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<identifier>oai:HAL:inserm-00821120v1</identifier>
<datestamp>2017-12-21</datestamp>
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<publisher>HAL CCSD</publisher>
<title lang=en>Aggregation of mononuclear and red blood cells through an {alpha}4{beta}1-Lu/basal cell adhesion molecule interaction in sickle cell disease.</title>
<title lang=en>Aggregation of mononuclear and red blood cells through an {alpha}4{beta}1-Lu/basal cell adhesion molecule interaction in sickle cell disease. : Mononuclear and sickle red blood cell interactions</title>
<creator>Chaar, Vicky</creator>
<creator>Picot, Julien</creator>
<creator>Renaud, Olivier</creator>
<creator>Bartolucci, Pablo</creator>
<creator>Nzouakou, Ruben</creator>
<creator>Bachir, Dora</creator>
<creator>Galactéros, Frédéric</creator>
<creator>Colin, Yves</creator>
<creator>Le Van Kim, Caroline</creator>
<creator>El Nemer, Wassim</creator>
<contributor>Protéines de la membrane érythrocytaire et homologues non-érythroides ; Université des Antilles et de la Guyane (UAG) - Institut National de la Transfusion Sanguine [Paris] (INTS) - Université Paris Diderot - Paris 7 (UPD7) - Université de la Réunion (UR) - Institut National de la Santé et de la Recherche Médicale (INSERM)</contributor>
<contributor>Imagopole (CITECH) ; Institut Pasteur [Paris]</contributor>
<contributor>Unité des maladies génétiques du globule rouge ; Assistance publique - Hôpitaux de Paris (AP-HP) - Hôpital Henri Mondor - Centre de référence des syndromes drépanocytaires majeurs - Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)</contributor>
<contributor>The investigation was supported by the Institut National de la Transfusion Sanguine (INTS), the Institut National de la Santé et de la Recherche Médicale (INSERM), Université Paris Diderot Paris 7, a grant from the Agence Nationale de la Recherche (ANR, SCADHESION 2007), two grants from Région Ile-de-France (SESAME 2007 no. F-08-1104/R and IMAGOPOLE Project 2007) and a fellowship "maladies rares" from the Société Française de Médecine Interne (SNFMI) and Actélion.</contributor>
<description>International audience</description>
<source>ISSN: 0390-6078</source>
<source>EISSN: 1592-8721</source>
<source>Haematologica</source>
<publisher>Ferrata Storti Foundation</publisher>
<identifier>inserm-00821120</identifier>
<identifier>http://www.hal.inserm.fr/inserm-00821120</identifier>
<identifier>http://www.hal.inserm.fr/inserm-00821120/document</identifier>
<identifier>http://www.hal.inserm.fr/inserm-00821120/file/1841.full.pdf</identifier>
<source>http://www.hal.inserm.fr/inserm-00821120</source>
<source>Haematologica, Ferrata Storti Foundation, 2010, 95 (11), pp.1841-8. 〈10.3324/haematol.2010.026294〉</source>
<identifier>DOI : 10.3324/haematol.2010.026294</identifier>
<relation>info:eu-repo/semantics/altIdentifier/doi/10.3324/haematol.2010.026294</relation>
<identifier>PUBMED : 20562314</identifier>
<relation>info:eu-repo/semantics/altIdentifier/pmid/20562314</relation>
<language>en</language>
<subject>[SDV.BC] Life Sciences [q-bio]/Cellular Biology</subject>
<type>info:eu-repo/semantics/article</type>
<type>Journal articles</type>
<description lang=en>BACKGROUND: Abnormal interactions between red blood cells, leukocytes and endothelial cells play a critical role in the occurrence of the painful vaso-occlusive crises associated with sickle cell disease. We investigated the interaction between circulating leukocytes and red blood cells which could lead to aggregate formation, enhancing the incidence of vaso-occlusive crises. DESIGN AND METHODS: Blood samples from patients with sickle cell disease (n=25) and healthy subjects (n=5) were analyzed by imaging and classical flow cytometry after density gradient separation. The identity of the cells in the peripheral blood mononuclear cell layer was determined using antibodies directed specifically against white (anti-CD45) or red (anti-glycophorin A) blood cells. RESULTS: Aggregates between red blood cells and peripheral blood mononuclear cells were visualized in whole blood from patients with sickle cell disease. The aggregation rate was 10-fold higher in these patients than in control subjects. Both mature red blood cells and reticulocytes were involved in these aggregates through their interaction with mononuclear cells, mainly with monocytes. The size of the aggregates was variable, with one mononuclear cell binding to one, two or several red blood cells. Erythroid Lu/basal cell adhesion molecule and α(4)β(1) integrin were involved in aggregate formation. The aggregation rate was lower in patients treated with hydroxycarbamide than in untreated patients. CONCLUSIONS: Our study gives visual evidence of the existence of circulating red blood cell-peripheral blood mononuclear cell aggregates in patients with sickle cell disease and shows that these aggregates are decreased during hydroxycarbamide treatment. Our results strongly suggest that erythroid Lu/basal cell adhesion molecule proteins are implicated in these aggregates through their interaction with α(4)β(1) integrin on peripheral blood mononuclear cells.</description>
<date>2010-11</date>
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