Shandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Science, Shandong University, Jinan, P. R. China.
Institute of Organic Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Jinan, P. R. China.
Autophagy. 2020 Jan;16(1):70-85. doi: 10.1080/15548627.2019.1598750. Epub 2019 Apr 7.
Vascular endothelial cells (VECs) that form the inner wall of blood vessels can be injured by high glucose-induced autophagy and apoptosis. Although the role of long noncoding RNA in regulating cell fate has received widespread attention, long noncoding RNAs (lncRNAs) that can both regulate autophagy and apoptosis need to be discovered. In this study, we identified that a small chemical molecule, 3-benzyl-5-([2-nitrophenoxy] methyl)-dihydrofuran-2(3H)-one (3BDO), synthesized by us, could inhibit VEC autophagy and apoptosis induced by a high concentration of glucose. To find new lncRNAs that regulate autophagy and apoptosis in VECs, we performed lncRNA microarray analysis. We found and verified an upregulated lncRNA named that was induced by a high concentration of glucose could be downregulated by 3BDO most obviously among all of the detected lncRNAs. Meanwhile, we investigated the mechanism of in regulating VEC autophagy and apoptosis. The results showed that facilitated endothelial autophagy and apoptosis as a competing endogenous RNA (ceRNA) by decoying and . Further study elucidated that could trigger the decrease of CTNNBIP1 (catenin beta interacting protein 1) by combining with its 3' UTR and then upregulating CTNNB1 (catenin beta 1); inhibited the phosphorylation of AMP-activated protein kinase (AMPK) by targeting and decreasing DPP4 (dipeptidyl peptidase 4). Therefore, and represent new signal pathways that regulate VEC autophagy and apoptosis under the high-glucose condition.: 3BDO: 3-benzyl-5-([2-nitrophenoxy] methyl)-dihydrofuran-2(3H)-one; 3' UTR: 3' untranslated region; AGO2: argonaute RISC catalytic component 2; AMPK: AMP-activated protein kinase/protein kinase AMP-activated; BAX/BCL2L4: BCL2 associated X, apoptosis regulator; BCL2: BCL2 apoptosis regulator; CASP3: caspase 3; ceRNA: competing endogenous RNA; CTNNB1: catenin beta 1; CTNNBIP1/ICAT: catenin beta interacting protein 1; DPP4: dipeptidyl peptidase 4; FGF2/FGF-2: fibroblast growth factor 2; HG: high concentration glucose (30 mM glucose); lncRNA: long noncoding RNA; MAP1LC3B/LC3B: microtubule associated protein 1 light chain 3 beta; miRNA: microRNA; : microRNA 4778-3p; : microRNA 561-3p; : microRNA 5680; : microRNA 877-3p; MTOR: mechanistic target of rapamycin kinase; Mut: mutant; NC: negative control; NG: normal concentration glucose (5.5 mM glucose); PARP1: poly(ADP-ribose) polymerase 1; qPCR: quantitative real-time PCR; RNA-FISH: RNA-fluorescence in situ hybridization; ROS: reactive oxygen species; RT-PCR: reverse transcription polymerase chain reaction; siRNA: small interfering RNA; SQSTM1: sequestosome 1; : TGFB2 overlapping transcript 1; TUNEL: terminal deoxynucleotidyl transferase dUTP nick end labeling; VECs: vascular endothelial cells; WT: wild type.
血管内皮细胞(VECs)形成血管的内壁,可被高葡萄糖诱导的自噬和细胞凋亡损伤。虽然长非编码 RNA 在调节细胞命运方面的作用已经引起了广泛的关注,但需要发现既能调节自噬又能调节凋亡的长非编码 RNA。在这项研究中,我们鉴定出一种小分子,3-苄基-5-([2-硝基苯氧基]甲基)-二氢呋喃-2(3H)-酮(3BDO),由我们合成,可以抑制高浓度葡萄糖诱导的 VEC 自噬和凋亡。为了寻找新的调节 VEC 自噬和凋亡的长非编码 RNA,我们进行了长非编码 RNA 微阵列分析。我们发现并验证了一个上调的长非编码 RNA,命名为,在所有检测到的长非编码 RNA 中,它被高浓度葡萄糖诱导,并且可被 3BDO 最明显地下调。同时,我们研究了在调节 VEC 自噬和凋亡中的作用机制。结果表明,作为竞争内源性 RNA(ceRNA),通过诱饵和 ,促进内皮细胞自噬和凋亡。进一步的研究阐明,通过与 3'UTR 结合并上调 CTNNB1(连接蛋白 beta 1),触发 CTNNBIP1(连接蛋白 beta 互作蛋白 1)的减少;通过靶向并减少 DPP4(二肽基肽酶 4)抑制 AMP 激活蛋白激酶(AMPK)的磷酸化。因此,和代表了在高葡萄糖条件下调节 VEC 自噬和凋亡的新信号通路。:3BDO:3-苄基-5-([2-硝基苯氧基]甲基)-二氢呋喃-2(3H)-酮;3'UTR:3'非翻译区;AGO2:argonaute RISC 催化成分 2;AMPK:AMP 激活蛋白激酶/蛋白激酶 AMP 激活;BAX/BCL2L4:BCL2 相关 X,凋亡调节因子;BCL2:BCL2 凋亡调节因子;CASP3:半胱天冬酶 3;ceRNA:竞争内源性 RNA;CTNNB1:连接蛋白 beta 1;CTNNBIP1/ICAT:连接蛋白 beta 互作蛋白 1;DPP4:二肽基肽酶 4;FGF2/FGF-2:成纤维细胞生长因子 2;HG:高浓度葡萄糖(30 mM 葡萄糖);lncRNA:长非编码 RNA;MAP1LC3B/LC3B:微管相关蛋白 1 轻链 3 beta;miRNA:微 RNA;:微 RNA 4778-3p;:微 RNA 561-3p;:微 RNA 5680;:微 RNA 877-3p;MTOR:雷帕霉素靶蛋白激酶;Mut:突变;NC:阴性对照;NG:正常浓度葡萄糖(5.5 mM 葡萄糖);PARP1:多聚(ADP-核糖)聚合酶 1;qPCR:实时定量 PCR;RNA-FISH:RNA-fluorescence 原位杂交;ROS:活性氧;RT-PCR:逆转录聚合酶链反应;siRNA:小干扰 RNA;SQSTM1:自噬体 1;:TGFB2 重叠转录本 1;TUNEL:末端脱氧核苷酸转移酶 dUTP 缺口末端标记;VECs:血管内皮细胞;WT:野生型。