酸性神经酰胺酶缺陷小鼠心功能障碍及基因表达改变。

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Annie Kleynerman, Jitka Rybova, William M McKillop, Theresa A Dlugi, Mary L Faber, Maria Fuller, Caitlin C O'Meara, Jeffrey A Medin
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引用次数: 0

摘要

法伯病(FD)是一种由ASAH1基因突变引起的超罕见常染色体隐性溶酶体储存疾病。FD的特点是酸性神经酰胺酶(ACDase)缺乏,神经酰胺在各组织中积累。典型FD患者的典型症状包括脂肪肉芽肿病、呼吸系统并发症和神经功能障碍,常导致婴儿期死亡。一些FD患者的心脏异常已被描述;然而,尚未对FD患者的心脏病理进行详细检查。在这里,我们报告了我们产生的新的P361R-FD小鼠ACDase缺乏症模型的明显心脏病理生理学。P361R-FD小鼠表现出较小的心脏,改变的心肌细胞结构,破坏的组织组成和包含巨噬细胞。超声心动图提示心室萎缩,瓣膜功能障碍,心排血量减少,每搏容量降低。肌钙蛋白I在P361R-FD小鼠中显著升高。P361R-FD小鼠的心脏发现神经酰胺、胆固醇和其他脂质增加。新生儿P361R-FD小鼠心脏组织的组织病理学分析显示,溶酶体早在出生后第1天就出现了破坏。最后,我们报道了P361R-FD小鼠心脏发育过程中心脏传导、横纹肌收缩和鞘脂稳态基因表达的差异。总之,我们在ACDase缺乏的小鼠模型中研究了心脏,证明了ACDase缺乏会导致溶酶体功能障碍、鞘脂和胆固醇失衡、组织破坏和显著炎症,导致这些动物的心功能受损。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiac dysfunction and altered gene expression in acid ceramidase-deficient mice.

Farber disease (FD) is an ultrarare, autosomal-recessive, lysosomal storage disorder attributed to ASAH1 gene mutations. FD is characterized by acid ceramidase (ACDase) deficiency and the accumulation of ceramide in various tissues. Classical FD patients typically manifest symptoms including lipogranulomatosis, respiratory complications, and neurological deficits, often leading to mortality during infancy. Cardiac abnormalities in several FD patients have been described; however, a detailed examination of cardiac pathology in FD has not been conducted. Here we report pronounced cardiac pathophysiology in a new P361R-FD mouse model of ACDase deficiency that we generated. P361R-FD mice displayed smaller hearts, altered cardiomyocyte architecture, disrupted tissue composition, and inclusion-containing macrophages. Echocardiography suggested ventricular atrophy, valve dysfunction, decreased cardiac output, and lowered stroke volumes. Troponin I was significantly elevated in P361R-FD mice. Hearts from P361R-FD mice were found to have increased ceramide, cholesterol, and other lipids. Histopathological analysis of heart tissue from neonatal P361R-FD mice revealed lysosomal disruption as early as postnatal day 1. Finally, we report cardiac conduction, striated muscle contraction, and sphingolipid homeostasis gene expression differences during cardiac development in P361R-FD mice. In summary, we investigated the heart in a mouse model of ACDase deficiency, demonstrating that ACDase deficiency induced lysosomal dysfunction, sphingolipid and cholesterol imbalances, tissue disruption, and significant inflammation, leading to impaired cardiac function in these animals.NEW & NOTEWORTHY This is the first characterization of cardiac function and histopathology in a mouse model of acid ceramidase deficiency. We report physiologic disruption suggestive of heart failure with preserved ejection fraction, progressive histopathology, and aberrant gene expression. We found significant lysosomal disruption at both neonatal and adult ages, suggesting a crucial role of acid ceramidase, and potentially ceramides, in cardiac development and function.

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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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