Bmx tyrosine kinase is specifically expressed in the endocardium and the endothelium of large arteries

被引:69
作者
Ekman, N [1 ]
Lymboussaki, A [1 ]
Vastrik, I [1 ]
Sarvas, K [1 ]
Kaipainen, A [1 ]
Alitalo, K [1 ]
机构
[1] UNIV HELSINKI, MOLEC CANC BIOL LAB, HAARTMAN INST, FIN-00014 HELSINKI, FINLAND
关键词
genes; signal transduction; endocardium; endothelium;
D O I
10.1161/01.CIR.96.6.1729
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The growth and differentiation of endothelial cells are regulated by signal transduction through tyrosine protein kinases. Recently, a novel cytoplasmic tyrosine kinase gene, Bmx (Bone Marrow tyrosine kinase gene in chromosome X), was identified in human bone marrow RNA and found to be expressed predominantly in myeloid hematopoietic cell lineages. Our preliminary analyses indicated that the Bmx gene was also highly expressed in human heart. Methods and Results Mouse Bmx cDNA was isolated, sequenced, and found to encode a polypeptide approximate to 91% identical to the human Bmx tyrosine kinase. Northern blotting and in situ hybridization of tissue sections indicated that Bmx mRNA is specifically expressed in the endocardium of the developing heart as well as in the endocardium of the left ventricle and in the endothelium of large arteries in adult mice. A weak signal was seen also in coronary arterial endothelium. Conclusions Bmx shows a unique specificity of expression among tyrosine kinase genes and may be involved in signal transduction in endocardial and arterial endothelial cells. The results suggest that specific signal transduction mechanisms are present in such endothelia.
引用
收藏
页码:1729 / 1732
页数:4
相关论文
共 11 条
[1]   THE BRUTON TYROSINE KINASE GENE IS EXPRESSED THROUGHOUT B-CELL DIFFERENTIATION, FROM EARLY PRECURSOR B-CELL STAGES PRECEDING IMMUNOGLOBULIN GENE REARRANGEMENT UP TO MATURE B-CELL STAGES [J].
DEWEERS, M ;
VERSCHUREN, MCM ;
KRAAKMAN, MEM ;
MENSINK, RGJ ;
SCHUURMAN, RKB ;
VANDONGEN, JJM ;
HENDRIKS, RW .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (12) :3109-3114
[2]  
GIBSON S, 1993, BLOOD, V82, P1561
[3]   THE RELATED FLT4, FLT1, AND KDR RECEPTOR TYROSINE KINASES SHOW DISTINCT EXPRESSION PATTERNS IN HUMAN FETAL ENDOTHELIAL-CELLS [J].
KAIPAINEN, A ;
KORHONEN, J ;
PAJUSOLA, K ;
APRELIKOVA, O ;
PERSICO, MG ;
TERMAN, BI ;
ALITALO, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (06) :2077-2088
[4]  
Kaukonen J, 1996, BRIT J HAEMATOL, V94, P455
[5]  
MANO H, 1990, ONCOGENE, V5, P1781
[6]   THE PH DOMAIN - A COMMON PIECE IN THE STRUCTURAL PATCHWORK OF SIGNALING PROTEINS [J].
MUSACCHIO, A ;
GIBSON, T ;
RICE, P ;
THOMPSON, J ;
SARASTE, M .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (09) :343-348
[7]   ENDOTHELIAL RECEPTOR TYROSINE KINASES INVOLVED IN ANGIOGENESIS [J].
MUSTONEN, T ;
ALITALO, K .
JOURNAL OF CELL BIOLOGY, 1995, 129 (04) :895-898
[8]  
SOMMERS CL, 1995, ONCOGENE, V11, P245
[9]  
TAMAGNONE L, 1994, ONCOGENE, V9, P3683
[10]   BINDING OF BETA-GAMMA-SUBUNITS OF HETEROTRIMERIC G-PROTEINS TO THE PH DOMAIN OF BRUTON TYROSINE KINASE [J].
TSUKADA, S ;
SIMON, MI ;
WITTE, ON ;
KATZ, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (23) :11256-11260