Hirokawa N
Department of Anatomy and Cell Biology, Faculty of Medicine, University of Tokyo, Japan.
Curr Opin Cell Biol. 1994 Feb;6(1):74-81. doi: 10.1016/0955-0674(94)90119-8.
High-resolution microscopic analysis has precisely revealed the control of microtubule dynamics by individual microtubule-associated proteins (MAPs) in vitro. Furthermore, transfection of MAP cDNA into fibroblasts and subsequent analysis using microinjection of caged fluorescein-labeled tubulin and photoactivation have enabled the function of MAPs in microtubule dynamics to be studied in detail in vivo. Systematic, quantitative studies using transfection of various kinds of MAP cDNA deletion mutants have demonstrated the complex mechanism for microtubule bundling in vivo, and have shown the involvement in microtubule bundling of both microtubule binding and projection regions of MAPs. A similar approach, combined with detailed structural analysis, has indicated clearly that differences in the amino-terminal projection region of MAPs can determine differential organization of MT bundles, and thus influence the characteristic organization of microtubule domains in dendrites and axons.
高分辨率显微镜分析已精确揭示了体外单个微管相关蛋白(MAPs)对微管动力学的控制。此外,将MAP cDNA转染到成纤维细胞中,随后使用笼形荧光素标记微管蛋白的显微注射和光激活进行分析,使得能够在体内详细研究MAPs在微管动力学中的功能。使用各种MAP cDNA缺失突变体转染进行的系统定量研究已经证明了体内微管束形成的复杂机制,并表明MAPs的微管结合区和突出区均参与微管束形成。一种类似的方法,结合详细的结构分析,已清楚地表明MAPs氨基末端突出区的差异可决定微管束的不同组织方式,从而影响树突和轴突中微管结构域的特征性组织方式。