自噬
血管生成
槟榔碱
口腔粘膜下纤维性变
下调和上调
免疫印迹
脐静脉
新生血管
癌症研究
化学
死孢子体1
免疫组织化学
细胞生物学
病理
生物
医学
细胞凋亡
生物化学
受体
体外
基因
毒蕈碱乙酰胆碱受体
作者
Zhuo Dai,Bingyu Zhu,Huiqiao Yu,Xinchun Jian,Jieying Peng,Changyun Fang,Yingfang Wu
标识
DOI:10.1016/j.archoralbio.2019.03.021
摘要
To detect the expression of protein light chain 3 (LC3) and p62-SQSTM1 (p62) in the lamina propria of oral submucous fibrosis (OSF) and to determine the association of autophagy with OSF. To investigate the role of autophagy in angiogenesis of human umbilical vein endothelial cells (HUVECs) and to assess whether this effect was induced by arecoline. LC3 and p62 expression was detected in OSF tissue through immunohistochemistry (IHC). Transmission electron microscopy (TEM) and Western blot were used to investigate the expression of autophagy in HUVECs. The role of autophagy in angiogenesis in HUVECs was investigated using the Matrigel assay. 1: LC3 expression was upregulated in OSF samples. In contrast, p62 was downregulated in early and intermediate stages but upregulated in advanced stages of OSF. 2: HUVECs treated with arecoline exhibited increased autophagosomes, LC3 expression and reduced p62 expression, when co-treated with chloroquine (CQ), which is a specific autophagy inhibitor, revealed the opposite trend. 3: Autophagy inhibited angiogenesis in HUVECs. Our findings suggest that arecoline induces autophagy in HUVECs. The high level of autophagy could reduce cell viability and inhibit angiogenesis in HUVECs, potentially promoting the development of OSF.
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