Dendritic shrinkage after injury: a cellular killer or a necessity for axonal regeneration?

被引:13
作者
Beckers, An [1 ]
Moons, Lieve [1 ]
机构
[1] Katholieke Univ Leuven, Dept Biol, Neural Circuit Dev & Regenerat Res Grp, Leuven, Belgium
关键词
axonal regeneration; dendritic remodeling; retina; central nervous system; zebrafish; mitochondrial transport; mitochondrial dynamics; energy supply; MITOCHONDRIAL TRANSPORT;
D O I
10.4103/1673-5374.253505
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dendrites form an essential component of the neuronal circuit have been largely overlooked in regenerative research. Nevertheless, subtle changes in the dendritic arbors of neurons are one of the first stages of various neurodegenerative diseases, leading to dysfunctional neuronal networks and ultimately cellular death. Maintaining dendrites is therefore considered an essential neuroprotective strategy. This mini-review aims to discuss an intriguing hypothesis, which postulates that dendritic shrinkage is an important stimulant to boost axonal regeneration, and thus that preserving dendrites might not be the ideal therapeutic method to regain a full functional network upon central nervous system damage. Indeed, our study in zebrafish, a versatile animal model with robust regenerative capacity recently unraveled that dendritic retraction is evoked prior to axonal regrowth after optic nerve injury. Strikingly, inhibiting dendritic pruning upon damage perturbed axonal regeneration. This constraining effect of dendrites on axonal regrowth has sporadically been proposed in literature, as summarized in this short narrative. In addition, the review discusses a plausible underlying mechanism for the observed antagonistic axon-dendrite interplay, which is based on energy restriction inside neurons. Axonal injury indeed leads to a high local energy demand in which efficient axonal energy supply is fundamental to ensure regrowth. At the same time, axonal lesion is known to induce mitochondrial depolarization, causing energy depletion in the axonal compartment of damaged neurons. Mitochondria, however, become mostly stationary after development, which has been proposed as a potential underlying reason for the low regenerative capacity of adult mammals. Per contra, upon reduced neuronal activity, mitochondrial mobility enhances. In this view, dendritic shrinkage after axonal injury in zebrafish could result in less synaptic input and hence, a release of mitochondria within the soma-dendrite compartment that then translocate to the axonal growth cone to stimulate axonal regeneration. If this hypothesis proofs to be correct, i.e. dendritic remodeling serving as fuel for axonal regeneration, we envision a major shift in the research focus within the neuroregenerative field and in the potential uncovering of various novel therapeutic targets.
引用
收藏
页码:1313 / 1316
页数:4
相关论文
共 14 条
[1]   Insulin signalling promotes dendrite and synapse regeneration and restores circuit function after axonal injury [J].
Agostinone, Jessica ;
Alarcon-Martinez, Luis ;
Gamlin, Clare ;
Yu, Wan-Qing ;
Wong, Rachel O. L. ;
Di Polo, Adriana .
BRAIN, 2018, 141 :1963-1980
[2]   An Antagonistic Axon-Dendrite Interplay Enables Efficient Neuronal Repair in the Adult Zebrafish Central Nervous System [J].
Beckers, An ;
Van Dyck, Annelies ;
Bollaerts, Ilse ;
Van houcke, Jessie ;
Lefevere, Evy ;
Andries, Lien ;
Agostinone, Jessica ;
Van Hove, Inge ;
Di Polo, Adriana ;
Lemmens, Kim ;
Moons, Lieve .
MOLECULAR NEUROBIOLOGY, 2019, 56 (05) :3175-3192
[3]   Mitochondrial transport and docking in axons [J].
Cai, Qian ;
Sheng, Zu-Hang .
EXPERIMENTAL NEUROLOGY, 2009, 218 (02) :257-267
[4]   The Mammalian-Specific Protein Armcx1 Regulates Mitochondrial Transport during Axon Regeneration (vol 92, pg 1294, 2016) [J].
Cartoni, Romain ;
Norsworthy, Michael W. ;
Bei, Fengfeng ;
Wang, Chen ;
Li, Siwei ;
Zhang, Yiling ;
Gabel, Christopher V. ;
Schwarz, Thomas L. ;
He, Zhigang .
NEURON, 2017, 94 (03) :689-689
[5]   Novel DLK-independent neuronal regeneration in Caenorhabditis elegans shares links with activity-dependent ectopic outgrowth [J].
Chung, Samuel H. ;
Awal, Mehraj R. ;
Shay, James ;
McLoed, Melissa M. ;
Mazur, Eric ;
Gabel, Christopher V. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (20) :E2852-E2860
[6]   Effects of intravitreal injection of a Rho-GTPase inhibitor (BA-210), or CNTF combined with an analogue of cAMP, on the dendritic morphology of regenerating retinal ganglion cells [J].
Drummond, Eleanor S. ;
Rodger, Jennifer ;
Penrose, Marissa ;
Robertson, Donald ;
Hu, Ying ;
Harvey, Alan R. .
RESTORATIVE NEUROLOGY AND NEUROSCIENCE, 2014, 32 (03) :391-402
[7]   Mitochondria Localize to Injured Axons to Support Regeneration [J].
Han, Sung Min ;
Baig, Huma S. ;
Hammarlund, Marc .
NEURON, 2016, 92 (06) :1308-1323
[8]   The fusogen AFF-1 can rejuvenate the regenerative potential of adult dendritic trees by self-fusion [J].
Kravtsov, Veronika ;
Oren-Suissa, Meital ;
Podbilewicz, Benjamin .
DEVELOPMENT, 2017, 144 (13) :2364-2374
[9]   CNS Axons Globally Increase Axonal Transport after Peripheral Conditioning [J].
Mar, Fernando M. ;
Simoes, Anabel R. ;
Leite, Sergio ;
Morgado, Marlene M. ;
Santos, Telma E. ;
Rodrigo, Ines S. ;
Teixeira, Carla A. ;
Misgeld, Thomas ;
Sousa, Monica M. .
JOURNAL OF NEUROSCIENCE, 2014, 34 (17) :5965-5970
[10]   Restoration of Dendritic Complexity, Functional Connectivity, and Diversity of Regenerated Retinal Bipolar Neurons in Adult Zebrafish [J].
McGinn, Timothy E. ;
Mitchell, Diana M. ;
Meighan, Peter C. ;
Partington, Natalie ;
Leoni, Dylan C. ;
Jenkins, Christina E. ;
Varnum, Michael D. ;
Stenkamp, Deborah L. .
JOURNAL OF NEUROSCIENCE, 2018, 38 (01) :120-136