Expression of tenascin C in cardiovascular lesions of Kawasaki disease.


Journal

Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
ISSN: 1879-1336
Titre abrégé: Cardiovasc Pathol
Pays: United States
ID NLM: 9212060

Informations de publication

Date de publication:
Historique:
received: 16 04 2018
revised: 05 10 2018
accepted: 13 10 2018
pubmed: 13 11 2018
medline: 15 3 2019
entrez: 13 11 2018
Statut: ppublish

Résumé

To examine tenascin C (TN-C) expression in coronary artery lesions (CALs) and myocardial lesions (MLs) in Kawasaki disease (KD). Twenty-five KD autopsy cases (post-KD-onset range of 6 days to 17 years) were examined in this study. Time-course analysis based on the disease day was performed of the histological findings for the CALs and MLs, as well as the localization and intensity of expression of TN-C. TN-C expression was observed to coincide with the areas where inflammatory cell infiltration was present in both coronary arteries and myocardium during the acute stage of KD, and the intensity of its expression correlated with the degree of inflammation. Obvious TN-C expression persisted in the thickened intima and media of CALs even after Disease Day 27. However, in spite of the presence of inflammatory cell infiltration, TN-C expression became weaker in the adventitia and surrounding connective tissue. After 8 months or more, TN-C was not expressed in the vasculitis scars of most cases, but expression was observed around newly formed vessels in the thickened intima and around recanalized vessels after thrombotic occlusion. The findings suggest a correlation between the degree of inflammation and TN-C expression in the cardiovascular lesions of acute-stage Kawasaki disease.

Sections du résumé

BACKGROUND/OBJECTIVE OBJECTIVE
To examine tenascin C (TN-C) expression in coronary artery lesions (CALs) and myocardial lesions (MLs) in Kawasaki disease (KD).
METHODS AND RESULTS RESULTS
Twenty-five KD autopsy cases (post-KD-onset range of 6 days to 17 years) were examined in this study. Time-course analysis based on the disease day was performed of the histological findings for the CALs and MLs, as well as the localization and intensity of expression of TN-C. TN-C expression was observed to coincide with the areas where inflammatory cell infiltration was present in both coronary arteries and myocardium during the acute stage of KD, and the intensity of its expression correlated with the degree of inflammation. Obvious TN-C expression persisted in the thickened intima and media of CALs even after Disease Day 27. However, in spite of the presence of inflammatory cell infiltration, TN-C expression became weaker in the adventitia and surrounding connective tissue. After 8 months or more, TN-C was not expressed in the vasculitis scars of most cases, but expression was observed around newly formed vessels in the thickened intima and around recanalized vessels after thrombotic occlusion.
CONCLUSIONS CONCLUSIONS
The findings suggest a correlation between the degree of inflammation and TN-C expression in the cardiovascular lesions of acute-stage Kawasaki disease.

Identifiants

pubmed: 30419479
pii: S1054-8807(18)30108-X
doi: 10.1016/j.carpath.2018.10.005
pii:
doi:

Substances chimiques

Biomarkers 0
TNC protein, human 0
Tenascin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

25-30

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Yuki Yokouchi (Y)

Department of Surgical Pathology, Toho University Ohashi Medical Center, Tokyo, Japan. Electronic address: tyuki@med.toho-u.ac.jp.

Toshiaki Oharaseki (T)

Department of Surgical Pathology, Toho University Ohashi Medical Center, Tokyo, Japan.

Yasunori Enomoto (Y)

Department of Surgical Pathology, Toho University Ohashi Medical Center, Tokyo, Japan.

Wakana Sato (W)

Department of Surgical Pathology, Toho University Ohashi Medical Center, Tokyo, Japan.

Kyoko Imanaka-Yoshida (K)

Department of Pathology and Matrix Biology, Mie University Graduate School of Medicine, Mie, Japan; Mie University Research Center for Matrix Biology, Mie, Japan.

Kei Takahashi (K)

Department of Surgical Pathology, Toho University Ohashi Medical Center, Tokyo, Japan.

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Classifications MeSH