Abstract
Selective inheritance of sub-cellular components has emerged as a mechanism guiding stem cell fate after asymmetric cell divisions. Peroxisomes play a crucial role in multiple metabolic processes such as fatty acid metabolism and reactive oxygen species detoxification, but the apportioning of peroxisomes during stem cell division remains understudied. Here, we develop a mouse model and labeling technique to follow the dynamics of distinct peroxisome age-classes, and find that old peroxisomes are inherited by the daughter cell retaining full stem cell potency in mammary and epidermal stem cell divisions. Old peroxisomes carry Glucose-6-phosphate-dehydrogenase, whose specific location on the peroxisomal membrane promotes stem cell function by facilitating peroxisomal ether lipid synthesis. Our study demonstrates age-selective apportioning of peroxisomes in vivo, and unveils how functional heterogeneity of peroxisomes is utilized by asymmetrically dividing cells to metabolically divert the fate of the two daughter cells.
© 2025. The Author(s).
MeSH terms
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Animals
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Asymmetric Cell Division* / physiology
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Cell Self Renewal*
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Epithelial Cells* / cytology
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Epithelial Cells* / metabolism
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Female
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Glucosephosphate Dehydrogenase* / genetics
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Glucosephosphate Dehydrogenase* / metabolism
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Mammary Glands, Animal / cytology
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Mice
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Mice, Inbred C57BL
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Peroxisomes* / enzymology
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Peroxisomes* / metabolism
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Stem Cells* / cytology
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Stem Cells* / metabolism
Substances
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Glucosephosphate Dehydrogenase
Grants and funding
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ERC, #677809, and #101045009/EC | EC Seventh Framework Programm | FP7 Ideas: European Research Council (FP7-IDEAS-ERC - Specific Programme: "Ideas" Implementing the Seventh Framework Programme of the European Community for Research, Technological Development and Demonstration Activities (2007 to 2013))
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#266869, #304591, #312436, #320185/Academy of Finland (Suomen Akatemia)
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2018-03078, 2018-02963, 2022-01304/Vetenskapsrådet (Swedish Research Council)
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190634, 180681, and 222499/Cancerfonden (Swedish Cancer Society)
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KAW 2014.0207 and 20220054/Knut och Alice Wallenbergs Stiftelse (Knut and Alice Wallenberg Foundation)