期刊文献+

转录因子基因在大鼠肝再生中的表达方式和作用分析

EXPRESSION PATTERNS AND ROLES OF TRANSCRIPTION FACTOR GENES IN RAT LIVER REGENERATION
下载PDF
导出
摘要 目的探讨转录因子基因在肝再生中的表达变化及作用。方法经查阅网站资料和相关论文获得转录因子基因及其参与的生理活动,用大鼠基因组230 2.0芯片检测转录因子基因在大鼠再生肝中的表达,用手术组和假手术组比较的方法确定肝再生相关基因。结果初步证实上述基因中有320个基因与肝再生相关,涉及细胞代谢、增殖、分化、凋亡等16种生理活动。它们在肝再生中的表达分为41种方式,表明肝再生中细胞生理生化活动具有阶段性、多样性和复杂性。其中,肝再生早期[部分肝切除(PH)后0.5~4h]和前期(PH后6~12h)糖类合成,脂类代谢和炎症反应相关转录因子基因表达增强,中期和后期细胞增殖、生长、分化和凋亡相关转录因子基因表达增强。结论肝再生的生理生化活动受多种转录因子基因调控。其中,e2f1、fos、copeb等转录因子基因发挥关键作用。 Objective To study the expression changes of transcription factor genes and their underlying involvement in rat liver regeneration (LR) at transcription level. Methods The transcription factor genes and their function were collected by referring to the putative literatures and databases. Then, their expression in rat LR were checked by Rat Genome 230 2.0 array. LR-related genes were identified through the comparison of discrepancies in gene expression between partial hepateetomy (PH) and sham-operation (SO) groups. Results 320 genes were determined to be LR-related, which were involved in 16 biological processes, such as cellular metabolism, proliferation, differentiation, apoptosis, etc. Expression profiles of above genes were classified into 41 categories according to their functions and expression trends, implying their diversity and complexity during LR. The expression of transcription factor genes that were involved in carbohydrate biosynthesis, lipid metabolism, and inflammatory response was enhanced in the forepart (0.5-4 hours after PH) and prophase (6-12 hours after FH) of LR. Cellular proliferation, growth, differentiation and apoptosis related transcription factor genes were promoted in the metaphase ( 16-66 hours after FH) and anaphase (72-168 hours after PH). Conclusion Physiological and biochemical activities in LR were regulated by multiple transcription factor genes, and e2fl, fos, copeb, etc. played key roles in it.
出处 《解剖学报》 CAS CSCD 北大核心 2008年第3期323-328,共6页 Acta Anatomica Sinica
基金 国家973计划前期研究专项(2006CB708506)资助
关键词 部分肝切除 转录因子 肝再生相关基因 基因组2302.0芯片 大鼠 Partial hepatectomy Transcription factor Liver regeneration-related gene Genome 230 2.0 array Rat
  • 相关文献

参考文献5

二级参考文献42

  • 1Bian-Hong Fu, Ze-Zhi Wu and Cheng Dong Chongqing, China College of Bioengineering, Key Lab for Biomechanics and Tissue Engineering under the State Ministry of Education and College of Resources & Environmental Science , Chongqing University, Chongqing 400044, China,Bioengineering Pro- gram, Pennsylvania State University, 205 Hallowell Building, University Park, Pennsylvania 16802-6804, USA.Integrin betal mediates hepatocellular carcinoma cells chemotaxis to laminin[J].Hepatobiliary & Pancreatic Diseases International,2004,3(4):548-551. 被引量:4
  • 2Bao-Hua Zhang,Han Chen,Xiao-Ping Yao,Wen-Ming Cong,Meng-Chao Wu From the Eastern Hepatobiliary Surgery Hospital, Second Military Medical University of PLA, Shanghai 200438, China.E-selectin and its ligand-sLeX in the metastasis of hepatocellular carcinoma[J].Hepatobiliary & Pancreatic Diseases International,2002,1(1):80-82. 被引量:6
  • 3孙秀菊,郝冬梅,郑志红,付浩,徐惠绵,王梅先,孙开来.胃癌发生发展相关基因筛选与表达分析[J].中华医学遗传学杂志,2005,22(1):31-34. 被引量:7
  • 4Cun-ShuanXu,Cui-FangChang,Jin-YunYuan,Wen-QiangLi,Hong-PengHan,Ke-JinYang,Li-FengZhao,Yu-ChangLi,Hui-YongZhang,SalmanRahman,Jing-BoZhang.Expressed genes in regenerating rat liver after partial hepatectomy[J].World Journal of Gastroenterology,2005,11(19):2932-2940. 被引量:16
  • 5Yoshiyuki Takahara,Mitsuo Takahashi,Hiroki Wagatsuma,Fumihiko Yokoya,Qing-Wei Zhang,Mutsuyo Yamaguchi,Hiroyuki Aburatani,Norifumi Kawada.Gene expression profiles of hepatic cell-type specific marker genes in progression of liver fibrosis[J].World Journal of Gastroenterology,2006,12(40):6473-6499. 被引量:5
  • 6Izawa, Y., M. Yoshizumi, Y. Fujita, N. Ali, Y. Kanematsu, K. Ishizawa, K. Tsuchiya, T. Obata, Y. Ebina, S. Tomita & T. Tamaki, 2005, ERK1/2 activation by angiotensin Ⅱ inhibits insulin-induced glucose uptake in vascular smooth muscle cells. Exp Cell Res., 308: 291- 299.
  • 7Cheng, X & J. H. Jaggar, 2006, Genetic ablation of caveolin-1 modifies Ca^2+ spark coupling in murine arterial smooth muscle cells. Am J Physiol Heart Circ Physiol., 290: 2309-2319.
  • 8Moiseeva, E. P., Q. Javed, E. L. Spring & D. P. de Bono, 2000, Galectin 1 is involved in vascular smooth muscle cell proliferation. Cardiovasc Res., 45: 493-502.
  • 9Jain, M.K., K. P. Fujita, C.M. Hsieh, W. O. Endege, N.E. Sibinga, S. F. Yet, S. Kashiki, W. S. Lee, M. A. Perrella, E. Haber& M. E. Lee, 1996, Molecular cloning and characterization of SmLIM, a developmentally regulated LIM protein preferentially expressed in aortic smooth muscle cells. J Biol Chem., 271 : 10 194-10 199.
  • 10Blayney, L., P. Gapper & C. Rix, 1998, Identification of phospholipase C beta isoforms and their location in cultured vascular smooth muscle cells of pig, human and rat. Cardiovasc Res., 40: 564-572.

共引文献23

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部