Immunofluorescence Analysis of Villous Trophoblasts: A Tool for Prenatal Diagnosis of Inherited Epidermolysis Bullosa with Pyloric Atresia  Marina D'Alessio,

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Immunofluorescence Analysis of Villous Trophoblasts: A Tool for Prenatal Diagnosis of Inherited Epidermolysis Bullosa with Pyloric Atresia  Marina D'Alessio, Giovanna Zambruno, Alexandra Charlesworth, Jean-Philippe Lacour, Guerrino Meneguzzi  Journal of Investigative Dermatology  Volume 128, Issue 12, Pages 2815-2819 (December 2008) DOI: 10.1038/jid.2008.143 Copyright © 2008 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 1 Immunofluorescence staining pattern of integrin α6β4 and plectin in chorionic villous samples. Immunofluorescence labeling of frozen chorionic villous samples of (a–c) a healthy control and (d–i) pregnancies at risk for PA-EB using (a, d, g) monoclonal antibodies G0H3, (b, e, h) 3E1, and (c, f, i) 10F6 to integrins α6, β4, and plectin, respectively. In the chorionic villi of the healthy 11-week-gestation fetus, a comparable and intense staining signal for integrins (a) α6, (b) β4, the α6β4 heterodimer (not shown) and (c) plectin localizes at the cytotrophoblast surface and concentrates at the basement membrane zone. In the trophoblasts of the 28- and the 37-week fetuses (Table 1, samples 23, 25, respectively), the immunofluorescence analysis showed a strong reduction of (d) integrin α6 or (h) integrin β4, respectively, thus indicating PA-JEB. The immunolabeling of (e) integrin β4 and (f) plectin of the 28-week fetus, and (g) of integrin α6 and (i) plectin of the 35-week fetus was similar with the controls. The corresponding fetuses resulted homozygous and compound heterozygous for nonsense mutations in the ITGA6 or the ITGB4 genes, respectively. Bar=68μm. Journal of Investigative Dermatology 2008 128, 2815-2819DOI: (10.1038/jid.2008.143) Copyright © 2008 The Society for Investigative Dermatology, Inc Terms and Conditions