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大鼠肝脏再生过程中抑制素1的亚细胞分布及其细胞意义

Subcellular distribution of prohibitin 1 in rat liver during liver regeneration and its cellular implication.

作者信息

Sun Qing-Ju, Liu Tao

机构信息

Department of Clinical Laboratory, Navy No. 971 Hospital, Qingdao 266072, Shandong Province, China.

Department of Infectious Diseases, Navy No. 971 Hospital, Qingdao 266071, Shandong Province, China.

出版信息

World J Hepatol. 2024 Jan 27;16(1):65-74. doi: 10.4254/wjh.v16.i1.65.

Abstract

BACKGROUND

The function of prohibitin 1 (Phb1) during liver regeneration (LR) remains relatively unexplored. Our previous research identified downregulation of Phb1 in rat liver mitochondria 24 h after 70% partial hepatectomy (PHx), as determined by subcellular proteomic analysis.

AIM

To investigate the potential role of Phb1 during LR.

METHODS

We examined changes in Phb1 mRNA and protein levels, subcellular distribution, and abundance in rat liver during LR following 70% PHx. We also evaluated mitochondrial changes and apoptosis using electron microscopy and flow cytometry. RNA-interference-mediated knockdown of Phb1 (PHBi) was performed in BRL-3A cells.

RESULTS

Compared with sham-operation control groups, Phb1 mRNA and protein levels in 70% PHx test groups were downregulated at 24 h, then upregulated at 72 and 168 h. Phb1 was mainly located in mitochondria, showed a reduced abundance at 24 h, significantly increased at 72 h, and almost recovered to normal at 168 h. Phb1 was also present in nuclei, with continuous increase in abundance observed 72 and 168 h after 70% PHx. The altered ultrastructure and reduced mass of mitochondria during LR had almost completely recovered to normal at 168 h. PHBi in BRL-3A cells resulted in increased S-phase entry, a higher number of apoptotic cells, and disruption of mitochondrial membrane potential.

CONCLUSION

Phb1 may contribute to maintaining mitochondrial stability and could play a role in regulating cell proliferation and apoptosis of rat liver cells during LR.

摘要

背景

在肝脏再生(LR)过程中,抑制素1(Phb1)的功能仍相对未被充分研究。我们之前的研究通过亚细胞蛋白质组学分析确定,在70%部分肝切除术(PHx)后24小时,大鼠肝脏线粒体中Phb1表达下调。

目的

研究Phb1在肝脏再生过程中的潜在作用。

方法

我们检测了70% PHx后大鼠肝脏再生过程中Phb1 mRNA和蛋白水平、亚细胞分布及丰度的变化。我们还使用电子显微镜和流式细胞术评估了线粒体变化和细胞凋亡情况。在BRL-3A细胞中进行了RNA干扰介导的Phb1基因敲低(PHBi)。

结果

与假手术对照组相比,70% PHx试验组中Phb1 mRNA和蛋白水平在24小时时下调,然后在72小时和168小时时上调。Phb1主要定位于线粒体,其丰度在24小时时降低,在72小时时显著增加,在168小时时几乎恢复正常。Phb1也存在于细胞核中,在70% PHx后72小时和168小时观察到其丰度持续增加。肝脏再生过程中线粒体超微结构改变和质量减少在168小时时几乎完全恢复正常。BRL-3A细胞中的PHBi导致S期进入增加、凋亡细胞数量增多以及线粒体膜电位破坏。

结论

Phb1可能有助于维持线粒体稳定性,并可能在肝脏再生过程中调节大鼠肝细胞的增殖和凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d82/10835489/d5b279fef8a7/WJH-16-65-g001.jpg

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