Cholesterol Depletion Regulates Axonal Growth and Enhances Central and Peripheral Nerve Regeneration
Axonal growth during normal development and axonal regeneration rely on the action of many receptor signaling systems and complexes, most of them located in specialized raft membrane microdomains with a precise lipid composition. Cholesterol is a component of membrane rafts and the integrity of thes...
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Published in | Frontiers in cellular neuroscience Vol. 13; p. 40 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Research Foundation
12.02.2019
Frontiers Media Frontiers Media S.A |
Subjects | |
Online Access | Get full text |
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Summary: | Axonal growth during normal development and axonal regeneration rely on the action of many receptor signaling systems and complexes, most of them located in specialized raft membrane microdomains with a precise lipid composition. Cholesterol is a component of membrane rafts and the integrity of these structures depends on the concentrations present of this compound. Here we explored the effect of cholesterol depletion in both developing neurons and regenerating axons. First, we show that cholesterol depletion
in developing neurons from the central and peripheral nervous systems increases the size of growth cones, the density of filopodium-like structures and the number of neurite branching points. Next, we demonstrate that cholesterol depletion enhances axonal regeneration after axotomy
both in a microfluidic system using dissociated hippocampal neurons and in a slice-coculture organotypic model of axotomy and regeneration. Finally, using axotomy experiments in the sciatic nerve, we also show that cholesterol depletion favors axonal regeneration
. Importantly, the enhanced regeneration observed in peripheral axons also correlated with earlier electrophysiological responses, thereby indicating functional recovery following the regeneration. Taken together, our results suggest that cholesterol depletion
is able to promote axonal growth in developing axons and to increase axonal regeneration
and
both in the central and peripheral nervous systems. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Stefania Raimondo, University of Turin, Italy These authors have contributed equally to this work Present address: Ramón Martínez-Mármol, Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia Reviewed by: Mehmet Emin Onger, Ondokuz Mayıs University, Turkey; Petr Dubový, Masaryk University, Czechia |
ISSN: | 1662-5102 1662-5102 |
DOI: | 10.3389/fncel.2019.00040 |