Molecular Endocrinology Laboratory, Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee -247667, Uttarakhand, India.
Division of Bacteriology and Mycology, Indian Veterinary Research Institute, Izatnagar-, Bareilly -243122, Uttar Pradesh, India.
J Nutr Biochem. 2018 Jul;57:212-227. doi: 10.1016/j.jnutbio.2018.02.017. Epub 2018 Mar 2.
Kaempferol, a natural flavonoid, has the beneficial effects of preserving pancreatic β-cell mass and function, but its action on β-cell lipid metabolism still remains elusive. Recently, autophagy has been reported to play a major role in lipid metabolism in various cell types, but its role in pancreatic β-cell's lipid metabolism is rarely reported. Here, we investigated the role of kaempferol-induced autophagy in inhibition of lipid stores, ER stress and β-cell dysfunction in palmitic acid-challenged RIN-5F cells and isolated pancreatic islets. The lipid-lowering effect of kaempferol was determined by Oil Red O staining, triglyceride assay, BODIPY labeling, RT-PCR and immunoblot analysis of PLIN2 (the lipid droplet coat protein) expression. Further, the involvement of AMPK/mTOR-mediated lipophagy was established by pharmacological and genetic inhibitors of autophagy and AMPK. The co-localization studies of lipid droplets with autophagosomes/lysosomes by BODIPY-MDC-LysoTracker co-staining, LC3/BODIPY labeling and LC3/PLIN2 double immunolabeling further strengthened the findings. Kaempferol treatment exhibited decreased lipid stores and increased co-localization of lipid droplets with autophagosomes and lysosomes in palmitic acid-challenged β-cells. Moreover, inhibition of autophagy led to decreased co-localization and increased lipid droplets accumulation. Kaempferol-induced alleviation of ER stress and β-cell dysfunctions was established by immunoblot analysis of CHOP-10 (a key mediator of cell death in response to ER stress) and insulin content/secretion analysis respectively. Together, these findings suggest that kaempferol prevents ectopic lipid accumulation and ER stress, thus restoring β-cell function through AMPK-mediated lipophagy. The current data implies that kaempferol may be a potential therapeutic candidate to prevent obesity-linked diabetic complications.
山奈酚是一种天然类黄酮,具有保护胰岛β细胞数量和功能的有益作用,但它对β细胞脂质代谢的作用仍不清楚。最近,自噬被报道在各种细胞类型的脂质代谢中发挥重要作用,但它在胰岛β细胞脂质代谢中的作用很少有报道。在这里,我们研究了山奈酚诱导的自噬在抑制棕榈酸挑战的 RIN-5F 细胞和分离的胰岛中的脂质蓄积、内质网应激和β细胞功能障碍中的作用。通过油红 O 染色、甘油三酯测定、BODIPY 标记、PLIN2(脂滴包被蛋白)表达的 RT-PCR 和免疫印迹分析来确定山奈酚的降脂作用。此外,通过自噬和 AMPK 的药理学和遗传抑制剂确定了 AMPK/mTOR 介导的脂噬作用的参与。通过 BODIPY-MDC-LysoTracker 共染色、LC3/BODIPY 标记和 LC3/PLIN2 双重免疫标记研究脂质滴与自噬体/溶酶体的共定位进一步加强了这一发现。山奈酚处理表现出减少的脂质蓄积和增加的脂滴与自噬体和溶酶体的共定位在棕榈酸挑战的β细胞中。此外,自噬的抑制导致共定位减少和脂质滴积累增加。通过免疫印迹分析 CHOP-10(细胞死亡反应中内质网应激的关键介质)和胰岛素含量/分泌分析分别建立了山奈酚诱导的内质网应激和β细胞功能障碍的缓解作用。总之,这些发现表明,山奈酚可预防异位脂质蓄积和内质网应激,从而通过 AMPK 介导的脂噬恢复β细胞功能。目前的数据表明,山奈酚可能是预防肥胖相关糖尿病并发症的潜在治疗候选物。