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Combination of PDGF-BB and adipose-derived stem cells accelerated wound healing through modulating PTEN/AKT pathway
被引:4
|作者:
Lai, Fangyuan
[1
]
Dai, Shijie
[2
]
Zhao, Ye
[1
]
Sun, Yi
[1
]
机构:
[1] Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Ctr Plast & Reconstruct Surg, Dept Plast & Reconstruct Surg,Affiliated Peoples H, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Chinese Med Univ, Coll Pharm, Hangzhou, Zhejiang, Peoples R China
来源:
关键词:
Adipose-derived stem cells;
PDGF-BB;
PRP;
Wound healing;
PLATELET-RICH PLASMA;
STROMAL CELLS;
SKIN;
FAT;
D O I:
10.1016/j.injury.2023.02.027
中图分类号:
R4 [临床医学];
学科分类号:
1002 ;
100602 ;
摘要:
Adipose-derived stem cells (ADSCs) have been widely proven to facilitate wound healing. Our study aimed to estimate the influence of combined ADSCs and platelet-derived growth factor-BB (PDGF-BB) on wound healing. We utilized 4 healthy SD rats to isolate ADSCs. Platelet-rich plasma (PRP) was ac-quired utilizing a two-step centrifugation technology. The role of PRP, PDGF-BB, and PDGF-BB combined with a PI3k inhibitor LY294002 on the viability, migration, and PTEN/AKT pathway in ADSCs were exam-ined utilizing CCK-8, Transwell, and western blot assays. Then, we constructed an open trauma model in SD rats. Effects of ADSCs treated with PDGF-BB on pathological changes, CD31, and PTEN/AKT pathway of wound closure were assessed by hematoxylin & eosin (H&E) staining, Masson staining, immunohisto-chemical, and western blot assays, respectively. PRP and PDGF-BB intensified the viability and migration of ADSCs by modulating the PTEN/AKT pathway. Interestingly, LY294002 reversed the role of PDGF-BB on ADSCs. In vivo experiments, combined intervention with ADSCs plus PDGF-BB/PRP facilitated wound closure and ameliorated histological injury. Moreover, combined intervention with ADSCs and PDGF-BB attenuated the PTEN level and elevated the CD31 level as well as the ratio of p-AK T/AK T in the skin tis-sues. A combination of ADSCs and PDGF-BB facilitated wound healing might associate with the regulation of the PTEN/AKT pathway. (c) 2023 Published by Elsevier Ltd.
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页码:1451 / 1461
页数:11
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