DSpace UNL

RUN >
Faculdade de Ciências e Tecnologia (FCT) >
FCT Departamentos >
FCT: Departamento de Ciências da Vida >
FCT: DCV - Dissertações de Mestrado >

Please use this identifier to cite or link to this item: http://hdl.handle.net/10362/6710

Título: Dissecting neuronal development deficits by inflammation: from morphology to cytoskeleton dynamics
Autor: Frias, Cátia Sofia Pereira
Orientador: Brites, Dora
Borralho, Adelaide
Palavras-chave: Neuroinflammation
Hippocampal neurons
Neuronal arborization
Growth cone
Synaptogenesis
Cytoskeleton
Issue Date: Dec-2011
Editora: FCT-UNL
Resumo: Neuroinflammation, a response of the nervous system to injury, results in the release of pro-inflammatory mediators, as interleukin-1β (IL-1β) and tumor necrosis factor-alpha (TNF-α). Exposure of nerve cells to a neuroinflammatory environment was shown to change the normal neurodevelopment, which can be linked to the appearance of neurological disabilities. In this work, we aimed to assess the effects of moderate levels of IL-1β and TNF-α in the establishment of neuronal arborization, growth cone morphology and synaptogenesis. An early exposure of embryonic hippocampal neurons to cytokines delay neuronal development, with an increase in the number of non-polarized cells, stage 2 of development. When analyzing stage 3 neurons, IL-1β showed to decrease total arborization, in particular at the axonal level, while TNF-α increased dendritic arborization. In fact, IL-1β reduces dendritic and axonal length and the number of axonal branches, whereas it increases the extent of dendritic and axonal branches, probably to compensate the other effects. In contrast, TNF-α increases the number of primary dendrites and dendritic branches, as well as their length. By next analyzing microtubule dynamics as the ratio of acetylated- (old) vs. tyrosinated-tubulin (newly-formed), we found that IL-1β and TNF-α induce microtubule stabilization, which may be related to a deficient axonal outgrowth. In addition, both cytokines reduced the area of growth cones, with an increase in the immunofluorescence of F-actin, indicating alterations at the cytoskeleton which may compromise axonal elongation and branching. Regarding neuronal connectivity, we demonstrated that both cytokines not only reduced the density of dendritic spines and synapses, but also the maturity of dendritic spines, suggesting a reduction in the synaptic strength. These findings establish a relation between neuroinflammation in fetal life and the emergence of neuronal damage, similar to those observed in neurodevelopmental disorders, as schizophrenia.
Descrição: Dissertação para obtenção do Grau de Mestre em Genética Molecular e Biomedicina
URI: http://hdl.handle.net/10362/6710
Appears in Collections:FCT: DCV - Dissertações de Mestrado

Files in This Item:

File Description SizeFormat
Frias_2011.pdf1,98 MBAdobe PDFView/Open
Statistics
FacebookTwitterDeliciousLinkedInDiggGoogle BookmarksMySpaceOrkut
Formato BibTex mendeley Endnote Logotipo do DeGóis 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

Universidade Nova de Lisboa  - Feedback
Promotores do RCAAP   Financiadores do RCAAP

Fundação para a Ciência e a Tecnologia Universidade do Minho   Governo Português Ministério da Educação e Ciência PO Sociedade do Conhecimento (POSC) Portal oficial da União Europeia