Collagen XIV is important for growth and structural integrity of the myocardium

纤维发生 细胞外基质 细胞生物学 结缔组织 胚胎干细胞 纤维 基质金属蛋白酶 胚胎心脏 胶原蛋白,I型,α1 化学 心脏发育 形态发生 生物 内分泌学 内科学 病理 生物化学 医学 基因
作者
Ge Tao,Agata Levay,Jacqueline D. Peacock,Danielle J. Huk,Sarah N. Both,Nicole H. Purcell,José R. Pinto,Maarten L. Galantowicz,Manuel Koch,Pamela A. Lucchesi,David E. Birk,Joy Lincoln
出处
期刊:Journal of Molecular and Cellular Cardiology [Elsevier]
卷期号:53 (5): 626-638 被引量:62
标识
DOI:10.1016/j.yjmcc.2012.08.002
摘要

Collagen XIV is a fibril-associated collagen with an interrupted triple helix (FACIT). Previous studies have shown that this collagen type regulates early stages of fibrillogenesis in connective tissues of high mechanical demand. Mice null for Collagen XIV are viable, however formation of the interstitial collagen network is defective in tendons and skin leading to reduced biomechanical function. The assembly of a tightly regulated collagen network is also required in the heart, not only for structural support but also for controlling cellular processes. Collagen XIV is highly expressed in the embryonic heart, notably within the cardiac interstitium of the developing myocardium, however its role has not been elucidated. To test this, we examined cardiac phenotypes in embryonic and adult mice devoid of Collagen XIV. From as early as E11.5, Col14a1−/− mice exhibit significant perturbations in mRNA levels of many other collagen types and remodeling enzymes (MMPs, TIMPs) within the ventricular myocardium. By post natal stages, collagen fibril organization is in disarray and the adult heart displays defects in ventricular morphogenesis. In addition to the extracellular matrix, Col14a1−/− mice exhibit increased cardiomyocyte proliferation at post natal, but not E11.5 stages, leading to increased cell number, yet cell size is decreased by 3 months of age. In contrast to myocytes, the number of cardiac fibroblasts is reduced after birth associated with increased apoptosis. As a result of these molecular and cellular changes during embryonic development and post natal maturation, cardiac function is diminished in Col14a1−/− mice from 3 months of age; associated with dilation in the absence of hypertrophy, and reduced ejection fraction. Further, Col14a1 deficiency leads to a greater increase in left ventricular wall thickening in response to pathological pressure overload compared to wild type animals. Collectively, these studies identify a new role for type XIV collagen in the formation of the cardiac interstitium during embryonic development, and highlight the importance of the collagen network for myocardial cell survival, and function of the working myocardium after birth.
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