APOLIPOPROTEIN E EFFECT ON THE CNS IMMUNE RESPONSE
APOLIPOPROTEIN E EFFECT ON THE CNS IMMUNE RESPONSE
批准号:
6187508
负责人:
DANIEL T LASKOWITZ
金额:
$10.9万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-07-01 至 2001-06-30
关键词:
amyloid proteins apolipoprotein E brain injury cellular immunity central nervous system cerebral ischemia /hypoxia cytokine disease /disorder model encephalomyelitis gene targeting genetically modified animals glia human genetic material tag inflammation interferon gamma laboratory mouse lipopolysaccharides macroglobulins neuroimmunomodulation nitric oxide phosphorylation protein structure function receptor binding second messengers tissue /cell culture
中文摘要
载脂蛋白E (apoE)是一种含有299个氨基酸的蛋白质
英文摘要
Apolipopoprotein E (apoE) is a 299 amino acid protein with multiple
biological properties, including a role in cholesterol trafficking,
immumomodulation, and a putative role in nerve injury and repair.
Recent evidence suggests that the one of the three common apoE isoforms,
E4 is associated with increased risk for developing Alzheimer's disease
(sporadic and late onset familial), and poor prognosis after a variety
of acute neurological insults, including closed head injury,
intracranial, hemorrhage, and cerebral ischemia. We will test the
hypothesis that apoE is a biologically relevant mediator of the CNS
response to acute and chronic injury. We will also test the hypothesis
that there are isoform-specific differences in these immunoregulatory
functions. Our preliminary evidence suggests that apoE suppresses the
endogenous inflammatory response mediated by glial cells, and may also
inhibit the cellular immune response when the blood-brain barrier is
compromised. We have also demonstrated that apoE modulates the CNS
reaction to focal ischemia in vivo, and our preliminary observations are
consistent with the possibility that these effects are isoform-specific.
We propose to characterize the role of apoE in modulating the CNS
inflammatory response by utilizing apoE deficient mice and mice
expressing the human E2, E3, and E4 transgenes to prepare cell culture
models and in vivo models of CNS injury and inflammation. This
supervised research experience will be integrated with advanced didactic
coursework in immunology and neurobiology. In the latter part of the
grant period, we will examine the molecular basis by which apoE affects
the immune response.
Specifically, we will focus on receptor interactions and modulation of
signal transduction pathways. During this period, the focus will be on
developing more sophisticated research skill to facilitate independence.
In summary, this proposal will examine the role of apoE in modulating
the CNS immune response and will provide the fundamental training in
immunology and neurobiology necessary for developing and independent
research career in neuroimmunology.
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依托单位:
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依托单位:
海外基金