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Cytoplasmic structure in rapid-frozen axons.

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TLDR
It is proposed that the longitudinally oriented microtubule domains are channels within which organelles are transported and may constitute the myriad enzymes and other nonfibrous components that slowly move down the axon.
Abstract
Turtle optic nerves were rapid-frozen from the living state, fractured, etched, and rotary shadowed. Stereo views of fractured axons show that axoplasm consists of three types of longitudinally oriented domains. One type consists of neurofilament bundles in which individual filaments are interconnected by a cross-bridging network. Contiguous to neurofilament domains are domains containing microtubules suspended in a loose, granular matrix. A third domain is confined to a zone, 80-100 nm wide, next to the axonal membrane and consists of a dense filamentous network connecting the longitudinal elements of the axonal cytoskeleton to particles on the inner surface of the axolemma. Three classes of membrane-limited organelles are distinguished: axoplasmic reticulum, mitochondria, and discrete vesicular organelles. The vesicular organelles must include lysosomes, multivesicular bodies, and vesicles which are retrogradely transported in axons, though some vesicular organelles may be components of the axoplasmic reticulum. Organelles in each class have a characteristic relationship to the axonal cytoskeleton. The axoplasmic reticulum enters all three domains of axoplasm, but mitochondria and vesicular organelles are excluded from the neurofilament bundles, a distribution confirmed in thin sections of cryoembedded axons. Vesicular organelles differ from mitochondria in at least three ways with respect to their relationships to adjacent axoplasm: (a) one, or sometimes both, of their ends are associated with a gap in the surrounding granular axoplasm; (b) an appendage is typically associated with one of their ends; and (c) they are not attached or closely apposed to microtubules. Mitochondria, on the other hand, are only rarely associated with gaps in the axoplasm, do not have an appendage, and are virtually always attached to one or more microtubules by an irregular array of side-arms. We propose that the longitudinally oriented microtubule domains are channels within which organelles are transported. We also propose that the granular material in these channels may constitute the myriad enzymes and other nonfibrous components that slowly move down the axon.

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Citations
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Journal ArticleDOI

Actin, Spectrin, and Associated Proteins Form a Periodic Cytoskeletal Structure in Axons

TL;DR: Surprisingly, while actin in dendrites formed long filaments, the act in axons was organized into evenly spaced ringlike structures at the axon circumference that wrapped around the circumference of axons and were evenly spaced along axonal shafts with a periodicity of ~180 to 190 nanometers.
Journal ArticleDOI

Cytoskeletal dynamics and transport in growth cone motility and axon guidance

TL;DR: A working model for cytoskeletal regulation of directed axon outgrowth is presented and an important goal for the future will be to understand the coordinated response of the cytoskeleton to signaling cascades induced by guidance receptor activation.
Journal ArticleDOI

A novel brain ATPase with properties expected for the fast axonal transport motor

TL;DR: The identification and partial characterization of an ATPase activity from brain whose binding to microtubules is stabilized by AMP-PNP is reported, and this novel ATPase fraction has the predicted characteristics of the motor involved in fast axonal transport.
References
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Journal ArticleDOI

The Fine Structure of the Nervous System.

TL;DR: This is the first atlas of the ultrastructure of the mature nervous system and it is a relatively complete collection of elegant micrographs with an accompanying text that explores the role that thin astrocytic processes may play in isolating receptive surfaces, thereby preventing axon terminals from influencing.
Journal ArticleDOI

Synaptic vesicle exocytosis captured by quick freezing and correlated with quantal transmitter release.

TL;DR: The utility of quick- freezing as a technique to capture biological processes as evanescent as synaptic transmission as well as physiological demonstrations that quanta are discharged independently has been established.
Journal ArticleDOI

Filament organization revealed in platinum replicas of freeze-dried cytoskeletons.

TL;DR: Freeze-dried cytoskeletons provide an opportunity to study--at high resolution and in the absence of problems caused by chemical fixation--the detailed organization of filaments in different regions of the cytoplasm and at different stages of cell development.
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