DISTRIBUTION OF VITRONECTIN MESSENGER-RNA DURING MURINE DEVELOPMENT

被引:52
作者
SEIFFERT, D
IRUELAARISPE, ML
SAGE, EH
LOSKUTOFF, DJ
机构
[1] HARVARD UNIV, SCH MED, DEPT PATHOL, BOSTON, MA USA
[2] BETH ISRAEL HOSP, BOSTON, MA 02215 USA
[3] UNIV WASHINGTON, DEPT BIOL STRUCT, SEATTLE, WA USA
关键词
VITRONECTIN; ADHESIVE GLYCOPROTEINS; COAGULATION SYSTEM; COMPLEMENT SYSTEM; FIBRINOLYTIC SYSTEM;
D O I
10.1002/aja.1002030108
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
Vitronectin (Vn) is not only a major adhesive glycoprotein in plasma but also regulates cell-mediated proteolytic enzyme cascades, including the complement, coagulation, and fibrinolytic systems. This broad functional activity suggests that Vn may also play a critical role in development. To bean to investigate this possibility, we studied Vn gene expression during murine embryogenesis, In situ hybridization analysis of embryonic tissues revealed Vn mRNA primarily in the liver and the central nervous system (CNS). In the liver, Vn mRNA was detected by day 10, the level increasing at later developmental stages. In the CNS, Vn mRNA was also detected as early as day 10 and was confined to the floor plate. However, as development proceeded, high levels of Vn transcripts became prominent in the meninges of the cortex and spinal cord, and in close proximity to brain capillaries. The perikarya of most neurons lacked Vn mRNA. Unexpectedly, high levels of Vn mRNA were associated with capillaries of the CNS, but not with blood vessels of peripheral organs. These results indicate that Vn is expressed in a spatially and temporally distinct pattern during murine embryogenesis, and suggest that the Vn transcript may be a CNS-specific vascular marker. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:71 / 79
页数:9
相关论文
共 24 条
[1]   REQUIREMENT OF VASCULAR INTEGRIN ALPHA(V)BETA(3) FOR ANGIOGENESIS [J].
BROOKS, PC ;
CLARK, RAF ;
CHERESH, DA .
SCIENCE, 1994, 264 (5158) :569-571
[2]  
Chromczynski P, 1987, ANAL BIOCHEM, V162, P156
[3]  
CIAMBRONE GJ, 1992, J BIOL CHEM, V267, P13617
[4]  
COOPER S, 1993, INT CONGR SER, V1042, P83
[5]   PLASMINOGEN ACTIVATORS, TISSUE DEGRADATION, AND CANCER [J].
DANO, K ;
ANDREASEN, PA ;
GRONDAHLHANSEN, J ;
KRISTENSEN, P ;
NIELSEN, LS ;
SKRIVER, L .
ADVANCES IN CANCER RESEARCH, 1985, 44 :139-266
[6]  
Ganong W, 1991, REV MED PHYSL
[7]  
Gilbert S. F., 1991, DEV BIOL
[8]   ANALYSIS OF CYTOKINE MESSENGER-RNA AND DNA - DETECTION AND QUANTITATION BY COMPETITIVE POLYMERASE CHAIN-REACTION [J].
GILLILAND, G ;
PERRIN, S ;
BLANCHARD, K ;
BUNN, HF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) :2725-2729
[9]   VITRONECTIN IS THE MAJOR SERUM-PROTEIN ESSENTIAL FOR NGF-MEDIATED NEURITE OUTGROWTH FROM PC12 CELLS [J].
GRABHAM, PW ;
GALLIMORE, PH ;
GRAND, RJA .
EXPERIMENTAL CELL RESEARCH, 1992, 202 (02) :337-344
[10]   INTEGRINS - VERSATILITY, MODULATION, AND SIGNALING IN CELL-ADHESION [J].
HYNES, RO .
CELL, 1992, 69 (01) :11-25