Reparative mechanisms in the cerebellar cortex

被引:71
作者
Carulli, D
Buffo, A
Strata, P
机构
[1] Univ Turin, Dept Neurosci, Rita Levi Montalcini Ctr Brain Repair, I-10125 Turin, Italy
[2] IRCCS, Fdn Santa Lucia, Rome, Italy
关键词
D O I
10.1016/j.pneurobio.2004.03.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the adult brain, different neuronal populations display different degrees of plasticity. Here, we describe the highly different plastic properties of inferior olivary neurones and Purkinje cells. Olivary neurones show a basal expression of growth-associated proteins, such as GAP-43 and Krox24/EGR-1, and remarkable remodelling capabilities of their terminal arbour. They also regenerate their transected neurites into growth-permissive territories and may reinnervate the lost target. Sprouting and regrowing olivary axons are able to follow specific positional information cues to establish new connections according to the original projection map. In addition, they set a strong cell body reaction to injury, which in specific olivary subsets is regulated by inhibitory target-derived cues. In contrast, Purkinje cells do not have a constitutive level of growth-associated genes, and show little cell body reaction, no axonal regeneration after axotomy, and weak sprouting capabilities. Block of myelin-derived signals allows terminal arbour remodelling, but not regeneration, while selective over-expression of GAP-43 induces axonal sprouting along the axonal surface and at the level of the lesion. We suggest that the high constitutive intrinsic plasticity of the inferior olive neurones allows their terminal arbour to sustain the activity-dependent ongoing competition with the parallel fibres in order to maintain the post-synaptic territory, and possibly underlies mechanisms of learning and memory. Such a plasticity is used also as a reparative mechanism following axotomy. In contrast, in Purkinje cells, poor intrinsic regenerative capabilities and myelin-derived signals stabilise the mature connectivity and prevent axonal regeneration after lesion. (C) 2004 Elsevier Ltd. All rights reserved.
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页码:373 / 398
页数:26
相关论文
共 279 条
[121]  
Inamura N, 2000, J NEUROSCI RES, V60, P450, DOI 10.1002/(SICI)1097-4547(20000515)60:4<450::AID-JNR3>3.3.CO
[122]  
2-G
[123]  
Ito M., 1984, CEREBELLUM NEURAL CO
[124]  
JACOBON M, 1991, DEV NEUROBIOLOGY
[125]   EXPRESSION OF C-JUN AS A RESPONSE TO DORSAL-ROOT AND PERIPHERAL-NERVE SECTION IN DAMAGED AND ADJACENT INTACT PRIMARY SENSORY NEURONS IN THE RAT [J].
JENKINS, R ;
MCMAHON, SB ;
BOND, AB ;
HUNT, SP .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1993, 5 (06) :751-759
[126]  
Jörntell H, 2003, J NEUROSCI, V23, P9620
[127]   Sensory loss and cortical reorganization in mature primates [J].
Kaas, JH .
PLASTICITY IN THE ADULT BRAIN: FROM GENES TO NEUROTHERAPY, 2002, 138 :167-176
[128]   INVERSE PATTERNS OF MYELINATION AND GAP-43 EXPRESSION IN THE ADULT CNS - NEURITE GROWTH-INHIBITORS AS REGULATORS OF NEURONAL PLASTICITY [J].
KAPFHAMMER, JP ;
SCHWAB, ME .
JOURNAL OF COMPARATIVE NEUROLOGY, 1994, 340 (02) :194-206
[129]   INCREASED EXPRESSION OF THE GROWTH-ASSOCIATED PROTEIN GAP-43 IN THE MYELIN-FREE RAT SPINAL-CORD [J].
KAPFHAMMER, JP ;
SCHWAB, ME .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1994, 6 (03) :403-411
[130]   Retrograde repression of growth-associated protein-43 mRNA expression in rat cortical neurons [J].
Karimi-Abdolrezaee, S ;
Schreyer, DJ .
JOURNAL OF NEUROSCIENCE, 2002, 22 (05) :1816-1822