Waterman-Storer C M, Gregory J, Parsons S F, Salmon E D
Marine Biological Laboratory, Woods Hole, Massachusetts 02543, USA.
J Cell Biol. 1995 Sep;130(5):1161-9. doi: 10.1083/jcb.130.5.1161.
We discovered by using high resolution video microscopy, that membranes become attached selectively to the growing plus ends of microtubules by membrane/microtubule tip attachment complexes (TACs) in interphase-arrested, undiluted, Xenopus egg extracts. Persistent plus end growth of stationary microtubules pushed the membranes into thin tubules and dragged them through the cytoplasm at the approximately 20 microns/min velocity typical of free plus ends. Membrane tubules also remained attached to plus ends when they switched to the shortening phase of dynamic instability at velocities typical of free ends, 50-60 microns/min. Over time, the membrane tubules contacted and fused with one another along their lengths, forming a polygonal network much like the distribution of ER in cells. Several components of the membrane networks formed by TACs were identified as ER by immunofluorescent staining using antibodies to ER-resident proteins. TAC motility was not inhibited by known inhibitors of microtubule motor activity, including 5 mM AMP-PNP, 250 microM orthovanadate, and ATP depletion. These results show that membrane/microtubule TACs enable polymerizing ends to push and depolymerizing ends to pull membranes into thin tubular extensions and networks at fast velocities.
我们通过高分辨率视频显微镜观察发现,在间期停滞、未稀释的非洲爪蟾卵提取物中,膜通过膜/微管末端附着复合物(TACs)选择性地附着于微管不断生长的正端。静止微管的持续正端生长将膜推成细管,并以游离正端典型的约20微米/分钟的速度将它们拖过细胞质。当膜细管转变为动态不稳定性的缩短阶段时,其速度为游离末端典型的50 - 60微米/分钟,此时膜细管也仍附着于正端。随着时间的推移,膜细管沿其长度相互接触并融合,形成一个多边形网络,非常类似于细胞内质网的分布。使用针对内质网驻留蛋白的抗体进行免疫荧光染色,由TACs形成的膜网络的几个成分被鉴定为内质网。TAC的运动不受已知的微管运动活性抑制剂的抑制,包括5 mM AMP - PNP、250 microM原钒酸盐和ATP耗竭。这些结果表明,膜/微管TACs使聚合端能够推动、解聚端能够拉动膜,从而快速形成细管状延伸和网络。