Genre
- Journal Article
Understanding the mechanisms that regulate nephron progenitors during kidney development should aid development of therapies for renal failure. MicroRNAs, which modulate gene expression through post-transcriptional repression of specific target mRNAs, contribute to the differentiation of stem cells, but their role in nephrogenesis is incompletely understood. Here, we found that the loss of miRNAs in nephron progenitors results in a premature depletion of this population during kidney development. Increased apoptosis and expression of the pro-apoptotic protein Bim accompanied this depletion. Profiling of miRNA expression during nephrogenesis identified several highly expressed miRNAs (miR-10a, miR-106b, miR-17-5p) in nephron progenitors that are either known or predicted to target Bim. We propose that modulation of apoptosis by miRNAs may determine congenital nephron endowment. Furthermore, our data implicate the pro-apoptotic protein Bim as a miRNA target in nephron progenitors.
Department of Medicine, Children's Hospital Boston, MA, USA.
United States
American Society of Nephrology : Washington, DC
Accession Number: 21546576. Language: English. Language Code: eng. Date Revised: 20120601. Date Created: 20110601. Date Completed: 20110825. Update Code: 20120604. Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't. Journal ID: 9013836. Publication Model: Print-Electronic. Cited Medium: Internet. NLM ISO Abbr: J. Am. Soc. Nephrol. PubMed Central ID: PMC3103725 Linking ISSN: 10466673. Subset: IM. Date of Electronic Publication: 2011 May 05; ID: 21546576
Language
- English
Subjects
- Apoptosis Regulatory Proteins/genetics
- Kidney/cytology
- Mice, Transgenic
- Cell Proliferation
- Gene Expression Profiling
- MicroRNAs/*physiology
- Apoptosis/physiology
- Stem Cells/*physiology
- Membrane Proteins/genetics
- animals
- Stem Cells/cytology
- Membrane Proteins/*physiology
- Male
- Models, Animal
- Proto-Oncogene Proteins/genetics
- Apoptosis Regulatory Proteins/*physiology
- Kidney/*embryology
- Pregnancy
- Mice
- Cell Differentiation/physiology
- Proto-Oncogene Proteins/*physiology
- Kidney/*physiology
- Mice, Mutant Strains
- Female