Structure and organization of membrane organelles along distal microtubule segments in growth cones
- 1 September 1991
- journal article
- Published by Wiley in Journal of Neuroscience Research
- Vol. 30 (1) , 242-258
- https://doi.org/10.1002/jnr.490300125
Abstract
Advance and stabilization of organelle‐rich cytoplasm within the neuronal growth cone is coupled to axon elongation (Goldberg and Burmeister, 1986; Aletta and Greene, 1988), and this involves forward movement of organelles from the growth cone base along distinct tracks toward the leading edge. Membrane‐bound organelles that advance first within the growth cone often make transient excursions toward the leading edge, and at the light microscope level these leading organelles appear to colocalize with distal microtubule (MX) segments (Dailey and Bridgman, 1989). We have used electron microscopy (EM) to identify the membranous organelles adjacent to distal MT segments, and to examine their structural interactions with MTs. In both glutaraldehyde‐fixed and rapid frozen whole‐mount growth cones, attenuated endoplasmic reticulum (ER)‐like membrane elements were the most common organelle type located adjacent to distal MX segments. These ER‐like membrane elements coursed roughly parallel to MTs and frequently terminated within an electron‐dense bulb at the MX tip. Blind‐ended membrane tubes, dense‐core vesicles, clear vesicles, and vacuoles were also found adjacent to distal MX segments. Quantitative analyses of organelle‐MT associations suggest that elements of the ER‐like membrane system may frequently advance ahead of other membrane‐bound organelles. Freeze‐etch EM revealed crossbridging structures between MTs and membranous organelles, which is consistent with the idea that advance of leading membrane organelles into the growth cone periphery is mediated by microtubule‐based motor transport mechanisms. The results suggest that distal microtubule segments serve as transport elements for advance of membrane organelles into more peripheral growth cone regions, and together MTs and ER‐like membrane organelles may initiate the conversion of dynamic F‐actin‐rich cytoplasm to more stable organelle‐rich cytoplasm (i.e., axoplasm).Keywords
This publication has 53 references indexed in Scilit:
- Submolecular domains of bovine brain kinesin identified by electron microscopy and monoclonal antibody decorationCell, 1989
- The organization of myosin and actin in rapid frozen nerve growth cones.The Journal of cell biology, 1989
- The ultrastructure of the neuronal growth cone: New insights from subcellular fractionation and rapid freezing studiesElectron Microscopy Reviews, 1988
- MAP 1C is a microtubule-activated ATPase which translocates microtubules in vitro and has dynein-like properties.The Journal of cell biology, 1987
- Neuronal calcium homeostasisTrends in Neurosciences, 1987
- Assembly of microtubules at the tip of growing axonsNature, 1986
- Cross-bridges mediate anterograde and retrograde vesicle transport along microtubules in squid axoplasm.The Journal of cell biology, 1985
- Polarized compartmentalization of organelles in growth cones from developing optic tectum.The Journal of cell biology, 1985
- COLCHICINE INHIBITION OF NERVE FIBER FORMATION IN VITROThe Journal of cell biology, 1972
- The mechanism of the fixation of tissue components by osmium tetroxide via hydrogen bondingJournal of Ultrastructure Research, 1972