Expression of cell adhesion molecules in dilated cardiomyopathy - Evidencefor endothelial activation in inflammatory cardiomyopathy

Citation
M. Noutsias et al., Expression of cell adhesion molecules in dilated cardiomyopathy - Evidencefor endothelial activation in inflammatory cardiomyopathy, CIRCULATION, 99(16), 1999, pp. 2124-2131
Citations number
24
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
CIRCULATION
ISSN journal
00097322 → ACNP
Volume
99
Issue
16
Year of publication
1999
Pages
2124 - 2131
Database
ISI
SICI code
0009-7322(19990427)99:16<2124:EOCAMI>2.0.ZU;2-#
Abstract
Background-Dilated cardiomyopathy (DCM) is pathogenically linked to inflamm atory cardiomyopathy (InfCM), which is characterized by intramyocardial inf iltration. The transendothelial migration of immunocompetent cells is media ted by cell adhesion;molecules (CAMs). Methods and Results-We investigated the expression pattern of CAMs (immunog lobulin superfamily, 32 selectins, and beta(1)- and beta(2)-integrins) in e ndomyocardial biopsies from DCM patients (n=152; left ventricular ejection fraction <40%) using immunohistochemistry. Whereas few specimens obtained a t autopsy (controls; n=14) presented enhanced expression regarding single e ndothelial CAMs (human leukocyte antigen [HLA] class I, 7%; HLA-DR, 14%; CD 29, 14%), none demonstrated concurrent abundance of >3 CAMs (inflammatory e ndothelial activation), nor did any control tissue prove positive for InfCM (>7.0 CD3+ lymphocytes per 1 mm(2)). In comparison, 64% (n=97) of the DCM biopsies were evaluated positive for InfCM and 67% (n=101:) for inflammator y endothelial activation, respectively, Whereas expression of HLA class I, HLA-DR, intercellular cell adhesion molecule-1, and CD29 was distributed ho mogeneously within a patient's serial sections, immunoreactivity:of vascula r cell adhesion molecule-1, lymphocyte function antigen-3, and the selectin s was accentuated on single vascular endothelia. Sixty-six percent of the D CM biopsies presented CD29 abundance also within the extracellular matrix a nd the sarcolemma. CD62P and CD62E were present in 16% and 40% of the DCM p atients, respectively. Endothelial CAM representatives correlated with one another (P<0.05), except for CD62P with HLA. Endothelial CAM expression cor related with intramyocardial infiltrates phenotyped by the corresponding co unterreceptors. Conclusions-Inflammatory endothelial activation is present in 67% of DCM pa tients. Because CAM expression correlates with the immunohistological diagn osis of InfCM and counterreceptor-bearing intramyocardial infiltrates, eval uation of endothelial CAMs might be of diagnostic significance in InfCM.