Characterization of the glial scar tissue in a murine model of spinal cord compression, with focus on hyaluronan

Spinal cord injury (SCI) is a devastating neurological disorder that affects thousands of people each year. Although in recent decades significant progress has been made in relation to understanding the molecular and cellular events underlying the nervous damage, spinal cord injury is still a highly disabling condition for which there is no curative therapy. People affected by spinal cord injuries manifested dysfunction or loss, temporary or permanent, of motor, sensory and / or autonomic functions depending on the spinal lesion damaged. Currently, the incidence rate of this type of injury is approximately 15-40 cases per million people worldwide. At the origin of these lesions are: road accidents, falls, interpersonal violence and the practice of sports. In this work we placed the hypothesis that HA is one of the component of the scar tissue formed after a compressive SCI, that it is likely synthetised by the perilesional glial cells and that it might support the permeation of the glial scar during the late phase of SCI. Nowadays, much focus is drawn on the recovery of CNS function, made impossible after SCI due to the high content of sulfated proteoglycans in the extracellular matrix. Counterbalancing the ratio between these proteoglycans and hyaluronic acid could be one of the experimental therapy to re-permeate the glial scar tissue formed after SCI, making possible axonal regrowth and functional recovery. Therefore, we established a model of spinal cord compression in mice and studied the glial scar tissue, particularly through the characterization of the expression of enzymes related to the metabolism of HA and the subsequent concentration thereof at different distances of the lesion epicenter. Our results show that the lesion induced in mice shows results similar to those produced in human lesions, in terms of histologic similarities and behavioral results. but these animals demonstrate an impressive spontaneous reorganization mechanism of the spinal cord tissue that occurs after injury and allows for partial recovery of the functions of the CNS. As regards the study of the glial scar, changes were recorded at the level of mRNA expression of enzymes metabolizing HA i.e., after injury there was a decreased expression of HA synthases 1-2 (HAS 1-2) and an increase of the expression HAS3 synthase mRNA, as well as the enzymes responsible for the HA catabolism, HYAL 1-2. But the amount of HA measured through the ELISA test was found unchanged after injury, it is not possible to explain this fact only with the change of expression of enzymes. At two weeks and in response to SCI, we found synthesized HA by reactive astrocytes and probably by others like microglial cells as it was advanced by the HA/GFAP+ and HA/IBA1+ cells co-location.

Proposta de uma matriz de indicadores de sustentabilidade para Estarreja

Esta dissertação centra-se na elaboração de uma proposta de matriz de indicadores de sustentabilidade a aplicar ao município de Estarreja. Apesar dos mais recentes desafios e requisitos em matéria de monitorização de planos, projectos e actividades com implicações sobre o ambiente e a sustentabilidade, o acompanhamento da evolução económica, social e ambiental, de uma forma integrada, pelo município tem sido escasso. A literatura da especialidade bem como diversas experiencias municipais nacionais e internacionais têm revelado que a adopção de sistemas de indicadores de sustentabilidade tem um grande potencial não apenas para avaliar o progresso dos municípios em direcção à sustentabilidade ambiental, mas também para induzir melhores formas de governação local. O principal objectivo desta dissertação é a construção de uma matriz de indicadores que avalie a sustentabilidade do município de Estarreja ao nível ambiental. A metodologia adoptada neste trabalho consiste em cinco fases, sendo a primeira fase, a revisão da literatura, através da análise de artigos científicos da especialidade. Na segunda fase é feito o enquadramento legislativo das responsabilidades de monitorização ambiental que cabem aos municípios portugueses. Numa terceira fase, desenvolve-se o levantamento e análise de indicadores sectoriais existentes, já recolhidos e tratados por instituições do Concelho de Estarreja. Na quarta fase procede-se à construção da matriz de indicadores de sustentabilidade, agregando os indicadores já recolhidos pelas iniciativas municipais a um novo conjunto de indicadores de sustentabilidade capazes de analisar a evolução do município no que respeita às pressões sobre o ambiente e sobre os níveis de qualidade ambiental. Na quinta fase são apresentadas as principais conclusões do trabalho e feitas recomendações para tornar exequível e eficiente a monitorização da matriz. O trabalho está organizado em cinco capítulos sendo estes coincidentes com as cinco fases da metodologia. A região de Estarreja tem implantado no seu concelho um dos maiores complexos industriais do país e, em consequência disso, tem vindo a sofrer ao longo dos anos o impacto das actividades industrial e urbana. O procedimento para a construção do sistema de indicadores, bem como a identificação dos eixos temáticos necessários para descrever o contexto que influencia a sustentabilidade do desenvolvimento local, teve por base outros sistemas de indicadores de sustentabilidade local e fornece uma ampla avaliação das características ambientais do município. As dimensões ambientais incluem água, gestão de resíduos, solos, ruído, protecção da natureza, biodiversidade, qualidade do ar, energia e espaços verdes e estão distribuídas por 60 indicadores. Entre estes, 32 já estão a ser monitorizados e 28 foram acrescentados no âmbito deste trabalho. A monitorização dos indicadores propostos não exige grande investimento em capital humano e financeiro, no entanto, constitui um desafio, uma vez que pressupõe a interacção, partilha de informação e transparência por parte das diferentes entidades e empresas municipais.

APP RERMS enriched matrix as an adhesion substrate for neuritic outgrowth

Specific domains can determine protein structural functional relationships. For the Alzheimer’s Amyloid Precursor Protein (APP) several domains have been described, both in its intracellular and extracellular fragments. Many functions have been attributed to APP including an important role in cell adhesion and cell to cell recognition. This places APP at key biological responses, including synaptic transmission. To fulfil these functions, extracellular domains take on added significance. The APP extracellular domain RERMS is in fact a likely candidate to be involved in the aforementioned physiological processes. A multidisciplinary approach was employed to address the role of RERMS. The peptide RERMS was crosslinked to PEG (Polyethylene glycol) and the reaction validated by FTIR (Fourier transform infrared spectrometry). FTIR proved to be the most efficient at validating this reaction because it requires only a drop of sample, and it gives information about the reactions occurred in a mixture. The data obtained consist in an infrared spectra of the sample, where peaks positions give information about the structure of the molecules, and the intensity of peaks is related to the concentration of the molecules. Subsequently substrates of PEG impregnated with RERMS were prepared and SH-SY5Y (human neuroblastoma cell line) cells were plated and differentiated on the latter. Several morphological alterations were clearly evident. The RERMS peptide provoked cells to take on a flatter appearance and the cytoskeletal architecture changed, with the appearance of stress fibres, a clear indicator of actin reorganization. Given that focal adhesions play a key role in determining cellular structure the latter were directly investigated. Focal adhesion kinase (FAK) is one of the most highly expressed proteins in the CNS (central nervous system) during development. It has been described to be crucial for radial migration of neurons. FAK can be localized in growth cones and mediated the response to attractive and repulsive cues during migration. One of the mechanisms by which FAK becomes active is by auto phosphorylation at tyrosine 397. It became clearly evident that in the presence of the RERMS peptide pFAK staining at focal adhesions intensified and more focal adhesions became apparent. Furthermore speckled structures in the nucleus, putatively corresponding to increased expression activity, also increased with RERMS. Taken together these results indicate that the RERMS domain in APP plays a critical role in determining cellular physiological responses. Here is suggested a model by which RERMS domain is recognized by integrins and mediate intracellular responses involving FAK, talin, actin filaments and vinculin. This mechanism probably is responsible for mediating cell adhesion and neurite outgrowth on neurons.