Kreidberg J A, Donovan M J, Goldstein S L, Rennke H, Shepherd K, Jones R C, Jaenisch R
Division of Nephrology, Children's Hospital, Boston, MA 02115, USA.
Development. 1996 Nov;122(11):3537-47. doi: 10.1242/dev.122.11.3537.
A mutation was targeted to the murine alpha3 integrin gene. Homozygous mutant mice survived to birth, but died during the neonatal period. The mutation caused abnormal kidney and lung development. Mutant kidneys displayed decreased branching of the medullary collecting ducts, although the number of nephrons was not altered. Proximal tubules exhibited two distinct subsets of abnormalities, with the epithelial cells either containing excess lysosomes or becoming microcystic. In addition, glomerular development was markedly affected. In mutant kidneys, the extent of branching of glomerular capillary loops was decreased, with capillary lumina being wider than normal. The glomerular basement membrane was disorganized and glomerular podocytes were unable to form mature foot processes. Branching of the bronchi in lungs of mutant mice was also decreased and the large bronchi extended to the periphery. These results indicate a role for integrin receptors in basement membrane organization and branching morphogenesis.
一个突变被定位到小鼠α3整合素基因上。纯合突变小鼠存活至出生,但在新生儿期死亡。该突变导致肾脏和肺部发育异常。突变的肾脏显示髓质集合管分支减少,尽管肾单位数量未改变。近端小管表现出两种不同的异常亚群,上皮细胞要么含有过多的溶酶体,要么变成微囊状。此外,肾小球发育受到明显影响。在突变的肾脏中,肾小球毛细血管袢的分支程度降低,毛细血管腔比正常的宽。肾小球基底膜紊乱,肾小球足细胞无法形成成熟的足突。突变小鼠肺部支气管的分支也减少,大支气管延伸到外周。这些结果表明整合素受体在基底膜组织和分支形态发生中起作用。