Suppr超能文献

缺血再灌注在体内和体外均可诱导肾髓质厚壁升支细胞表达G-CSF基因。

Ischemia-reperfusion induces G-CSF gene expression by renal medullary thick ascending limb cells in vivo and in vitro.

作者信息

Zhang Ying, Woodward Vanessa K, Shelton John M, Richardson James A, Zhou Xin J, Link Daniel, Kielar Mariusz L, Jeyarajah D Rohan, Lu Christopher Y

机构信息

Div. of Nephrology (Internal Medicine Univ. of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-8856, USA.

出版信息

Am J Physiol Renal Physiol. 2004 Jun;286(6):F1193-201. doi: 10.1152/ajprenal.00379.2002. Epub 2004 Jan 20.

Abstract

Ischemic acute renal failure involves not only the kidney but also extrarenal organs such as the bone marrow that produces inflammatory cells. By ELISA and RNase protection assays, we now show that renal ischemia-reperfusion increases serum concentrations of granulocyte macrophage colony-stimulating factor (G-CSF) protein and increases both G-CSF mRNA and protein in the ischemic kidney. In situ hybridization localized the increased G-CSF mRNA to tubule cells, including medullary thick ascending limb cells (mTAL), in the outer medulla. We also show that mTAL produce G-CSF protein and increase G-CSF mRNA after stimulation by reactive oxygen species in vitro. The production of G-CSF by the kidney after ischemia-reperfusion provides a means of communication from the injured kidney to the bone marrow. This supports the known inflammatory response to ischemia.

摘要

缺血性急性肾衰竭不仅累及肾脏,还涉及肾外器官,如产生炎症细胞的骨髓。通过酶联免疫吸附测定法(ELISA)和核糖核酸酶保护试验,我们现在发现肾缺血再灌注会增加血清中粒细胞巨噬细胞集落刺激因子(G-CSF)蛋白的浓度,并使缺血肾脏中的G-CSF信使核糖核酸(mRNA)和蛋白均增加。原位杂交将增加的G-CSF mRNA定位于外髓质的肾小管细胞,包括髓袢升支粗段(mTAL)细胞。我们还发现,体外经活性氧刺激后,mTAL会产生G-CSF蛋白并增加G-CSF mRNA。缺血再灌注后肾脏产生G-CSF为受损肾脏与骨髓之间提供了一种通讯方式。这支持了已知的对缺血的炎症反应。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验