A function for filamentous alpha-smooth muscle actin: Retardation of motility in fibroblasts

被引:189
作者
RonnovJessen, L
Petersen, OW
机构
[1] UNIV COPENHAGEN, PANUM INST, INST MED ANAT, STRUCT CELL BIOL UNIT, DK-2200 COPENHAGEN N, DENMARK
[2] DANISH CANC SOC, DIV CANC BIOL, DEPT TUMOR ENDOCRINOL, RES CTR, DK-2100 COPENHAGEN O, DENMARK
关键词
D O I
10.1083/jcb.134.1.67
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 mu m/h, respectively. To knock out the alpha-sm actin protein, several antisense phosphorothioate oligodeoxynucleotide (ODNs) were tested. One of these, 3'UT1, 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'UT1 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 beta-integrin. We propose that an important function of filamentous alpha-sm actin is to immobilize the cells.
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收藏
页码:67 / 80
页数:14
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