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本文引用的文献

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Culturing muscle fibres in hanging drop: a novel approach to solve an old problem.悬滴法培养肌纤维:解决老问题的新方法。
Biol Cell. 2014 Feb;106(2):72-82. doi: 10.1111/boc.201300028. Epub 2014 Jan 10.
2
Mouse and human pluripotent stem cells and the means of their myogenic differentiation.小鼠和人类多能干细胞及其向肌源性分化的方法。
Results Probl Cell Differ. 2012;55:321-56. doi: 10.1007/978-3-642-30406-4_18.
3
Cell-surface proteomics identifies lineage-specific markers of embryo-derived stem cells.细胞表面蛋白质组学鉴定胚胎来源干细胞的谱系特异性标记物。
Dev Cell. 2012 Apr 17;22(4):887-901. doi: 10.1016/j.devcel.2012.01.005. Epub 2012 Mar 15.
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Efficient and scalable purification of cardiomyocytes from human embryonic and induced pluripotent stem cells by VCAM1 surface expression.通过 VCAM1 表面表达从人胚胎和诱导多能干细胞中高效且规模化纯化心肌细胞。
PLoS One. 2011;6(8):e23657. doi: 10.1371/journal.pone.0023657. Epub 2011 Aug 18.
5
Cell cycle regulation during proliferation and differentiation of mammalian muscle precursor cells.哺乳动物肌肉前体细胞增殖和分化过程中的细胞周期调控。
Results Probl Cell Differ. 2011;53:473-527. doi: 10.1007/978-3-642-19065-0_20.
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Membrane vesicles, current state-of-the-art: emerging role of extracellular vesicles.膜泡,当前的最新进展:细胞外囊泡的新兴作用。
Cell Mol Life Sci. 2011 Aug;68(16):2667-88. doi: 10.1007/s00018-011-0689-3. Epub 2011 May 11.
7
Functional myogenic engraftment from mouse iPS cells.来自小鼠诱导多能干细胞的功能性肌源性植入。
Stem Cell Rev Rep. 2011 Nov;7(4):948-57. doi: 10.1007/s12015-011-9258-2.
8
Therapeutic approaches to muscular dystrophy.肌肉萎缩症的治疗方法。
Hum Mol Genet. 2011 Apr 15;20(R1):R69-78. doi: 10.1093/hmg/ddr105. Epub 2011 Mar 24.
9
MyoD gene suppression by Oct4 is required for reprogramming in myoblasts to produce induced pluripotent stem cells.肌节同源盒蛋白基因(MyoD)的抑制是 Oct4 在成肌细胞中重编程为诱导多能干细胞所必需的。
Stem Cells. 2011 Mar;29(3):505-16. doi: 10.1002/stem.598.
10
Assessment of the myogenic stem cell compartment following transplantation of Pax3/Pax7-induced embryonic stem cell-derived progenitors.评估 Pax3/Pax7 诱导的胚胎干细胞衍生祖细胞移植后的成肌干细胞隔室。
Stem Cells. 2011 May;29(5):777-90. doi: 10.1002/stem.625.

体外培养的小鼠胚胎干细胞进行成肌分化及与成肌细胞融合的能力。

Competence of in vitro cultured mouse embryonic stem cells for myogenic differentiation and fusion with myoblasts.

作者信息

Archacka Karolina, Denkis Agnieszka, Brzóska Edyta, Świerczek Barbara, Tarczyluk Marta, Jańczyk-Ilach Katarzyna, Ciemerych Maria A, Moraczewski Jerzy

机构信息

Department of Cytology, Faculty of Biology, University of Warsaw , Warsaw, Poland .

出版信息

Stem Cells Dev. 2014 Oct 15;23(20):2455-68. doi: 10.1089/scd.2013.0582. Epub 2014 Jun 18.

DOI:10.1089/scd.2013.0582
PMID:24940624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4186807/
Abstract

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.

摘要

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。