哈卡特
光老化
化学
丙二醛
富血小板血浆
PI3K/AKT/mTOR通路
蛋白激酶B
超氧化物歧化酶
MAPK/ERK通路
药理学
癌症研究
氧化应激
细胞凋亡
免疫学
信号转导
生物化学
医学
血小板
皮肤病科
体外
作者
Xiao Cui,Yongshi Ma,Hong Wang,Jianfang Huang,Linlin Li,Jianbing Tang,Biao Cheng
摘要
Abstract Platelet‐rich plasma (PRP) has seen wide clinical use owing to its regenerative and repair abilities. Objective: To investigate the anti‐photoaging effects of pre‐ and post‐treatment of PRP on UVB‐damaged HaCaT cells. Methods: HaCaT cells were irradiated with 80 mJ/cm 2 UVB, before or after PRP treatment (1000 × 10 7 /L), and following measurements were taken: survival rate of UVB‐irradiated HaCaT cells, malondialdehyde (MDA) content and activities of glutathione peroxidase (GSH‐Px), superoxide dismutase (SOD) and catalase (CAT). Western blot was used to determine the effect of different PRP intervention on the expression of PI3K, AKT, ERK, MMP‐1, MMP‐9, TIMP‐1 and γ‐H2AX in the UVB‐irradiated HaCaT cells. Results: pre‐ and post‐PRP treatment reduced MDA content and increased the activities of GSH‐Px, SOD and CAT in photoaged HaCaT cells. These changes resulted in reduced cytotoxic effects. Besides, different PRP intervention promoted cell proliferation via PI3K/AKT pathway. Furthermore, PRP application suppressed the expression of γ‐H2AX. Also, PRP intervention alleviated photoaging effects by upregulating the expression level of tissue inhibitor of metalloproteinases‐1 (TIMP‐1) while downregulating matrix metalloproteinase (MMP) expression level in photoaged HaCaT cells. Conclusion: pre‐ and post‐PRP treatment play anti‐photoaging role through strengthening cellular oxidative defense capacity, mitigating MMP expression, alleviating DNA damages and promoting proliferation of UVB‐irradiated HaCaT cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI