scherer, SS ;
Peles, E .
JOURNAL OF CELL BIOLOGY, 2002, 159 (02) :361-371
[73]   ALTERNATIVE SPLICE FORM OF TYPE-II PROCOLLAGEN MESSENGER-RNA (IIA) IS PREDOMINANT IN SKELETAL PRECURSORS AND NON-CARTILAGINOUS TISSUES DURING EARLY MOUSE DEVELOPMENT [J].
SANDELL, LJ ;
NALIN, AM ;
REIFE, RA .
DEVELOPMENTAL DYNAMICS, 1994, 199 (02) :129-140
[74]   IN-SITU EXPRESSION OF COLLAGEN AND PROTEOGLYCAN GENES IN NOTOCHORD AND DURING SKELETAL DEVELOPMENT AND GROWTH [J].
SANDELL, LJ .
MICROSCOPY RESEARCH AND TECHNIQUE, 1994, 28 (06) :470-482
[75]  
SCHERER SS, 2001, GLIAL CELL DEV, P229
[76]   Specific disruption of a Schwann cell dystrophin-related protein complex in a demyelinating neuropathy [J].
Sherman, DL ;
Fabrizi, C ;
Gillespie, CS ;
Brophy, PJ .
NEURON, 2001, 30 (03) :677-687
[77]  
Shy ME, 1996, J NEUROSCI RES, V43, P511, DOI 10.1002/(SICI)1097-4547(19960301)43:5<511::AID-JNR1>3.0.CO
[78]  
2-L
[79]   Developmental regulation and overexpression of the transcription factor AP-2, a potential regulator of the timing of Schwann cell generation [J].
Stewart, HJS ;
Brennan, A ;
Rahman, M ;
Zoidl, G ;
Mitchell, PJ ;
Jessen, KR ;
Mirsky, R .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 14 (02) :363-372
[80]   EXPRESSION OF C-JUN, JUN-B, JUN-D AND CAMP RESPONSE ELEMENT-BINDING PROTEIN BY SCHWANN-CELLS AND THEIR PRECURSORS IN-VIVO AND IN-VITRO [J].
STEWART, HJS .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1995, 7 (06) :1366-1375