State Key Laboratory of Food Science and Technology, China-Canada Joint Lab of Food Science and Technology (Nanchang), Nanchang University, 235 Nanjing East Road, Nanchang, Jiangxi 330047, China.
Key Laboratory of Coarse Cereal Processing (Ministry of Agriculture and Rural Affairs), School of Food and Biological Engineering, Chengdu University, Chengdu 610106, China.
Food Funct. 2021 Nov 1;12(21):10524-10537. doi: 10.1039/d1fo00987g.
The release of lysosomal hydrolase into the cytoplasm is accompanied by several systems of apoptosis signal transduction, and the imbalance between cell viability and apoptosis induces tumorigenesis. Tea polysaccharides (TPs) are the main bioactive components in green tea with hopeful anti-tumor efficacy, while their mechanism is still unclear. Here, TPs significantly promoted the death of colon cancer cell line CT26. RNA-seq results showed that the signal pathways up-regulated by TPs included lysosome pathways, apoptosis, the release of mitochondrial pigment c and programmed cell death. Among them, the results of AO-EB and annexin V-FITC/PI double staining indicated that TPs significantly up-regulated apoptosis. In addition, TPs significantly disrupted the function of lysosomes, which would cause mitochondrial damage. Intriguingly, TPs treatment increased the expression of Bak1, cleaved caspase-9 and cleaved caspase-3, but decreased the level of Bcl-2 and mitochondrial membrane potential, which indicated that TPs induced mitochondrial-mediated apoptosis. Moreover, TPs ameliorated the reduced lysosomal numbers by Baf A1 (lysosomal inhibitor). Therefore, our data indicated that TPs targeted lysosomes and induced apoptosis by a lysosomal-mitochondrial pathway mediated caspase cascade, thereby inhibiting the proliferation of CT26 cells. In short, the data would help the development of TPs as potential cancer drug therapeutics.
溶酶体水解酶释放到细胞质中伴随着几种细胞凋亡信号转导系统,细胞活力和细胞凋亡之间的失衡会导致肿瘤的发生。茶多糖(TPs)是绿茶中主要的生物活性成分,具有有希望的抗肿瘤功效,但其作用机制尚不清楚。在这里,TPs 显著促进了结肠癌细胞系 CT26 的死亡。RNA-seq 结果表明,TPs 上调的信号通路包括溶酶体途径、细胞凋亡、线粒体色素 c 的释放和程序性细胞死亡。其中,AO-EB 和 annexin V-FITC/PI 双重染色的结果表明 TPs 显著促进了细胞凋亡。此外,TPs 显著破坏了溶酶体的功能,从而导致线粒体损伤。有趣的是,TPs 处理增加了 Bak1、cleaved caspase-9 和 cleaved caspase-3 的表达,但降低了 Bcl-2 和线粒体膜电位的水平,这表明 TPs 诱导了线粒体介导的细胞凋亡。此外,TPs 改善了 Baf A1(溶酶体抑制剂)引起的溶酶体数量减少。因此,我们的数据表明,TPs 通过溶酶体-线粒体途径介导的半胱天冬酶级联反应靶向溶酶体并诱导细胞凋亡,从而抑制 CT26 细胞的增殖。总之,这些数据有助于将 TPs 开发为潜在的癌症药物治疗剂。