Rose O, Rohwedel J, Reinhardt S, Bachmann M, Cramer M, Rotter M, Wobus A, Starzinski-Powitz A
Institut der Anthropologie und Humangenetik für Biologen, Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany.
Dev Dyn. 1994 Nov;201(3):245-59. doi: 10.1002/aja.1002010308.
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.
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。