Angiogenin Expression during Early Human Placental Development; Association with Blood Vessel Formation.

Abstract : The placenta is a transient organ essential for fetal development. During human placental development, chorionic villi grow in coordination with a large capillary network resulting from both vasculogenesis and angiogenesis. Angiogenin is one of the most potent inducers of neovascularisation in experimental models in vivo. We and others have previously mapped angiogenin expression in the human term placenta. Here, we explored angiogenin involvement in early human placental development. We studied, angiogenin expression by in situ hybridisation and/or by RT-PCR in tissues and primary cultured trophoblastic cells and angiogenin cellular distribution by coimmunolabelling with cell markers: CD31 (PECAM-1), vascular endothelial cadherin (VE-cadherin), vascular endothelial growth factor receptor-2 (VEGF-R2), Tie-2, von Willebrand factor, CD34, erythropoeitin receptor (Epo-R), alpha-smooth muscle actin, CD45, cytokeratin 7, and Ki-67. Extravillous and villous cytotrophoblasts, isolated and differentiated in vitro, expressed and secreted angiogenin. Angiogenin was detected in villous trophoblastic layers, and structured and nascent fetal vessels. In decidua, it was expressed by glandular epithelial cells, vascular cells and macrophages. The observed pattern of angiogenin expression is compatible with a role in blood vessel formation and in cross-talk between trophoblasts and endothelial cells. In view of angiogenin properties, we suggest that angiogenin may participate in placental vasculogenesis and organogenesis.
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BioMed Research International , Hindawi Publishing Corporation, 2014, 2014, pp.781632. 〈10.1155/2014/781632〉
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Nadine Pavlov, Jean-Louis Frendo, Jean Guibourdenche, Séverine Degrelle, Danièle Evain-Brion, et al.. Angiogenin Expression during Early Human Placental Development; Association with Blood Vessel Formation.. BioMed Research International , Hindawi Publishing Corporation, 2014, 2014, pp.781632. 〈10.1155/2014/781632〉. 〈inserm-01019883〉

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