Tsang Hiu-Gwen, Clark Emily L, Markby Greg R, Bush Stephen J, Hume David A, Corcoran Brendan M, MacRae Vicky E, Summers Kim M
The Roslin Institute and R(D)SVS, The University of Edinburgh, Edinburgh, United Kingdom.
Nuffield Department of Clinical Medicine, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
Front Genet. 2020 Sep 8;11:919. doi: 10.3389/fgene.2020.00919. eCollection 2020.
The maintenance of a healthy cardiovascular system requires expression of genes that contribute to essential biological activities and repression of those that are associated with functions likely to be detrimental to cardiovascular homeostasis. Vascular calcification is a major disruption to cardiovascular homeostasis, where tissues of the cardiovascular system undergo ectopic calcification and consequent dysfunction, but little is known about the expression of calcification genes in the healthy cardiovascular system. Large animal models are of increasing importance in cardiovascular disease research as they demonstrate more similar cardiovascular features (in terms of anatomy, physiology and size) to humans than do rodent species. We used RNA sequencing results from the sheep, which has been utilized extensively to examine calcification of prosthetic cardiac valves, to explore the transcriptome of the heart and cardiac valves in this large animal, in particular looking at expression of calcification and extracellular matrix genes. We then examined genes implicated in the process of vascular calcification in a wide array of cardiovascular tissues and across multiple developmental stages, using RT-qPCR. Our results demonstrate that there is a balance between genes that promote and those that suppress mineralization during development and across cardiovascular tissues. We show extensive expression of genes encoding proteins involved in formation and maintenance of the extracellular matrix in cardiovascular tissues, and high expression of hematopoietic genes in the cardiac valves. Our analysis will support future research into the functions of implicated genes in the development of valve calcification, and increase the utility of the sheep as a large animal model for understanding ectopic calcification in cardiovascular disease. This study provides a foundation to explore the transcriptome of the developing cardiovascular system and is a valuable resource for the fields of mammalian genomics and cardiovascular research.
维持健康的心血管系统需要表达有助于基本生物活动的基因,并抑制那些与可能损害心血管稳态的功能相关的基因。血管钙化是对心血管稳态的重大破坏,心血管系统的组织会发生异位钙化并随之出现功能障碍,但关于健康心血管系统中钙化基因的表达情况却知之甚少。大型动物模型在心血管疾病研究中的重要性日益增加,因为与啮齿类动物相比,它们在心血管特征(在解剖学、生理学和大小方面)上与人类更为相似。我们利用绵羊的RNA测序结果(绵羊已被广泛用于研究人工心脏瓣膜的钙化)来探索这种大型动物心脏和心脏瓣膜的转录组,特别关注钙化和细胞外基质基因的表达。然后,我们使用RT-qPCR在多种心血管组织和多个发育阶段检测了与血管钙化过程相关的基因。我们的结果表明,在发育过程中和整个心血管组织中,促进矿化的基因和抑制矿化的基因之间存在平衡。我们展示了心血管组织中参与细胞外基质形成和维持的蛋白质编码基因的广泛表达,以及心脏瓣膜中造血基因的高表达。我们的分析将支持未来对相关基因在瓣膜钙化发育中的功能研究,并提高绵羊作为理解心血管疾病异位钙化的大型动物模型的实用性。这项研究为探索发育中的心血管系统的转录组提供了基础,是哺乳动物基因组学和心血管研究领域的宝贵资源。