期刊文献+

PAX2与急慢性肾脏疾病研究进展 被引量:1

The role of PAX2 in acute kidney injury and chronic kidney disease
原文传递
导出
摘要 配对盒基因2(paired box2,PAX2)是一种核转录因子,表达在发育期肾脏。研究表明PAX2通过与PTIP的相互作用使染色质处于可转录状态,与Grg4的相互作用削弱了其与PTIP结合而抑制转录。 PAX2在急性肾损伤时再表达,参与促进细胞增殖修复。先天PAX2基因突变与先天性肾脏输尿管异常密切相关。在慢性肾脏疾病,PAX2起到促进增殖及囊肿形成的作用。该文就PAX2的功能及其在急性肾损伤和慢性肾脏疾病中作用的相关研究进行综述。 Paired box2 ( PAX2 ) is a transciption factor which mainly expressed in the developing kid-ney. Researches indicate that PAX2 promote the transcription through interactions with the adaptor PAX transac-tivation domain interacting protein(PTIP). Otherwise,PAX2 protein can lead to chromatin compaction and gene silencing through interactions with Grg4. PAX2 reexpressed in acute kidney injury and involved in promoting cell proliferation. Congenital PAX2 gene mutation is closely related to congenital abnormalies of the kidney and uri-nary tract. In chronic kidney disease,PAX2 promote proliferation and cyst formation. Here,the recent researches on the function of PAX2 and its role in acute kidney injury and chronic kidney disease are reviewed.
出处 《国际儿科学杂志》 2016年第1期-,共5页 International Journal of Pediatrics
基金 辽宁省科技厅科学技术计划项目,辽宁省科学计划项目(2013021099)Fund program:Science and Technology Planning Project of Liaoning Science and Technology Commi-ssion(2013225086). Science and Technology Planning Project of Liaoning Province
关键词 PAX2 急性肾损伤 慢性肾脏疾病 PAX2 Acute kidney injury Chronic kidney disease
  • 相关文献

参考文献1

二级参考文献34

  • 1Bechtel W, Mcgoohan S, Zeisberg EM, et al. Methylation determines fibroblast activation and fibroganesis in the kidney [ J ]. Nat Med, 2010,16 (5) :544-550. 被引量:1
  • 2Borges b'T, Melo SA, Ozdemir BC, et al. TGF-131-Containing exo- somes from injured epithelial cells activate fibroblasts to initiate tissue regenerative responses and fibrosis [ J ]. Am Soc Nephrol, 2013,24 (3) :385-392. 被引量:1
  • 3Lebleu VS ,Taduri G,O'connell J,et al. Origin and function of myofi- broblasts in kidney fibrosis[ J]. Nat Med,2013,19 (8) :1047-1053. 被引量:1
  • 4Bird A. Perceptions of epigenetics [ J ]. Nature, 2007,447 ( 7143 ) : 396-398. 被引量:1
  • 5Portela A, Esteller M. Epigenetic modifications and human disease [ J]. Nat Biotechno1,2010,28 (10) : 1057-1068. 被引量:1
  • 6Liu Y. Renal fibrosis:new insights into the pathogenesis and thera- peutics[ J]. Kidney Int,2006,69(2) :213-217. 被引量:1
  • 7Song CX, He C. Potential functional roles of DNA demethylation intermediates[J]. Trends Biochem Sci,2013,38 (10) :480-484. 被引量:1
  • 8Jones PA. Functions of DNA methylation: islands, start sites, gene bodies and beyond[ J]. Nat Rev Ganet,2012,13 (7) :484-492. 被引量:1
  • 9Estecio MR, Issa JP. Dissecting DNA hypermethylation in cancer [J]. FEBS Lett,2011,585 (13) :2078-2086. 被引量:1
  • 10Mohn F, Weber M, Rebhan M, et al. Lineage-specific polycomb targets and de novo DNA methylation define restriction and potential of neuronal progenitors[ J]. Mol Ce11,2008,30 (6) :755-766. 被引量:1

共引文献2

同被引文献4

引证文献1

二级引证文献2

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