Becker Katrin
Cardiovascular Research Laboratory, Department of Cardiology, Pulmonary Diseases and Vascular Medicine, Medical Faculty, University Hospital Düsseldorf, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Institute for Molecular Cardiology, Medical Faculty, University Hospital Düsseldorf, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Cells. 2025 Jun 11;14(12):883. doi: 10.3390/cells14120883.
BACKGROUND/OBJECTIVES: While the presence of inflammatory processes in stenotic aortic valves is acknowledged, no systematic characterization of the systemic immune reaction upon aortic valve stenosis (AS) has been performed yet. The hypothesis of this study was that AS induces a systemic inflammatory reaction linked with local processes in the heart. METHODS: Murine wire injury (WI) to induce AS, or sham surgery, were performed prior to the 4-week assessment of AS severity, left ventricular (LV) function and hypertrophy with echocardiography (echo). Organ weights, levels of leukocytes, cytokines and costimulatory molecules in blood, heart, and peripheral immune organs (spleen, liver, lymph nodes), and immune cell uptake of Cy5-labelled perfluorocarbon nanoemulsions were measured. RESULTS: Trends towards correlation were found between organ weights, myocardial immune cells and echo. Cytokine mRNA levels trended mainly towards an increase in heart and regional lymph nodes and a reduction in spleen and liver, and correlation with echo was more homogeneous after WI. Unchanged cytokine protein levels in myocardium and plasma trended to correlate with echo. A homogeneous pattern was found for echo and costimulatory molecule correlation, while PFC uptake by lymphatic cells was reduced upon AS. CONCLUSIONS: The results suggest a link between number and activation state of leukocytes in peripheral organs and cardiac processes in AS. Considering the pathological value of inflammation, it is crucial that future studies investigate if a modulation of the systemic inflammatory reaction relieves severity of AS and opposes development of heart failure.
背景/目的:虽然人们认识到狭窄主动脉瓣中存在炎症过程,但尚未对主动脉瓣狭窄(AS)时的全身免疫反应进行系统表征。本研究的假设是,AS会引发与心脏局部过程相关的全身炎症反应。 方法:在通过超声心动图(echo)对AS严重程度、左心室(LV)功能和肥大进行4周评估之前,进行小鼠钢丝损伤(WI)以诱导AS或假手术。测量器官重量、血液中白细胞、细胞因子和共刺激分子的水平、心脏和外周免疫器官(脾脏、肝脏、淋巴结),以及Cy5标记的全氟碳纳米乳剂的免疫细胞摄取量。 结果:在器官重量、心肌免疫细胞和echo之间发现了相关性趋势。细胞因子mRNA水平主要呈现出心脏和局部淋巴结增加、脾脏和肝脏减少的趋势,WI后与echo的相关性更一致。心肌和血浆中细胞因子蛋白水平不变,其趋势与echo相关。在echo和共刺激分子相关性方面发现了一致的模式,而AS时淋巴细胞对PFC的摄取减少。 结论:结果表明外周器官中白细胞的数量和激活状态与AS中的心脏过程之间存在联系。考虑到炎症的病理价值,未来研究调查全身炎症反应的调节是否能减轻AS的严重程度并对抗心力衰竭的发展至关重要。
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