帕金
粒体自噬
品脱1
迷迭香酸
细胞生物学
生物
小发夹RNA
乳酰丝汀
张力素
分子生物学
自噬
生物化学
化学
基因敲除
蛋白酶体
蛋白酶体抑制剂
PI3K/AKT/mTOR通路
信号转导
PTEN公司
细胞凋亡
医学
抗氧化剂
疾病
病理
帕金森病
作者
Cheng Cheng,Zhou Sha,Xiang Chen,Wei Zhang,Liyun Shi
出处
期刊:PubMed
日期:2022-12-01
卷期号:47 (23): 6450-6456
被引量:3
标识
DOI:10.19540/j.cnki.cjcmm.20220726.401
摘要
This study aims to explore the molecular mechanism through which rosmarinic acid up-regulates mitophagy and enhances antibacterial immunity activity of macrophages. To be specific, RAW264.7 macrophages were treated with rosmarinic acid and then infected with Staphylococcus aureus. The total mRNA and proteins of the cells were then extracted. The mRNA and protein levels of phosphatase and tensin homolog(PTEN)-induced putative kinase 1(PINK1) were detected by q-PCR and Western blot, respectively. Cell mitochondria isolation kit was employed to isolate mitochondria in macrophages. Recruitment of E3 ubiquitin ligase Parkin to mitochondria and the phosphorylation of Parkin were detected by Western blot. Co-immunoprecipitation and laser confocal microscopy were employed to observe the co-localization of PINK1 and Parkin. Mitochondrial division inhibitor 1(Mdivi-1), small interfering RNA(siRNA)-directed gene knockdown, and plate-colony counting were used to detect the levels of inflammatory cytokines and the intracellular antibacterial ability, in an attempt to confirm that rosmarinic acid promotes antibacterial immunity activity of macrophages through strengthening PINK1/Parkin-mediated mitophagy. The results showed that rosmarinic acid up-regulated the mRNA and protein expression of PINK1, promoted the recruitment of Parkin from cytoplasm to mitochondria and the phosphorylation, and enhanced the interaction between PINK1 and Parkin and their co-localization in macrophages. Blocking mitophagy or knocking PINK1 significantly abrogated the promotion of macrophage antibacterial immune response by rosmarinic acid. In summary, rosmarinic acid enhances antibacterial immunity activity of macrophages through up-regulating PINK1/Parkin-mediated mitophagy.
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