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Pod1 is required in stromal cells for glomerulogenesis
Author(s) -
Cui Shiying,
Schwartz Lois,
Quaggin Susan E.
Publication year - 2003
Publication title -
developmental dynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.634
H-Index - 141
eISSN - 1097-0177
pISSN - 1058-8388
DOI - 10.1002/dvdy.10244
Subject(s) - biology , mesenchyme , stromal cell , ureteric bud , microbiology and biotechnology , embryonic stem cell , in situ hybridization , population , mesenchymal stem cell , kidney development , gene , genetics , gene expression , cancer research , demography , sociology
Pod1 (capsulin/epicardin/Tcf21) is a basic‐helix‐loop‐helix transcription factor that is highly expressed in the mesenchyme of developing organs that include the kidney, lung, gut, and heart. Null Pod1 mice are born but die shortly after birth due to a lack of alveoli in the lungs and cardiac defects. In addition, the kidneys are hypoplastic and demonstrate disrupted branching morphogenesis of the ureteric bud epithelium, a marked reduction in the number of nephrons, a delay in glomerulogenesis, and blood vessel abnormalities. To further dissect the cellular function of Pod1 during kidney development, chimeric mice were generated through aggregations of null Pod1 embryonic stem cells and murine embryos ubiquitously expressing enhanced green fluorescent protein (GFP). Histologic, immunohistochemical, and in situ hybridization analysis of the resulting chimeric offspring demonstrated both cell autonomous and non–cell autonomous roles for Pod1 in the differentiation of specific renal cell lineages that include peritubular interstitial cells and pericytes. Most strikingly, the glomerulogenesis defect was rescued by the presence of wild‐type stromal cells, suggesting a non–cell autonomous role for Pod1 in this cell population. © 2003 Wiley‐Liss, Inc.