INT180238
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
The requirement of NFAT for induction of twist1 expression in Th1 cells distinguishes control of twist1 expression in Th cells from its control in fibroblasts, where TNF-? | |||||||||||||||
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Th cellspecific twist1 expression in vivo | |||||||||||||||
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Imprinting of the twist1 gene for reexpression in Th1 cells is reflected by increased acetylation of histone H3 and trimethylated histone H3 at lysine 4, in both resting and reactivated Th1 cells, as compared with Th2 cells (Fig. | |||||||||||||||
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Their imprinting for increased twist1 expression, maintained over time in individual patients, indicates a history of repeated restimulation and an endogenous regulation of proinflammatory effector functions under the control of NFAT and NF-? | |||||||||||||||
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Remarkably, expression of twist1 is highly up-regulated in CD3+CD4+ T cells isolated from inflamed tissues of patients with chronic inflammation of joints or gut. | |||||||||||||||
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The key role of twist1 expression by Th1 cells for the self-limitation of Th1-induced inflammation is evident from the present analysis of murine models of inflammation. | |||||||||||||||
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For the initial expression of twist1 in Th1 cells, and its imprinting for reexpression in further restimulations, the concerted action of activated STAT4, NFAT1, and NF-? | |||||||||||||||
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Why is expression of twist1 up-regulated gradually? | |||||||||||||||
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Furthermore, the cell viabilities decreased in a dose-dependent manner of Pa-PDT with IC50 value of 0.6 ? | |||||||||||||||
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In a murine transfer model of OVA-specific DTH, the effect of twist1 expression on the inflammation induced by transferred Th1 cells was analyzed. | |||||||||||||||
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Control of twist1 expression in Th1 lymphocytes | |||||||||||||||
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The data illustrated in Fig. 2a show that there is no significant difference in survival of cells exposed to ETXp-PCI and PDT, suggesting that the observed cytotoxicity in both groups was due entirely to the PDT effect. | |||||||||||||||
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Finally, LTM is likely represented by LTP3 which should be influenced by cAMP-specific PDE inhibition | |||||||||||||||
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PDE Pyridoxine-dependent epilepsy | |||||||||||||||
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Chronic PDE inhibition, via the persistent activation of PDE5 promoters, may up-regulate PDE expression and, therefore, be associated with the development of drug tachyphylaxis (Moreland et al 1999). | |||||||||||||||
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General Comments
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