Zhu Chunhui, Zhao Ying, Pei Dandan, Liu Zhongbo, Liu Jin, Li Ye, Yu Shuchen, Ma Lingyan, Sun Junyi, Li Ang
Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, No. 98, Xiwu Road, Xincheng District, Xi'an, 710004, China.
Department of Periodontology, College of Stomatology, Xi'an Jiaotong University, Xi'an, China.
BMC Oral Health. 2022 Apr 26;22(1):144. doi: 10.1186/s12903-022-02167-5.
Oxidative stress mediated by hyperglycemia damages cell-reparative processes such as mitophagy. Down-regulation of mitophagy is considered to be a susceptible factor for diabetes mellitus (DM) and its complications. However, the role of mitophagy in DM-associated periodontitis has not been fully elucidated. Apoptosis of human gingival epithelial cells (hGECs) is one of the representative events of DM-associated periodontitis. Thus, this study aimed to investigate PTEN-induced putative kinase 1 (PINK1)-mediated mitophagy activated in the process of high glucose (HG)-induced hGECs apoptosis.
For dose-response studies, hGECs were incubated in different concentrations of glucose (5.5, 15, 25, and 50 mmol/L) for 48 h. Then, hGECs were challenged with 25 mmol/L glucose for 12 h and 48 h, respectively. Apoptosis was detected by TdT-mediated dUTP nick end labeling (TUNEL), caspase 9 and mitochondrial membrane potential (MMP). Subsequently, autophagy was evaluated by estimating P62, LC3 II mRNA levels, LC3 fluorescent puncta and LC3-II/I ratio. Meanwhile, the involvement of PINK1-mediated mitophagy was assessed by qRT-PCR, western blotting and immunofluorescence. Finally, hGECs were transfected with shPINK1 and analyzed by MMP, caspase 9 and annexin V-FITC apoptosis.
The number of TUNEL-positive cells and caspase 9 protein were significantly increased in cells challenged with HG (25 mmol/L) for 48 h (HG 48 h). MMP was impaired both at HG 12 h and HG 48 h, but the degree of depolarization was more serious at HG 48 h. The autophagy improved as the amount of LC3 II increased and p62 decreased in HG 12 h. During this process, HG 12 h treatment induced PINK1-mediated mitophagy. PINK1 silencing with HG 12 h resulted in MMP depolarization and cell apoptosis.
These results suggested that loss of the PINK1 gene may cause mitochondrial dysfunction and increase sensitivity to HG-induced apoptosis of hGECs at the early stage. PINK1 mediated mitophagy attenuates early apoptosis of gingival epithelial cells induced by high glucose.
高血糖介导的氧化应激会损害细胞修复过程,如线粒体自噬。线粒体自噬下调被认为是糖尿病及其并发症的一个易感因素。然而,线粒体自噬在糖尿病相关性牙周炎中的作用尚未完全阐明。人牙龈上皮细胞(hGECs)凋亡是糖尿病相关性牙周炎的代表性事件之一。因此,本研究旨在探讨磷酸酶和张力蛋白同源物(PTEN)诱导的假定激酶1(PINK1)介导的线粒体自噬在高糖(HG)诱导的hGECs凋亡过程中的激活情况。
在剂量反应研究中,将hGECs在不同浓度的葡萄糖(5.5、15、25和50 mmol/L)中孵育48小时。然后,分别用25 mmol/L葡萄糖处理hGECs 12小时和48小时。通过末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法(TUNEL)、半胱天冬酶9和线粒体膜电位(MMP)检测细胞凋亡。随后,通过评估P62、微管相关蛋白1轻链3 II(LC3 II)mRNA水平、LC3荧光斑点和LC3-II/I比值来评估自噬。同时,通过定量逆转录聚合酶链反应(qRT-PCR)、蛋白质印迹法和免疫荧光评估PINK1介导的线粒体自噬的参与情况。最后,用短发夹RNA靶向PINK1(shPINK1)转染hGECs,并通过MMP、半胱天冬酶9和膜联蛋白V-异硫氰酸荧光素(annexin V-FITC)凋亡分析。
在25 mmol/L高糖处理48小时(HG 48小时)的细胞中,TUNEL阳性细胞数量和半胱天冬酶9蛋白显著增加。在HG 12小时和HG 48小时时MMP均受损,但在HG 48小时时去极化程度更严重。在HG 12小时时,随着LC3 II含量增加和p62减少,自噬得到改善。在此过程中,HG 12小时处理诱导了PINK1介导的线粒体自噬。在HG 12小时时沉默PINK1导致MMP去极化和细胞凋亡。
这些结果表明,PINK1基因缺失可能导致线粒体功能障碍,并在早期增加hGECs对HG诱导凋亡的敏感性。PINK1介导的线粒体自噬减轻了高糖诱导的牙龈上皮细胞早期凋亡。