大鼠肝再生的肝细胞凋亡中Kruppel样因子4 mRNA、微小RNA-881-3p、环状RNA_20298和环状RNA_14826的表达变化与作用

林凯琳 杨献光 王子慧 臧夏炎 薛奇杰 韩璐 张春博 赵志虎 徐存拴

解剖学报 ›› 2023, Vol. 54 ›› Issue (4) : 420-424.

PDF(2042 KB)
欢迎访问《解剖学报》官方网站!今天是 English
PDF(2042 KB)
解剖学报 ›› 2023, Vol. 54 ›› Issue (4) : 420-424. DOI: 10.16098/j.issn.0529-1356.2023.04.007

大鼠肝再生的肝细胞凋亡中Kruppel样因子4 mRNA、微小RNA-881-3p、环状RNA_20298和环状RNA_14826的表达变化与作用

  • 林凯琳1,2 杨献光1,2 王子慧1,2 臧夏炎1,2 薛奇杰1,2 韩璐1,2 张春博1,2 赵志虎3*  徐存拴1,2*
作者信息 +

Expression change and role of Kruppel-like factor 4 mRNA, microRNA-881-3p, circular RNA_20298 and circular RNA_14826 in the hepatocyte apoptosis during the rat liver regeneration 

  • LIN Kai-lin1,2  YANG Xian-guang1,2  WANG Zi-hui1,2  ZANG Xia-yan1,2  XUE Qi-jie1,2  HAN Lu1,2  ZHANG Chun-bo1,2  ZHAO Zhi-hu3*  XU Cun-shuan1,2*
Author information +
文章历史 +

摘要

目的  了解大鼠肝再生(LR)0 h和120 h时Kruppel样因子4(KLF4)基因及其mRNA相互作用的微小RNA(miRNA)和环状RNA(circRNA)的表达变化、相互作用和调节肝细胞凋亡的途径与方式。  方法  按Higgins等方法制备大鼠2/3肝切除(PH)模型,按Smedsrod等方法分离肝细胞,用大规模定量检测技术测定大鼠肝再生中肝细胞的mRNA、miRNA和circRNA合称内源竞争RNA(ceRNA)表达变化,用Cytoscape 3.2软件构建ceRNA的相互作用网络,用ceRNA综合分析等方法解析它们的表达相关性和作用相关性。   结果  PH后0 h和120 h时,KLF4 mRNA的比值为1.00±0.16和3.14±0.27,miR.881.3p为18.30±1.44和0.47±0.02,circRNA_20298为0.32±0.10和4.24±0.22,circRNA_14826为0.42±0.13和0.61±0.08。同时,PH后0 h时,KLF4促进的肾上腺素受体β 2(ADRB2)、二甲基精氨酸二甲基氨基水解酶 2(DDAH2)、膜联蛋白A5(ANXA5)等4个细胞凋亡相关基因表达下调,抑制的细胞凋亡相关基因突触核蛋白γ(synuclein gamma,SNCG)、谷胱甘肽二硫化物还原酶(GSR)、FYVE、RhoGEF和PH结构域包含 4(FGD4)表达上调。PH后120 h时,KLF4促进的细胞凋亡相关基因ANXA5和胸腺素beta 10(TMSB10)表达上调,抑制的细胞凋亡相关基因氯化物细胞内通道4(CLIC4)和紫杉素3(ATXN3)表达下调。   结论  上述circRNA抑制的miRNA、miRNA抑制的KLF4 mRNA以及KLF4调节的细胞凋亡相关基因的表达相关性和作用相关性有利于PH后0 h时肝细胞保持活性状态和PH后120 h时肝细胞处于凋亡状态。

