Increased M1 Macrophages Infiltration Is Associated with Thrombogenesis in Rheumatic Mitral Stenosis Patients with Atrial Fibrillation

Autor: Suhui Zhu, Jun Xie, Guixin He, Bingjian Wang, Biao Xu, Guannan Li, Wei Tan, Jianzhou Chen
Rok vydání: 2016
Předmět:
Male
0301 basic medicine
Pathology
Inflammasomes
Interleukin-1beta
lcsh:Medicine
Apoptosis
030204 cardiovascular system & hematology
Pathology and Laboratory Medicine
Biochemistry
White Blood Cells
0302 clinical medicine
Animal Cells
Atrial Fibrillation
Medicine and Health Sciences
Mitral Valve Stenosis
Myocytes
Cardiac

Cardiac Atria
lcsh:Science
Immune Response
Stenosis
Immune System Proteins
Multidisciplinary
Cell Death
Heart
Atrial fibrillation
Middle Aged
M2 Macrophage
Thrombosis
Cell Processes
cardiovascular system
Cardiology
Female
Cellular Types
Anatomy
medicine.symptom
Arrhythmia
Research Article
Adult
medicine.medical_specialty
Patients
Immune Cells
Immunology
Inflammation
Proinflammatory cytokine
03 medical and health sciences
Signs and Symptoms
Mitral valve stenosis
Internal medicine
NLR Family
Pyrin Domain-Containing 3 Protein

medicine
Humans
cardiovascular diseases
Thrombus
Blood Cells
business.industry
Macrophages
lcsh:R
Rheumatic Heart Disease
Biology and Life Sciences
Proteins
Cell Biology
medicine.disease
Health Care
030104 developmental biology
Cardiovascular Anatomy
lcsh:Q
Carrier Proteins
business
Zdroj: PLoS ONE, Vol 11, Iss 3, p e0149910 (2016)
PLoS ONE
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0149910
Popis: Atrial fibrillation (AF) is the most common arrhythmia. In patients with AF, the role of macrophage subsets in thrombogenesis is unclear. In the present study, we analyzed the role of M1 and M2 macrophages and related cytokines in thrombogenesis of AF. Immunohistochemistry, Western blot, and TUNEL assay were used to detect M1/M2 macrophage infiltration, the expression pattern of IL-1β and inflammasome components, and apoptosis of cardiomyocytes in 71 specimens obtained from the left atrial appendage of patients with rheumatic mitral stenosis (MS) with or without thrombosis. We demonstrated that proinflammatory M1 macrophages were predominant in the atrium of MS patients with AF and thrombus. NLRP3 inflammasomes and IL-1β, which are primarily functional in macrophages, were activated in those patients. We also showed that increased cell death was associated with thrombogenesis in MS patients. These data indicate that infiltration of M1 macrophages and over-activation of NLRP3 inflammasomes may play a role in progressive atrial inflammation and thrombogenesis in rheumatic mitral stenosis patients with AF.
Databáze: OpenAIRE