Von Hippel-Lindau Acts as a Metabolic Switch Controlling Nephron Progenitor Differentiation
Author(s) -
Kasey R. Cargill,
Shelby L. Hemker,
Andrew Clugston,
Anjana Murali,
Elina Mukherjee,
Jiao Liu,
Daniel Bushnell,
Andrew J. Bodnar,
Zubaida Saifudeen,
Jacqueline Ho,
Carlton M. Bates,
Dennis Kostka,
Eric S. Goetzman,
Sunder SimsLucas
Publication year - 2019
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.2018111170
Subject(s) - nephron , progenitor cell , progenitor , medicine , microbiology and biotechnology , endocrinology , cancer research , biology , kidney , stem cell
Nephron progenitors, the cell population that give rise to the functional unit of the kidney, are metabolically active and self-renew under glycolytic conditions. A switch from glycolysis to mitochondrial respiration drives these cells toward differentiation, but the mechanisms that control this switch are poorly defined. Studies have demonstrated that kidney formation is highly dependent on oxygen concentration, which is largely regulated by von Hippel-Lindau (VHL; a protein component of a ubiquitin ligase complex) and hypoxia-inducible factors (a family of transcription factors activated by hypoxia).
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