FGF-2-responsive neural stem cell proliferation requires CCg, a novel autocrine/paracrine cofactor

被引:260
作者
Taupin, P
Ray, J
Fischer, WH
Suhr, ST
Hakansson, K
Grubb, A
Gage, FH
机构
[1] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, Peptide Biol Lab, La Jolla, CA 92037 USA
[3] Univ Lund Hosp, Dept Clin Chem, S-22185 Lund, Sweden
关键词
D O I
10.1016/S0896-6273(00)00119-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have purified and characterized a factor, from the conditioned medium of neural stem cell cultures, which is required for fibroblast growth factor 2's (FGF-2) mitogenic activity on neural stem cells. This autocrine/paracrine cofactor is a glycosylated form of cystatin C (CCg), whose N-glycosylation is required for its activity. We further demonstrated that, both in vitro and in vivo, neural stem cells undergoing cell division are immunopositive for cystatin C. Finally, we showed in vivo functional activity of CCg by demonstrating that the combined delivery of FGF-2 and CCg to the adult dentate gyrus stimulated neurogenesis. We propose that the process of neurogenesis is controlled by the cooperation between trophic factors and autocrine/paracrine cofactors, of which CCS is a prototype.
引用
收藏
页码:385 / 397
页数:13
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