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Cystic fibrosis transmembrane conductance regulator (CFTR) regulates the production of osteoprotegerin (OPG) and prostaglandin (PG) E2 in human bone.
Le Heron L., Guillaume C., Velard F., Braux J., Touqui L., Moriceau S., Sermet-Gaudelus I., Laurent-Maquin D., Jacquot J.
Journal of Cystic Fibrosis 9, 1 (2010) 69-72 - http://www.hal.inserm.fr/inserm-00501818
(20005786)
Cystic fibrosis transmembrane conductance regulator (CFTR) regulates the production of osteoprotegerin (OPG) and prostaglandin (PG) E2 in human bone.
Louis Le Heron1, Christine Guillaume1, Frédéric Velard1, Julien Braux1, Lhousseine Touqui2, Sandra Moriceau3, Isabelle Sermet-Gaudelus3, Dominique Laurent-Maquin1, Jacky Jacquot () 1
1 :  Interface biomatériaux/Tissus hôtes
INSERM : U926 – Université de Reims - Champagne Ardenne
UFR Pharmacie 1, rue du maréchal Juin, 51095 Reims
France
2 :  Défense innée et inflammation
INSERM : U874 – Institut Pasteur de Paris
25, rue du Docteur Roux 75724 PARIS CEDEX 15
France
3 :  Centre de recherche Croissance et signalisation
INSERM : U845 – Université Paris V - Paris Descartes
Fac de médecine Necker-enfants malades 156, rue de vaugirard 75730 PARIS CEDEX 15
France
Bone loss is an important clinical issue in patients with cystic fibrosis (CF). Whether the cystic fibrosis transmembrane conductance regulator (CFTR) plays a direct role in bone cell function is yet unknown. In this study, we provide evidence that inhibition of CFTR-Cl(-) channel function results in a significant decrease of osteoprotegerin (OPG) secretion accompanied with a concomitant increase of prostaglandin (PG) E(2) secretion of primary human osteoblast cultures (n=5). Our data therefore suggest that in bone cells of CF patients, the loss of CFTR activity may result in an increased inflammation-driven bone resorption (through both the reduced OPG and increased PGE(2) production), and thus might contribute to the early bone loss reported in young children with CF.
Sciences du Vivant/Médecine humaine et pathologie/Pneumologie et système respiratoire
Sciences du Vivant/Médecine humaine et pathologie/Rhumatologie et système ostéo-articulaire
Sciences du Vivant/Biochimie, Biologie Moléculaire
Anglais
1873-5010

Articles dans des revues avec comité de lecture
10.1016/j.jcf.2009.11.005
Journal of Cystic Fibrosis (J Cyst Fibros)
Publisher Elsevier
ISSN 1569-1993 
internationale
01/2010
14/12/2009
9
1
69-72

CFTR – human bone – OPG – PGE2 – osteoclatogenesis
Aged – Bone Resorption – Cells – Cultured – Cystic Fibrosis – Cystic Fibrosis Transmembrane Conductance Regulator – Dinoprostone – Female – Humans – Middle Aged – Osteoblasts – Osteoprotegerin – RNA – Messenger – Reverse Transcriptase Polymerase Chain Reaction