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产前小鼠发育过程中肌源性细胞及培养的胚胎干细胞分化过程中M-钙黏蛋白的表达。

Expression of M-cadherin protein in myogenic cells during prenatal mouse development and differentiation of embryonic stem cells in culture.

作者信息

Rose O, Rohwedel J, Reinhardt S, Bachmann M, Cramer M, Rotter M, Wobus A, Starzinski-Powitz A

机构信息

Institut der Anthropologie und Humangenetik für Biologen, Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany.

出版信息

Dev Dyn. 1994 Nov;201(3):245-59. doi: 10.1002/aja.1002010308.

Abstract

Molecules regulating morphogenesis by cell-cell interactions are the cadherins, a class of calcium-dependent adhesion molecules. One of its members, M-cadherin, has been isolated from a myoblast cell line (Donalies et al. [1991] Proc. Natl. Acad. Sci. U.S.A. 88:8024-8028). In mouse development, expression of M-cadherin mRNA first appears at day 8.5 of gestation (E8.5) in somites and has been postulated to be down-regulated in developing muscle masses (Moore and Walsh [1993] Development 117:1409-1420). Affinity-purified polyclonal M-cadherin antibodies, detecting a protein of approximately 120 kDa, were used to study the cell expression pattern of M-cadherin protein. It was first visualized in somites at E10 1/3 and could be confined to desmin positive, myotomal cells. At all subsequent prenatal stages, M-cadherin was only found in myogenic cells of somitic origin. The detection of the protein at E10 1/3 suggests a translational delay of M-cadherin mRNA of 1 to 2 days (E8.5 vs. E10 1/3). This was further supported by the finding that during differentiation of ES cell line BLC6 into skeletal muscle cells in culture, expression of M-cadherin mRNA can be detected 2 days prior to M-cadherin protein. During prenatal development, the pattern of M-cadherin expression changes: In E10 1/3 embryos and also in myotomal cells of later stages, M-cadherin is evenly distributed on the cell surface. In developing muscle masses (tested at E16 to E18), however, M-cadherin protein becomes clustered most likely at sites of cell-cell contact as indicated by double-labelling experiments: M-cadherin-staining is the positive image of laminin negative areas excluding the presence of a basal lamina at M-cadherin positive sites. Furthermore, M-cadherin is coexpressed with the neuronal cell adhesion molecule N-CAM which has been shown to mediate cell-cell contact in myogenic cells. In summary, our results are in line with the idea that M-cadherin might play a central role in myogenic morphogenesis.

摘要

通过细胞间相互作用调节形态发生的分子是钙黏着蛋白,这是一类钙依赖性黏附分子。其成员之一,M-钙黏着蛋白,已从成肌细胞系中分离出来(多纳利斯等人[1991]《美国国家科学院院刊》88:8024 - 8028)。在小鼠发育过程中,M-钙黏着蛋白mRNA的表达首先出现在妊娠第8.5天(E8.5)的体节中,据推测在发育中的肌肉块中表达下调(摩尔和沃尔什[1993]《发育》117:1409 - 1420)。亲和纯化的多克隆M-钙黏着蛋白抗体,可检测到一种约120 kDa的蛋白质,用于研究M-钙黏着蛋白的细胞表达模式。它在E10 1/3时首次在体节中可见,并局限于结蛋白阳性的肌节细胞。在所有随后的产前阶段,M-钙黏着蛋白仅在体节来源的成肌细胞中发现。在E10 1/3时检测到该蛋白质表明M-钙黏着蛋白mRNA存在1至2天的翻译延迟(E8.5与E10 1/3相比)。这一发现得到了进一步支持,即在培养的胚胎干细胞系BLC6分化为骨骼肌细胞的过程中,M-钙黏着蛋白mRNA的表达比M-钙黏着蛋白蛋白质早2天被检测到。在产前发育过程中,M-钙黏着蛋白的表达模式发生变化:在E10 1/3胚胎以及后期的肌节细胞中,M-钙黏着蛋白均匀分布在细胞表面。然而,在发育中的肌肉块(在E16至E18检测)中,双标记实验表明M-钙黏着蛋白蛋白最有可能聚集在细胞间接触部位:M-钙黏着蛋白染色是层粘连蛋白阴性区域的阳性图像,排除了在M-钙黏着蛋白阳性部位存在基膜的情况。此外,M-钙黏着蛋白与神经元细胞黏附分子N-CAM共表达,N-CAM已被证明在成肌细胞中介导细胞间接触。总之,我们的结果与M-钙黏着蛋白可能在成肌形态发生中起核心作用的观点一致。

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