Commercially Available Angiotensin II At2 Receptor Antibodies Are Nonspecific

被引:61
作者
Hafko, Roman [1 ]
Villapol, Sonia [2 ,3 ]
Nostramo, Regina [4 ]
Symes, Aviva [2 ,3 ]
Sabban, Esther L. [4 ]
Inagami, Tadashi [5 ]
Saavedra, Juan M. [1 ]
机构
[1] NIMH, Pharmacol Sect, Div Intramural Res Programs, NIH, Bethesda, MD 20892 USA
[2] Ctr Neurosci & Regenerat Med, Bethesda, MD USA
[3] Uniformed Serv Univ Hlth Sci, Dept Pharmacol, Bethesda, MD 20814 USA
[4] New York Med Coll, Dept Biochem & Mol Biol, Valhalla, NY 10595 USA
[5] Vanderbilt Univ, Sch Med, Nashville, TN 37212 USA
关键词
TYPE-2 AT(2) RECEPTOR; MESSENGER-RNA; CONVERTING-ENZYME; BIOCHEMICAL-PROPERTIES; AT(1) RECEPTORS; ADRENAL-GLAND; RAT-BRAIN; EXPRESSION; SUBTYPES; SPECIFICITY;
D O I
10.1371/journal.pone.0069234
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Commercially available angiotensin II AT(2) 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 AT(2) 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 AT(2) 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 wildtype or AT(2) 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 AT(2) receptor binding or gene expression. We conclude that none of these commercially available AT(2) 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 AT(2) receptor expression.
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页数:12
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