Abstract

Objective  To explore the role pathway and pattern of the Kruppel-like factor 4 (KLF4) and its mRNA interaction with microRNA(miRNAs) and circular RNA(circRNAs) at 0 hour and the 120 th hour in the rat liver regeneration.    Methods  The rat 2/3 hepatectomy (partial hepatectomy, PH) model was prepared as described by Higgins, the hepatocytes were isolated according to the method  of Smedsrod et al, the expression changes of mRNA, miRNA and circRNA together named as competing endogenous RNA (ceRNA) were detected by the large-scale quantitative detection technology, the interaction network of ceRNA  was constructed by Cytoscape 3.2 software, and their correlation in expression and role were analyzed by ceRNA comprehensive analysis.    Results  It was found that at the 0 hour and the 120th hour PH, the ratio value of KLF4 mRNA showed 1.00±0.16 and 3.14±0.27, miR-881-3p displays 18.30±1.44 and 0.47±0.02, circRNA_20298 indicated 0.32±0.10 and 4.24±0.22, circRNA_14826 showed 0.42±0.13 and 0.61±0.08. At the same time, the four kinds of cell apoptosis-related genes adrenoceptor beta 2 (ADRB2), dimethylarginine dimethylaminohydrolase 2 (DDAH2), annexin A5 (ANXA5), ect, which were promoted in expression by KLF4, were down-regulated at 0 hour after PH, but the cell apoptosis-related genes synuclein gamma (SNCG), glutathione-disulfide reductase (GSR), FYVE, RhoGEF and PH domain containing 4 (FGD4), ect, which were inhibited in expression by KLF4, were upregulated at 0 hour after PH. On the other hand, the cell apoptosis-related genes ANXA5 and thymosin beta 10 (TMSB10), which are promoted in expression by KLF4, were up-regulated at the 120th hour after PH, but the cell apoptosis-related genes chloride intracellular channel 4 (CLIC4) and ataxin 3 (ATXN3), ect, which were inhibited in expression by KLF4, were down-regulated at the 120th hour after PH.    Conclusion  The correlation in expression and role of the miRNAs, which are inhibited by circRNAs, KLF4, its mRNA is inhibited by miRNAs, and the cell apoptosis-related genes, which are regulated by KLF4, are helpful for the hepatocyte to be in active state 0 hour after PH and to be in apoptotic state 120-hour after PH.

关键词

肝再生 / Kruppel样因子4 / 生物高通量检测 / 内源竞争RNA综合分析 / 大鼠

Key words

Liver regeneration / Kruppel like factor 4 / Biological high-throughput detection / Competing endogenous RNA comprehensive analysis / Rat

引用本文

导出引用
林凯琳 杨献光 王子慧 臧夏炎 薛奇杰 韩璐 张春博 赵志虎 徐存拴. 大鼠肝再生的肝细胞凋亡中Kruppel样因子4 mRNA、微小RNA-881-3p、环状RNA_20298和环状RNA_14826的表达变化与作用[J]. 解剖学报. 2023, 54(4): 420-424 https://doi.org/10.16098/j.issn.0529-1356.2023.04.007
LIN Kai-lin YANG Xian-guang WANG Zi-hui ZANG Xia-yan XUE Qi-jie HAN Lu ZHANG Chun-bo ZHAO Zhi-hu XU Cun-shuan. Expression change and role of Kruppel-like factor 4 mRNA, microRNA-881-3p, circular RNA_20298 and circular RNA_14826 in the hepatocyte apoptosis during the rat liver regeneration [J]. Acta Anatomica Sinica. 2023, 54(4): 420-424 https://doi.org/10.16098/j.issn.0529-1356.2023.04.007
中图分类号: Q257   

