Cystic fibrosis transmembrane conductance regulator (CFTR) regulates the production of osteoprotegerin (OPG) and prostaglandin (PG) E2 in human bone 

Slides:



Advertisements
Similar presentations
IL-18 Downregulates Collagen Production in Human Dermal Fibroblasts via the ERK Pathway  Hee Jung Kim, Seok Bean Song, Jung Min Choi, Kyung Moon Kim,
Advertisements

Inhibitory effect of troglitazone on TNF-α-induced expression of monocyte chemoattractant protein-1 (MCP-1) in human endothelial cells  Masayoshi Y Ohta,
A potential role of chondroitin sulfate on bone in osteoarthritis: inhibition of prostaglandin E2 and matrix metalloproteinases synthesis in interleukin-1β-
Bacterial contamination in the environment of hospitalised children with cystic fibrosis  Agnès Ferroni, Aurélie Werkhauser-Bertrand, Muriel Le Bourgeois,
Adenosine analogs and electromagnetic fields inhibit prostaglandin E2 release in bovine synovial fibroblasts  M. De Mattei, Ph.D., K. Varani, Ph.D., F.F.
Elevated hepatic SULT1E1 activity in mouse models of cystic fibrosis alters the regulation of estrogen responsive proteins  Li Li, Charles N. Falany 
Reduced levels of active GLP-1 in patients with cystic fibrosis with and without diabetes mellitus  Magnus Hillman, Leif Eriksson, Lena Mared, Karin Helgesson,
Persistent Bordetella bronchiseptica infection in a child with cystic fibrosis: Relationship to bacterial phenotype  Nevine El Khatib, Agnes Ferroni,
The hsa-miR-125a/hsa-let-7e/hsa-miR-99b cluster is potentially implicated in Cystic Fibrosis pathogenesis  Marie-Laure Endale Ahanda, Thierry Bienvenu,
Effect of ivacaftor on CFTR forms with missense mutations associated with defects in protein processing or function  Fredrick Van Goor, Haihui Yu, Bill.
Splicing defects in the CFTR gene: Minigene analysis of two mutations, G>C and A>G  Gwendal Dujardin, Diane Commandeur, Catherine Le Jossic-Corcos,
The hsa-miR-125a/hsa-let-7e/hsa-miR-99b cluster is potentially implicated in Cystic Fibrosis pathogenesis  Marie-Laure Endale Ahanda, Thierry Bienvenu,
NF-κBp65-specific siRNA inhibits expression of genes of COX-2, NOS-2 and MMP-9 in rat IL-1β-induced and TNF-α-induced chondrocytes  Dr C. Lianxu, Ph.D.,
A novel neutrophil derived inflammatory biomarker of pulmonary exacerbation in cystic fibrosis  Emer P. Reeves, David A. Bergin, Sean Fitzgerald, Elaine.
Induction of cathelicidin in normal and CF bronchial epithelial cells by 1,25- dihydroxyvitamin D3  Sunghan Yim, Puneet Dhawan, Chandran Ragunath, Sylvia.
Charlotte Andersson, Munir M. Zaman, Amanda B. Jones, Steven D
Interleukin-17 and Interferon-γ Synergize in the Enhancement of Proinflammatory Cytokine Production by Human Keratinocytes  Marcel B.M. Teunissen, Jan.
Avani C. Modi, Crystal S. Lim, Nami Yu, David Geller, Mary H
Oxidative stress in stable cystic fibrosis patients: Do we need higher antioxidant plasma levels?  Antonela Lezo, Fiorella Biasi, Paola Massarenti, Roberto.
Modulation of the expression of tissue plasminogen activator and its inhibitor by hypoxia in human peritoneal and adhesion fibroblasts  Ghassan M Saed,
Megan R. Nelson, Craig R. Adamski, Audrey Tluczek 
Urinary incontinence in 9���16��year olds with cystic fibrosis compared to other respiratory conditions and a normal group  W.J. Browne, C.J. Wood, M.
Measures of body habitus are associated with lung function in adults with cystic fibrosis: A population-based study  Doug L. Forrester, Alan J. Knox,
Expression and regulation of Toll-like receptor 2 by IL-1β and fibronectin fragments in human articular chondrocytes  S.-L. Su, M.S., C.-D. Tsai, Ph.D.,
Cirrhosis and other liver disease in cystic fibrosis
Ibuprofen rescues mutant cystic fibrosis transmembrane conductance regulator trafficking  Graeme W. Carlile, Renaud Robert, Julie Goepp, Elizabeth Matthes,
Controlled clinical trials in cystic fibrosis — are we doing better?
Should diffuse bronchiectasis still be considered a CFTR-related disorder?  Anne Bergougnoux, Victoria Viart, Julie Miro, Sébastien Bommart, Nicolas Molinari,
Anju Anand, Elizabeth Tullis, Anne Stephenson, Preyanka Abhyankar 
D. Stevens, P.J. Oades, N. Armstrong, C.A. Williams 
Claire J. Tipping, Rebecca L. Scholes, Narelle S. Cox 
DIO2 modifies inflammatory responses in chondrocytes
Cystic fibrosis mortality trend in Italy from 1970 to 2011
Disposition index identifies defective beta-cell function in cystic fibrosis subjects with normal glucose tolerance  L. Merjaneh, Q. He, Q. Long, L.S.
Selenomethionine inhibits IL-1β inducible nitric oxide synthase (iNOS) and cyclooxygenase 2 (COX2) expression in primary human chondrocytes  A.W.M. Cheng,
Clinical presentation of mild cystic fibrosis in a Serbian patient homozygous for the CFTR mutation c G>A  Aleksandra Nikolic, Nedeljko Radlovic,
Amyloidosis in cystic fibrosis: A case series
A.H. Gifford  Journal of Cystic Fibrosis 
Volume 54, Issue 2, Pages (August 1998)
Dr J. Deschner, D. M. D. , Ph. D. , Dr B. Rath-Deschner, D. M. D. , Ph
Osteoclast function, bone turnover and inflammatory cytokines during infective exacerbations of cystic fibrosis  Elizabeth F. Shead, Charles S. Haworth,
Inhalation solutions — Which ones may be mixed
Optimizing strategies for CFTR molecular testing
E. Tschiedel, H. Grasemann, F. Ratjen  Journal of Cystic Fibrosis 
Cystic fibrosis transmembrane conductance regulator gene variants are associated with autoimmune pancreatitis and slow response to steroid treatment 
Diagnostic multiplex PCR assay for the identification of the Liverpool, Midlands 1 and Manchester CF epidemic strains of Pseudomonas aeruginosa  Joanne.
Prevalence and risk factors for recovery of filamentous fungi in individuals with cystic fibrosis  Christopher R. Sudfeld, Elliott C. Dasenbrook, William.
Increased expression of Interleukin-13 but not Interleukin-4 in cystic fibrosis patients  Hans-Peter Hauber, Djalal Gholami, Gerhard Koppermann, Hans-Eberhard.
Chee Y. Ooi, Peter R. Durie  Journal of Cystic Fibrosis 
Effect of ivacaftor in patients with advanced cystic fibrosis and a G551D-CFTR mutation: Safety and efficacy in an expanded access program in the United.
Paternity in men with cystic fibrosis: a retrospective survey in France  Ingrid Duguépéroux, Dominique Hubert, Stéphane Dominique, Gil Bellis, Marc De.
Trends in pathogens colonising the respiratory tract of adult patients with cystic fibrosis, 1985–2005  F.A. Millar, N.J. Simmonds, M.E. Hodson  Journal.
IL-18 Downregulates Collagen Production in Human Dermal Fibroblasts via the ERK Pathway  Hee Jung Kim, Seok Bean Song, Jung Min Choi, Kyung Moon Kim,
J.E. Spahr, R.B. Love, M. Francois, K. Radford, K.C. Meyer 
Design of adult and paediatric studies investigating the efficacy and tolerability of ivacaftor [16, 17]. Design of adult and paediatric studies investigating.
Michael W. Konstan, David J. Pasta, Jeffrey S. Wagener, Donald R
Volume 64, Issue 6, Pages (December 2003)
C. R. Hansen, T. Pressler, K. G. Nielsen, P. Ø. Jensen, T
D.F. Waterhouse, A.M. McLaughlin, C.G. Gallagher 
CFTR modulators and pregnancy: Our work has only just begun
‘Peeling paint’ dermatitis as a presenting sign of cystic fibrosis
Lutz Goldbeck, Sven Zerrer, Tim G. Schmitz  Journal of Cystic Fibrosis 
Changes of CFTR functional measurements and clinical improvements in cystic fibrosis patients with non p.Gly551Asp gating mutations treated with ivacaftor 
Khin M. Gyi, Margaret E. Hodson, Magdi Y. Yacoub 
David Adeboyeku, Sandra Scott, Margaret E. Hodson 
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens  Hongjun.
Estrogen and selective estrogen receptor modulators regulate vascular endothelial growth factor and soluble vascular endothelial growth factor receptor.
Triptolide is a potent suppressant of C3, CD40 and B7h expression in activated human proximal tubular epithelial cells  Yuzhi Hong, Wuding Zhou, Ke Li,
Elisabeth P. Dellon, Margaret W. Leigh, James R. Yankaskas, Terry L
Improved early diagnosis of Pseudomonas aeruginosa by real-time PCR to prevent chronic colonisation in a paediatric cystic fibrosis population  Elaine.
Presentation transcript:

