Document Detail


Chemokines regulate small leucine-rich proteoglycans in the extracellular matrix of the pressure-overloaded right ventricle.
MedLine Citation:
PMID:  22345433     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Chemokines have been suggested to play a role during development of left ventricular failure, but little is known about their role during right ventricular (RV) remodeling and dysfunction. We have previously shown that the chemokine (C-X-C motif) ligand 13 (CXCL13) regulates small leucine-rich proteoglycans (SLRPs). We hypothesized that chemokines are upregulated in the pressure-overloaded RV, and that they regulate SLRPs. Mice with RV pressure overload following pulmonary banding (PB) had a significant increase in RV weight and an increase in liver weight after 1 wk. Microarray analysis (Affymetrix) of RV tissue from mice with PB revealed that CXCL10, CXCL6, chemokine (C-X3-C motif) ligand 1 (CX3CL1), chemokine (C-C motif) ligand 5 (CCL5), CXCL16, and CCL2 were the most upregulated chemokines. Stimulation of cardiac fibroblasts with these same chemokines showed that CXCL16 increased the expression of the four SLRPs: decorin, lumican, biglycan, and fibromodulin. CCL5 increased the same SLRPs, except decorin, whereas CX3CL1 increased the expression of decorin and lumican. CXCL16, CX3CL1, and CCL5 were also shown to increase the levels of glycosylated decorin and lumican in the medium after stimulation of fibroblasts. In the pressure-overloaded RV tissue, Western blotting revealed an increase in the total protein level of lumican and a glycosylated form of decorin with a higher molecular weight compared with control mice. Both mice with PB and patients with pulmonary stenosis had significantly increased circulating levels of CXCL16 compared with healthy controls measured by enzyme immunoassay. In conclusion, we have found that chemokines are upregulated in the pressure-overloaded RV and that CXCL16, CX3CL1, and CCL5 regulate expression and posttranslational modifications of SLRPs in cardiac fibroblasts. In the pressure-overloaded RV, protein levels of lumican were increased, and a glycosylated form of decorin with a high molecular weight appeared.
Authors:
Anne Waehre; Maria Vistnes; Ivar Sjaastad; Ståle Nygård; Cathrine Husberg; Ida Gjervold Lunde; Pål Aukrust; Arne Yndestad; Leif E Vinge; Dina Behmen; Christian Neukamm; Henrik Brun; Erik Thaulow; Geir Christensen
Related Documents :
8155443 - Haemodynamics of liver reperfusion: comparison of two anaesthetic techniques.
385143 - A computerised dichromatic earpiece densitometer for the measurement of cardiac output.
2240793 - Effect of endotoxin administration on equine digital hemodynamics and starling forces.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2012-02-16
Journal Detail:
Title:  Journal of applied physiology (Bethesda, Md. : 1985)     Volume:  112     ISSN:  1522-1601     ISO Abbreviation:  J. Appl. Physiol.     Publication Date:  2012 Apr 
Date Detail:
Created Date:  2012-04-16     Completed Date:  2012-09-17     Revised Date:  2013-09-26    
Medline Journal Info:
Nlm Unique ID:  8502536     Medline TA:  J Appl Physiol (1985)     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1372-82     Citation Subset:  IM    
Affiliation:
Institute for Experimental Medical Research, Oslo University Hospital and University of Oslo, Kirkeveien 166, Oslo, Norway. anne.wahre@medisin.uio.no
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Animals
Case-Control Studies
Chemokine CCL5 / metabolism
Chemokine CX3CL1 / metabolism
Chemokine CXCL6 / metabolism
Chemokines / metabolism*
Chemokines, CXC / metabolism
Child
Child, Preschool
Extracellular Matrix / metabolism*
Female
Fibroblasts / metabolism
Humans
Hypertrophy, Right Ventricular / metabolism*
Infant
Leucine / metabolism*
Male
Mice
Mice, Inbred C57BL
Models, Animal
Proteoglycans / metabolism*
Pulmonary Valve Stenosis / metabolism
Receptors, Scavenger / metabolism
Ventricular Dysfunction, Right / metabolism*
Chemical
Reg. No./Substance:
0/CXCL16 protein, human; 0/Ccl5 protein, mouse; 0/Chemokine CCL5; 0/Chemokine CX3CL1; 0/Chemokine CXCL6; 0/Chemokines; 0/Chemokines, CXC; 0/Cx3cl1 protein, mouse; 0/Cxcl16 protein, mouse; 0/Proteoglycans; 0/Receptors, Scavenger; 61-90-5/Leucine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Effects of lactate on the voltage-gated sodium channels of rat skeletal muscle: modulating current o...
Next Document:  Effect of rowing ergometry and oral volume loading on cardiovascular structure and function during b...