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Evidence for an Age-Dependent Decline in Axon Regeneration in the Adult Mammalian Central Nervous System.
- Source :
-
Cell reports [Cell Rep] 2016 Apr 12; Vol. 15 (2), pp. 238-46. Date of Electronic Publication: 2016 Mar 31. - Publication Year :
- 2016
-
Abstract
- How aging impacts axon regeneration after CNS injury is not known. We assessed the impact of age on axon regeneration induced by Pten deletion in corticospinal and rubrospinal neurons, two neuronal populations with distinct innate regenerative abilities. As in young mice, Pten deletion in older mice remains effective in preventing axotomy-induced decline in neuron-intrinsic growth state, as assessed by mTOR activity, neuronal soma size, and axonal growth proximal to a spinal cord injury. However, axonal regeneration distal to injury is greatly diminished, accompanied by increased expression of astroglial and inflammatory markers at the injury site. Thus, the mammalian CNS undergoes an age-dependent decline in axon regeneration, as revealed when neuron-intrinsic growth state is elevated. These results have important implications for developing strategies to promote axonal repair after CNS injuries or diseases, which increasingly affect middle-aged to aging populations.<br /> (Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Astrocytes pathology
Axotomy
Biomarkers metabolism
Down-Regulation
Gene Deletion
Inflammation pathology
Mice
PTEN Phosphohydrolase deficiency
PTEN Phosphohydrolase metabolism
Pyramidal Tracts pathology
Pyramidal Tracts physiopathology
Signal Transduction
Spinal Cord Injuries pathology
Spinal Cord Injuries physiopathology
TOR Serine-Threonine Kinases metabolism
Aging pathology
Axons pathology
Central Nervous System pathology
Mammals growth & development
Nerve Regeneration
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 15
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 27050519
- Full Text :
- https://doi.org/10.1016/j.celrep.2016.03.028