Advances and Limitations of Current Epigenetic Studies Investigating Mammalian Axonal Regeneration

被引:28
作者
Palmisano, Ilaria [1 ]
Di Giovanni, Simone [1 ]
机构
[1] Imperial Coll London, Div Brain Sci, Dept Med, Ctr Restorat Neurosci,Lab Neuroregenerat, London, England
关键词
Epigenetic; HDAC; HAT; Transcription; Axonal regeneration; Spinal cord injury; Nerve injury; DNA methylation; RNA; DNA METHYLTRANSFERASES DNMT3A; CENTRAL-NERVOUS-SYSTEM; CPG BINDING-PROTEINS; CHROMATIN ARCHITECTURE; PROMOTES REGENERATION; HISTONE MODIFICATIONS; TRANSCRIPTION FACTORS; MOLECULAR-MECHANISMS; FUNCTIONAL RECOVERY; INJURY RESPONSES;
D O I
10.1007/s13311-018-0636-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Axonal regeneration relies on the expression of regenerative associated genes within a coordinated transcriptional programme, which is finely tuned as a result of the activation of several regenerative signalling pathways. In mammals, this chain of events occurs in neurons following peripheral axonal injury, however it fails upon axonal injury in the central nervous system, such as in the spinal cord and the brain. Accumulating evidence has been suggesting that epigenetic control is a key factor to initiate and sustain the regenerative transcriptional response and that it might contribute to regenerative success versus failure. This review will discuss experimental evidence so far showing a role for epigenetic regulation in models of peripheral and central nervous system axonal injury. It will also propose future directions to fill key knowledge gaps and to test whether epigenetic control might indeed discriminate between regenerative success and failure.
引用
收藏
页码:529 / 540
页数:12
相关论文
共 137 条
[1]   Nerve injury signaling [J].
Abe, Namiko ;
Cavalli, Valeria .
CURRENT OPINION IN NEUROBIOLOGY, 2008, 18 (03) :276-283
[2]   Extrinsic and intrinsic factors controlling axonal regeneration after spinal cord injury [J].
Afshari, Fardad T. ;
Kappagantula, Sunil ;
Fawcett, James W. .
EXPERT REVIEWS IN MOLECULAR MEDICINE, 2009, 11
[3]  
Bartnik-Olson Brenda L, 2013, Front Neuroenergetics, V5, P8, DOI 10.3389/fnene.2013.00008
[4]   Phosphorylation of TET Proteins Is Regulated via O-GlcNAcylation by the O-Linked N-Acetylglucosamine Transferase (OGT) [J].
Bauer, Christina ;
Goebel, Klaus ;
Nagaraj, Nagarjuna ;
Colantuoni, Christian ;
Wang, Mengxi ;
Mueller, Udo ;
Kremmer, Elisabeth ;
Rottach, Andrea ;
Leonhardt, Heinrich .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (08) :4801-4812
[5]   YY1 and CTCF orchestrate a 3D chromatin looping switch during early neural lineage commitment [J].
Beagan, Jonathan A. ;
Duong, Michael T. ;
Titus, Katelyn R. ;
Zhou, Linda ;
Cao, Zhendong ;
Ma, Jingjing ;
Lachanski, Caroline V. ;
Gillis, Daniel R. ;
Phillips-Cremins, Jennifer E. .
GENOME RESEARCH, 2017, 27 (07) :1139-1152
[6]   TDP-43 Promotes Neurodegeneration by Impairing Chromatin Remodeling [J].
Berson, Amit ;
Sartoris, Ashley ;
Nativio, Raffaella ;
Van Deerlin, Vivianna ;
Toledo, Jon B. ;
Porta, Silvia ;
Liu, Shichong ;
Chung, Chia-Yu ;
Garcia, Benjamin A. ;
Lee, Virginia M. -Y. ;
Trojanowski, John Q. ;
Johnson, F. Brad ;
Berger, Shelley L. ;
Bonini, Nancy M. .
CURRENT BIOLOGY, 2017, 27 (23) :3579-+
[7]   The DNA methyltransferases of mammals [J].
Bestor, TH .
HUMAN MOLECULAR GENETICS, 2000, 9 (16) :2395-2402
[8]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[9]   Changes within maturing neurons limit axonal regeneration in the developing spinal cord [J].
Blackmore, M ;
Letourneau, PC .
JOURNAL OF NEUROBIOLOGY, 2006, 66 (04) :348-360
[10]   Multiscale 3D Genome Rewiring during Mouse Neural Development [J].
Bonev, Boyan ;
Cohen, Netta Mendelson ;
Szabo, Quentin ;
Fritsch, Lauriane ;
Papadopoulos, Giorgio L. ;
Lubling, Yaniv ;
Xu, Xiaole ;
Lv, Xiaodan ;
Hugnot, Jean-Philippe ;
Tanay, Amos ;
Cavalli, Giacomo .
CELL, 2017, 171 (03) :557-+