Defective Glomerulogenesis in the Absence of Laminin alpha 5 Demonstrates a Developmental Role for the Kidney Glomerular Basement Membrane
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...
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Veröffentlicht in: | Developmental biology 2000-01, Vol.217 (2), p.278-289 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 0012-1606 |
DOI: | 10.1006/dbio.1999.9546 |