Burgess D R
J Cell Biol. 1982 Dec;95(3):853-63. doi: 10.1083/jcb.95.3.853.
Various models have been put forward suggesting ways in which brush borders from intestinal epithelial cells may be motile. Experiments documenting putative brush border motility have been performed on isolated brush borders and have generated models suggesting microvillar retraction or microvillar rootlet interactions. The reported Ca++ ATP-induced retraction of microvilli has been shown, instead, to be microvillar dissolution in response to Ca++ and not active brush border motility. I report here studies on the reactivation of motility in intact sheets of isolated intestinal epithelium. Whole epithelial sheets were glycerinated, which leaves the brush border and intercellular junctions intact, and then treated with ATP, PPi, ITP, ADP, GTP, or delta S-ATP. Analysis by video enhanced differential interference-contrast microscopy and thin-section transmission electron microscopy reveals contractions in the terminal web region causing microvilli to be fanned apart in response to ATP and delta S-ATP but not in response to ADP, PPi, ITP, or GTP. Electron microscopy reveals that the contractions occur at the level of the intermediate junction in a circumferential constriction which can pull cells completely apart. This constriction occurs in a location occupied by an actin-containing circumferential band of filaments, as demonstrated by S-1 binding, which completely encircles the terminal web at the level of the intermediate junction. Upon contraction, this band becomes denser and thicker. Since myosin, alpha-actinin and tropomyosin, in addition to actin, have been localized to this region of the terminal web, it is proposed that the intestinal epithelial cell can be motile via a circumferential terminal web contractile ring analogous to the contractile ring of dividing cells.
已经提出了各种模型,提示小肠上皮细胞刷状缘可能具有运动性的方式。记录假定刷状缘运动性的实验是在分离的刷状缘上进行的,并产生了提示微绒毛回缩或微绒毛根丝相互作用的模型。相反,已表明所报道的钙离子ATP诱导的微绒毛回缩是微绒毛对钙离子的溶解,而非活跃的刷状缘运动。我在此报告关于分离的完整小肠上皮片层运动性重新激活的研究。将整个上皮片层用甘油处理,这使得刷状缘和细胞间连接保持完整,然后用ATP、焦磷酸(PPi)、肌苷三磷酸(ITP)、二磷酸腺苷(ADP)、鸟苷三磷酸(GTP)或δS-ATP处理。通过视频增强微分干涉相差显微镜和超薄切片透射电子显微镜分析显示,在终末网区域出现收缩,导致微绒毛在ATP和δS-ATP作用下呈扇形散开,但在ADP、PPi、ITP或GTP作用下则无此现象。电子显微镜显示,收缩发生在中间连接水平的环形缩窄处,该缩窄可将细胞完全拉开。如通过S-1结合所证明的,这种缩窄发生在由含肌动蛋白的环形丝状带所占据的位置,该带在中间连接水平完全环绕终末网。收缩时,这条带变得更致密和更厚。由于除肌动蛋白外,肌球蛋白、α-辅肌动蛋白和原肌球蛋白也已定位到终末网的这个区域,因此有人提出小肠上皮细胞可通过类似于分裂细胞收缩环的环形终末网收缩环进行运动。