Cloning of the mouse laminin alpha 4 cDNA. Expression in a subset of endothelium

被引:111
作者
Frieser, M
Nockel, H
Pausch, F
Roder, C
Hahn, A
Deutzmann, R
Sorokin, LM
机构
[1] UNIV ERLANGEN NURNBERG,INST EXPT MED,D-91045 ERLANGEN,GERMANY
[2] UNIV REGENSBURG,DEPT BIOCHEM,D-8400 REGENSBURG,GERMANY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1997年 / 246卷 / 03期
关键词
laminin isoforms; endothelial cell;
D O I
10.1111/j.1432-1033.1997.t01-1-00727.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endothelial cells express a 400-kDa or 240-kDa laminin alpha chain, depending on their tissue of origin or physiological state [1, 2]. Using differential display and subsequent screening of a mouse endothelial cell cDNA library we here identify the gene coding for the 240-kDa laminin chain as the laminin alpha 4 gene. The complete mouse laminin alpha 4 cDNA sequence is reported and compared with other laminin alpha chains. In situ hybridization of embryonic and new born mouse tissues revealed expression of laminin alpha 4 mRNA in a subset of endothelium, in particular aortic endothelium, endocardium and endothelium of blood vessels in the skin and in the brain. Strong laminin alpha 4 expression by aortic endothelia was confirmed by data obtained from cultured bovine aortic endothelial cells (BAEC). Isolation of laminin from BAEC conditioned medium revealed a Y-shaped molecule in rotary shadowing. Subsequent sequencing of BAEC laminin resulted in laminin alpha 4, beta 1 and gamma 1 amino acid sequences, confirming that laminin alpha 4 is one of the major laminin alpha chains expressed by aortic endothelium not only in the mouse. In addition, strong laminin alpha 4 mRNA expression occurred in peripheral nerves, cardiac muscle, fat, the dermis of the skin and lung stroma of mouse tissues. The data demonstrate a cytokine and progesterone-regulated differential expression of laminin alpha 4 mRNA in mouse endothelium, suggesting a distinct functional role for this laminin chain in endothelium.
引用
收藏
页码:727 / 735
页数:9
相关论文
共 31 条
[1]   HERLITZS JUNCTIONAL EPIDERMOLYSIS-BULLOSA IS LINKED TO MUTATIONS IN THE GENE (LAMC2) FOR THE GAMMA-2 SUBUNIT OF NICEIN/KALININ (LAMININ-5) [J].
ABERDAM, D ;
GALLIANO, MF ;
VAILLY, J ;
PULKKINEN, L ;
BONIFAS, J ;
CHRISTIANO, AM ;
TRYGGVASON, K ;
UITTO, J ;
EPSTEIN, EH ;
ORTONNE, JP ;
MENEGUZZI, G .
NATURE GENETICS, 1994, 6 (03) :299-304
[2]  
BECK K, 1992, J MOL BIOL, V231, P311
[3]   CLONING AND EXPRESSION OF LAMININ ALPHA-2 CHAIN (M-CHAIN) IN THE MOUSE [J].
BERNIER, SM ;
UTANI, A ;
SUGIYAMA, S ;
DOI, T ;
POLISTINA, C ;
YAMADA, Y .
MATRIX BIOLOGY, 1995, 14 (06) :447-455
[4]  
DELWEL GO, 1996, ADHESION RECEPTORS T, P9
[5]   STRUCTURAL STUDY OF LONG ARM FRAGMENTS OF LAMININ - EVIDENCE FOR REPETITIVE C-TERMINAL SEQUENCES IN THE A-CHAIN, NOT PRESENT IN THE B-CHAINS [J].
DEUTZMANN, R ;
HUBER, J ;
SCHMETZ, KA ;
OBERBAUMER, I ;
HARTL, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 177 (01) :35-45
[6]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[7]   SHAPES, DOMAIN ORGANIZATIONS AND FLEXIBILITY OF LAMININ AND FIBRONECTIN, 2 MULTIFUNCTIONAL PROTEINS OF THE EXTRACELLULAR-MATRIX [J].
ENGEL, J ;
ODERMATT, E ;
ENGEL, A ;
MADRI, JA ;
FURTHMAYR, H ;
ROHDE, H ;
TIMPL, R .
JOURNAL OF MOLECULAR BIOLOGY, 1981, 150 (01) :97-120
[8]  
Engel J., 1993, MOL CELLULAR ASPECTS, P147, DOI [10.1016/B978-0-12-593165-6.50014-0, DOI 10.1016/B978-0-12-593165-6.50014-0]
[9]   CLONING AND COMPLETE PRIMARY STRUCTURE OF THE MOUSE LAMININ ALPHA-3 CHAIN - DISTINCT EXPRESSION PATTERN OF THE LAMININ ALPHA-3A AND ALPHA-3B CHAIN ISOFORMS [J].
GALLIANO, MF ;
ABERDAM, D ;
AGUZZI, A ;
ORTONNE, JP ;
MENEGUZZI, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (37) :21820-21826
[10]  
HENCHCLIFFE C, 1993, DEVELOPMENT, V118, P325