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Omics profiling identifies the regulatory functions of the MAPK/ERK pathway in nephron progenitor metabolism

Authors :
Hyuk Nam Kwon
Kristen Kurtzeborn
Vladislav Iaroshenko
Xing Jin
Abigail Loh
Nathalie Escande-Beillard
Bruno Reversade
Sunghyouk Park
Satu Kuure
Veterinary Biosciences
Mitochondrial Morphogenesis
Kidney development
Helsinki Institute of Life Science HiLIFE
STEMM - Stem Cells and Metabolism Research Program
Helsinki Institute of Life Science HiLIFE, Infra
Biosciences
Reversade, Bruno
Kwon, H.N.
Kurtzeborn, K.
Laroshenko, V.
Jin, X.
Loh, A.
Escande-Beillard, N.
Park, S.
Kuure, S.
School of Medicine
Source :
Development
Publication Year :
2022

Abstract

Nephron endowment is defined by fetal kidney growth and crucially dictates renal health in adults. Defects in the molecular regulation of nephron progenitors contribute to only a fraction of reduced nephron mass cases, suggesting alternative causative mechanisms. The importance of MAPK/ERK activation in nephron progenitor maintenance has been previously demonstrated, and here, we characterized the metabolic consequences of MAPK/ERK deficiency. Liquid chromatography/mass spectrometry-based metabolomics profiling identified 42 reduced metabolites, of which 26 were supported by in vivo transcriptional changes in MAPK/ERK-deficient nephron progenitors. Among these, mitochondria, ribosome and amino acid metabolism, together with diminished pyruvate and proline metabolism, were the most affected pathways. In vitro cultures of mouse kidneys demonstrated a dosage-specific function for pyruvate in controlling the shape of the ureteric bud tip, a regulatory niche for nephron progenitors. In vivo disruption of proline metabolism caused premature nephron progenitor exhaustion through their accelerated differentiation in pyrroline-5-carboxylate reductases 1 (Pycr1) and 2 (Pycr2) double-knockout kidneys. Pycr1/Pycr2-deficient progenitors showed normal cell survival, indicating no changes in cellular stress. Our results suggest that MAPK/ERK-dependent metabolism functionally participates in nephron progenitor maintenance by monitoring pyruvate and proline biogenesis in developing kidneys.<br />This work was supported by funds from the Academy of Finland (309997 to S.K.), the Finnish Cultural Foundation (Suomen Kulttuurirahasto; to S.K. and H.N.K.), the Maud Kuistila Foundation (Maud Kuistilan Muistosa?a?tio?; to S.K. and K.K.), Pediatric Cancer Foundation Va?re (Lasten Syo?pa?sa?a?tio? Va?reen; to S.K.), Aamu Pediatric Cancer Foundation (S.K.) and the Orion Research Foundation (Orionin Tutkimussa?a?tio?; K.K.). Open Access funding provided by the Aamu Pediatric Cancer Foundation. Deposited in PMC for immediate release.

Details

Language :
English
Database :
OpenAIRE
Journal :
Development
Accession number :
edsair.doi.dedup.....e99ca7d4d51f452f2e53eaea760b9ddc