Expression of the human NOV gene in first trimester fetal tissues

被引:50
作者
Kocialkowski, S
Yeger, H
Kingdom, J
Perbal, B
Schofield, PN
机构
[1] Univ Cambridge, Dept Anat, Lab Stem Cell Biol, Cambridge CB2 3DY, England
[2] Univ Toronto, Toronto, ON, Canada
[3] Hosp Sick Children, Dept Pathol, Toronto, ON M5G 1X8, Canada
[4] Univ Toronto, Mt Sinai Hosp, Toronto, ON M5G 1X5, Canada
[5] Univ Paris 07, Lab Oncol Virale & Mol, UFR Biochim, F-75005 Paris, France
来源
ANATOMY AND EMBRYOLOGY | 2001年 / 203卷 / 06期
关键词
NOV; cell differentiation; muscle; motor neurone; ganglia; CNS; human; fetus; CCN;
D O I
10.1007/s004290100177
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
NOV, located on human chromosome 8q24.1, was originally cloned following discovery of its avian homolog as a consequence of over-expression in virally induced nephroblastoma. The gene product is a secreted, modular, protein and a member of the CCN gene family. Evidence to date indicates chat the expression of the wild type protein is associated with cellular quiescence in normal embryonic fibroblasts yet produces growth stimulatory effects on established murine NIH 3T3 cells. Here we report the expression of NOV in the first trimester of human embryogenesis, between 5 and 10 weeks. In situ hybridisation and immunohistochemistry reveal widespread expression in derivatives of all three germ layers. The most abundant sites of expression are in the motor neurons and floor plate of the spinal cord, adrenal cortex, fusing skeletal, and smooth muscle, the urogenital system and the developing heart. Additionally, expression is seen in the cranial ganglia, differentiating chondrocytes, gonads, and lung. The sites of expression suggest strongly that autocrine or paracrine expression of NOV is associated with the process of cell differentiation.
引用
收藏
页码:417 / 427
页数:11
相关论文
共 68 条
[1]  
ABRAHAMSON DR, 1991, SEMIN NEPHROL, V11, P375
[2]   Muscarinic acetylcholine receptors induce the expression of the immediate early growth regulatory gene CYR61 [J].
Albrecht, C ;
von der Kammer, H ;
Mayhaus, M ;
Klaudiny, J ;
Schweizer, M ;
Nitsch, RM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (37) :28929-28936
[3]   Insulin-like growth factor-binding protein-5 (IGFBP-5) stimulates phosphorylation of the IGFBP-5 receptor [J].
Andress, DL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1998, 274 (04) :E744-E750
[4]   CYR61, a product of a growth factor-inducible immediate early gene, promotes angiogenesis and tumor growth [J].
Babic, AM ;
Kireeva, ML ;
Kolesnikova, TV ;
Lau, LF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6355-6360
[5]   THE MODULAR ARCHITECTURE OF A NEW FAMILY OF GROWTH-REGULATORS RELATED TO CONNECTIVE-TISSUE GROWTH-FACTOR [J].
BORK, P .
FEBS LETTERS, 1993, 327 (02) :125-130
[6]   CONNECTIVE-TISSUE GROWTH-FACTOR - A CYSTEINE-RICH MITOGEN SECRETED BY HUMAN VASCULAR ENDOTHELIAL-CELLS IS RELATED TO THE SRC-INDUCED IMMEDIATE EARLY GENE-PRODUCT CEF-10 [J].
BRADHAM, DM ;
IGARASHI, A ;
POTTER, RL ;
GROTENDORST, GR .
JOURNAL OF CELL BIOLOGY, 1991, 114 (06) :1285-1294
[7]  
BRICE AL, 1989, DEVELOPMENT, V106, P543
[8]   The connective tissue growth factor cysteine-rich 61 nephroblastoma overexpressed (CCN) family [J].
Brigstock, DR .
ENDOCRINE REVIEWS, 1999, 20 (02) :189-206
[9]  
Burren CP, 1999, J CLIN ENDOCR METAB, V84, P1096
[10]   TISSUE-SPECIFIC EXPRESSION OF THE INSULIN-LIKE GROWTH-FACTOR BINDING-PROTEIN (IGFBP) MESSENGER-RNAS IN MOUSE AND RAT DEVELOPMENT [J].
CERRO, JA ;
GREWAL, A ;
WOOD, TL ;
PINTAR, JE .
REGULATORY PEPTIDES, 1993, 48 (1-2) :189-198