The tetraspanin CD9 controls migration and proliferation of parietal epithelial cells and glomerular disease progression

Hélène Lazareth(Centre National de la Recherche Scientifique), Carole Hénique(Inserm), Olivia Lenoir(Inserm), Victor G. Puelles(Universität Hamburg), Martin Flamant(Université Paris Cité), Guillaume Bollée(Inserm), Cécile Fligny(Inserm), Marine Camus(Inserm), Léa Guyonnet(Luxembourg Institute of Health), Corinne Millien(Inserm), F. Gaillard(Inserm), Anna Chipont(Inserm), Blaise Robin(Inserm), Sylvie Fabrega(Hôpital Necker-Enfants Malades), Neeraj Dhaun(Edinburgh Royal Infirmary), Eric Camerer(Inserm), Oliver Kretz(Universität Hamburg), Florian Grahammer(Universität Hamburg), Fabian Braun(Universität Hamburg), Tobias B. Huber(Universität Hamburg), Dominique Nochy(Assistance Publique – Hôpitaux de Paris), Chantal Mandet(Assistance Publique – Hôpitaux de Paris), Patrick Bruneval(Assistance Publique – Hôpitaux de Paris), Laurent Mesnard(Sorbonne Université), Éric Thervet(Inserm), Alexandre Karras(Inserm), François Le Naour(Université Paris-Sud), Eric Rubinstein(Université Paris-Sud), Claude Boucheix(Université Paris-Sud), Antigoni Alexandrou(Centre National de la Recherche Scientifique), Marcus J. Moeller(RWTH Aachen University), Cédric Bouzigues(Centre National de la Recherche Scientifique), Pierre‐Louis Tharaux(Inserm)
Nature Communications
July 24, 2019
Cited by 87Open Access
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Abstract

The mechanisms driving the development of extracapillary lesions in focal segmental glomerulosclerosis (FSGS) and crescentic glomerulonephritis (CGN) remain poorly understood. A key question is how parietal epithelial cells (PECs) invade glomerular capillaries, thereby promoting injury and kidney failure. Here we show that expression of the tetraspanin CD9 increases markedly in PECs in mouse models of CGN and FSGS, and in kidneys from individuals diagnosed with these diseases. Cd9 gene targeting in PECs prevents glomerular damage in CGN and FSGS mouse models. Mechanistically, CD9 deficiency prevents the oriented migration of PECs into the glomerular tuft and their acquisition of CD44 and β1 integrin expression. These findings highlight a critical role for de novo expression of CD9 as a common pathogenic switch driving the PEC phenotype in CGN and FSGS, while offering a potential therapeutic avenue to treat these conditions.


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