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Evidence for an Age-Dependent Decline in Axon Regeneration in the Adult Mammalian Central Nervous System
被引:114
作者:
Geoffroy, Cedric G.
[1
]
Hilton, Brett J.
[2
,3
]
Tetzlaff, Wolfram
[2
,3
,4
]
Zheng, Binhai
[1
]
机构:
[1] Univ Calif San Diego, Dept Med, Dept Neurosci, La Jolla, CA 92093 USA
[2] Univ British Columbia, Int Collaborat Repair Discoveries, Vancouver, BC V6T 1Z4, Canada
[3] Univ British Columbia, Dept Zool, 6270 Univ Blvd, Vancouver, BC V6T 1Z4, Canada
[4] Univ British Columbia, Dept Surg, Vancouver, BC V6T 1Z4, Canada
基金:
加拿大健康研究院;
美国国家卫生研究院;
关键词:
SPINAL-CORD-INJURY;
TUMOR-SUPPRESSOR GENE;
MOUSE;
PTEN;
NEURONS;
PROTEIN;
BRAIN;
CNS;
TRANSCRIPTOME;
ASTROCYTES;
D O I:
10.1016/j.celrep.2016.03.028
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
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.
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页码:238 / 246
页数:9
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