Regulation of glial development by cystatin C

被引:26
作者
Hasegawa, Akiko
Naruse, Masae
Hitoshi, Seiji
Iwasaki, Yasuno
Takebayashi, Hirohide
Ikenaka, Kazuhiro
机构
[1] Natl Inst Nat Sci, Div Neurobiol & Bioinformat, Natl Inst Physiol Sci, Okazaki, Aichi 4448787, Japan
[2] Grad Univ Adv Studies, SOKENADAI, Sch Life Sci, Dept Physiol Sci, Okazaki, Aichi, Japan
关键词
astrocyte; Cystatin C; gliogenesis; oligodendrocyte;
D O I
10.1111/j.1471-4159.2006.04169.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cystatin C (CysC) is an endogenous cysteine proteases inhibitor produced by mature astrocytes in the adult brain. Previously we isolated CysC as a factor activating the glial fibrillary acidic protein (GFAP) promoter, and showed that CysC is expressed in astrocyte progenitors during development. Here we show that protease inhibitor activity increased daily in conditioned medium, and that this activity was mainly a result of CysC released from primary cultured cells. Human CysC added to the culture medium of primary brain cells increased the number of GFAP-positive and nestin-positive cells. Human CysC also increased the number of neurospheres formed from embryonic brain, and thus it increases the number of neural stem/precursor cells in a manner similar to glycosylated rat CysC. The addition of a neutralizing antibody, on the other hand, greatly decreased the number of GFAP and glutamate aspartate transporter (GLAST)-positive astrocytes. This decrease was reversed by the addition of CysC but not by another cysteine protease inhibitor. Thus, the promotion of astrocyte development by CysC appears to be independent of its protease inhibitor activity. The antibody increased the number of oligodendrocytes and their precursors. Therefore, CysC modifies glial development in addition to its activity against neural stem/precursor cells.
引用
收藏
页码:12 / 22
页数:11
相关论文
共 32 条
[1]   EFFICIENT PRODUCTION OF NATIVE, BIOLOGICALLY-ACTIVE HUMAN CYSTATIN-C BY ESCHERICHIA-COLI [J].
ABRAHAMSON, M ;
DALBOGE, H ;
OLAFSSON, I ;
CARLSEN, S ;
GRUBB, A .
FEBS LETTERS, 1988, 236 (01) :14-18
[2]   THE CEREBRAL EXPRESSION OF PLASMA-PROTEIN GENES IN DIFFERENT SPECIES [J].
ALDRED, AR ;
BRACK, CM ;
SCHREIBER, G .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1995, 111 (01) :1-15
[3]   L-TRANS-EPOXYSUCCINYL-LEUCYLAMIDO(4-GUANIDINO)BUTANE (E-64) AND ITS ANALOGS AS INHIBITORS OF CYSTEINE PROTEINASES INCLUDING CATHEPSINS B, H AND L [J].
BARRETT, AJ ;
KEMBHAVI, AA ;
BROWN, MA ;
KIRSCHKE, H ;
KNIGHT, CG ;
TAMAI, M ;
HANADA, K .
BIOCHEMICAL JOURNAL, 1982, 201 (01) :189-198
[4]  
BARRETT AJ, 1986, BIOMED BIOCHIM ACTA, V45, P1363
[5]  
Bayer S.A, 1991, Neocortical development
[6]  
ESNARD F, 1990, BIOL CHEM H-S, V371, P161
[7]   Glia as neural progenitor cells [J].
Goldman, S .
TRENDS IN NEUROSCIENCES, 2003, 26 (11) :590-596
[8]   Spatial and temporal expression of S100B in cells of oligodendrocyte lineage [J].
Hachem, S ;
Aguirre, A ;
Vives, V ;
Marks, A ;
Gallo, V ;
Legraverend, C .
GLIA, 2005, 51 (02) :81-97
[9]  
Hall A, 1996, DEVELOPMENT, V122, P4085
[10]   Decreased metastatic spread in mice homozygous for a null allele of the cystatin C protease inhibitor gene [J].
Huh, CG ;
Håkansson, K ;
Nathanson, CM ;
Thorgeirsson, UP ;
Jonsson, N ;
Grubb, A ;
Abrahamson, M ;
Karlsson, S .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 1999, 52 (06) :332-340