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PDI-catalyzed oxidative protein folding mediates senescence by induction of ER-derived oxidative stress

ABSTRACT: Protein homeostasis is linked with aging and aging associated diseases. Oxidative protein folding occurs in the endoplasmic reticulum (ER) and produces H2O2 as a byproduct. The role of oxidative protein folding in human stem cells aging remains unknown. Here, we succeed to knockout protein disulfide isomerase (PDI), a key oxidoreductase for catalyzing oxidative protein folding, in human embryonic stem cells (hESCs) and human mesenchymal stem cells (hMSCs). Deletion of PDI does not affect the self-renewal of hESCs but significantly delays hMSCs senescence. Mechanistically, knockout of PDI slows down the rate of oxidative protein folding and decreases the leakage of ER-derived H2O2 into the nucleus, therefore alleviating oxidative stress and the secretory-associated senescence phenotype (SASP). Among the SASP-related genes, SERPINE1 is identified as a key driver for cell senescence. These findings establish a novel link between oxidative protein folding and aging. The previously unrecognized function of PDI in regulating cell senescence provides a potential target for aging and aging-related disease intervention.

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Stem Cell, Cell Culture

SUBMITTER: ji zhao

LAB HEAD: Qianzhao Ji

PROVIDER: PXD037244 | Pride | 2023-06-12

REPOSITORIES: Pride

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			Action	DRS
	BD005LQ_K5_1_P8_Slot2-28_1_14994.d.tar	Other
	BD005LQ_K5_2_P8_Slot2-29_1_14995.d.tar	Other
	BD005LQ_K5_3_P8_Slot2-30_1_14996.d.tar	Other
	BD005LQ_WT_1_P8_Slot2-25_1_14990.d.tar	Other
	BD005LQ_WT_2_P8_Slot2-26_1_14991.d.tar	Other

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