scholarly journals Bidirectional organelle transport can occur in cell processes that contain single microtubules.

1985 ◽  
Vol 100 (1) ◽  
pp. 322-326 ◽  
Author(s):  
M P Koonce ◽  
M Schliwa

Intracellular organelle transport was studied in a new model system, the giant freshwater ameba Reticulomyxa. The ameba extends a large reticulate network of cytoplasmic strands in which various phase-dense organelles can be seen to move at a rate of up to 25 microns/s. This combined light and high voltage electron microscopic study shows that organelles move bidirectionally in even the finest network strands that contain only a single microtubule. In terms of microtubule-associated intracellular transport, this observation defines a minimum set of conditions necessary for such movement. The implications of this finding for possible models of force generation are discussed.

1978 ◽  
Vol 57 (5-6) ◽  
pp. 708-708 ◽  
Author(s):  
T. Aoba ◽  
J. Takahashi ◽  
T. Yagi ◽  
M. Okazaki ◽  
Y. Moriwaki

Author(s):  
Michael Koonce

Pharmacological and correlative light and electron microscopic studies suggest that the two major cytoskeletal systems, the microtubules (MTs) and microfilaments (MFs), are involved in the directed transport of intracellular organelles. However, the details of organelle-cytoskeletal interactions and force generation are not known, nor is it clear whether transport is solely a MT or MF-based phenomenon, a coordinated effort, or if each system supports different classes of motility. Here I describe an isolated cytoskeletal “framework” derived from an unusual species of freshwater amoeba that provides a model system in which to examine these questions. We are intending to use this preparation to study the interactions with and movement of both isolated native and artificial organelles.


Author(s):  
A.S. Lossinsky ◽  
M.J. Song

Previous studies have suggested the usefulness of high-voltage electron microscopy (HVEM) for investigating blood-bram barrier (BBB) injury and the mechanism of inflammatory-cell (IC) attachment. These studies indicated that, in evaluating standard conventional thin sections, one might miss cellular attachment sites of ICs in their process of attaching to the luminal endothelial cell (EC) surface of cerebral blood vessels. Our current studies in animals subjected to autoimmune disease suggest that HVEM may be useful in localizing precise receptor sites involved in early IC attachment.Experimental autoimmune encephalomyelitis (EAE) was induced in mice and rats according to standard procedures. Tissue samples from cerebellum, thalamus or spinal cords were embedded in plastic following vascular perfusion with buffered aldehyde. Thick (0.5-0.7 μm) sections were cut on glass knives and collected on Formvar-coated slot grids stained with uranylacetate and lead citrate and examined with the AEI EM7 1.2 MV HVEM in Albany, NY at 1000 kV.


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