年龄相关性心脏和脾脏S100A9和NLRP3表达的性别差异。

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Kathleen Pappritz, Isabel Voss, Muhammad El-Shafeey, Sophie Van Linthout
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引用次数: 0

摘要

年龄是心血管疾病(CVD)的重要危险因素,并与全身性低度炎症有关,即所谓的“炎症”。我们的目的是研究年龄和性别对衰老过程早期炎症标志物S100A9和NLRP3炎症小体成分的影响,使用成熟的成年小鼠和中年/围绝经期小鼠。鉴于心脾轴在心力衰竭中的重要性,除左心室和心脏成纤维细胞外,还分析了脾脏。通过免疫组织化学、流式细胞术和基因表达分析,我们的研究表明,与年龄匹配的雄性和3个月大的雌性小鼠相比,围绝经期小鼠脾脏的炎症状态更高,而衰老与S100A9和NLRP3炎性小体成分的左心室基因表达升高有关,与性别无关。总之,我们的数据表明,脾脏和左心室的炎症特征在中年小鼠中已经有所不同,并且部分取决于性别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex differences in age-related cardiac and splenic S100A9 and NLRP3 expression.

Age is an important risk factor for cardiovascular diseases (CVD) and associated with a systemic, low-grade inflammation, so called "inflammaging". We aimed to investigate the impact of age and sex on the inflammatory markers S100A9 and components of the NLRP3 inflammasome at an early stage in the aging process, using mature adult and middle-aged/perimenopausal mice. Given the importance of the cardiosplenic axis in heart failure, the spleen was analyzed in addition to the left ventricle and cardiac fibroblasts. Using immunohistochemistry, flow cytometry and gene expression analysis, our study demonstrates a higher inflammatory state of the spleen in perimenopausal versus age-matched males and 3-months old female mice, whereas aging is associated with higher left ventricular gene expression of S100A9 and NLRP3 inflammasome components independent of sex. In conclusion, our data indicate that inflammatory signatures in the spleen and left ventricle already differ in middle-aged mice and are partly sex-dependent.

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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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