参考文献

[1]Fausto N, Campbell JS, Riehle KJ. Liver regeneration [J]. J Hepatol, 2006, 43(2 Suppl 1):S45-53. 
[2]Fausto N. Liver regeneration [J]. J Hepatol, 2000, 32(1 Suppl):19-31. 
[3]Fujiyoshi M, Ozaki M. Molecular mechanisms of liver regeneration and protection for treatment of liver dysfunction and diseases [J]. J Hepatobiliary Pancreat Sci,2011, 18(1):13-22. 
[4]Kim AR, Park JI, Oh HT, et al. TAZ stimulates liver regeneration through interleukin-6-induced hepatocyte proliferation and inhibition of cell death after liver injury [J]. FASEB J, 2019, 33(5):5914-5923.  
[5]Zhou Y, Xu JC, Jia YF, et al. Role of death receptors in the regulation of hepatocyte proliferation and apoptosis during rat liver regeneration [J]. Genet Mol Res, 2015, 14(4):14066-14075. 
[6]Fausto N, Laird AD, Webber EM. Liver regeneration.2.role of growth factors and cytokines in hepatic regeneration [J]. FASEB J, 1995, 9(15):1527-1536. 
  [7]Ghaleb AM, Yang VW. Krüppel-like factor 4 (KLF4): what we currently know [J]. Gene, 2017, 611:27-37. 
[8]Choi H, Roh J. Role of Klf4 in the regulation of apoptosis and cell cycle in rat granulosa cells during the periovulatory period [J]. Int J Mol Sci, 2018, 20(1):87. 
[9]Higgins GM, Anderson RM. Experimental pathology of the liver: restoration of the liver of the white rat following partial surgical removal [J]. Arch Pathol, 1931, 12:186-202. 
[10]Smedsrod B, Pertoft H, Eggertsen G. Functional and morphological characterization of cultures of Kupffer cells and liver endothelial cells prepared by means of density separation in Percoll, and selective substrate adhereence [J]. Cell Tissure Res, 1985, 241(3): 639-649. 
[11]Smedsrod B, Pertoft H. Preparation of pure hepatocytes and reticuloendothelial cells in high yield from a single rat liver by means of Percoll centrifugation and selective adhereence [J]. J Leukcyte Bio, 1985, 38: 213-231. 
[12]Zang XY, Wang ZH, Li YF, et al. Expression and role of CCAAT enhancer binding protein α mRNA, microRNA-144-3p and three kinds of circular RNAs of hepatocytes during the rat liver regeneration initiation [J]. Acta Anatomica Sinica, 2021, 52 (6): 904-908. (in Chinese)

臧夏炎,王子慧,李亚霏,等.大鼠肝再生启动阶段肝细胞CCAAT增强子结合蛋白α mRNA、微小RNA-144-3p和3种环状RNA的表达和作用[J].解剖学报, 2021, 52(6): 904-908. 

[13]Tang Q, Hann SS. Hotair: an oncogenic long non-coding RNA in human cancer [J]. Cell Physiol Biochem, 2018, 47(3):893-913. 

[14]Su Y, Wu HJ, Pavlosky A, et al. Regulatory non-coding RNA: new instruments in the orchestration of cell death [J]. Cell Death Dis, 2016, 7(8):e2333. 
[15]Wezyk M, Spólnicka M, Pospiech E, et al. Hypermethylation of TRIM59 and KLF14 influences cell death signaling in familial alzheimer’s disease [J]. Oxid Med Cell Longev, 2018, 2018:6918797. 
[16]Zhen K, Yan QM, Song YM, et al. TMSB10, a potential prognosis prediction biomarker, promotes the invasion and angiogenesis of gastric cancer [J]. Chinese Journal of Gastroenterology and Hepatology, 2021, 36(11):3102-3112. (in Chinese)
甄堃,颜巧梅,宋玉梅,等.TMSB10,一种潜在的促进胃癌的侵袭和血管生成预后标志物[J].胃肠病学和肝病学杂志,2021, 36(11):3102-3112. 
[17]Xiao RH, Shen ShCh, Yi Y, et al. TMSB10 promotes migration and invasion of cancer cells and is a novel prognostic marker for renal cell carcinoma [J]. Chinese Journal of Clinical and Experimental Pathology, 2019, 12(1):305-312. (in Chinese)
肖瑞海,沉少辰,易宇,等. TMSB10促进癌细胞的迁移和侵袭,是肾细胞癌的新型预后标志物[J]. 临床和实验病理学杂志,2019,12(1):305-312. 
[18]Yokoyama R, Kojima H, Takai R, et al. Effects of CLIC4 on fucoxanthinol-induced apoptosis in human colorectal cancer cells [J]. Nutr Cancer, 2021, 73(5):889-898. 
[19]Zou HJ, Chen HY, Zhou Zh, et al. ATXN3 promotes breast cancer metastasis by deubiquitinating KLF4 [J]. Cancer Lett, 2019, 467:19-28. (in Chinese)
邹浩景,陈红艳,周专,等. ATXN3通过去泛素化KLF4促进乳腺癌转移[J].癌症期刊,2019,467:19-28. 

PDF(2042 KB)

Accesses

Citation

Detail

段落导航
相关文章

/