Section on Pharmacology, DIRP, NIMH, NIH, 10 Center Drive, Bldg., 10, Room 2D-57, Bethesda, MD 20892, USA.
Cell Mol Neurobiol. 2012 Nov;32(8):1353-65. doi: 10.1007/s10571-012-9862-y. Epub 2012 Jul 28.
Commercially available Angiotensin II AT1 receptor antibodies are widely employed for receptor localization and quantification, but they have not been adequately validated. In this study, six commercially available AT1 receptor antibodies were characterized by established criteria: sc-1173 and sc-579 from Santa Cruz Biotechnology, Inc., AAR-011 from Alomone Labs, Ltd., AB15552 from Millipore, and ab18801 and ab9391 from Abcam. The immunostaining patterns observed were different for every antibody tested, and were unrelated to the presence or absence of AT1 receptors. The antibodies detected a 43 kDa band in western blots, corresponding to the predicted size of the native AT1 receptor. However, identical bands were observed in wild-type mice and in AT1A knock-out mice not expressing the target protein. Moreover, immunoreactivity detected in rat hypothalamic 4B cells not expressing AT1 receptors or transfected with AT1A receptor construct was identical, as revealed by western blotting and immunocytochemistry in cultured 4B cells. Additional prominent immunoreactive bands above and below 43 kDa were observed by western blotting in extracts from tissues of AT1A knock-out and wild-type mice and in 4B cells with or without AT1 receptor expression. In all cases, the patterns of immunoreactivity were independent of the AT1 receptor expression and different for each antibody studied. We conclude that, in our experimental setup, none of the commercially available AT1 receptor antibodies tested met the criteria for specificity and that competitive radioligand binding remains the only reliable approach to study AT1 receptor physiology in the absence of full antibody characterization.
市售的血管紧张素 II AT1 受体抗体广泛用于受体定位和定量,但尚未得到充分验证。在这项研究中,根据既定标准对六种市售 AT1 受体抗体进行了表征:Santa Cruz Biotechnology, Inc. 的 sc-1173 和 sc-579、Alomone Labs, Ltd. 的 AAR-011、Millipore 的 AB15552 以及 Abcam 的 ab18801 和 ab9391。每种测试的抗体观察到的免疫染色模式都不同,与 AT1 受体的存在与否无关。抗体在 Western blot 中检测到 43 kDa 的条带,与天然 AT1 受体的预测大小相对应。然而,在野生型小鼠和不表达靶蛋白的 AT1A 敲除小鼠中观察到相同的条带。此外,在不表达 AT1 受体的大鼠下丘脑 4B 细胞或转染 AT1A 受体构建体的 4B 细胞中,通过 Western blot 和免疫细胞化学检测到相同的免疫反应性。在 AT1A 敲除和野生型小鼠组织提取物以及具有或不具有 AT1 受体表达的 4B 细胞中,通过 Western blot 观察到 43 kDa 以上和以下的额外明显免疫反应性条带。在所有情况下,免疫反应性模式均与 AT1 受体表达无关,并且每种研究的抗体都不同。我们得出结论,在我们的实验设置中,测试的市售 AT1 受体抗体均不符合特异性标准,并且在没有充分抗体表征的情况下,竞争性放射性配体结合仍然是研究 AT1 受体生理学的唯一可靠方法。