Cystic fibrosis transmembrane conductance regulator (CFTR) regulates the production of osteoprotegerin (OPG) and prostaglandin (PG) E2 in human bone  Louis Le Heron, Christine Guillaume, Frédéric Velard, Julien Braux, Lhousseine Touqui, Sandra Moriceau, Isabelle Sermet-Gaudelus, Dominique Laurent-Maquin, Jacky Jacquot  Journal of Cystic Fibrosis  Volume 9, Issue 1, Pages 69-72 (January 2010) DOI: 10.1016/j.jcf.2009.11.005 Copyright © 2009 European Cystic Fibrosis Society. Terms and Conditions

Fig. 1 Panel A: CFTR mRNA expression of human osteoblasts in primary culture (lane 2) compared to positive control human bronchial cells (16HBE14-cell line, lane 1) analyzed by RT-PCR; PCR products were separated by 1% agarose gel electrophoresis and visualized with ethidium bromide with an ImageMaster® VDS (Pharmacia Biotech). Panel B: CFTR protein immunofluorescence in normal human osteoblasts (passage 3, 7week-culture). Journal of Cystic Fibrosis 2010 9, 69-72DOI: (10.1016/j.jcf.2009.11.005) Copyright © 2009 European Cystic Fibrosis Society. Terms and Conditions

Fig. 2 Panels A and B: Osteoprotegerin (OPG) and prostaglandin E2 (PGE2) secretion (pg/ml/106 cells) by cultured human osteoblasts and maintained for a 5-h period in the absence (−) and presence (+) of TNF-α (20ng/ml) following a 72-h pretreatment of 10μM of CFTR-inh172, respectively. ** Significantly different (p<0.05) from control (DMSO). Results are the mean and S.E. of five independent experiments (realized in triplicate). Journal of Cystic Fibrosis 2010 9, 69-72DOI: (10.1016/j.jcf.2009.11.005) Copyright © 2009 European Cystic Fibrosis Society. Terms and Conditions