Cerebrospinal fluid contains biologically active bone morphogenetic protein-7

被引:33
作者
Dattatreyamurty, B [1 ]
Roux, E
Horbinski, C
Kaplan, PL
Robak, LA
Beck, HN
Lein, P
Higgins, D
Chandrasekaran, V
机构
[1] Creat Biomol Inc, Hopkinton, MA 01748 USA
[2] SUNY Buffalo, Dept Pharmacol & Toxicol, Buffalo, NY 14214 USA
[3] Canisius Coll, Buffalo, NY 14208 USA
[4] Johns Hopkins Univ, Bloomburg Sch Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21136 USA
基金
美国国家科学基金会;
关键词
bone morphogenetic protein; cerebrospinal fluid; sympathetic neuron; dendrite; Smad-1; bovine;
D O I
10.1006/exnr.2001.7728
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Bone morphogenetic proteins (BMPs) regulate the development and function of many types of neurons. However, little is known of the actual concentrations of BMPs in the various parts of the brain. In this study, we considered the possibility that BMPs might be present in cerebrospinal fluid (CSF). Western blot analysis of normal adult bovine CSF revealed the presence of dimeric and monomeric forms of BMP-7, and the concentration of this molecule was found to be similar to12 ng/ml in a radioimmunoassay. Since BMP-7 is known to induce dendritic growth in rat sympathetic neurons, this was used as a bioassay to examine the biological activity of the BMP-7 present in CSF. Addition of normal bovine CSF to cultures of sympathetic neurons produced a dose-dependent increase in dendritic growth and the magnitude of this response approximated that obtained with maximally effective concentrations of exogenous BMP-7. Moreover, CSF-induced dendritic growth was inhibited by follistatin, a protein that can sequester BMPs, and by either of two monoclonal antibodies that react with BMP-7. These results show that, unlike most other neurotrophic factors, BMP-7 is a constituent of normal CSF and is present at concentrations sufficient to elicit a near maximal biological response. (C) 2001 Elsevier Science.
引用
收藏
页码:273 / 281
页数:9
相关论文
共 60 条
[1]   REGULATION OF GENE-EXPRESSION IN HIPPOCAMPAL-NEURONS BY DISTINCT CALCIUM SIGNALING PATHWAYS [J].
BADING, H ;
GINTY, DD ;
GREENBERG, ME .
SCIENCE, 1993, 260 (5105) :181-186
[2]  
BRACCI-LAUDIERO L, 1992, NEUROSCI LETT, V147, P9
[3]  
Chandrasekaran V, 2000, J NEUROBIOL, V42, P383, DOI 10.1002/(SICI)1097-4695(200003)42:4<383::AID-NEU1>3.0.CO
[4]  
2-9
[5]   Distribution of bone morphogenetic protein and bone morphogenetic protein receptor transcripts in the rodent nervous system and up-regulation of bone morphogenetic protein receptor type II in hippocampal dentate gyrus in a rat model of global cerebral ischemia [J].
Charytoniuk, DA ;
Traiffort, E ;
Pinard, E ;
Issertial, O ;
Seylaz, J ;
Ruat, M .
NEUROSCIENCE, 2000, 100 (01) :33-43
[6]  
DATTATREYAMURTY B, 1986, J BIOL CHEM, V261, P3104
[7]   IDENTIFICATION IN HUMAN OVARIAN FOLLICULAR-FLUID OF PROTEINS THAT SHARE AN EPITOPE REGION UNIQUE TO THE EXTRACELLULAR DOMAIN OF THE FOLLICLE-STIMULATING-HORMONE RECEPTOR [J].
DATTATREYAMURTY, B ;
SCHWEDER, CA ;
REICHERT, LE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (05) :1303-1309
[8]  
DELEAN A, 1978, AM J PHYSIOL, V235, P97
[9]   Microtubule binding to Smads may regulate TGFβ activity [J].
Dong, CM ;
Li, ZR ;
Alvarez, R ;
Feng, XH ;
Goldschmidt-Clermont, PJ .
MOLECULAR CELL, 2000, 5 (01) :27-34
[10]   A SOLUBLE FORM OF THE F3 NEURONAL CELL-ADHESION MOLECULE PROMOTES NEURITE OUTGROWTH [J].
DURBEC, P ;
GENNARINI, G ;
GORIDIS, C ;
ROUGON, G .
JOURNAL OF CELL BIOLOGY, 1992, 117 (04) :877-887