Takemura R, Masaki T, Hirokawa N
Department of Anatomy and Cell Biology, School of Medicine, University of Tokyo, Bunkyo-ku, Japan.
Cell Motil Cytoskeleton. 1988;9(4):299-311. doi: 10.1002/cm.970090403.
At the terminal web of chicken intestinal epithelial cell, the actin bundles are cross-linked by a fine filamentous network of actin-associated cross-linkers. Myosin, fodrin, and TW 260/240 have been identified as major components of the cross-linkers. We studied the development of the cross-linkers by quick-freeze, deep-etch electron microscopy, and the expression of cross-linker proteins (myosin, fodrin 240, and TW 260) by immunofluorescence and immunoblotting analysis during the embryogenesis. Microvilli start to form at 5-7 days, and the rootlets begin to elongate at 10 days. At an early stage of the development of the terminal web (13 days), fodrin 240 and a small amount of myosin are expressed, and a few actin-associated cross-linkers are present between the rootlets. However, TW 260 is not expressed at this stage. At an intermediate stage (19 days), the amount of myosin increases, and TW 260 begins to be expressed. The number of cross-linkers associated with the unit length of the rootlets is 24/microns. At the final stage of the terminal web formation (2 days after hatching), the amount of fodrin 240, myosin, and TW 260 is similar to the adult level, and the number of the actin-associated cross-linkers per unit length of the rootlet is 27/microns (approximately 85% of the adult). These results suggest that the synthesis of cross-linker proteins may be intricately regulated to achieve the desired density of cross-linkages at each developmental stage: at early and intermediate stages, sufficient and not an excess of cross-linkages are formed; and at a final stage, a higher complexity of cross-linkages is achieved. In addition, there is a differential expression of the components of the actin-associated cross-linkers: myosin and fodrin could be early components of the cross-linkers involved in the basic stabilization of the terminal web structure, whereas TW 260/240 becomes incorporated later, possibly involved in the stabilization preparatory to the rapid elongation of microvilli, which occurs after the formation of the terminal web.
在鸡肠上皮细胞的终末网处,肌动蛋白束通过与肌动蛋白相关的交联蛋白构成的精细丝状网络相互交联。肌球蛋白、血影蛋白和TW 260/240已被确定为交联蛋白的主要成分。我们通过快速冷冻、深度蚀刻电子显微镜研究了交联蛋白的发育过程,并通过免疫荧光和免疫印迹分析研究了胚胎发育过程中交联蛋白(肌球蛋白、血影蛋白240和TW 260)的表达情况。微绒毛在5 - 7天时开始形成,根丝在10天时开始伸长。在终末网发育的早期阶段(13天),血影蛋白240和少量肌球蛋白表达,根丝之间存在一些与肌动蛋白相关的交联蛋白。然而,此时TW 260不表达。在中间阶段(19天),肌球蛋白的量增加,TW 260开始表达。与根丝单位长度相关的交联蛋白数量为24/微米。在终末网形成的最后阶段(孵化后2天),血影蛋白240、肌球蛋白和TW 260的量与成年水平相似,根丝单位长度的肌动蛋白相关交联蛋白数量为27/微米(约为成年水平的85%)。这些结果表明,交联蛋白的合成可能受到复杂的调控,以在每个发育阶段达到所需的交联密度:在早期和中间阶段,形成足够但不过量的交联;在最后阶段,实现更高复杂性的交联。此外,肌动蛋白相关交联蛋白的成分存在差异表达:肌球蛋白和血影蛋白可能是参与终末网结构基本稳定的交联蛋白的早期成分,而TW 260/240稍后加入,可能参与终末网形成后微绒毛快速伸长之前的稳定过程。