PATHOGENESIS OF FEVER IN HUMANS
PATHOGENESIS OF FEVER IN HUMANS
批准号:
3480844
负责人:
Charles anthony Dinarello
金额:
$28.36万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1986
资助国家:
美国
项目状态:
已结题
起止时间:
1986-12-01 至 1992-11-30
关键词:
T lymphocyte acute phase protein binding proteins body temperature regulation cell type chemical structure function colchicine endotoxins gel electrophoresis gel filtration chromatography gene expression genetic transcription genetic translation hemodialysis human tissue hyperthermia immunofluorescence technique interleukin 1 ion exchange chromatography laboratory mouse laboratory rabbit lipoxygenase marine animal oil monoclonal antibody monocyte protein biosynthesis protein sequence pyrogens radioimmunoassay radiotracer synthetic peptide tissue /cell culture toxic shock syndrome tumor necrosis factor alpha
中文摘要
这项提议涉及到白介素1(IL-1)作为一种关键的
宿主对微生物入侵、炎症、免疫的反应
反应和损伤。IL-1是最早也是最突出的
在感染或损伤发生后合成的分子。
IL-1的S效应有很多与病理过程有关,
并且宿主具有合成、加工、
IL-1的转运和活性受到调控。这项建议
研究了这些不同的机制。实验是设计的
目的:探讨人血单核细胞产生IL-1的能力。至.为止
IL-1-β的总多聚腺苷RNA编码的5%
刺激后的单核细胞。机制控制着翻译
将这种RNA转化为IL-1蛋白,而其他机制似乎
控制将主要翻译产品处理为
具有生物活性的IL-1。转录、翻译和加工
IL-1在血液单核细胞中的表达与培养细胞中的不同
台词。因此,这些实验的重点是每一个
健康人体血液循环中产生IL-1的步骤,
在疾病中和在各种疾病修改的影响下
物质。将采用特殊方法防止
单核细胞表面黏附对IL-1转录的影响
两种新发展的IL-1-β和IL-1放射免疫分析方法
阿尔法将用于一项大型研究,以确定构成
“正常”的伊尔-1生产。免疫沉淀和
使用特异性、非交叉反应抗体的免疫荧光
将用于检测IL-1的大小和细胞定位。
IL-1的特定生物学活性与分子水平不同。
大小和结构-功能关系的研究
IL-1的提出是为了确定一个可能的活性部位(S)。
将对合成肽进行评估,并
与自然产生的单核细胞IL-1片段相关。
利用中毒性休克建立血流动力学休克动物模型
证候毒素可用来评价丹参的全身效应
IL-1及其片段和抑制其生物学活性的物质
活动。将使用两个临床模型来研究IL-1
补充鱼油对人体生殖功能的影响
饮食和血液透析。这些研究补充了基本的
IL-1产生的分子调控研究。
最后,这些研究检查了IL-1的产生和活性
在内源性放大和抑制模型中。
英文摘要
This proposal concerns interleukin-1 (IL-1) as a key mediator of
host responses to microbial invasion, inflammation, immunological
reaction and injury. IL-1 is one of the first and most prominent
molecular synthesized following the onset of infection or injury.
Many of IL-1's effects are involved with pathological processes,
and the host has mechanisms by which synthesis, processing,
transport and activities of IL-1 are regulated. This proposal
studies these various mechanisms. The experiments are designed
to explore IL-1 production from human blood monocytes. Up to
5% of the total polyadenylated RNA codes for IL-1-beta in
monocytes after stimulation. Mechanisms control the translation
of this RNA into IL-1 protein whereas other mechanisms seem to
control processing of the primary translation product into
biologically active IL-1. Transcription, translation and processing
of IL-1 are different in blood monocytes than in cultured cells
lines. Therefore, these experiments are focused on each of the
steps of IL-1 production in circulating human blood cells in health,
in disease and under the influence of various disease modifying
substances. special methods will be employed that prevent the
transcription of Il-1 in monocytes due to adherence to surfaces.
Two newly developed radioimmunoassays for IL-1-beta and Il-1-
alpha will be used in a large study to establish what constitutes
"normal" Il-1 production. Immunoprecipitation and
immunofluorescence using specific, non-cross reacting antibodies
will be used to detect the sizes and cellular localization of IL-1.
The specific biological activities of Il-1 differ with the molecular
size and hence studies on the structure-function relationship of
IL-1 are proposed in order to identify a putative active site(s).
The evaluation of synthetic peptides will be performed and
correlated with naturally occurring fragments of monocyte Il-1.
An animal model of hemodynamic shock using toxic shock
syndrome toxin is to be used to evaluate the systemic effects of
Il-1, its fragments and substances that inhibit its biological
activities. Two clinical models will be used to study Il-1
production in human subjects: the effect of supplemental fish oil
diet and hemodialysis. These studies complement the basic
investigations on the molecular control of IL-1 production.
Finally, these studies examine the production and activity of IL-1
in models of endogenous amplification and inhibition.
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海外基金