Can molecular motors drive distance measurements in injured neurons?

Injury to nerve axons induces diverse responses in neuronal cell bodies, some of which are influenced by the distance from the site of injury. This suggests that neurons have the capacity to estimate the distance of the injury site from their cell body. Recent work has shown that the molecular motor...

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Main Authors: Naaman Kam, Yitzhak Pilpel, Mike Fainzilber
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-08-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC2718615?pdf=render
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spelling doaj-2c9872771a2f400682cc2f87fa9dcc692020-11-25T01:13:56ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582009-08-0158e100047710.1371/journal.pcbi.1000477Can molecular motors drive distance measurements in injured neurons?Naaman KamYitzhak PilpelMike FainzilberInjury to nerve axons induces diverse responses in neuronal cell bodies, some of which are influenced by the distance from the site of injury. This suggests that neurons have the capacity to estimate the distance of the injury site from their cell body. Recent work has shown that the molecular motor dynein transports importin-mediated retrograde signaling complexes from axonal lesion sites to cell bodies, raising the question whether dynein-based mechanisms enable axonal distance estimations in injured neurons? We used computer simulations to examine mechanisms that may provide nerve cells with dynein-dependent distance assessment capabilities. A multiple-signals model was postulated based on the time delay between the arrival of two or more signals produced at the site of injury-a rapid signal carried by action potentials or similar mechanisms and slower signals carried by dynein. The time delay between the arrivals of these two types of signals should reflect the distance traversed, and simulations of this model show that it can indeed provide a basis for distance measurements in the context of nerve injuries. The analyses indicate that the suggested mechanism can allow nerve cells to discriminate between distances differing by 10% or more of their total axon length, and suggest that dynein-based retrograde signaling in neurons can be utilized for this purpose over different scales of nerves and organisms. Moreover, such a mechanism might also function in synapse to nucleus signaling in uninjured neurons. This could potentially allow a neuron to dynamically sense the relative lengths of its processes on an ongoing basis, enabling appropriate metabolic output from cell body to processes.http://europepmc.org/articles/PMC2718615?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Naaman Kam
Yitzhak Pilpel
Mike Fainzilber
spellingShingle Naaman Kam
Yitzhak Pilpel
Mike Fainzilber
Can molecular motors drive distance measurements in injured neurons?
PLoS Computational Biology
author_facet Naaman Kam
Yitzhak Pilpel
Mike Fainzilber
author_sort Naaman Kam
title Can molecular motors drive distance measurements in injured neurons?
title_short Can molecular motors drive distance measurements in injured neurons?
title_full Can molecular motors drive distance measurements in injured neurons?
title_fullStr Can molecular motors drive distance measurements in injured neurons?
title_full_unstemmed Can molecular motors drive distance measurements in injured neurons?
title_sort can molecular motors drive distance measurements in injured neurons?
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2009-08-01
description Injury to nerve axons induces diverse responses in neuronal cell bodies, some of which are influenced by the distance from the site of injury. This suggests that neurons have the capacity to estimate the distance of the injury site from their cell body. Recent work has shown that the molecular motor dynein transports importin-mediated retrograde signaling complexes from axonal lesion sites to cell bodies, raising the question whether dynein-based mechanisms enable axonal distance estimations in injured neurons? We used computer simulations to examine mechanisms that may provide nerve cells with dynein-dependent distance assessment capabilities. A multiple-signals model was postulated based on the time delay between the arrival of two or more signals produced at the site of injury-a rapid signal carried by action potentials or similar mechanisms and slower signals carried by dynein. The time delay between the arrivals of these two types of signals should reflect the distance traversed, and simulations of this model show that it can indeed provide a basis for distance measurements in the context of nerve injuries. The analyses indicate that the suggested mechanism can allow nerve cells to discriminate between distances differing by 10% or more of their total axon length, and suggest that dynein-based retrograde signaling in neurons can be utilized for this purpose over different scales of nerves and organisms. Moreover, such a mechanism might also function in synapse to nucleus signaling in uninjured neurons. This could potentially allow a neuron to dynamically sense the relative lengths of its processes on an ongoing basis, enabling appropriate metabolic output from cell body to processes.
url http://europepmc.org/articles/PMC2718615?pdf=render
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