26 research outputs found
Unveiling the cellular and molecular players involved in methamphetamine - induced neuroinflammation: focus on astrocyte - microglial crosstalk
Neuron-Microglia Contact-Dependent Mechanisms Attenuate Methamphetamine-Induced Microglia Reactivity and Enhance Neuronal Plasticity
Exposure to methamphetamine (Meth) has been classically associated with damage to neuronal terminals. However, it is now becoming clear that addiction may also result from the interplay between glial cells and neurons. Recently, we demonstrated that binge Meth administration promotes microgliosis and microglia pro-inflammation via astrocytic glutamate release in a TNF/IP(3)R2-Ca2+-dependent manner. Here, we investigated the contribution of neuronal cells to this process. As the crosstalk between microglia and neurons may occur by contact-dependent and/or contact-independent mechanisms, we developed co-cultures of primary neurons and microglia in microfluidic devices to investigate how their interaction affects Meth-induced microglia activation. Our results show that neurons exposed to Meth do not activate microglia in a cell-autonomous way but require astrocyte mediation. Importantly, we found that neurons can partially prevent Meth-induced microglia activation via astrocytes, which seems to be achieved by increasing arginase 1 expression and strengthening the CD200/CD200r pathway. We also observed an increase in synaptic individual area, as determined by co-localization of pre- and post-synaptic markers. The present study provides evidence that contact-dependent mechanisms between neurons and microglia can attenuate pro-inflammatory events such as Meth-induced microglia activation
Microglia dysfunction caused by the loss of Rhoa disrupts neuronal physiology and leads to neurodegeneration
© 2020 The Author(s). Creative Commons Attribution (CC BY 4.0)Nervous tissue homeostasis requires the regulation of microglia activity. Using conditional gene targeting in mice, we demonstrate that genetic ablation of the small GTPase Rhoa in adult microglia is sufficient to trigger spontaneous microglia activation, producing a neurological phenotype (including synapse and neuron loss, impairment of long-term potentiation [LTP], formation of β-amyloid plaques, and memory deficits). Mechanistically, loss of Rhoa in microglia triggers Src activation and Src-mediated tumor necrosis factor (TNF) production, leading to excitotoxic glutamate secretion. Inhibiting Src in microglia Rhoa-deficient mice attenuates microglia dysregulation and the ensuing neurological phenotype. We also find that the Rhoa/Src signaling pathway is disrupted in microglia of the APP/PS1 mouse model of Alzheimer disease and that low doses of Aβ oligomers trigger microglia neurotoxic polarization through the disruption of Rhoa-to-Src signaling. Overall, our results indicate that disturbing Rho GTPase signaling in microglia can directly cause neurodegeneration.The authors acknowledge the support of the following i3S Scientific Platforms: Animal Facility, Translational Cytometry Unit (TraCy), BioSciences Screening (BS) and Advanced Light Microscopy (ALM), and members of the national infrastructure PPBI-Portuguese Platform of BioImaging (supported by POCI-01–0145-FEDER-022122). FCT Portugal ( PTDC/MED-NEU/31318/2017-031318 ) supported work in the J.B.R. lab. FCT Portugal , PEst ( UID/NEU/04539/2013 ), COMPETE-FEDER ( POCI-01-0145-FEDER-007440 ), Centro 2020 Regional Operational Programme ( CENTRO-01-0145-FEDER-000008 : BrainHealth 2020), and Strategic Project UIDB/04539/2020 and UIDP/04539/2020 (CIBB) supported work in the A.F.A. lab.
C.C.P. and R.S. hold employment contracts financed by national funds through FCT (Fundação para a Ciência e a Tecnologia, I.P.) in the context of the program contract described in paragraphs 4, 5, and 6 of article 23 of law no. 57/2016, of August 29th, as amended by law no. 57/2017 of July 19th.info:eu-repo/semantics/publishedVersio
Caracterização molecular dos doentes portugueses com miocardiopatia dilatada
Introduction: Dilated cardiomyopathy (DCM) is a disease of the heart muscle characterized
by ventricular dilatation and impaired systolic function. Familial forms account for 30-50%
of cases. Autosomal dominant inheritance is the predominant pattern of transmission. Causal
genetic variants have been identified in several genes and molecular diagnosis has implications
for genetic counseling and risk stratification.
Objective: We aimed to estimate the frequency of genetic variants and the molecular basis of
DCM in Portugal.
Methods: We performed a multicenter study of unrelated patients, recruited between 2013 and
2014. Variants in 15 genes were screened using PCR with direct sequencing (next-generation
sequencing with at least 30-fold coverage combined with Sanger sequencing).
