Dynamic instability and motile events of native microtubules from squid axoplasm
- 1 January 1988
- journal article
- axoplasmic transport
- Published by Wiley in Cell Motility
- Vol. 10 (1-2) , 285-295
- https://doi.org/10.1002/cm.970100133
Abstract
Native microtubules from extruded axoplasm of squid giant axons were used as a paradigm to characterize the motion of organelles along free microtubules and to study the dynamics of microtubule length changes. The motion of large round organelles was visualized by AVEC‐DIC microscopy and analyzed at a temporal resolution of 10 frames per second. The movements were smooth and showed no major changes in velocity or direction. During translocation, the organelles paused very rarely. Superimposed on the rather constant mean velocity was a velocity fluctuation, which indicated that the organelles are subject to considerable thermal motion during translocation. Evidence for a regular low‐frequency oscillation was not found. The thermal motion was anisotropic such that axial motion was less restricted than lateral motion. We conclude that the crossbridge connecting the moving organelle to the microtubule has a flexible region that behaves like a hinge, which permits preferential movement in the direction parallel to the microtubule. The dynamic changes in length of native microtubules were studied at a temporal resolution of 1 Hz. About 98% of the native microtubules maintained their length (“stable” microtubules), while 2% showed phases of growing and/or shrinking typical for dynamic instability (“dynamic” microtubules). Gliding and organelle motion were not influenced by dynamic length changes. Transitions between growing and shrinking phases were low‐frequency events (1–10 minutes per cycle). However, a new type of microtubule length fluctuation, which occurred at a high frequency (a few seconds per cycle), was detected. The length changes were in the 1–3 μm range. The latter events were very prominent at the (+) ends. It appears that the native axonal microtubules are much more stable than the purified microtubules and the microtubules of cultured cells that have been studied thus far. Potential mechanisms accounting for the three states of microtubule stability are discussed. These studies show that the native microtubules from squid giant axons are a very useful paradigm for studying microtubule‐related motility events and microtubule dynamics.Keywords
This publication has 44 references indexed in Scilit:
- Dynamic instability of native microtubules from squid axons is rare and independent of gliding and vesicle transportExperimental Cell Research, 1988
- MAP 1C is a microtubule-activated ATPase which translocates microtubules in vitro and has dynein-like properties.The Journal of cell biology, 1987
- Correlation between the ATPase and microtubule translocating activities of sea urchin egg kinesinNature, 1987
- Microtubule dynamics in vivo: a test of mechanisms of turnover.The Journal of cell biology, 1987
- Microtubule‐Associated Proteins (MAPs) of Dogfish Brain and Squid Optic GangliaaAnnals of the New York Academy of Sciences, 1986
- Microtubule dynamics in interphase cells.The Journal of cell biology, 1986
- Polarized microtubule gliding and particle saltations produced by soluble factors from sea urchin eggs and embryosCell Motility, 1986
- The determination of the instantaneous velocity of axonally transported organelles from filmed records of their motionCanadian Journal of Physiology and Pharmacology, 1982
- Stable polymers of the axonal cytoskeleton: the axoplasmic ghost.The Journal of cell biology, 1982
- Microtubule Formation in vitro in Solutions Containing Low Calcium ConcentrationsScience, 1972