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男性心脏中β-连环蛋白、CacyBP/SIP、半乳糖凝集素-3 和免疫蛋白酶体亚基 LMP7 水平与年龄相关的变化。

Ageing-related changes in the levels of β-catenin, CacyBP/SIP, galectin-3 and immunoproteasome subunit LMP7 in the heart of men.

机构信息

Department of Histology and Cytophysiology, Medical University of Białystok, Białystok, Poland.

Department of Neurosurgery, Medical University of Bialystok, Białystok, Poland.

出版信息

PLoS One. 2020 Mar 2;15(3):e0229462. doi: 10.1371/journal.pone.0229462. eCollection 2020.

Abstract

Aging is a major risk factor for morbidity and mortality from cardiovascular causes in men. To better understand the cellular processes related to age-related cardiac complications, we undertook research aimed at comparative evaluation of genes expression and distribution of β-catenin, CacyBP/SIP, galectin-3 and LMP7 in the heart of healthy men in different age groups. The study was conducted on the hearts of 12 men (organ donors) without a history of cardiovascular disease, who were divided into two age groups: men under and men over 45 years of age. On paraffin sections, immunohistochemical reactions were performed to detect β-catenin, CacyBP/SIP, galectin-3 and immunoproteasome subunit LMP7. The expression of genes coding β-catenin, CacyBP/SIP, galectin-3 and LMP7 was also evaluated by real-time PCR method. In the heart of men over 45 years old, both gene expression and immunoreactivity of β-catenin, CacyBP/SIP, galectin-3 and LMP7 were stronger compared to younger individuals. The results of the presented studies suggest that β-catenin, CacyBP/SIP, galectin-3 and immunoproteasomes might be involved in the internal regulation of heart homeostasis during ageing.

摘要

衰老是男性心血管疾病发病率和死亡率的一个主要危险因素。为了更好地了解与年龄相关的心脏并发症相关的细胞过程,我们进行了研究,旨在比较评估不同年龄组健康男性心脏中β-连环蛋白、CacyBP/SIP、半乳糖凝集素-3 和 LMP7 的基因表达和分布。该研究在 12 名(器官捐献者)男性的心脏上进行,这些男性没有心血管疾病史,他们被分为两个年龄组:45 岁以下和 45 岁以上的男性。在石蜡切片上,进行免疫组织化学反应以检测β-连环蛋白、CacyBP/SIP、半乳糖凝集素-3 和免疫蛋白酶体亚单位 LMP7。还通过实时 PCR 方法评估编码β-连环蛋白、CacyBP/SIP、半乳糖凝集素-3 和 LMP7 的基因的表达。在 45 岁以上的男性心脏中,β-连环蛋白、CacyBP/SIP、半乳糖凝集素-3 和 LMP7 的基因表达和免疫反应性均强于年轻个体。本研究的结果表明,β-连环蛋白、CacyBP/SIP、半乳糖凝集素-3 和免疫蛋白酶体可能参与衰老过程中心脏内稳态的内部调节。

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