Results: A total of 107 patients were included, 64 (60%) men, mean age at diagnosis
38±13 years, with 48 (45%) familial cases. In total, 31 rare variants in eight genes (mainly
in MYBPC3, TNNT2 and LMNA) were identified, in 28 patients (26%). Only four variants had been
previously described in association with DCM, 11 with hypertrophic cardiomyopathy, and nine
variants were novel. Four variants were likely pathogenic and the remainder were of uncertain
significance. We found no major differences in the main clinical and imaging characteristics
between patients with or without rare variants and patients with likely pathogenic variants.
Conclusions: Our results reflect the complexity and diversity of DCM genetics. For better inter-pretation of the pathogenicity of the variants found and their causative roles in DCM, molecularcascade screening of families is imperative. Further insight into genotype-phenotype correla-tions and risk stratification is desirable.Introdução: A miocardiopatia dilatada (MCD) é uma doença do músculo cardíaco caracterizada por dilatação ventricular e compromisso da função sistólica. As formas familiares são responsáveis por 30 a 50% dos casos. O padrão de hereditariedade predominante é o autossómicodominante. Variantes genéticas causais foram identificadas em vários genes e o diagnósticomolecular tem implicac¸ões para o aconselhamento genético e estratificação de risco.Objetivo: Avaliar a base molecular da MCD em Portugal.Métodos: Estudo multicêntrico de doentes não relacionados, recrutados entre 2013 e 2014.Foram analisados 15 genes, através da técnica de PCR com sequenciac¸ão direta (NGS com pelomenos uma cobertura de 30 vezes combinada com sequenciac¸ão de Sanger).Resultados: Foram incluídos 107 pacientes, 64 (60%) homens, idade média ao diagnóstico de38 ± 13 anos, com 48 (45%) casos familiares. Foram identificadas 31 variantes raras, em oitogenes, (principalmente MYBPC3, TNNT2 e LMNA) em 28 pacientes (26%). Apenas quatro variantestinham sido previamente descritas em associac¸ão com MCD, 11 com miocardiopatia hipertró-fica e nove variantes eram novas. Quatro variantes foram classificadas como provavelmentepatogénicas e as restantes de significado incerto. Não encontrámos diferenc¸as significativas nasprincipais características clínicas e imagiológicas entre doentes com ou sem variantes raras e doentes com variantes provavelmente patogénicas.
Conclusões: Estes resultados refletem a complexidade e diversidade genética da MCD. Para uma melhor interpretação da patogenicidade das variantes e potencial causalidade, o rastreio molecular das famílias é imperativo. Uma visão mais aprofundada das correlações genótipo-fenótipo e da estratificação de risco é desejável
La democracia desde los márgenes : transformaciones en el campo político boliviano
Uno de los rasgos característicos de la política es que se trata de una cuestión de sujetos y, en consecuencia, de la existencia de una pluralidad de sujetos.
Este libro preparado por el equipo dirigido por Marité Zegada es el mapeo y reconstrucción analítica más amplios que se han hecho sobre esta diversidad de espacios, de sujetos y de instituciones políticas que existen en el país, sobre todo para los últimos años. Ésta es la virtud más general de este trabajo: pensar la política dando cuenta de la pluralidad. Por un lado, hace un mapeo de espacios,fuerzas e instituciones pero no lo hace de una manera meramente descriptiva, sino que lo hace a través de una reconstrucción analítica que va revisando el tipo de discursos, de estrategias, es decir, de prácticas e ideas políticas que despliega cada uno de estos sujetos.Índice
Prólogo 5
Introducción 9 1
Capítulo i 15
Elementos para (re)pensar el campo político boliviano:
poder, política y democracia
Algunas consideraciones históricas sobre la democracia 19
Lecturas de la democracia y la crisis de sus paradigmas 20
Nuevas articulaciones conceptuales de la democracia 22
Discursos y contenido de la democracia 25
Capítulo ii 29
Campos de conflicto:
la crisis del Estado y su reconfiguración
Elementos estructurales de la crisis estatal 29
La emergencia de nuevos elementos constitutivos
del campo político 39
Campos de conflicto y dinámica sociopolítica en el
gobierno de Evo Morales 44
Capítulo iii 99
¿Qué cambió en el campo político boliviano?
