TY - JOUR
T1 - C-type natriuretic peptide in human coronary atherosclerotic lesions
AU - Naruko, Takahiko
AU - Ueda, Makiko
AU - Van der Wal, Allard C.
AU - Van der Loos, Chris M.
AU - Itoh, Hiroshi
AU - Nakao, Kazuwa
AU - Becker, Anton E.
PY - 1996
Y1 - 1996
N2 - Background: C-type natriuretic peptide (CNP) belongs to the natriuretic peptide family and is considered to have regulatory effects on vascular tone and smooth muscle growth. Since these features play a role in atherogenesis, the presence of CNP at such sites was studied. Methods and Results: Thirty- three coronary artery segments were harvested at autopsy: 10 normal, with diffuse intimal thickening, and 23 atherosclerotic lesions. Samples were snap-frozen and processed for immunohistochemical staining. For the identification of CNP, a mouse monoclonal antibody (KY-CNP-1) was used. 1A4, EBM-11 (CD68), and von Willebrand factor antibodies were used to stain smooth muscle cells, macrophages, and endothelial cells, respectively. CNP is present in several cell types. Normal arterial segments show CNP-positive endothelial cells. Hypercellular atherosclerotic lesions show distinct CNP positivity of smooth muscle cells and macrophages but a decrease in positivity of endothelial cells. Advanced atherosclerotic lesions contain CNP-positive macrophages, but the smooth muscle cells within the fibrous cap and the surface endothelial cells are almost all CNP negative. Conclusions: These observations suggest that CNP has functional significance in atherogenesis.
AB - Background: C-type natriuretic peptide (CNP) belongs to the natriuretic peptide family and is considered to have regulatory effects on vascular tone and smooth muscle growth. Since these features play a role in atherogenesis, the presence of CNP at such sites was studied. Methods and Results: Thirty- three coronary artery segments were harvested at autopsy: 10 normal, with diffuse intimal thickening, and 23 atherosclerotic lesions. Samples were snap-frozen and processed for immunohistochemical staining. For the identification of CNP, a mouse monoclonal antibody (KY-CNP-1) was used. 1A4, EBM-11 (CD68), and von Willebrand factor antibodies were used to stain smooth muscle cells, macrophages, and endothelial cells, respectively. CNP is present in several cell types. Normal arterial segments show CNP-positive endothelial cells. Hypercellular atherosclerotic lesions show distinct CNP positivity of smooth muscle cells and macrophages but a decrease in positivity of endothelial cells. Advanced atherosclerotic lesions contain CNP-positive macrophages, but the smooth muscle cells within the fibrous cap and the surface endothelial cells are almost all CNP negative. Conclusions: These observations suggest that CNP has functional significance in atherogenesis.
KW - atherosclerosis
KW - muscle, smooth
KW - natriuretic peptides
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U2 - 10.1161/01.CIR.94.12.3103
DO - 10.1161/01.CIR.94.12.3103
M3 - Article
C2 - 8989116
AN - SCOPUS:0030452795
SN - 0009-7322
VL - 94
SP - 3103
EP - 3108
JO - Circulation
JF - Circulation
IS - 12
ER -