Yuan S H, Liang H, Cai M Y, Xu F, Yuan D, Zheng X B, Li Mxy, Weng J P
Department of Endocrinology, Third Affiliated Hospital, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Diabetology, Guangzhou 510630, China.
Zhonghua Yi Xue Za Zhi. 2016 May 24;96(19):1535-9. doi: 10.3760/cma.j.issn.0376-2491.2016.19.016.
To explore the influence of patatin-like phospholipase domain-containing protein 3 (PNPLA3) on palmitic acid (PA)-induced hepatocyte apoptosis and its mechanism.
Human hepatocarcinoma cell line HepG2 cells were transfected with PNPLA3(WT)-pcDNA3.1 (PNPLA3(WT) group) and PNPLA3(I148M)-pcDNA3.1 (PNPLA3(I148M) group) plasmids respectively to overexpress wild type or mutant type PNPLA3, and cells transfected with empty vector pcDNA3.1 (NC group) were set as control group.After 24 h PA incubation, Oil red staining was used to determine lipid deposition, and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling assay (TUNEL) was used to measure apoptosis.Western blot was used to detect the protein level of endoplasmic reticulum (ER) stress and associated apoptosis.Enzyme-linked immunosorbent assay (ELISA) was used to test lysolecithin (LPC) levels in the cellular supernatant.
After 24 h PA incubation, there was no significant difference in lipid deposition among three groups.Compared to NC group, the cell apoptosis rates of PNPLA3(WT) and PNPLA3(I148M) groups were increased by 2 times and 3 times respectively.The levels of ER stress PRKR-like endoplasmic reticulum kinase (PERK) pathway associated proteins, immunoglobulin-binding protein (BIP), p-PERK, p-eIF2α, and ER stress associated apoptosis pathway proteins, CCAAT/enhancer binding homologous protein (CHOP), p53 upregulated modulator of apoptosis (PUMA), Bax, caspase-3 were higher, and were more significant in PNPLA3(I148M) group.The LPC level in the supernatant of PNPLA3(WT) and PNPLA3(I148M) groups were about 5 times and 1.5 times of NC group respectively after PA incubation.
PNPLA3 may be involved in palmitic acid-induced apoptosis mediated by hepatocyte ER stress through regulating LPC metabolism.
探讨含patatin样磷脂酶结构域蛋白3(PNPLA3)对棕榈酸(PA)诱导的肝细胞凋亡的影响及其机制。
分别用PNPLA3(野生型)-pcDNA3.1(PNPLA3(野生型)组)和PNPLA3(I148M)-pcDNA3.1(PNPLA3(I148M)组)质粒转染人肝癌细胞系HepG2细胞,以过表达野生型或突变型PNPLA3,将转染空载体pcDNA3.1的细胞(NC组)设为对照组。PA孵育24 h后,采用油红染色检测脂质沉积,采用末端脱氧核苷酸转移酶介导的dUTP-生物素缺口末端标记法(TUNEL)检测细胞凋亡。采用蛋白质印迹法检测内质网(ER)应激及相关凋亡的蛋白水平。采用酶联免疫吸附测定(ELISA)检测细胞上清液中溶血卵磷脂(LPC)水平。
PA孵育24 h后,三组脂质沉积无显著差异。与NC组相比,PNPLA3(野生型)组和PNPLA3(I148M)组细胞凋亡率分别增加了2倍和3倍。ER应激蛋白激酶样内质网激酶(PERK)途径相关蛋白、免疫球蛋白结合蛋白(BIP)、p-PERK、p-eIF2α的水平,以及ER应激相关凋亡途径蛋白CCAAT/增强子结合同源蛋白(CHOP)、p53上调凋亡调节因子(PUMA)、Bax、半胱天冬酶-3的水平均升高,且在PNPLA3(I148M)组更显著。PA孵育后,PNPLA3(野生型)组和PNPLA3(I148M)组细胞上清液中LPC水平分别约为NC组的5倍和1.5倍。
PNPLA3可能通过调节LPC代谢参与PA诱导的、由肝细胞ER应激介导的凋亡。