Serpin B1 defect and increased apoptosis of neutrophils in Cohen syndrome neutropenia

• Published in: Journal of molecular medicine (Berlin, Germany) Vol. 97; no. 5; pp. 633 - 645
• Main Authors: Duplomb, Laurence, Rivière, Julie, Jego, Gaëtan, Da Costa, Romain, Hammann, Arlette, Racine, Jessica, Schmitt, Alain, Droin, Nathalie, Capron, Claude, Gougerot-Pocidalo, Marie-Anne, Dubrez, Laurence, Aral, Bernard, Lafon, Arnaud, Edery, Patrick, Ghoumid, Jamal, Blair, Edward, El Chehadeh-Djebbar, Salima, Carmignac, Virginie, Thevenon, Julien, Guy, Julien, Girodon, François, Bastie, Jean-Noël, Delva, Laurent, Faivre, Laurence, Thauvin-Robinet, Christel, Solary, Eric
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.05.2019; Springer Nature B.V; Springer Verlag
• Subjects: Apoptosis; Biomedical and Life Sciences; Biomedicine; Cell death; Cohen syndrome; Elastase; Endoplasmic reticulum; Genetic disorders; Glycosylation; Golgi apparatus; Human Genetics; Intercellular adhesion molecule 1; Internal Medicine; Leukocyte migration; Leukocytes (neutrophilic); Life Sciences; Localization; Molecular Medicine; Neutropenia; Neutrophils; Original Article; Cohen syndrome; Neutropenia; Apoptosis; Serpin B1
• ISSN: 0946-2716; 1432-1440
• DOI: 10.1007/s00109-019-01754-4

Cohen syndrome (CS) is a rare genetic disorder due to mutations in VPS13B gene. Among various clinical and biological features, CS patients suffer from inconsistent neutropenia, which is associated with recurrent but minor infections. We demonstrate here that this neutropenia results from an exaggerate rate of neutrophil apoptosis. Besides this increased cell death, which occurs in the absence of any endoplasmic reticulum stress or defect in neutrophil elastase (ELANE) expression or localization, all neutrophil functions appeared to be normal. We showed a disorganization of the Golgi apparatus in CS neutrophils precursors, that correlates with an altered glycosylation of ICAM-1 in these cells, as evidenced by a migration shift of the protein. Furthermore, a striking decrease in the expression of SERPINB1 gene, which encodes a critical component of neutrophil survival, was detected in CS neutrophils. These abnormalities may account for the excessive apoptosis of neutrophils leading to neutropenia in CS. Key messages Cohen syndrome patients’ neutrophils display normal morphology and functions. Cohen syndrome patients’ neutrophils have an increased rate of spontaneous apoptosis compared to healthy donors’ neutrophils. No ER stress or defective ELA2 expression or glycosylation was observed in Cohen syndrome patients’ neutrophils. SerpinB1 expression is significantly decreased in Cohen syndrome neutrophils as well as in VPS13B-deficient cells.