RESUMEN
The orphan nuclear receptor TLX (Nr2e1) is a key regulator of hippocampal neurogenesis. Impaired adult hippocampal neurogenesis has been reported in neurodegenerative and psychiatric conditions including dementia and stress-related depression. Neuroinflammation is also implicated in the neuropathology of these disorders, and has been shown to negatively affect hippocampal neurogenesis. To investigate a role for TLX in hippocampal neuroinflammation, we assessed microglial activation in the hippocampus of mice with a spontaneous deletion of TLX. Results from our study suggest that a lack of TLX is implicated in deregulation of microglial phenotype and that consequently, the survival and function of newborn cells in the hippocampus is impaired. TLX may be an important target in understanding inflammatory-associated impairments in neurogenesis.
Asunto(s)
Hipocampo/patología , Microglía/fisiología , Neurogénesis/fisiología , Receptores Citoplasmáticos y Nucleares/deficiencia , Animales , Supervivencia Celular , Giro Dentado/metabolismo , Giro Dentado/patología , Proteína Doblecortina , Hipocampo/metabolismo , Inflamación , Interleucina-1beta/biosíntesis , Interleucina-1beta/genética , Masculino , Ratones , Ratones Noqueados , Receptores Citoplasmáticos y Nucleares/fisiología , Nicho de Células MadreRESUMEN
Deficits in cognitive function are associated with neuroinflammatory changes, typified by activation of glial cells and an alteration of the pro- and anti-inflammatory cytokine balance in the brain. Although there is evidence to suggest that activation of microglia is regulated by interaction with other cell types in the brain, the mechanism(s) involved is poorly understood. Here, we provide evidence that interaction between CD200 and its receptor plays a role in modulating microglial activation under conditions of chronic and acute inflammation of the brain. We report that interleukin-4 (IL-4) plays a central role in modulating expression of CD200 and identify a mechanism by which IL-4 directly controls microglial cell activation. Our findings provide the first demonstration of a role for IL-4 in modulating CD200 expression and suggest a mechanism for regulation of microglial activation in the intact CNS under inflammatory conditions.
Asunto(s)
Antígenos CD/metabolismo , Interleucina-4/fisiología , Glicoproteínas de Membrana/metabolismo , Microglía/metabolismo , Microglía/patología , Enfermedad Aguda , Animales , Enfermedad Crónica , Inflamación/metabolismo , Ligandos , Masculino , Glicoproteínas de Membrana/fisiología , Ratones , Ratones Endogámicos C57BL , Ratas , Ratas WistarRESUMEN
Kefir is a fermented milk beverage consumed for nutritional and health tonic benefits in many parts of the world. It is produced by the fermentation of milk with a consortium of bacteria and yeast embedded within a polysaccharide matrix. This consortium is not well defined and can vary substantially between kefir grains. There are little data on the microbial stability of kefir grains, nor on interactions between microbes in the grain and in the milk. To study this, a grain was split, with one half of each stored at -20°C and the other half passaged repeatedly in whole unpasteurised milk. Grains passaged in the unpasteurised milk recovered vigour and acquired the yeast Kluyveromyces marxainus from the milk which was confirmed to be the same strain by molecular typing. Furthermore, these passaged grains produced kefir that was distinguished chemically and organoleptically from the stored grains. Some changes in ultrastructure were also observed by scanning electron microscopy. The study showed that kefir grains can acquire yeast from their environment and the final product can be influenced by these newly acquired yeasts. Kluyveromyces marxianus is considered to be responsible for some of the most important characteristics of kefir so the finding that this yeast is part of the less stable microbiota is significant.
Asunto(s)
Calidad de los Alimentos , Kéfir/microbiología , Kluyveromyces/metabolismo , Leche/microbiología , Saccharomyces cerevisiae/metabolismo , Animales , Productos Lácteos Cultivados/microbiología , Fermentación , Humanos , Kluyveromyces/genética , Consorcios Microbianos , Pasteurización , GustoRESUMEN
This paper presents a method for semi-automatic analysis of morphometry in image cytometry studies. We examine morphological changes in neuroblastoma cells caused by a toxin. Nuclei are automatically recognized from images using a constrained seeded region growing algorithm. The shape of the nuclei is quantified by fitting ellipses to the identified regions. Features such as centroids, elongation, orientation and size are extracted from this fitting process. Under certain assumptions, it is demonstrated that the log elongation measurement has an asymptotically normal distribution whose variance is dependent only on object size. This allows weighted linear models to be fitted to elongation measurements. Hypothesis tests show that over time, there is a significant elongation due to application of the toxin. The other variables are not significant, but there is a significant 'image' effect. The scientific implications of these findings are considered.