Archacka Karolina, Denkis Agnieszka, Brzóska Edyta, Świerczek Barbara, Tarczyluk Marta, Jańczyk-Ilach Katarzyna, Ciemerych Maria A, Moraczewski Jerzy
Department of Cytology, Faculty of Biology, University of Warsaw , Warsaw, Poland .
Stem Cells Dev. 2014 Oct 15;23(20):2455-68. doi: 10.1089/scd.2013.0582. Epub 2014 Jun 18.
Pluripotent stem cells are a potential source of various cell types for use in regenerative medicine. Despite accumulating knowledge, there is currently no efficient and reproducible protocol that does not require genetic manipulation for generation of myogenic cells from pluripotent stem cells. Here, we examined whether mouse embryonic stem (ES) cells are able to undergo myogenic differentiation and fusion in response to signals released by differentiating myoblasts. Using ES cells expressing the histone 2B-green fluorescent fusion protein, we were able to detect hybrid myotubes formed by ES cells and differentiating myoblasts. ES cells that fused with myoblasts downregulated the expression of pluripotency markers and induced the expression of myogenic markers, while unfused ES cells did not exhibit this expression pattern. Thus, the signals released by myoblasts were not sufficient to induce myogenic differentiation of ES cells. Although ES cells synthesize many proteins involved in myoblast adhesion and fusion, we did not observe any myotubes formed exclusively by ES cells. We found that ES cells lacked M-cadherin and vascular cell adhesion molecule-1, which may account for the low frequency of hybrid myotube formation in ES cell-myoblast co-cultures and the inability of ES cells alone to form myotubes.
多能干细胞是再生医学中各种细胞类型的潜在来源。尽管已有越来越多的知识积累,但目前尚无一种高效且可重复的方案,能够在不进行基因操作的情况下从多能干细胞生成肌细胞。在此,我们研究了小鼠胚胎干细胞(ES细胞)是否能够响应分化中的成肌细胞释放的信号而进行肌源性分化和融合。利用表达组蛋白2B-绿色荧光融合蛋白的ES细胞,我们能够检测到由ES细胞和分化中的成肌细胞形成的杂种肌管。与成肌细胞融合的ES细胞下调了多能性标志物的表达,并诱导了肌源性标志物的表达,而未融合的ES细胞则未表现出这种表达模式。因此,成肌细胞释放的信号不足以诱导ES细胞的肌源性分化。尽管ES细胞合成了许多参与成肌细胞黏附和融合的蛋白质,但我们未观察到仅由ES细胞形成的任何肌管。我们发现ES细胞缺乏M-钙黏蛋白和血管细胞黏附分子-1,这可能解释了ES细胞-成肌细胞共培养中杂种肌管形成频率较低以及ES细胞单独无法形成肌管的原因。