Exendin-4 impairs the autophagic flux to induce apoptosis in pancreatic acinar AR42J cells by down-regulating LAMP

被引:8
|
作者
Li, Zhiqiang [1 ]
Zhu, Shaihong [1 ]
Huang, Lihua [2 ]
Shang, Mingming [1 ]
Yu, Can [1 ]
Zhu, Hongwei [1 ]
Han, Duo [1 ]
Huang, Hui [1 ]
Yu, Xiao [1 ]
Li, Xia [3 ]
机构
[1] Cent S Univ, Xiangya Hosp 3, Dept Hepatopancreatobiliary Surg, Tongzipo Rd 138, Changsha 410013, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp 3, Ctr Med Expt, Changsha 410013, Hunan, Peoples R China
[3] Cent S Univ, Xiangya Hosp 3, Dept Endocrinol, Tongzipo Rd 138, Changsha 410013, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Exendin-4; Pancreas; Impaired autophagy; Apoptosis; RECEPTOR ACTIVATION; GLP-1R AGONIST; THERAPIES; CANCER; TISSUE; DAMAGE; DEATH; RATS; MICE; P62;
D O I
10.1016/j.bbrc.2018.01.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study aimed to explore the mechanism of impaired autophagy flux induced by exendin-4 and its role on cell apoptosis in pancreatic AR42J cells. The AR42J cells were treated with various concentration of exendin-4 for several time points to assess its cytotoxicity by MU assay. Then the AR42J cells were treated by 10pM exendin-4 for 72 h, the cell death was analyzed by flow cytometry and caspase-3 level was examined by Western blot with or without the pretreatment of z-VAD-fmk to testify whether exendin-4 induces the cell apoptosis. The protein levels of LOB, p62 and LAMP-2 were assessed by Western blot, the mRNA level of LAMP-2 was quantified by quantitative PCR in the absence or presence of LAMP-2 over-expression plasmid and the expression and activity of CatB and CatL were tested by ELISA or activity assay methods in AR42J cells treated by exendin-4. The normal rats and the diabetes-model rats by high-fat and high-sugar diet for two month then with streptozotocin intraperitoneally were subcutaneously injected with exendin-4 for 10 weeks to test the expression of LAMP-2 mRNA and protein in the pancreas. Cells pretreated with Bafilomycin A1 were detected for LOB and p62 expressions by Western blot. Cells pretreated by 3-MA were used to assess whether 3-MA can protect from exendin-4 cytotoxicity. We found that exendin-4 can decrease the AR42J cell viability as well as increase the cell death and cleaved caspase-3 level, which all can be inhibited by z-VAD-fmk. Exendin-4 can downregulate the expression of LAMP-2 and then impair the autophagy flux to induce the accumulation of LC3B-II and p62, but cannot change the expression and activity of CatB and CatL Bafilomycin Al almostly have no impact on the change of LOB and p62 protein levels induced by exendin-4. Both 3-MA and overexpressed LAMP-2 can reduce the cytotoxicity of exendin-4. Therefore, we considered the down-regulation of LAMP-2 which can impair the autophagy flux by inhibiting the fusion of autophagosomes with lysosomes to induce the AR42J cell apoptosis as the potential mechanism of chronic pancreatitis induced by exendin-4. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:294 / 301
页数:8
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