Validation of commercial Mas receptor antibodies for utilization in Western Blotting, immunofluorescence and immunohistochemistry studies

NATALIA C FERNANDEZ; DIEGO T QUIROGA; MICHAEL BADER; MARINA CECILIA MUÑOZ; VALERIA BURGHI ; VERÓNICA G PIAZZA; JANAÍNA FELIX BRAGA; FERNANDO P DOMINICI; YAMILA B GÁNDOLA; ERICA MARIO GUILHEN; ROBSON A SANTOS

PLOS ONE

PUBLIC LIBRARY SCIENCE

Lugar: San Francisco; Año: 2017

1932-6203

Mas receptor (MasR) is a G protein-coupled receptor proposed as a candidate formediating the angiotensin (Ang)-converting enzyme 2-Ang (1-7) protective axis ofrenin-angiotensin system. Because the role of this receptor is not definitively clarified,determination of MasR tissue distribution and expression levels constitutes a criticalknowledge to fully understanding its function. Commercially available antibodies havebeen widely employed for MasR protein localization and quantification, but they havenot been adequately validated. In this study, we carried on an exhaustive evaluation offour commercial MasR antibodies, following previously established criteria. WesternBlotting (WB) and immunohistochemistry studies starting from hearts and kidneys fromwild type (WT) mice revealed that antibodies raised against different MasR domainsyielded different patterns of reactivity. Furthermore, staining patterns appearedidentical in samples from MasR knockout (MasR-KO) mice. We verified by polymerasechain reaction analysis that the MasR-KO mice used were truly deficient in thisreceptor as MAS transcripts were undetectable in either heart or kidney from thisanimal model. In addition, we evaluated the ability of the antibodies to detect thehuman c-myc-tagged MasR overexpressed in human embryonic kidney cells. Threeantibodies were capable of detecting the MasR either by WB or byimmunofluorescence, reproducing the patterns obtained with an anti c-myc antibody. Inconclusion, although three of the selected antibodies were able to detect MasR proteinat high expression levels observed in a transfected cell line, they failed to detect thisreceptor in mice tissues at physiological expression levels. As a consequence,validated antibodies that can recognize and detect the MasR at physiological levels arestill lacking.