Literature DB >> 1282329

Organelles in fast axonal transport. What molecules do they carry in anterograde vs retrograde directions, as observed in mammalian systems?

A B Dahlström1, A J Czernik, J Y Li.   

Abstract

The present minireview describes experiments carried out, in short-term crush-operated rat nerves, using immunofluorescence and cytofluorimetric scanning techniques to study endogenous substances in anterograde and retrograde fast axonal transport. Vesicle membrane components p38 (synaptophysin) and SV2 are accumulating on both sides of a crush, but a larger proportion of p38 (about 3/4) than of SV2 (about 1/2) is recycling toward the cell body, compared to the amount carried with anterograde transport. Matrix peptides, such as CGRP, ChRA, VIP, and DBH are recycling to a minor degree, although only 10-20% of surface-associated molecules, such as synapsins and kinesin, appear to recycle. The described methodological approach to study the composition of organelles in fast axonal transport, anterograde as compared to retrograde, is shown to be useful for investigating neurobiological processes. We make use of the "in vivo chromatography" process that the fast axonal transport system constitutes. Only substances that are in some way either stored in, or associated with, transported organelles can be clearly observed to accumulate relative to the crush region. Emphasis in this paper was given to the synapsins, because of diverging results published concerning the degree of affiliation with various neuronal organelles. Our previously published results have indicated that in the living axons the SYN I is affiliated with mainly anterogradely fast transported organelles. Therefore, some preliminary, previously unpublished results on the accumulations of the four different synapsins (SYN Ia, SYN Ib, SYN IIa, and SYN IIb), using antisera specific for each of the four members of the synapsin family, are described. It was found that SYN Ib clearly has a stronger affiliation to anterogradely transported organelles than SYN Ia, and that both SYN IIa and SYN IIb are bound to some degree to transported organelles.

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Year:  1992        PMID: 1282329     DOI: 10.1007/BF02780550

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  78 in total

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  10 in total

1.  Neurosecretory granule formation in ligated axons: additional arguments for a local differentiation from a Golgi apparatus extension.

Authors:  J R Quatacker
Journal:  Histochem J       Date:  2001-03

2.  Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy.

Authors:  Natalie Vavlitou; Irene Sargiannidou; Kyriaki Markoullis; Kyriacos Kyriacou; Steven S Scherer; Kleopas A Kleopa
Journal:  J Neuropathol Exp Neurol       Date:  2010-09       Impact factor: 3.685

3.  Fast vesicle transport is required for the slow axonal transport of synapsin.

Authors:  Yong Tang; David Scott; Utpal Das; Daniel Gitler; Archan Ganguly; Subhojit Roy
Journal:  J Neurosci       Date:  2013-09-25       Impact factor: 6.167

Review 4.  Membrane composition of adrenergic large and small dense cored vesicles and of synaptic vesicles: consequences for their biogenesis.

Authors:  H Winkler
Journal:  Neurochem Res       Date:  1997-08       Impact factor: 3.996

5.  Localization of synapsin I in normal fibers and regenerating axonal sprouts of the rat sciatic nerve.

Authors:  S Akagi; A Mizoguchi; K Sobue; H Nakamura; C Ide
Journal:  Histochem Cell Biol       Date:  1996-05       Impact factor: 4.304

6.  Immunohistochemical characterisation of differentiated CAD cells: expression of peptides and chromogranins.

Authors:  Yongling Li; Linda Xiu-E Hou; Annika Aktiv; Annica Dahlström
Journal:  Histochem Cell Biol       Date:  2005-07-09       Impact factor: 4.304

Review 7.  Molecular analysis of a secretory organelle: structure and function of synaptic vesicle-specific proteins.

Authors:  K M Buckley
Journal:  J Membr Biol       Date:  1994-04       Impact factor: 1.843

8.  Plus-end motors override minus-end motors during transport of squid axon vesicles on microtubules.

Authors:  V Muresan; C P Godek; T S Reese; B J Schnapp
Journal:  J Cell Biol       Date:  1996-10       Impact factor: 10.539

9.  Spontaneous murine neuroaxonal dystrophy: a model of infantile neuroaxonal dystrophy.

Authors:  D M Bouley; J J McIntire; B T Harris; R J Tolwani; G M Otto; R H DeKruyff; S J Hayflick
Journal:  J Comp Pathol       Date:  2006-03-20       Impact factor: 1.311

10.  Tri-partite complex for axonal transport drug delivery achieves pharmacological effect.

Authors:  Aaron G Filler; Garth T Whiteside; Mark Bacon; Martyn Frederickson; Franklyn A Howe; Miri D Rabinowitz; Alan J Sokoloff; Terrence W Deacon; Chris Abell; Raj Munglani; John R Griffiths; B Anthony Bell; Andrew M L Lever
Journal:  BMC Neurosci       Date:  2010-01-20       Impact factor: 3.288

  10 in total

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