Anuria, omphalocele, and perinatal lethality in mice lacking the CD34-related protein podocalyxin

被引:254
作者
Doyonnas, R
Kershaw, DB
Duhme, C
Merkens, H
Chelliah, S
Graf, T
McNagny, KM
机构
[1] Univ British Columbia, Biomed Res Ctr, Vancouver, BC V6T 1Z3, Canada
[2] Univ Michigan, Med Ctr, Dept Pediat, Ann Arbor, MI 48109 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Bronx, NY 10461 USA
关键词
sialomucin; umbilical hernia; podocyte; hematopoiesis; vascular endothelium;
D O I
10.1084/jem.194.1.13
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Podocalyxin is a CD34-related sialomucin that is expressed at high levels by podocytes, and also by mesothelial cells, vascular endothelia, platelets, and hematopoietic stem cells. To elucidate the function of podocalyxin, we generated podocalyxin-deficient (podxl(-/-)) mice by homologous recombination. Null mice exhibit profound defects in kidney development and die with 24 hours of birth with anuric renal failure. Although podocytes are present in the glomeruli of the podxl(-/-) mice, they fail to form a foot processes and slit diaphragms and instead exhibit cell-cell junctional complexes (tight and adherens junctions). The corresponding reduction in permeable, glomerular filtration surface area presumably leads to the observed block in urine production. In addition, podxl(-/-) mice frequently display herniation of the gut (omphalocele), suggesting that podocalyxin may be required for retraction of the gut from the umbilical cord during development. Hematopoietic and vascular endothelial cells develop normally in the podocalyxin-deficient mice, possibly through functional compensation by other sialomucins (such as CD34). Our results provide the first example of an essential role for a sialomucin in development and suggest that defects in podocalyxin could play a role in a podocyte dysfunction in renal failure and omphalocele in humans.
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收藏
页码:13 / 27
页数:15
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