Serum Response Factor (SRF) mediated gene activity in physiological and pathological processes of neuronal motility

In recent years, the transcription factor SRF (serum response factor) was shown to contribute to various physiological processes linked to neuronal motility. The latter include cell migration, axon guidance and e.g. synapse function relying on cytoskeletal dynamics, neurite outgrowth, axonal and den...

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Main Author: Bernd eKnoll
Format: Article
Language:English
Published: Frontiers Media S.A. 2011-12-01
Series:Frontiers in Molecular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnmol.2011.00049/full
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spelling doaj-0f52e41d13bd465a80550cd8c964af942020-11-25T00:14:45ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992011-12-01410.3389/fnmol.2011.0004916355Serum Response Factor (SRF) mediated gene activity in physiological and pathological processes of neuronal motilityBernd eKnoll0Ulm UniversityIn recent years, the transcription factor SRF (serum response factor) was shown to contribute to various physiological processes linked to neuronal motility. The latter include cell migration, axon guidance and e.g. synapse function relying on cytoskeletal dynamics, neurite outgrowth, axonal and dendritic differentiation, growth cone motility and neurite branching. SRF teams up with MRTFs (myocardin related transcription factors) and TCFs (ternary complex factors) to mediate cellular actin cytoskeletal dynamics and the immediate-early gene (IEG) response, a bona fide indicator of neuronal activation. Herein, I will discuss how SRF and cofactors might modulate physiological processes of neuronal motility. Further, potential mechanisms engaged by neurite growth promoting molecules and axon guidance cues to target SRF’s transcriptional machinery in physiological neuronal motility will be presented. Of note, altered cytoskeletal dynamics and rapid initiation of an IEG response are a hallmark of injured neurons in various neurological disorders. Thus, SRF and its MRTF and TCF cofactors might emerge as a novel trio modulating peripheral and central axon regeneration.http://journal.frontiersin.org/Journal/10.3389/fnmol.2011.00049/fullRegenerationActinGrowth coneImmediate early GeneMRTFNeurite outgrowth
collection DOAJ
language English
format Article
sources DOAJ
author Bernd eKnoll
spellingShingle Bernd eKnoll
Serum Response Factor (SRF) mediated gene activity in physiological and pathological processes of neuronal motility
Frontiers in Molecular Neuroscience
Regeneration
Actin
Growth cone
Immediate early Gene
MRTF
Neurite outgrowth
author_facet Bernd eKnoll
author_sort Bernd eKnoll
title Serum Response Factor (SRF) mediated gene activity in physiological and pathological processes of neuronal motility
title_short Serum Response Factor (SRF) mediated gene activity in physiological and pathological processes of neuronal motility
title_full Serum Response Factor (SRF) mediated gene activity in physiological and pathological processes of neuronal motility
title_fullStr Serum Response Factor (SRF) mediated gene activity in physiological and pathological processes of neuronal motility
title_full_unstemmed Serum Response Factor (SRF) mediated gene activity in physiological and pathological processes of neuronal motility
title_sort serum response factor (srf) mediated gene activity in physiological and pathological processes of neuronal motility
publisher Frontiers Media S.A.
series Frontiers in Molecular Neuroscience
issn 1662-5099
publishDate 2011-12-01
description In recent years, the transcription factor SRF (serum response factor) was shown to contribute to various physiological processes linked to neuronal motility. The latter include cell migration, axon guidance and e.g. synapse function relying on cytoskeletal dynamics, neurite outgrowth, axonal and dendritic differentiation, growth cone motility and neurite branching. SRF teams up with MRTFs (myocardin related transcription factors) and TCFs (ternary complex factors) to mediate cellular actin cytoskeletal dynamics and the immediate-early gene (IEG) response, a bona fide indicator of neuronal activation. Herein, I will discuss how SRF and cofactors might modulate physiological processes of neuronal motility. Further, potential mechanisms engaged by neurite growth promoting molecules and axon guidance cues to target SRF’s transcriptional machinery in physiological neuronal motility will be presented. Of note, altered cytoskeletal dynamics and rapid initiation of an IEG response are a hallmark of injured neurons in various neurological disorders. Thus, SRF and its MRTF and TCF cofactors might emerge as a novel trio modulating peripheral and central axon regeneration.
topic Regeneration
Actin
Growth cone
Immediate early Gene
MRTF
Neurite outgrowth
url http://journal.frontiersin.org/Journal/10.3389/fnmol.2011.00049/full
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