Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/53714
Type: Artigo de periódico
Title: A role for MHC class I molecules in synaptic plasticity and regeneration of neurons after axotomy
Author: Oliveira, ALR
Thams, S
Lidman, O
Piehl, F
Hokfelt, T
Karre, K
Linda, H
Cullheim, S
Abstract: Recently, MHC class I molecules have been shown to be important for the retraction of synaptic connections that normally occurs during development [Huh, G.S., Boulanger, L. M., Du, H., Riquelme, P. A., Brotz, T. M. & Shatz, C. J. (2000) Science 290, 2155-2158]. In the adult CNS, a classical response of neurons to axon lesion is the detachment of synapses from the cell body and dendrites. We have investigated whether MHC I molecules are involved also in this type of synaptic detachment by studying the synaptic input to sciatic motoneurons at 1 week after peripheral nerve transection in beta2-microglobulin or transporter associated with antigen processing 1-null mutant mice, in which cell surface MHC I expression is impaired. Surprisingly, lesioned motoneurons in mutant mice showed more extensive synaptic detachments than those in wildtype animals. This surplus removal of synapses was entirely directed toward inhibitory synapses assembled in clusters. In parallel, a significantly smaller population of motoneurons reinnervated the distal stump of the transected sciatic nerve in mutants. MHC I molecules, which traditionally have been linked with immunological mechanisms, are thus crucial for a selective maintenance of synapses during the synaptic removal process in neurons after lesion, and the lack of MHC I expression may impede the ability of neurons to regenerate axons.
Subject: beta(2)-microglobulin
motoneuron
spinal cord
synapse elimination
nerve lesion
Country: EUA
Editor: Natl Acad Sciences
Rights: fechado
Identifier DOI: 10.1073/pnas.0408154101
Date Issue: 2004
Appears in Collections:Unicamp - Artigos e Outros Documentos

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