Their response to maturation stimuli is weak in the absence of IL

Their response to maturation stimuli is weak in the absence of IL-4 but these cells retain the ability to differentiate into fully functional mature dendritic cells upon IL-4 treatment. We suggest that these cells may provide a useful model to investigate tolerogenic function as a developmental feature of

DC and to understand molecular events involved in IL-4 priming for maturation. (C) 2007 Elsevier B.V. All rights reserved.”
“The amyloid-beta protein (A beta)-containing neuritic plaques and hyperphosphorylated tau-containing neurofibrillary tangles are two invariable characteristics of Alzheimer’s disease (AD). Three genes encoding amyloid-beta protein precursor (A beta PP), presenilin MLN8237 (PS) 1 and 2 are linked to early onset familial AD, and the apolipoprotein E (ApoE) epsilon 4 allele is a major risk factor for sporadic AD. The zebrafish A beta PP, PS, and ApoE genes have been identified, and the essential components of the gamma-secretase complex

that mediates cleavage of A beta PP to generate A beta have been examined in zebrafish. A RepSox transgenic zebrafish expressing mutant tau has been created, and the transgenic animals exhibit a neurodegeneraton phenotype The use of zebrafish as a model system for AD research has expanded our knowledge of A beta and tau.”
“Toxins are potent molecules used by various bacteria to interact with a host organism. Some of them specifically act on neuronal cells (clostridial neurotoxins) leading to characteristics neurological affections. But many other toxins are multifunctional and recognize a wider range of cell types including neuronal cells. Various enterotoxins interact with the enteric nervous system, for example by stimulating afferent neurons or inducing neurotransmitter release from enterochromaffin cells which result either in vomiting, in amplification of the diarrhea, or in intestinal inflammation process. Other toxins can pass the blood brain barrier

and directly act on specific neurons.”
“Serotonin type 3 (5-HT3) receptors are ligand-gated ion channels built by five subunits GSI-IX concentration of diverse composition. In humans, five subunits exist (5-HT3A-E) which are encoded by the genes HTR3A-E and are expressed in various isoforms. Recently, the importance of factors influencing receptor expression became clear, such as chaperones and microRNAs.Owing to their expression profile and physiological functions, 5-HT3 receptors have been implicated in irritable bowel syndrome (IBS) and psychiatric disorders. Interestingly, HTR3 variants have now been shown to be associated with these conditions. This underlines the potential of 5-HT3 receptors as therapeutic targets and may enable personalised therapies in the future.

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