Popescu Laurențiu M, Fertig Emanuel T, Gherghiceanu Mihaela
Department of Advanced Studies, 'Victor Babeş' National Institute of Pathology, Bucharest, Romania.
Department of Cellular and Molecular Medicine, 'Carol Davila' University of Medicine and Pharmacy, Bucharest, Romania.
J Cell Mol Med. 2016 Feb;20(2):370-80. doi: 10.1111/jcmm.12719. Epub 2015 Nov 5.
Telocytes (TCs) were previously shown by our group to form a tandem with stem/progenitor cells in cardiac stem cell (CSC) niches, fulfilling various roles in cardiac renewal. Among these, the ability to 'nurse' CSCs in situ, both through direct physical contact (junctions) as well as at a distance, by paracrine signalling or through extracellular vesicles containing mRNA. We employed electron microscopy to identify junctions (such as gap or adherens junctions) in a co-culture of cardiac TCs and CSCs. Gap junctions were observed between TCs, which formed networks, however, not between TCs and CSCs. Instead, we show that TCs and CSCs interact in culture forming heterocellular adherens junctions, as well as non-classical junctions such as puncta adherentia and stromal synapses. The stromal synapse formed between TCs and CSCs (both stromal cells) was frequently associated with the presence of electron-dense nanostructures (on average about 15 nm in length) connecting the two opposing membranes. The average width of the synaptic cleft was 30 nm, whereas the average length of the intercellular contact was 5 μm. Recent studies have shown that stem cells fail to adequately engraft and survive in the hostile environment of the injured myocardium, possibly as a result of the absence of the pro-regenerative components of the secretome (paracrine factors) and/or of neighbouring support cells. Herein, we emphasize the similarities between the junctions described in co-culture and the junctions identified between TCs and CSCs in situ. Reproducing a CSC niche in culture may represent a viable alternative to mono-cellular therapies.
我们团队之前的研究表明,在心源性干细胞(CSC)龛中,间质细胞(TCs)与干/祖细胞形成串联,在心脏更新中发挥多种作用。其中包括通过直接物理接触(连接)以及远距离通过旁分泌信号传导或含有mRNA的细胞外囊泡“滋养”原位CSC的能力。我们采用电子显微镜来鉴定心脏TCs和CSC共培养物中的连接(如缝隙连接或黏附连接)。在形成网络的TCs之间观察到了缝隙连接,然而,在TCs和CSC之间未观察到。相反,我们发现TCs和CSC在培养中相互作用,形成异细胞黏附连接以及诸如点状黏附连接和基质突触等非经典连接。在TCs和CSC(两者均为基质细胞)之间形成的基质突触经常与连接两个相对膜的电子致密纳米结构(平均长度约为15nm)的存在相关。突触间隙的平均宽度为30nm,而细胞间接触的平均长度为5μm。最近的研究表明,干细胞在受损心肌的恶劣环境中无法充分植入并存活,这可能是由于缺乏分泌组(旁分泌因子)的促再生成分和/或邻近支持细胞的结果。在此,我们强调共培养中描述的连接与原位TCs和CSC之间鉴定的连接的相似性。在培养中重现CSC龛可能是单细胞疗法的可行替代方案。