Tenascin C in stem cell niches: Redundant, permissive or instructive?

被引:45
作者
von Holst, Alexander [1 ]
机构
[1] Ruhr Univ Bochum, Dept Cell Morphol & Mol Neurobiol, DE-44780 Bochum, Germany
关键词
stem cell niche; forebrain; gene trap;
D O I
10.1159/000112848
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The stem cell niche provides the specialized environment that is able to sustain the lifelong maintenance of stem cells in their discrete locations within organs. The niche is usually composed of several different cell types and a specialized extracellular matrix consisting of many different constituents. Additionally, a variety of growth factors are secreted into the extracellular space and contribute to the functional organization of the niche. Here, I will concentrate on the multimodular extracellular matrix glycoprotein tenascin C (Tnc) and discuss it as an exemplary molecule that is present in several stem cell niches. In spite of its intuitively suggestive presence, it has been difficult to provide functional evidence for the importance of Tnc in the context of stem cells. In the nervous system, the careful analysis of Tnc-deficient mice has revealed that the developmental program neural stem cell pass-through is delayed due to changes in growth factor responsiveness. To gain further insight, we have employed the gene trap technology in neural stem cells to identify potential Tnc target genes. This approach has surfaced 2 interesting candidates that may contribute to a better understanding of the signal(s) elicited by Tnc in neural stem/progenitor cells in the niche. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:170 / 177
页数:8
相关论文
共 81 条
[11]   A niche for adult neural stem cells [J].
Doetsch, F .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (05) :543-550
[12]  
Evers MR, 2002, J NEUROSCI, V22, P7177
[13]   J1-TENASCIN IS A REPULSIVE SUBSTRATE FOR CENTRAL-NERVOUS-SYSTEM NEURONS [J].
FAISSNER, A ;
KRUSE, J .
NEURON, 1990, 5 (05) :627-637
[14]   An induction gene trap screen in embryonic stem cells: Identification of genes that respond to retinoic acid in vitro [J].
Forrester, LM ;
Nagy, A ;
Sam, M ;
Watt, A ;
Stevenson, L ;
Bernstein, A ;
Joyner, AL ;
Wurst, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) :1677-1682
[15]   Skin wounds and severed nerves heal normally in mice lacking tenascin-C [J].
Forsberg, E ;
Hirsch, E ;
Frohlich, L ;
Meyer, M ;
Ekblom, P ;
Aszodi, A ;
Werner, S ;
Fassler, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (13) :6594-6599
[16]   Socializing with the neighbors: Stem cells and their niche [J].
Fuchs, E ;
Tumbar, T ;
Guasch, G .
CELL, 2004, 116 (06) :769-778
[17]   Abnormal behavior and neurotransmissions of tenascin gene knockout mouse [J].
Fukamauchi, F ;
Mataga, N ;
Wang, YJ ;
Sato, S ;
Yoshiki, A ;
Kusakabe, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 221 (01) :151-156
[18]   Tyrosine hydroxylase activity and its mRNA level in dopaminergic neurons of tenascin gene knockout mouse [J].
Fukamauchi, F ;
Mataga, N ;
Wang, YJ ;
Sato, S ;
Yoshiki, A ;
Kusakabe, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 231 (02) :356-359
[19]   Deregulation of dorsoventral patterning by FGF confers trilineage differentiation capacity on CNS stem cells in vitro [J].
Gabay, L ;
Lowell, S ;
Rubin, LL ;
Anderson, DJ .
NEURON, 2003, 40 (03) :485-499
[20]   Mammalian neural stem cells [J].
Gage, FH .
SCIENCE, 2000, 287 (5457) :1433-1438