Rønnov-Jessen L, Petersen O W
Structural Cell Biology Unit, Institute of Medical Anatomy, the Panum Institute, Copenhagen, Denmark.
J Cell Biol. 1996 Jul;134(1):67-80. doi: 10.1083/jcb.134.1.67.
Actins are known to comprise six mammalian isoforms of which beta- and gamma-nonmuscle actins are present in all cells, whereas alpha-smooth muscle (alpha-sm) actin is normally restricted to cells of the smooth muscle lineages. alpha-Sm actin has been found also to be expressed transiently in certain nonmuscle cells, in particular fibroblasts, which are referred to as myofibroblasts. The functional significance of alpha-sm actin in fibroblasts is unknown. However, myofibroblasts appear to play a prominent role in stromal reaction in breast cancer, at the site of wound repair, and in fibrotic reactions. Here, we show that the presence of alpha-sm actin is a signal for retardation of migratory behavior in fibroblasts. Comparison in a migration assay of fibroblast cell strains with and without alpha-sm actin revealed migratory restraint in alpha-sm actin-positive fibroblasts. Electroporation of monoclonal antibody (mAb) 1A4, which recognizes specifically the NH2-terminal Ac-EEED sequence of alpha-sm actin, significantly increased the frequency of migrating cells over that obtained with an unrelated antibody or a mAb against beta-actin. Time-lapse video microscopy revealed migratory rates of 4.8 and 3.0 microns/h, respectively. To knock out the alpha-sm actin protein, several antisense phosphorothioate oligodeoxynucleotide (ODNs) were tested. One of these, 3'UTI, which is complementary to a highly evolutionary conserved 3' untranslated (3'UT) sequence of alpha-sm actin mRNA, was found to block alpha-sm actin synthesis completely without affecting the synthesis of any other proteins as analyzed by two-dimensional gel electrophoresis. Targeting by antisense 3'UTI significantly increased motility compared with the corresponding sense ODN. alpha-Sm actin inhibition also led to the formation of less prominent focal adhesions as revealed by immunofluorescence staining against vinculin, talin, and beta1-integrin. We propose that an important function of filamentous alpha-sm actin is to immobilize the cells.
肌动蛋白已知由六种哺乳动物同工型组成,其中β - 和γ - 非肌肉肌动蛋白存在于所有细胞中,而α - 平滑肌(α - sm)肌动蛋白通常局限于平滑肌谱系的细胞。人们还发现α - sm肌动蛋白在某些非肌肉细胞中短暂表达,特别是成纤维细胞,这些细胞被称为肌成纤维细胞。α - sm肌动蛋白在成纤维细胞中的功能意义尚不清楚。然而,肌成纤维细胞似乎在乳腺癌的基质反应、伤口修复部位以及纤维化反应中起重要作用。在此,我们表明α - sm肌动蛋白的存在是成纤维细胞迁移行为迟缓的信号。对有和没有α - sm肌动蛋白的成纤维细胞系进行迁移试验比较,发现α - sm肌动蛋白阳性的成纤维细胞存在迁移抑制。电穿孔特异性识别α - sm肌动蛋白NH2末端Ac - EEED序列的单克隆抗体(mAb)1A4,与使用无关抗体或抗β - 肌动蛋白的单克隆抗体相比,显著提高了迁移细胞的频率。延时视频显微镜显示迁移速率分别为4.8和3.0微米/小时。为了敲除α - sm肌动蛋白蛋白,测试了几种反义硫代磷酸酯寡脱氧核苷酸(ODN)。其中之一3'UTI,它与α - sm肌动蛋白mRNA高度进化保守的3'非翻译(3'UT)序列互补,被发现完全阻断α - sm肌动蛋白的合成,二维凝胶电泳分析显示不影响任何其他蛋白质的合成。与相应的正义ODN相比,反义3'UTI靶向显著增加了细胞运动性。α - sm肌动蛋白抑制还导致通过针对纽蛋白、踝蛋白和β1整合素的免疫荧光染色显示的粘着斑不那么明显。我们提出丝状α - sm肌动蛋白的一个重要功能是使细胞固定。