Department of Cellular and Molecular Medicine, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
J Cell Mol Med. 2011 Nov;15(11):2284-96. doi: 10.1111/j.1582-4934.2011.01449.x.
We used rat experimental myocardial infarction to study the ultrastructural recovery, especially neo-angiogenesis in the infarction border zone. We were interested in the possible role(s) of telocytes (TCs), a novel type of interstitial cell very recently discovered in myocardim (see http://www.telocytes.com). Electron microscopy, immunocytochemistry and analysis of several proangiogenic microRNAs provided evidence for TC involvement in neo-angiogenesis after myocardial infarction. Electron microscopy showed the close spatial association of TCs with neoangiogenetic elements. Higher resolution images provided the following information: (a) the intercellular space between the abluminal face of endothelium and its surrounding TCs is frequently less than 50 nm; (b) TCs establish multiple direct nanocontacts with endothelial cells, where the extracellular space seems obliterated; such nanocontacts have a length of 0.4-1.5 μm; (c) the absence of basal membrane on the abluminal face of endothelial cell. Besides the physical contacts (either nanoscopic or microscopic) TCs presumably contribute to neo-angiognesis via paracrine secretion (as shown by immunocytochemistry for VEGF or NOS2). Last but not least, TCs contain measurable quantities of angiogenic microRNAs (e.g. let-7e, 10a, 21, 27b, 100, 126-3p, 130a, 143, 155, 503). Taken together, the direct (physical) contact of TCs with endothelial tubes, as well as the indirect (chemical) positive influence within the 'angiogenic zones', suggests an important participation of TCs in neo-angiogenesis during the late stage of myocardial infarction.
我们使用大鼠实验性心肌梗死模型来研究梗死边缘区的超微结构恢复,尤其是新血管生成。我们对新近在心肌中发现的一种新型间质细胞—— 间质细胞(telocytes,TCs)——的可能作用很感兴趣(参见 http://www.telocytes.com)。电镜、免疫细胞化学和几种促血管生成 microRNAs 的分析为 TCs 在心肌梗死后新血管生成中的作用提供了证据。电镜显示 TCs 与新生血管生成元素密切的空间关联。更高分辨率的图像提供了以下信息:(a)内皮细胞的基底外侧面与其周围 TCs 之间的细胞间隙经常小于 50nm;(b)TCs 与内皮细胞建立了多个直接的纳米接触,其中细胞外空间似乎被消除;这种纳米接触的长度为 0.4-1.5μm;(c)内皮细胞基底外侧面缺乏基膜。除了物理接触(无论是纳米级还是微观级),TCs 可能通过旁分泌(如免疫细胞化学检测到的 VEGF 或 NOS2)促进新血管生成。最后但并非最不重要的是,TCs 含有可测量数量的血管生成 microRNAs(例如 let-7e、10a、21、27b、100、126-3p、130a、143、155、503)。总之,TCs 与内皮管的直接(物理)接触,以及在“血管生成区”内的间接(化学)积极影响,提示 TCs 在心肌梗死后晚期的新血管生成中具有重要作用。