Department of Histology and Embryology, Faculty of Medicine in Hradec Kralove, Charles University, Hradec Kralove, Czech Republic.
Department of Physiology, Faculty of Science, Charles University, Prague, Czech Republic.
J Muscle Res Cell Motil. 2024 Jun;45(2):41-51. doi: 10.1007/s10974-023-09641-9. Epub 2023 Jan 24.
Nestin is a unique intermediate filament expressed for a short period in the developing heart. It was also documented in several cell types of the adult myocardium under pathological conditions such as myocardial infarction or fibrosis. However, circumstances of nestin re-occurrence in the diseased or aging heart have not been elucidated yet. In this work we immunohistochemically detected nestin to determine its expression and distribution pattern in the left ventricular myocardium of normotensive Wistar Kyoto (WKY) rats and in the hypertrophic ones of spontaneously hypertensive (SHR) rats, both at the age of 1 and 1.5 year. No nestin cells were identified in the intact myocardium of 1-year-old WKY rats, whereas in the aged 1.5-year-old WKY rats nestin endothelial cells in some blood vessels were discovered. In the hypertrophic myocardium of all SHR rats, nestin was rarely detected in desmin vimentin cardiomyocytes and in some vimentin interstitial cells often accumulated in clusters, varying in intensity of desmin immunoreactivity. Moreover, nestin was infrequently expressed in the endothelial cells of some myocardial blood vessels in 1-year-old SHR rats, but not in 1.5-year-old ones. Quantitative image analysis of nestin expression in the myocardium confirmed significant increase in 1.5-year-old WKY rats and in SHR rats of both ages compared to the intact 1-year-old WKY rats. This study firstly documents nestin re-expression indicating cytoskeletal remodelling in different cell types of the aging intact and chronically pressure over-loaded hypertrophied myocardium. Our findings confirm nestin involvement in complex changes during myocardial hypertrophy and progressive aging.
巢蛋白是一种在发育中的心脏中短暂表达的独特中间丝。在心肌梗死或纤维化等病理条件下,它也被记录在成年心肌的几种细胞类型中。然而,巢蛋白在病变或衰老心脏中重新出现的情况尚未阐明。在这项工作中,我们通过免疫组织化学检测巢蛋白,以确定其在正常血压 Wistar Kyoto(WKY)大鼠左心室心肌中和自发性高血压(SHR)大鼠肥厚心肌中的表达和分布模式,大鼠年龄分别为 1 岁和 1.5 岁。在 1 岁的 WKY 大鼠完整心肌中未发现巢蛋白细胞,而在 1.5 岁的老年 WKY 大鼠中,发现一些血管中的巢蛋白内皮细胞。在所有 SHR 大鼠的肥厚心肌中,巢蛋白在 desmin vimentin 心肌细胞中很少被检测到,而在一些 vimentin 间质细胞中则经常聚集在一起,其 desmin 免疫反应强度不同。此外,在 1 岁的 SHR 大鼠的一些心肌血管内皮细胞中,巢蛋白表达也很少,但在 1.5 岁的大鼠中则没有。巢蛋白在心肌中表达的定量图像分析证实,与完整的 1 岁 WKY 大鼠相比,1.5 岁的 WKY 大鼠和两个年龄段的 SHR 大鼠的表达均显著增加。这项研究首次记录了巢蛋白的重新表达,表明在衰老的完整和慢性压力超负荷肥厚心肌的不同细胞类型中发生了细胞骨架重塑。我们的发现证实了巢蛋白参与心肌肥厚和进行性衰老过程中的复杂变化。