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正常大鼠肾脏近端小管段血管紧张素原 mRNA 和蛋白的定位差异。

Divergent localization of angiotensinogen mRNA and protein in proximal tubule segments of normal rat kidney.

机构信息

Department of Physiology, Hypertension and Renal Center of Excellence, Tulane University Health Sciences Center, New Orleans, Louisiana, USA.

出版信息

J Hypertens. 2012 Dec;30(12):2365-72. doi: 10.1097/HJH.0b013e3283598eed.

Abstract

OBJECTIVES

Angiotensinogen in the kidneys is formed primarily in the proximal tubule cells and is secreted into the tubular fluid. Structurally, proximal tubules can be divided into three segments. The first segment, segment 1 (S1) is mainly confined to the pars convoluta, the second segment, segment 2 (S2) comprises the end of pars convoluta, and the third segment, segment 3 (S3) includes the major part of the pars recta. There are some reports describing angiotensinogen localization in kidneys; however, it remains uncertain which proximal tubule segments express angiotensinogen. To determine the detailed localization of angiotensinogen in the three proximal tubule segments, we established multistaining methods using segment-specific protein markers.

METHODS

Using kidneys from Wistar-Kyoto rats, we performed immunohistochemistry and double or triple staining by fluorescence in-situ hybridization and/or immunofluorescence.

RESULTS

Our results show that angiotensinogen mRNA and protein are expressed in the cortex and outer medulla of the normal rat kidney. Angiotensinogen mRNA was hardly detected in S1, detected weakly in S2 and strongly in S3 segments. In contrast, angiotensinogen protein was detected in S1 at high levels and less in S2 and S3 segments.

CONCLUSION

These data indicate divergence of angiotensinogen mRNA transcription and angiotensinogen protein synthesis and metabolism in different segments of the normal rat proximal tubules.

摘要

目的

肾脏中的血管紧张素原主要在近端肾小管细胞中形成,并分泌到管状液中。从结构上看,近端小管可分为三个节段。第一段,节段 1(S1)主要局限于回旋部,第二段,节段 2(S2)包括回旋部的末端,第三段,节段 3(S3)包括直部的主要部分。有一些报道描述了血管紧张素原在肾脏中的定位;然而,目前尚不确定哪些近端小管节段表达血管紧张素原。为了确定血管紧张素原在三个近端小管节段中的详细定位,我们使用节段特异性蛋白标记物建立了多染色方法。

方法

使用 Wistar-Kyoto 大鼠的肾脏,我们通过荧光原位杂交和/或免疫荧光进行免疫组织化学和双或三染色。

结果

我们的结果表明,血管紧张素原 mRNA 和蛋白在正常大鼠肾脏的皮质和外髓质中表达。血管紧张素原 mRNA 在 S1 中几乎检测不到,在 S2 中弱表达,在 S3 中强表达。相比之下,血管紧张素原蛋白在 S1 中高水平表达,在 S2 和 S3 中表达水平较低。

结论

这些数据表明,正常大鼠近端小管不同节段的血管紧张素原 mRNA 转录和血管紧张素原蛋白合成和代谢存在差异。

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