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MAST CELL SPECIFIC REGULATION OF IL4 GENE EXPRESSION

MAST CELL SPECIFIC REGULATION OF IL4 GENE EXPRESSION
IL4 基因表达的肥大细胞特异性调控
批准号:
2003936
负责人:
Melissa A Brown
金额:
$17.91万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1993
资助国家:
美国
项目状态:
已结题
起止时间:
1993-05-01 至 2001-08-31

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中文摘要
翻译
描述:(改编自申请人摘要)白细胞介素-4 (IL-4)
英文摘要
DESCRIPTION: (Adapted from the applicant's abstract) Interleukin-4 (IL-4) is an important immunoregulatory cytokine with diverse effects on immune system maturation and function. Two major cell types are known to produce IL-4, T cells and mast cells. The regulation of IL-4 gene expression in these cell types has been shown to be different and a regulatory element in the second intron of the gene is mast cell specific, contributing to the different mechanisms of regulation in the two cell types. This project is based on a report that mast cells express a truncated IL-4 mRNA, encompassing only exons 3 and 4. This truncated mRNA was only detected by RNAse protection assays as Northern blot analysis was not sufficiently sensitive to distinguish the truncated mRNA from the full length mRNA. Analysis of intronic DNA has revealed the presence of a "TATA-less" promoter elements, suggesting that transcription of this truncated mRNA may initiate in this intronic regulatory element. This project is focused on further characterizing this truncated transcript and assessing the possible biological consequences of its expression. The aims are: 1) to assess the expression profile of the truncated transcript; 2) to assess the function of the transcript and 3) to define the regulatory elements within the intron that regulate transcription of the truncated mRNA. As it is possible that this novel transcript may represent an important mechanism for regulating IL-4 gene expression and for understanding the mechanisms behind its expression and by which it may regulate IL-4 biological activity.
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Distinct mast cell responses in male and female SJL mice underlie sex dimorphic EAE susceptibility
Mechanisms Regulating Reduced c-Kit-Dependent EAE Susceptibility in Male SJL Mice
Mechanisms Regulating Reduced c-Kit-Dependent EAE Susceptibility in Male SJL Mice
Ikaros in mast vs. basophil lineage choice
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