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模拟微重力通过下调 LMO2 和 EZH2 改变库普弗细胞的基因表达谱,并在早期抑制其增殖。

Simulated microgravity altered the gene expression profiles and inhibited the proliferation of Kupffer cells in the early phase by downregulating LMO2 and EZH2.

机构信息

Department of General Surgery, The 306th Hospital of PLA-Peking University Teaching Hospital, Beijing, 100101, China.

Department of General Surgery, Strategic Support Force Medical Center, Beijing, 100101, China.

出版信息

Life Sci Space Res (Amst). 2024 Feb;40:21-34. doi: 10.1016/j.lssr.2023.11.002. Epub 2023 Nov 17.

DOI:10.1016/j.lssr.2023.11.002
PMID:38245345
Abstract

Microgravity is a primary challenge that need to overcome, when human travel to space. Our study provided evidence that Kupffer cells (KCs) are sensitive to simulated microgravity (SMG), and no similar research report has been found in the literature. Using transcriptome sequencing technology, it was showed that 631 genes were upregulated and 801 genes were downregulated in KCs after treatment under SMG for 3 days. The GO analysis indicated that the proliferation of KCs was affected when exposed to SMG for 3 days. CCK-8 assay confirmed that the proliferation of KCs was inhibited in the third day under the environment of SMG. Furthermore, we identified 8 key genes that affect the proliferation of KCs and predicted 2 transcription factors (TFs) that regulate the 8 key genes. Significantly, we found that microgravity could affect the expression of LMO2 and EZH2 to reduce the transcription of Racgap1, Ccna2, Nek2, Aurka, Plk1, Haus4, Cdc20, Bub1b, which resulting in the reduction in KCs proliferation. These finding suggested that the inhibition of KCs proliferation under microgravity may influence the homeostasis of liver, and LMO2 and EZH2 can be the targets in management of KCs' disturbance in the future practice of space medicine.

摘要

微重力是人类太空旅行需要克服的主要挑战。我们的研究提供了证据表明枯否细胞(KCs)对模拟微重力(SMG)敏感,文献中没有类似的研究报告。使用转录组测序技术,发现在 SMG 处理 3 天后,KCs 中有 631 个基因上调和 801 个基因下调。GO 分析表明,KCs 在暴露于 SMG 3 天后增殖受到影响。CCK-8 测定证实,在 SMG 环境下第 3 天 KCs 的增殖受到抑制。此外,我们鉴定出 8 个影响 KCs 增殖的关键基因,并预测了调节这 8 个关键基因的 2 个转录因子(TFs)。重要的是,我们发现微重力可能会影响 LMO2 和 EZH2 的表达,从而降低 Racgap1、Ccna2、Nek2、Aurka、Plk1、Haus4、Cdc20、Bub1b 的转录,导致 KCs 增殖减少。这些发现表明,微重力下 KCs 增殖的抑制可能会影响肝脏的内稳态,LMO2 和 EZH2 可能成为未来太空医学实践中管理 KCs 紊乱的靶点。

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