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睫状神经营养因子及其受体在实验性梗阻性肾病中的表达

Expression of ciliary neurotrophic factor and its receptor in experimental obstructive nephropathy.

作者信息

Lee Byoung-Seung, Choi Jae-Youn, Cha Jung-Ho

机构信息

Department of Anatomy, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Anat Cell Biol. 2011 Jun;44(2):85-97. doi: 10.5115/acb.2011.44.2.85. Epub 2011 Jun 30.

Abstract

Ciliary neurotrophic factor (CNTF) is well known as a growth/survival factor of neuronal tissue. We investigated the expression of CNTF and its specific receptor alpha (CNTFRα) in a unilateral ureteral obstruction (UUO) model. Complete UUO was produced by left ureteral ligation in Sprague-Dawley rats. The animals were sacrificed on days 1, 3, 5, 7, 14, 21, and 28 after UUO. The kidneys were fixed, and processed for both immunohistochemistry and in situ hybridization. CNTF immunoreactivity in sham-operated kidneys was observed only in the descending thin limb (DTL) of the loop of Henle. In UUO kidneys, CNTF expression was induced in the S3 segment (S3s) of the proximal tubule from day 1, and progressively expanded into the entire S3s and a part of the convoluted proximal tubules, distal tubules (DT), and glomerular parietal epithelium up to day 7. Upregulated CNTF expression was maintained to day 28. From day 14, the inner medullary collecting duct showed weak CNTF immunoreactivity. The CNTFRα mRNA hybridization signal in sham-operated kidneys was weakly detected in the DTL, DT, medullary thick ascending limb, and in a few S3s cells. After UUO, CNTFRα mRNA expression increased progressively in both the renal cortex and the medulla up to day 7 and increased expression was maintained until day 28. The results suggest that the S3s may be the principal induction site for CNTF in response to renal injury, and that CNTF may play a role in chronic renal injury.

摘要

睫状神经营养因子(CNTF)作为神经组织的生长/存活因子广为人知。我们在单侧输尿管梗阻(UUO)模型中研究了CNTF及其特异性受体α(CNTFRα)的表达。通过在Sprague-Dawley大鼠中结扎左输尿管造成完全性UUO。在UUO后的第1、3、5、7、14、21和28天处死动物。将肾脏固定,并进行免疫组织化学和原位杂交处理。在假手术肾脏中,仅在髓袢降支细段(DTL)观察到CNTF免疫反应性。在UUO肾脏中,从第1天开始,近端小管的S3段(S3s)诱导出CNTF表达,并逐渐扩展至整个S3s以及部分近曲小管、远曲小管(DT)和肾小球壁层上皮,直至第7天。CNTF表达上调一直维持到第28天。从第14天开始,内髓集合管显示出较弱的CNTF免疫反应性。在假手术肾脏中,在DTL、DT、髓质厚升支和少数S3s细胞中微弱检测到CNTFRα mRNA杂交信号。UUO后,直至第7天,肾皮质和髓质中的CNTFRα mRNA表达均逐渐增加,且表达增加一直维持到第28天。结果表明,S3s可能是肾损伤时CNTF的主要诱导部位,并且CNTF可能在慢性肾损伤中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d55/3145847/99c7473b5a48/acb-44-85-g001.jpg

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