MitoSwap – Mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiation

Differentiating stem cells must adapt their mitochondrial metabolism to fit the needs of the mature differentiated cell. In a recent study, we observed that during differentiation to an endothelial phenotype, pluripotent stem cell mitochondria are removed by mitophagy, triggering compensatory mitoch...

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Main Authors: Priyanka Gajwani, Jalees Rehman
Format: Article
Language:English
Published: Taylor & Francis Group 2022-12-01
Series:Autophagy Reports
Subjects:
Online Access:http://dx.doi.org/10.1080/27694127.2022.2071549
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author Priyanka Gajwani
Jalees Rehman
author_facet Priyanka Gajwani
Jalees Rehman
author_sort Priyanka Gajwani
collection DOAJ
description Differentiating stem cells must adapt their mitochondrial metabolism to fit the needs of the mature differentiated cell. In a recent study, we observed that during differentiation to an endothelial phenotype, pluripotent stem cell mitochondria are removed by mitophagy, triggering compensatory mitochondrial biogenesis to replenish the mitochondrial pool. We identified the mitochondrial phosphatase PGAM5 as the link between mitophagy and transcription of the mitochondrial biogenesis regulator PPARGC1A/PGC1α in the nucleus. Swapping of mitochondria through the coupled processes of mitophagy and mitochondrial biogenesis lead to enhanced metabolic reprogramming in the differentiated cell.
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spelling doaj.art-1f3563376ea047729a2c74752fa9f4492023-09-14T13:24:40ZengTaylor & Francis GroupAutophagy Reports2769-41272022-12-011121021310.1080/27694127.2022.20715492071549MitoSwap – Mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiationPriyanka Gajwani0Jalees Rehman1University of Illinois, College of MedicineUniversity of Illinois, College of MedicineDifferentiating stem cells must adapt their mitochondrial metabolism to fit the needs of the mature differentiated cell. In a recent study, we observed that during differentiation to an endothelial phenotype, pluripotent stem cell mitochondria are removed by mitophagy, triggering compensatory mitochondrial biogenesis to replenish the mitochondrial pool. We identified the mitochondrial phosphatase PGAM5 as the link between mitophagy and transcription of the mitochondrial biogenesis regulator PPARGC1A/PGC1α in the nucleus. Swapping of mitochondria through the coupled processes of mitophagy and mitochondrial biogenesis lead to enhanced metabolic reprogramming in the differentiated cell.http://dx.doi.org/10.1080/27694127.2022.2071549ctnnb1/β-catenindifferentiationendotheliummitochondrial biogenesismitofusin 2mitophagypink1ppargc1a/pgc1αstem cells
spellingShingle Priyanka Gajwani
Jalees Rehman
MitoSwap – Mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiation
Autophagy Reports
ctnnb1/β-catenin
differentiation
endothelium
mitochondrial biogenesis
mitofusin 2
mitophagy
pink1
ppargc1a/pgc1α
stem cells
title MitoSwap – Mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiation
title_full MitoSwap – Mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiation
title_fullStr MitoSwap – Mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiation
title_full_unstemmed MitoSwap – Mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiation
title_short MitoSwap – Mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiation
title_sort mitoswap mitophagy partnered with compensatory mitochondrial biogenesis during stem cell differentiation
topic ctnnb1/β-catenin
differentiation
endothelium
mitochondrial biogenesis
mitofusin 2
mitophagy
pink1
ppargc1a/pgc1α
stem cells
url http://dx.doi.org/10.1080/27694127.2022.2071549
work_keys_str_mv AT priyankagajwani mitoswapmitophagypartneredwithcompensatorymitochondrialbiogenesisduringstemcelldifferentiation
AT jaleesrehman mitoswapmitophagypartneredwithcompensatorymitochondrialbiogenesisduringstemcelldifferentiation