Literature DB >> 3693400

Rapidly transported organelles containing membrane and cytoskeletal components: their relation to axonal growth.

P J Hollenbeck1, D Bray.   

Abstract

We have examined the movements, composition, and cellular origin of phase-dense varicosities in cultures of chick sympathetic and sensory neurons. These organelles are variable in diameter (typically between 0.2 and 2 microns) and undergo saltatory movements both towards and away from the neuronal cell body. Their mean velocities vary inversely with the size of the organelle and are greater in the retrograde than the anterograde direction. Organelles stain with the lipophilic dye 1, 1'-dioctadecyl-3,3,3',3'-tetramethyl-indocarbocyanine and with antibodies to cytoskeletal components. In cultures double-stained with antibodies to alpha-tubulin and 70-kD neurofilament protein (NF-L), approximately 40% of the organelles stain for tubulin, 30% stain for NF-L, 10% stain for both tubulin and NF-L, and 40% show no staining with either antibody. The association of cytoskeletal proteins with the organelles shows that these proteins are able to move by a form of rapid axonal transport. Under most culture conditions the predominant direction of movement is towards the cell body, suggesting that the organelles are produced at or near the growth cone. Retrograde movements continue in culture medium lacking protein or high molecular mass components and increase under conditions in which the advance of the growth cone is arrested. There is a fourfold increase in the number of organelles moving retrogradely in neurites that encounter a substratum-associated barrier to elongation; retrograde movements increase similarly in cultures exposed to cytochalasin at levels known to block growth cone advance. No previously described organelle shows behavior coordinated with axonal growth in this way. We propose that the organelles contain membrane and cytoskeletal components that have been delivered to the growth cone, by slow or fast anterograde transport, in excess of the amounts required to synthesize more axon. In view of their rapid mobility and variable contents, we suggest that they be called "neuronal parcels."

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Year:  1987        PMID: 3693400      PMCID: PMC2114729          DOI: 10.1083/jcb.105.6.2827

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  22 in total

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Journal:  J Supramol Struct       Date:  1976

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Authors:  K Weber; P C Rathke; M Osborn
Journal:  Proc Natl Acad Sci U S A       Date:  1978-04       Impact factor: 11.205

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Authors:  M A Ludueña
Journal:  Dev Biol       Date:  1973-08       Impact factor: 3.582

Review 4.  Intracellular transport in neurons.

Authors:  B Grafstein; D S Forman
Journal:  Physiol Rev       Date:  1980-10       Impact factor: 37.312

5.  Lateral transport of a lipid probe and labeled proteins on a cell membrane.

Authors:  J Schlessinger; D Axelrod; D E Koppel; W W Webb; E L Elson
Journal:  Science       Date:  1977-01-21       Impact factor: 47.728

6.  A simple method of reducing the fading of immunofluorescence during microscopy.

Authors:  G D Johnson; G M Nogueira Araujo
Journal:  J Immunol Methods       Date:  1981       Impact factor: 2.303

7.  Slow components of axonal transport: two cytoskeletal networks.

Authors:  M M Black; R J Lasek
Journal:  J Cell Biol       Date:  1980-08       Impact factor: 10.539

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Authors:  M G Honig; R I Hume
Journal:  J Cell Biol       Date:  1986-07       Impact factor: 10.539

9.  The movement of membranous organelles in axons. Electron microscopic identification of anterogradely and retrogradely transported organelles.

Authors:  S Tsukita; H Ishikawa
Journal:  J Cell Biol       Date:  1980-03       Impact factor: 10.539

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Authors:  P N Hoffman; R J Lasek
Journal:  J Cell Biol       Date:  1975-08       Impact factor: 10.539

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  33 in total

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2.  Rapid intermittent movement of axonal neurofilaments observed by fluorescence photobleaching.

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Journal:  Mol Biol Cell       Date:  2001-10       Impact factor: 4.138

3.  Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport.

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4.  An actin-associated protein present in the microtubule organizing center and the growth cones of PC-12 cells.

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5.  KIF1A/UNC-104 Transports ATG-9 to Regulate Neurodevelopment and Autophagy at Synapses.

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6.  Local modulation of plus-end transport targets herpesvirus entry and egress in sensory axons.

Authors:  G A Smith; L Pomeranz; S P Gross; L W Enquist
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7.  Synthesis of beta-tubulin, actin, and other proteins in axons of sympathetic neurons in compartmented cultures.

Authors:  H Eng; K Lund; R B Campenot
Journal:  J Neurosci       Date:  1999-01-01       Impact factor: 6.167

Review 8.  The cell biology of the nerve terminal.

Authors:  R B Kelly
Journal:  Neuron       Date:  1988-08       Impact factor: 17.173

9.  Expression levels of B-50/GAP-43 in PC12 cells are decisive for the complexity of their neurites and growth cones.

Authors:  E R Jap Tjoen San; A J van Rozen; H B Nielander; A B Oestreicher; W H Gispen; P Schotman
Journal:  J Mol Neurosci       Date:  1995       Impact factor: 3.444

10.  Real-time imaging of the axonal transport of granules containing a tissue plasminogen activator/green fluorescent protein hybrid.

Authors:  J E Lochner; M Kingma; S Kuhn; C D Meliza; B Cutler; B A Scalettar
Journal:  Mol Biol Cell       Date:  1998-09       Impact factor: 4.138

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