Un nuevo andamiaje constitucional
Propuestas de las organizaciones sociales, indígenas y
partidos políticos 99
Forma o carácter del Estado 100
Tipo de gobierno, modelo de democracia
y régimen político 104
Poderes u órganos del Estado 106
Sistema de representación política 113
Análisis comparativo de la Constitución de 1967 y
la de 2009 116
Capítulo iv 141
La democracia boliviana y sus (re)significaciones
Estado Plurinacional y democracia 143
La autonomía: una estrategia de democratización del poder 151
Democracia participativa y democracia representativa
en la nueva Constitución 155
La democracia comunitaria como forma de
ejercicio del poder 164
Capítulo v 199
Movimientos sociales y nuevas formas de
articulación de la política
Movimientos sociales en el campo político 200
Viejos y nuevos sujetos políticos 206
Nuevas estrategias y repertorios de acción política 233
Capítulo vi 243
El gobierno de los movimiento sociales:
una nueva práctica política-estatal
Conformación de gobierno 243
Procesos de toma de decisiones 249
Mandar obedeciendo o los dos cerebros 254
Política y pragmatismo entre el sueño y la oportunidad 256
El mito del gobierno de los movimientos sociales 270
Discursos ideológicos y procesos de auto identificación 285
Evo es como yo: indigenismo, nacionalismo y socialismo
Riesgos y potencialidades en el derrotero del gobierno 297
Conclusiones 303
Bibliografía 323
Anexos 33
Perception of Nursing Activities That Contribute to the Quality of Care: Validity and Reliability Testing of the French Version
Background and purpose: Measuring nurses' perceptions of the activities contributing to the quality of care needs to be emphasized, providing visibility to professional practice and their contributions to achieving health quality. This study aimed to translate, validate, and culturally adapt the "Perception of Nursing Activities that Contribute to the Quality of Care" (EPAECQC), scale to provide a reliable instrument to assist nurse managers in measuring nurses' perceptions of their activities in French reality. Methods: A quantitative, descriptive, and cross-sectional study, in two phases, was conducted. First, by translation and cultural adaptation, and second, through the validation of the scale. Results: The factor structure of the final version was reduced to 22 items. Content and construct validity and reliability were supported by internal consistency (Cronbachs' alpha = .913). Conclusions: The results show that the final version is a reliable and valid instrument, showing a high potential to be used in research and clinical practice.info:eu-repo/semantics/publishedVersio
RhoA balances microglial reactivity and survival during neuroinflammation
Abstract Microglia are the largest myeloid cell population in the brain. During injury, disease, or inflammation, microglia adopt different functional states primarily involved in restoring brain homeostasis. However, sustained or exacerbated microglia inflammatory reactivity can lead to brain damage. Dynamic cytoskeleton reorganization correlates with alterations of microglial reactivity driven by external cues, and proteins controlling cytoskeletal reorganization, such as the Rho GTPase RhoA, are well positioned to refine or adjust the functional state of the microglia during injury, disease, or inflammation. Here, we use multi-biosensor-based live-cell imaging approaches and tissue-specific conditional gene ablation in mice to understand the role of RhoA in microglial response to inflammation. We found that a decrease in RhoA activity is an absolute requirement for microglial metabolic reprogramming and reactivity to inflammation. However, without RhoA, inflammation disrupts Ca2+ and pH homeostasis, dampening mitochondrial function, worsening microglial necrosis, and triggering microglial apoptosis. Our results suggest that a minimum level of RhoA activity is obligatory to concatenate microglia inflammatory reactivity and survival during neuroinflammation
Papeles salmantinos de educación
Resumen basado en el de la publicaciónTítulo, resumen y palabras clave en español y en inglésEl Virus de la Inmunodeficiencia Humana (VIH) se convirtió en los años 80 en España en un problema de salud pública por sus elevados índices de morbi-mortalidad, consecuencia en esos primeros momentos del desconocimiento del virus y sus vías de transmisión, y por la tardía respuesta institucional para impulsar
programas destinados a disminuir las conductas que implican riesgo de infección en los sectores poblacionales más afectados. El aumento de consumidores de drogas por vía parenteral hizo de este sector poblacional el más afectado, y si bien los daños asociados al consumo de sustancias eran evidentes, fue el SIDA la causa mayoritaria de mortalidad. En este contexto, se impulsaron los Programas de Reducción del Daño, entre los cuáles destacaron los destinados a la Captación Activa e Intervención en Medio Abierto, con el objetivo de acceder a las “poblaciones ocultas” de drogodependientes, facilitar material higiénico para el consumo, así como retirar el ya utilizado, trabajando así mismo la disminución de los riesgos con mensajes de salud y facilidades para el acercamiento a la red asistencial.ES