Volume 22 Issue 6
Jun.  2024
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GAO Jie, LI Jiangyan, HUANG Hua, ZHANG Lunjun, DENG Rong. Effects of exosomes derived from hepatocellular carcinoma cells on their biological behaviors of proliferation, apoptosis and autophagy[J]. Chinese Journal of General Practice, 2024, 22(6): 936-939. doi: 10.16766/j.cnki.issn.1674-4152.003538
Citation: GAO Jie, LI Jiangyan, HUANG Hua, ZHANG Lunjun, DENG Rong. Effects of exosomes derived from hepatocellular carcinoma cells on their biological behaviors of proliferation, apoptosis and autophagy[J]. Chinese Journal of General Practice, 2024, 22(6): 936-939. doi: 10.16766/j.cnki.issn.1674-4152.003538

Effects of exosomes derived from hepatocellular carcinoma cells on their biological behaviors of proliferation, apoptosis and autophagy

doi: 10.16766/j.cnki.issn.1674-4152.003538
Funds:

 82200661

 2020byzd059

 2020byzd029

  • Received Date: 2024-03-04
    Available Online: 2024-07-22
  •   Objective  Exosomes play an important role in the occurrence and development of hepatocellular carcinoma. This study aims to investigate the effects of exosomes on the proliferation, apoptosis, autophagy, and exosome release of HepG2 hepatocellular carcinoma cells and the related mechanisms.  Methods  Exosomes of HepG2 cells were extracted by ultrafast centrifugation. Exosome morphology, diameter distribution and marker protein expression of HepG2 cells were analyzed by transmission electron microscopy, nanoparticle tracking and Western blotting analysis. After the co-culture of exosomes and HepG2 cells, a CCK-8 kit was used to detect the proliferation of HepG2 cells, the apoptosis of HepG2 cells was detected by flow cytometry, and the expressions of apoptosis-related proteins (Bax, Bcl-2) and autophagy-related proteins (LC3-Ⅱ/LC3-Ⅰ, p62, Beclin-1) were detected by Western blotting.  Results  The morphology of exosomes extracted from HepG2 cells was consistent with the characteristics of exosomes, and the diameter between 30 and 150 nm. The marker proteins Alix and CD63 were significantly expressed. The results of CCK-8 showed that the absorbance of HepG2 cells in the 24 h exosome group was not significantly different from that in the control group(P > 0.05), but the absorbance of the exosome group at 48 hours and 72 hours were higher than that of the control group (P < 0.05). Flow cytometry showed that the apoptosis rate was (14.96±0.28) % in the control group and (11.16±0.50) % in the exosome group, and the apoptosis rate decreased (t=11.485, P < 0.001). Western blotting results showed that compared with the control group, the expression of apoptosis-related protein Bcl-2 in exosome group was up-regulated (P < 0.01), and the expression of Bax was down-regulated (P < 0.01). Autophagy associated protein LC3-Ⅱ/LC3-Ⅰ expression was up-regulated (P < 0.01), Beclin-1 expression was up-regulated (P < 0.05), and p62 expression was down-regulated (P < 0.01).  Conclusion  Exosomes derived from HepG2 cells can promote cell proliferation and inhibit apoptosis by inducing up-regulation of autophagy.

     

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