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Human embryonic stem cell-derived exosomes promote pressure ulcer healing in aged mice by rejuvenating senescent endothelial cells
- Source :
- Stem Cell Research & Therapy, Vol 10, Iss 1, Pp 1-17 (2019), Stem Cell Research & Therapy
- Publication Year :
- 2019
- Publisher :
- BMC, 2019.
-
Abstract
- Background Angiogenesis, as an endogenous repair mechanism, plays crucial roles in wound healing and tissue regeneration. However, this process is impaired in the elderly due to aging-related vascular endothelial dysfunction. This study was aimed to explore the pro-angiogenic effects of exosomes from human embryonic stem cells (ESC-Exos) in aged mice of pressure-induced ulcer model and the underlying mechanism. Methods Pressure ulcer wounds were created on the back of d-galactose-induced aging mice. ESC-Exos were locally applied onto the wound beds, with PBS as control. The effects of ESC-Exos on wound healing were analyzed by measuring wound closure rates, histological and immunofluorescence analyses. Then, the anti-aging effect of ESC-Exos on vascular endothelial cells was tested in an in vitro d-galactose-induced HUVEC senescence model. Results ESC-Exos could accelerate wound closure and enhance angiogenesis, and the senescence of vascular endothelial cells was significantly ameliorated after ESC-Exos treatment. In vitro, ESC-Exos could rejuvenate the senescence of endothelial cells and recover compromised proliferation, migratory capacity, and tube formation. This recovery was Nrf2-activation-dependent, since cotreatment with Nrf2 inhibitor Brusatol could abolish the rejuvenative effects of ESC-Exos. Further study revealed that miR-200a was highly enriched in ESC-Exos and played a crucial role in ESC-Exos-mediated rejuvenation through downregulating Keap1, which negatively regulates Nrf2 expression. Conclusions ESC-Exos ameliorate endothelial senescence by activating Nrf2 and recover aging-related angiogenic dysfunction, thereby accelerating wound healing in aged mice. ESC-Exos might be a natural nano-biomaterial for aging-related diseases therapy. Electronic supplementary material The online version of this article (10.1186/s13287-019-1253-6) contains supplementary material, which is available to authorized users.
- Subjects :
- 0301 basic medicine
Cancer Research
Angiogenesis
Human Embryonic Stem Cells
Medicine (miscellaneous)
Endogeny
Exosomes
Mice
0302 clinical medicine
Immunology and Allergy
lcsh:QD415-436
Endothelial dysfunction
Genetics (clinical)
Cellular Senescence
reproductive and urinary physiology
Pressure Ulcer
Tube formation
lcsh:R5-920
Kelch-Like ECH-Associated Protein 1
Gene Expression Regulation, Developmental
Cell biology
Oncology
030220 oncology & carcinogenesis
embryonic structures
Molecular Medicine
Stem cell
biological phenomena, cell phenomena, and immunity
lcsh:Medicine (General)
Senescence
Embryonic stem cells
NF-E2-Related Factor 2
Immunology
Neovascularization, Physiologic
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Nrf2
lcsh:Biochemistry
03 medical and health sciences
Human Umbilical Vein Endothelial Cells
medicine
Animals
Humans
Regeneration
Transplantation
Wound Healing
business.industry
Research
fungi
Endothelial Cells
Cell Biology
medicine.disease
Embryonic stem cell
Microvesicles
carbohydrates (lipids)
MicroRNAs
030104 developmental biology
Cancer research
business
Wound healing
Subjects
Details
- Language :
- English
- ISSN :
- 17576512
- Volume :
- 10
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Stem Cell Research & Therapy
- Accession number :
- edsair.doi.dedup.....66478fe8eb66d98cab0a212b3012e1df
- Full Text :
- https://doi.org/10.1186/s13287-019-1253-6