Weisshaar B, Doll T, Matus A
Friedrich Miescher Institute, Basel, Switzerland.
Development. 1992 Dec;116(4):1151-61. doi: 10.1242/dev.116.4.1151.
Microtubule-associated protein 2c (MAP2c) is one of a set of embryonic MAP forms that are expressed during neuronal differentiation in the developing nervous system. We have investigated its mode of action by expressing recombinant protein in non-neuronal cell lines using cell cDNA transfection techniques. At every level of expression, all the MAP2c was bound to cellular microtubules. At low MAP2c levels, the microtubules retained their normal arrangement, radiating from the centrosomal microtubule-organising centre (MTOC) but at higher levels an increasing proportion of microtubules occurred independently of the MTOC. In most cells, radially oriented microtubules still attached to the MTOC co-existed with detached microtubules, suggesting that the primary effect of MAP2 is to increase the probability that tubulin polymerisation will occur independently of the MTOC. The MTOC-independent microtubules formed bundles whose distribution depended on their length in relation to the diameter of the transfected cell. Short bundles were attached to the cell cortex at one end and followed a straight course through the cytoplasm, whereas longer bundles followed a curved path around the periphery of the cell. By comparing these patterns to those produced by two chemical agents that stabilise microtubules, taxol and dimethyl sulphoxide, we conclude that effects of MAP2c arise from two sources. It stabilises microtubules without providing assembly initiation sites and as a result produces relatively few, long microtubule bundles. These bend only when they encounter the restraining influence of the cortical cytoskeleton of the cell, indicating that MAP2c also imparts stiffness to them. By conferring these properties of stability and stiffness to neuronal microtubules MAP2c contributes to supporting the structure of developing neurites.
微管相关蛋白2c(MAP2c)是在发育中的神经系统神经元分化过程中表达的一组胚胎MAP形式之一。我们使用细胞cDNA转染技术在非神经元细胞系中表达重组蛋白,研究了其作用方式。在每个表达水平上,所有的MAP2c都与细胞微管结合。在低MAP2c水平时,微管保持其正常排列,从中心体微管组织中心(MTOC)放射状延伸,但在较高水平时,越来越多的微管独立于MTOC出现。在大多数细胞中,径向排列且仍附着于MTOC的微管与脱离的微管共存,这表明MAP2的主要作用是增加微管蛋白聚合独立于MTOC发生的概率。独立于MTOC的微管形成束,其分布取决于它们相对于转染细胞直径的长度。短束的一端附着于细胞皮质,在细胞质中呈直线延伸,而较长的束则沿着细胞周边呈弯曲路径延伸。通过将这些模式与两种稳定微管的化学试剂紫杉醇和二甲基亚砜产生的模式进行比较,我们得出结论,MAP2c的作用源于两个方面。它稳定微管而不提供组装起始位点,结果产生相对较少的长微管束。这些微管束只有在遇到细胞皮质细胞骨架的限制影响时才会弯曲,这表明MAP2c也赋予它们刚性。通过赋予神经元微管这些稳定性和刚性特性,MAP2c有助于支持发育中神经突的结构。