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Development of a Specific Monoclonal Antibody to Detect Male Cells Expressing the RPS4Y1 Protein
Authors:Silvia Spena  Chiara Cordiglieri  Isabella Garagiola  Flora Peyvandi
Affiliation:1.Department of Pathophysiology and Transplantation, Università degli Studi di Milano, 20122 Milan, Italy;2.Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Fondazione Luigi Villa, 20122 Milan, Italy;3.National Institute of Molecular Genetics “Romeo e Enrica Invernizzi”—INGM, 20122 Milan, Italy;
Abstract:Hemophilia is an X-linked recessive bleeding disorder. In pregnant women carrier of hemophilia, the fetal sex can be determined by non-invasive analysis of fetal DNA circulating in the maternal blood. However, in case of a male fetus, conventional invasive procedures are required for the diagnosis of hemophilia. Fetal cells, circulating in the maternal bloodstream, are an ideal target for a safe non-invasive prenatal diagnosis. Nevertheless, the small number of cells and the lack of specific fetal markers have been the most limiting factors for their isolation. We aimed to develop monoclonal antibodies (mAbs) against the ribosomal protein RPS4Y1 expressed in male cells. By Western blotting, immunoprecipitation and immunofluorescence analyses performed on cell lysates from male human hepatoma (HepG2) and female human embryonic kidney (HEK293) we developed and characterized a specific monoclonal antibody against the native form of the male RPS4Y1 protein that can distinguish male from female cells. The availability of the RPS4Y1-targeting monoclonal antibody should facilitate the development of novel methods for the reliable isolation of male fetal cells from the maternal blood and their future use for non-invasive prenatal diagnosis of X-linked inherited disease such as hemophilia.
Keywords:hemophilia   male cells   male marker   ribosomal protein   RPS4Y1   monoclonal antibody   diagnosis   fetal cells
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