Department of Anesthesiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China 524001.
Department of Anesthesiology, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan, China 570311.
Oxid Med Cell Longev. 2022 Mar 30;2022:2109891. doi: 10.1155/2022/2109891. eCollection 2022.
Evidence reveals that propofol protects cells via suppressing excessive autophagy induced by hypoxia/reoxygenation (H/R). Previously, we found in a genome-wide microRNA profile analysis that several autophagy-related microRNAs were significantly altered during the process of H/R in the presence or absence of propofol posthypoxia treatment (P-PostH), but how these microRNAs work in P-PostH is still largely unknown. Here, we found that one of these microRNAs, microRNA-30b (miR-30b), in human umbilical vein endothelial cells (HUVECs) was downregulated by H/R treatment but significantly upregulated by 100 M propofol after H/R treatment. miR-30b showed similar changes in open heart surgery patients. By dual-luciferase assay, we found that Beclin-1 is the direct target of miR-30b. This conclusion was also supported by knockdown or overexpression of miR-30b. Further studies showed that miR-30b inhibited H/R-induced autophagy activation. Overexpression or knockdown of miR-30b regulated autophagy-related protein gene expression in vitro. To clarify the specific role of propofol in the inhibition of autophagy and distinguish the induction of autophagy from the damage of autophagy flux, we used bafilomycin A1. LC3-II levels were decreased in the group treated with propofol combined with bafilomycin A1 compared with the group treated with bafilomycin A1 alone after hypoxia and reoxygenation. Moreover, HUVECs transfected with Ad-mCherry-GFP-LC3b confirmed the inhibitory effect of miR-30b on autophagy flux. Finally, we found that miR-30b is able to increase the cellular viability under the H/R condition, partially mimicking the protective effect of propofol which suppressed autophagy via enhancing miR-30b and targeting Beclin-1. Therefore, we concluded that propofol upregulates miR-30b to repress excessive autophagy via targeting Beclin-1 under H/R condition. Thus, our results revealed a novel mechanism of the protective role of propofol during anesthesia. . This trial is registered with ChiCTR-IPR-14005470. The name of the trial register: Propofol Upregulates MicroRNA-30b to Repress Beclin-1 and Inhibits Excessive Autophagy and Apoptosis.
证据表明,异丙酚通过抑制缺氧/复氧(H/R)诱导的过度自噬来保护细胞。先前,我们在全基因组 microRNA 谱分析中发现,在存在或不存在缺氧后异丙酚处理(P-PostH)的情况下,几种自噬相关的 microRNA 在 H/R 过程中显著改变,但这些 microRNA 在 P-PostH 中的作用仍知之甚少。在这里,我们发现其中一种 microRNA,即 microRNA-30b(miR-30b),在人脐静脉内皮细胞(HUVECs)中,H/R 处理后下调,但 H/R 处理后 100 μM 异丙酚显著上调。miR-30b 在心脏手术患者中也表现出类似的变化。通过双荧光素酶报告基因实验,我们发现 Beclin-1 是 miR-30b 的直接靶基因。这一结论也得到了 miR-30b 敲低或过表达的支持。进一步的研究表明,miR-30b 抑制 H/R 诱导的自噬激活。miR-30b 的过表达或敲低可调节体外自噬相关蛋白基因的表达。为了阐明异丙酚在抑制自噬中的具体作用,并区分自噬诱导和自噬流损伤,我们使用了巴弗洛霉素 A1。与单独用巴弗洛霉素 A1 处理的组相比,缺氧和复氧后用异丙酚联合巴弗洛霉素 A1 处理的组中 LC3-II 水平降低。此外,用 Ad-mCherry-GFP-LC3b 转染的 HUVECs 证实了 miR-30b 对自噬流的抑制作用。最后,我们发现 miR-30b 能够在 H/R 条件下增加细胞活力,部分模拟异丙酚通过增强 miR-30b 并靶向 Beclin-1 抑制自噬的保护作用。因此,我们得出结论,异丙酚在 H/R 条件下通过上调 miR-30b 抑制过度自噬,靶向 Beclin-1。因此,我们的结果揭示了异丙酚在麻醉期间发挥保护作用的一种新机制。该试验在中国临床试验注册中心注册,注册号为 ChiCTR-IPR-14005470。试验名称:异丙酚上调 microRNA-30b 抑制 Beclin-1 并抑制过度自噬和细胞凋亡。