Defective glomerulogenesis in the absence of laminin α5 demonstrates a developmental role for the kidney glomerular basement membrane

被引:203
作者
Miner, JH [1 ]
Li, C [1 ]
机构
[1] Washington Univ, Sch Med, Dept Internal Med, Div Renal, St Louis, MO 63110 USA
关键词
laminin; basement membrane; development; kidney glomerulus; urogenital abnormalities;
D O I
10.1006/dbio.1999.9546
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Laminins are major components of all basement membranes. They are a diverse group of alpha/beta/gamma heterotrimers formed from five alpha, three beta, and three gamma chains. Laminin alpha 5 is a widely expressed chain found in many embryonic and adult basement membranes. During embryogenesis, alpha 5 has a role in disparate developmental processes, including neural tube closure, digit septation, and placentation. Here, we analyzed kidney development in Lama5 mutant embryos and found a striking defect in glomerulogenesis associated with an abnormal glomerular basement membrane (GBM). This correlates with failure of the developmental switch in laminin alpha chain deposition in which alpha 5 replaces alpha 1 in the GBM at the capillary loop stage of glomerulogenesis. In the absence of a normal GBM, glomerular epithelial cells were in disarray, and endothelial and mesangial cells were extruded from within the constricting glomerulus, leading to a complete absence of vascularized glomeruli. In addition, a minority of Lama5 mutant mice lacked one or both kidneys, indicating that laminin alpha 5 is also important in earlier kidney development. Our results demonstrate a dual role for laminin alpha 5 in kidney development, illustrate a novel defect in glomerulogenesis, and indicate a heretofore unappreciated developmental role for the GBM in influencing the behavior of epithelial and endothelial cells. (C) 2000 Academic Press.
引用
收藏
页码:278 / 289
页数:12
相关论文
共 55 条
[2]   SELECTIVE IMMUNOREACTIVITIES OF KIDNEY BASEMENT-MEMBRANES TO MONOCLONAL-ANTIBODIES AGAINST LAMININ - LOCALIZATION OF THE END OF THE LONG ARM AND THE SHORT ARMS TO DISCRETE MICRODOMAINS [J].
ABRAHAMSON, DR ;
IRWIN, MH ;
STJOHN, PL ;
PERRY, EW ;
ACCAVITTI, MA ;
HECK, LW ;
COUCHMAN, JR .
JOURNAL OF CELL BIOLOGY, 1989, 109 (06) :3477-3491
[3]   The role of laminins in basement membrane function [J].
Aumailley, M ;
Smyth, N .
JOURNAL OF ANATOMY, 1998, 193 :1-21
[4]   TOWARDS A GENETIC-BASIS FOR KIDNEY DEVELOPMENT [J].
BARD, JBL ;
MCCONNELL, JE ;
DAVIES, JA .
MECHANISMS OF DEVELOPMENT, 1994, 48 (01) :3-11
[5]   IDENTIFICATION OF MUTATIONS IN THE COL4A5 COLLAGEN GENE IN ALPORT SYNDROME [J].
BARKER, DF ;
HOSTIKKA, SL ;
ZHOU, J ;
CHOW, LT ;
OLIPHANT, AR ;
GERKEN, SC ;
GREGORY, MC ;
SKOLNICK, MH ;
ATKIN, CL ;
TRYGGVASON, K .
SCIENCE, 1990, 248 (4960) :1224-1227
[6]  
BERNSTEIN J, 1981, LAB INVEST, V45, P183
[7]   Renal agenesis in mice homozygous for a gene trap mutation in the gene encoding heparan sulfate 2-sulfotransferase [J].
Bullock, SL ;
Fletcher, JM ;
Beddington, RSP ;
Wilson, VA .
GENES & DEVELOPMENT, 1998, 12 (12) :1894-1906
[8]   Self-assembly of laminin isoforms [J].
Cheng, YS ;
Champliaud, MF ;
Burgeson, RE ;
Marinkovich, MP ;
Yurchenco, PD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (50) :31525-31532
[9]   Laminin polymerization induces a receptor-cytoskeleton network [J].
Colognato, H ;
Winkelmann, DA ;
Yurchenco, PD .
JOURNAL OF CELL BIOLOGY, 1999, 145 (03) :619-631
[10]   Collagen COL4A3 knockout: A mouse model for autosomal Alport syndrome [J].
Cosgrove, D ;
Meehan, DT ;
Grunkemeyer, JA ;
Kornak, JM ;
Sayers, R ;
Hunter, WJ ;
Samuelson, GC .
GENES & DEVELOPMENT, 1996, 10 (23) :2981-2992