Literature DB >> 29664188

Can Chromatin Accessibility be Exploited for Axon Regeneration?

Matt C Danzi1,2,3, Nick O'Neill1,3, John L Bixby1,3,4, Vance P Lemmon1,2,3.   

Abstract

Several studies have demonstrated that the intrinsic ability of neurons to regenerate their axons can be stimulated by maneuvers that favor the open state of chromatin, such as inhibiting histone deacetylase activity or increasing histone acetyltransferase activity. Taken together, these experiments suggest that axon regenerative ability can be increased by promoting chromatin accessibility. In this article, we assess the direct evidence in the literature for this hypothesis and re-examine other axon regeneration-promoting manipulations to see if they provide additional support. We find that several interventions known to enhance intrinsic axonal growth capability also increase chromatin accessibility. Although the support for this correlation is strong in the literature, we conclude with a word of caution about therapeutics attempting to exploit this relationship.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  PTEN; TET3; epigenetics; neuron; neuronal activity

Mesh:

Substances:

Year:  2018        PMID: 29664188      PMCID: PMC6556782          DOI: 10.1002/dneu.22598

Source DB:  PubMed          Journal:  Dev Neurobiol        ISSN: 1932-8451            Impact factor:   3.964


  52 in total

1.  Brief electrical stimulation promotes the speed and accuracy of motor axonal regeneration.

Authors:  A A Al-Majed; C M Neumann; T M Brushart; T Gordon
Journal:  J Neurosci       Date:  2000-04-01       Impact factor: 6.167

2.  The language of covalent histone modifications.

Authors:  B D Strahl; C D Allis
Journal:  Nature       Date:  2000-01-06       Impact factor: 49.962

3.  ACETYLATION AND METHYLATION OF HISTONES AND THEIR POSSIBLE ROLE IN THE REGULATION OF RNA SYNTHESIS.

Authors:  V G ALLFREY; R FAULKNER; A E MIRSKY
Journal:  Proc Natl Acad Sci U S A       Date:  1964-05       Impact factor: 11.205

4.  Retrograde axonal transport of JNK signaling molecules influence injury induced nuclear changes in p-c-Jun and ATF3 in adult rat sensory neurons.

Authors:  Charlotta Lindwall; Martin Kanje
Journal:  Mol Cell Neurosci       Date:  2005-06       Impact factor: 4.314

Review 5.  Chromatin remodeling and cancer, Part II: ATP-dependent chromatin remodeling.

Authors:  Gang G Wang; C David Allis; Ping Chi
Journal:  Trends Mol Med       Date:  2007-09-05       Impact factor: 11.951

6.  HDAC inhibition promotes neuronal outgrowth and counteracts growth cone collapse through CBP/p300 and P/CAF-dependent p53 acetylation.

Authors:  P Gaub; A Tedeschi; R Puttagunta; T Nguyen; A Schmandke; S Di Giovanni
Journal:  Cell Death Differ       Date:  2010-01-22       Impact factor: 15.828

7.  Promoting axon regeneration in the adult CNS by modulation of the PTEN/mTOR pathway.

Authors:  Kevin Kyungsuk Park; Kai Liu; Yang Hu; Patrice D Smith; Chen Wang; Bin Cai; Bengang Xu; Lauren Connolly; Ioannis Kramvis; Mustafa Sahin; Zhigang He
Journal:  Science       Date:  2008-11-07       Impact factor: 47.728

8.  The transcription factors c-JUN, JUN D and CREB, but not FOS and KROX-24, are differentially regulated in axotomized neurons following transection of rat sciatic nerve.

Authors:  T Herdegen; C E Fiallos-Estrada; W Schmid; R Bravo; M Zimmermann
Journal:  Brain Res Mol Brain Res       Date:  1992-07

Review 9.  Axon regeneration in the peripheral and central nervous systems.

Authors:  Eric A Huebner; Stephen M Strittmatter
Journal:  Results Probl Cell Differ       Date:  2009

10.  mTOR binds to the promoters of RNA polymerase I- and III-transcribed genes.

Authors:  Chi Kwan Tsang; Hui Liu; X F Steven Zheng
Journal:  Cell Cycle       Date:  2010-03-07       Impact factor: 4.534

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.