Abstract

Commercially available angiotensin II AT2 receptor antibodies are widely employed for receptor localization and quantification, but they have not been adequately validated. In this study, we characterized three commercially available AT2 receptor antibodies: 2818-1 from Epitomics, sc-9040 from Santa Cruz Biotechnology, Inc., and AAR-012 from Alomone Labs. Using western blot analysis the immunostaining patterns observed were different for every antibody tested, and in most cases consisted of multiple immunoreactive bands. Identical immunoreactive patterns were present in wild-type and AT2 receptor knockout mice not expressing the target protein. In the mouse brain, immunocytochemical studies revealed very different cellular immunoreactivity for each antibody tested. While the 2818-1 antibody reacted only with endothelial cells in small parenchymal arteries, the sc-9040 antibody reacted only with ependymal cells lining the cerebral ventricles, and the AAR-012 antibody reacted only with multiple neuronal cell bodies in the cerebral cortex. Moreover, the immunoreactivities were identical in brain tissue from wild-type or AT2 receptor knockout mice. Furthermore, in both mice and rat tissue extracts, there was no correlation between the observed immunoreactivity and the presence or absence of AT2 receptor binding or gene expression. We conclude that none of these commercially available AT2 receptor antibodies tested met the criteria for specificity. In the absence of full antibody characterization, competitive radioligand binding and determination of mRNA expression remain the only reliable approaches to study AT2 receptor expression.

Highlights

  • Circulating and local Renin-Angiotensin Systems (RAS) control multiple functions in many peripheral organs and in the brain [1,2,3,4]

  • AT2, Angiotensin II receptor type 2; GAPDH, Glyceraldehyde-3-phosphate dehydrogenase. * AT2 primers targeting mRNA sequence corresponding to the non-disrupted part of AT2 receptor gene. ** AT2 primers targeting mRNA corresponding to the part of the gene in intron III that was deleted in AT2 receptor knockouts

  • Angiotensin II receptor mRNA expression and AT2 receptor binding in wild-type and AT2 knockout mice

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Summary

Introduction

Circulating and local Renin-Angiotensin Systems (RAS) control multiple functions in many peripheral organs and in the brain [1,2,3,4]. Stimulation of AT2 receptors plays a protective role under pathological circumstances in the heart, kidney and brain, opposing AT1 receptor activation by increasing vasodilation and natriuresis and reducing brain ischemia and neuronal injury [8,9,10,11,12]. It appears that AT2 receptors contribute to control of AT1 receptor expression. In adult AT2 receptor knockout mice, AT1 receptor expression increases in the brain, adrenal gland, kidney, spleen and lung [13,14,15,16]

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