4.6 Article

HucMSC exosome-delivered 14-3-3ζ alleviates ultraviolet radiation-induced photodamage via SIRT1 pathway modulation

Journal

AGING-US
Volume 13, Issue 8, Pages 11542-11563

Publisher

IMPACT JOURNALS LLC

Keywords

exosomes; SIRT1; mesenchymal stem cells; DNA damage; oxidative stress

Funding

  1. National Natural Science Foundation of China [81971757, 82003379]
  2. Zhenjiang Key Laboratory of High Technology Research on Exosomes Foundation and Transformation Application [ss2018003]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions (Phase III)
  4. Tai Shan Young Scholar Foundation of Shandong Province [tsqn201909192]
  5. Shandong Provincial Natural Science Foundation [ZR2020YQ59]

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Research has found that exosomes derived from human umbilical cord mesenchymal stem cells (hucMSC-ex) have antioxidant and anti-inflammatory effects against UV radiation-induced skin photodamage by activating SIRT1 to reduce oxidative stress and promote autophagy, thereby alleviating cytotoxic damage. The delivery of 14-3-3 zeta protein by hucMSC-ex plays a cytoprotective role through modulation of a SIRT1-dependent antioxidant pathway. Overall, hucMSC-ex may serve as a potential agent for preventing or treating UV radiation-induced skin photodamage and aging.
Exosomes derived from human umbilical cord mesenchymal stem cells (hucMSC-ex) are nano-sized membrane-bound vesicles that have been reported to facilitate skin regeneration and repair. However, the roles played by hucMSC-ex in ultraviolet (UV) radiation-induced skin photodamage and the underlying mechanisms remain unknown. To investigate the functions of hucMSC-ex in a rat model of acute skin photodamage, immunofluorescence and immunohistochemical staining, quantitative real-time-polymerase chain reaction (qRT-PCR), western blot, and gene silencing assays were performed. We found that the in vivo subcutaneous injection of hucMSC-ex elicited antioxidant and anti-inflammatory effects against UV radiation-induced DNA damage and apoptosis. Further studies showed that the sirtuin 1 (SIRT1) expression level in skin keratinocytes (HaCaT) decreased in a time- and dose-dependent manner under in vitro UV radiation induced-oxidative stress conditions, which could be reversed by treatment with hucMSC-ex. The activation of SIRT1 significantly attenuated UV- and H2O2-induced cytotoxic damage by inhibiting oxidative stress and promoting the activation of autophagy. Our study found that 14-3-3 zeta protein, which was delivered by hucMSC-ex, exerted a cytoprotective function via the modulation of a SIRT1-dependent antioxidant pathway. Collectively, our findings indicated that hucMSC-ex might represent a new potential agent for preventing or treating UV radiation-induced skin photodamage and aging.

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