Receptor-type protein-tyrosine phosphatase μ is expressed in specific vascular endothelial beds in vivo

被引:36
作者
Bianchi, C
Sellke, FW
Del Vecchio, RL
Tonks, NK
Neel, BG
机构
[1] Beth Israel Deaconess Med Ctr, Canc Biol Program, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[3] Beth Israel Deaconess Med Ctr, Dept Surg, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Boston, MA 02215 USA
[5] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
关键词
signal transduction; angiogenesis; tyrosyl phosphorylation; contact inhibition; cell junctions;
D O I
10.1006/excr.1999.4428
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated the localization of receptor-type protein-tyrosine phosphatase mu (RPTP mu) in tissues by immunofluorescence. RPTP mu immunoreactivity was found almost exclusively within vascular endothelial cells. RPTP mu was more abundant in the arterial tree than in the venous circulation. This pattern of expression was opposite to that of the von Willebrand factor and demonstrated a lack of difference in expression of VE-cadherin. RPTP mu was undetectable in the endocardium, In agreement with previous work on nonendothelial cell lines, RPTP mu was exclusively at the lateral aspects of endothelial cells in vivo and at cell-cell contacts as well as ex vivo in two- or three-dimensional endothelial cell cultures, and expression levels were upregulated by cell density. RPTP mu was detected in few other cells: bronchial and biliary epithelia and cardiocytes (intercalated discs). Our results identify RPTP mu as a new marker of endothelial cell heterogeneity and suggest a possible role in endothelial-specific functions, involving cell-cell contact. (C) 1999 Academic Press.
引用
收藏
页码:329 / 338
页数:10
相关论文
共 28 条
[1]  
[Anonymous], 1988, Antibodies: A Laboratory Manual
[2]  
Ayalon O, 1997, J CELL SCI, V110, P547
[3]   Dynamic interaction of PTPμ with multiple cadherins in vivo [J].
Brady-Kalnay, SM ;
Mourton, T ;
Nixon, JP ;
Pietz, GE ;
Kinch, M ;
Chen, HY ;
Brackenbury, R ;
Rimm, DL ;
Del Vecchio, RL ;
Tonks, NK .
JOURNAL OF CELL BIOLOGY, 1998, 141 (01) :287-296
[4]   HOMOPHILIC BINDING OF PTP-MU, A RECEPTOR-TYPE PROTEIN-TYROSINE-PHOSPHATASE, CAN MEDIATE CELL-CELL AGGREGATION [J].
BRADYKALNAY, SM ;
FLINT, AJ ;
TONKS, NK .
JOURNAL OF CELL BIOLOGY, 1993, 122 (04) :961-972
[5]   RECEPTOR PROTEIN-TYROSINE-PHOSPHATASE PTP-MU ASSOCIATES WITH CADHERINS AND CATENINS IN-VIVO [J].
BRADYKALNAY, SM ;
RIMM, DL ;
TONKS, NK .
JOURNAL OF CELL BIOLOGY, 1995, 130 (04) :977-986
[6]   Antigen retrieval in cryostat tissue sections and cultured cells by treatment with sodium dodecyl sulfate (SDS) [J].
Brown, D ;
Lydon, J ;
McLaughin, M ;
StuartTilley, A ;
Tyszkowski, R ;
Alper, S .
HISTOCHEMISTRY AND CELL BIOLOGY, 1996, 105 (04) :261-267
[7]   Increased proteolytic processing of protein tyrosine phosphatase mu in confluent vascular endothelial cells: The role of PC5, a member of the subtilisin family [J].
Campan, M ;
Yoshizumi, M ;
Seidah, NG ;
Lee, ME ;
Bianchi, C ;
Haber, E .
BIOCHEMISTRY, 1996, 35 (12) :3797-3802
[8]  
DAMORE PA, 1992, AM J RESP CELL MOL, V6, P1
[9]  
DUMONT DJ, 1992, ONCOGENE, V7, P1471
[10]   DOMINANT-NEGATIVE AND TARGETED NULL MUTATIONS IN THE ENDOTHELIAL RECEPTOR TYROSINE KINASE, TEK, REVEAL A CRITICAL ROLE IN VASCULOGENESIS OF THE EMBRYO [J].
DUMONT, DJ ;
GRADWOHL, G ;
FONG, GH ;
PURI, MC ;
GERTSENSTEIN, M ;
AUERBACH, A ;
BREITMAN, ML .
GENES & DEVELOPMENT, 1994, 8 (16) :1897-1909