Ratner S, Sherrod W S, Lichlyter D
Breast Cancer Research Program, Barbara Ann Karmanos Cancer Institute, Detroit, MI 48201, USA.
J Immunol. 1997 Aug 1;159(3):1063-7.
Spherical circulating T cells must polarize to extravasate. We have found that the polarization process includes a drastic reconfiguration of the tubulin cytoskeleton. In spherical T cells, the nucleus is surrounded by microtubules radiating from the microtubule organizing center (MTOC). During polarization the uropod (a slender posterior appendage) forms at the site of the MTOC. As the uropod buds out, the MTOC is carried in its distal tip. The attached microtubules retract into the uropod lumen, collapsing like the spokes of an umbrella into a compact sheaf. Experiments with microtubule inhibitors show that the retracted microtubules do not support the uropod or produce motive force. Instead, the data suggest that retraction of the relatively rigid microtubules into the streamlined uropod increases T cell deformability, thereby facilitating migration through constricted spaces. Microtubule retraction, therefore, may prove to be a strategy for accelerating extravasation without disassembly of the microtubule-based transport system.
球形循环T细胞必须极化才能渗出。我们发现,极化过程包括微管细胞骨架的剧烈重新配置。在球形T细胞中,细胞核被从微管组织中心(MTOC)辐射出的微管所包围。在极化过程中,尾足(一个细长的后部附属物)在MTOC的位置形成。当尾足芽出时,MTOC被携带在其远端尖端。附着的微管缩回到尾足腔内,像伞的辐条一样折叠成一个紧凑的束。用微管抑制剂进行的实验表明,缩回的微管不支持尾足或产生动力。相反,数据表明,相对刚性的微管缩回到流线型的尾足中会增加T细胞的可变形性,从而促进其通过狭窄空间的迁移。因此,微管回缩可能是一种在不解散基于微管的运输系统的情况下加速渗出的策略。