Cyr J L, Brady S T
Department of Cell Biology and Neuroscience, University of Texas Southwestern Medical Center, Dallas 75235-9039.
Mol Neurobiol. 1992 Summer-Fall;6(2-3):137-55. doi: 10.1007/BF02780549.
Neurons require a large amount of intracellular transport. Cytoplasmic polypeptides and membrane-bounded organelles move from the perikaryon, down the length of the axon, and to the synaptic terminals. This movement occurs at distinct rates and is termed axonal transport. Axonal transport is divided into the slow transport of cytoplasmic proteins including glycolytic enzymes and cytoskeletal structures and the fast transport of membrane-bounded organelles along linear arrays of microtubules. The polypeptide compositions of the rate classes of axonal transport have been well characterized, but the underlying molecular mechanisms of this movement are less clear. Progress has been particularly slow toward understanding force-generation in slow transport, but recent developments have provided insight into the molecular motors involved in fast axonal transport. Recent advances in the cellular and molecular biology of one fast axonal transport motor, kinesin, have provided a clearer understanding of organelle movement along microtubules. The availability of cellular and molecular probes for kinesin and other putative axonal transport motors have led to a reevaluation of our understanding of intracellular motility.
神经元需要大量的细胞内运输。细胞质多肽和膜结合细胞器从胞体沿着轴突的长度移动到突触终末。这种移动以不同的速率发生,被称为轴突运输。轴突运输分为细胞质蛋白(包括糖酵解酶和细胞骨架结构)的慢速运输以及膜结合细胞器沿微管线性阵列的快速运输。轴突运输速率类别的多肽组成已得到很好的表征,但这种移动的潜在分子机制尚不清楚。在理解慢速运输中的力产生方面进展特别缓慢,但最近的进展为参与快速轴突运输的分子马达提供了见解。一种快速轴突运输马达驱动蛋白在细胞和分子生物学方面的最新进展,使人们对细胞器沿微管的移动有了更清晰的认识。用于驱动蛋白和其他假定的轴突运输马达的细胞和分子探针的可用性,促使我们重新评估对细胞内运动性的理解。