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Cardiac renewing: interstitial Cajal-like cells nurse cardiomyocyte progenitors in epicardial stem cell niches

机译:心脏更新:间质性Cajal样细胞在心外膜干细胞壁nurse中调节心肌祖细胞

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摘要

Recent studies suggested that various cell lineages exist within the subepicardium and we supposed that this area could host cardiac stem cell niches >(CSCNs). Using transmission electron microscopy, we have found at least 10 types of cells coexisting in the subepicardium of normal adult mice: adipocytes, fibroblasts, Schwann cells and nerve fibres, isolated smooth muscle cells, mast cells, macrophages, lymphocytes, interstitial Cajal-like cells >(ICLCs) and cardiomyocytes progenitors >(CMPs). The latter cells, sited in the area of origin of coronary arteries and aorta, showed typical features of either very immature or developing cardiomyocytes. Some of these cells were connected to each other to form columns surrounded by a basal lamina and embedded in a cellular network made by ICLCs. Complex intercellular communication occurs between the ICLCs and CMPs through electron-dense nanostructures or through shed vesicles. We provide here for the first time the ultrastructural description of >CSCN in the adult mice myocardium, mainly containing >ICLCs and >CMPs. The existence of resident CMPs in different developmental stages proves that cardiac renewing is a continuous process. We suggest that ICLCs might act as supporting nurse cells of the cardiac niches and may be responsible for activation, commitment and migration of the stem cells out of the niches. Briefly, not only resident cardiac stem cells but also ICLCs regulate myocyte turnover and contribute to both cardiac cellular homeostasis and endogenous repair/remodelling after injuries.
机译:最近的研究表明,皮下层内存在各种细胞谱系,我们认为该区域可以容纳心脏干细胞壁 strong>(CSCNs)。使用透射电子显微镜,我们发现正常成年小鼠的皮下膜中共存至少10种细胞类型:脂肪细胞,成纤维细胞,雪旺氏细胞和神经纤维,分离的平滑肌细胞,肥大细胞,巨噬细胞,淋巴细胞,间质性Cajal样细胞>(ICLCs)和心肌祖细胞>(CMPs)。后者的细胞位于冠状动脉和主动脉的起源区域,表现出非常不成熟或发育中的心肌细胞的典型特征。这些单元格中的一些单元格相互连接,形成由基底层包围的圆柱体,并嵌入由ICLC制成的蜂窝网络中。复杂的细胞间通讯通过电子致密的纳米结构或脱落的囊泡在ICLC和CMP之间发生。我们首次在成年小鼠心肌中提供> CSCN 的超微结构描述,其中主要包含> ICLC 和> CMP 。处于不同发育阶段的常驻CMP的存在证明了心脏更新是一个连续的过程。我们建议,ICLC可能充当心脏小生境的支持细胞,并可能负责干细胞的激活,定型和迁移。简而言之,不仅常驻心脏干细胞,而且ICLC都调节心肌细胞更新,并有助于心脏细胞稳态和损伤后内源性修复/重塑。

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