NF-KAPPA BS IN VIVO ROLE IN DERMATITIS AND ANGIOGENESIS
NF-KAPPA BS IN VIVO ROLE IN DERMATITIS AND ANGIOGENESIS
批准号:
2468652
负责人:
JOHN F KLEMENT
金额:
$8.04万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-09-20 至 2000-08-31
关键词:
RNase protection assay angiogenesis cell adhesion molecules chemokine disease /disorder model endopeptidases extracellular matrix gel mobility shift assay gene induction /repression genetically modified animals immunity immunocytochemistry immunogenetics inflammation keratinocyte laboratory mouse leukocytes model design /development northern blottings nuclear factor kappa beta skin disorder tetracyclines vascular endothelial growth factors
中文摘要
描述(来自申请书):
英文摘要
DESCRIPTION (from the application):
The pleiotropic transcription factor NF-kappaB is a major component of the
immune response and inflammation. Several of the genes involved in
angiogenesis and leukocyte evascularization (vegf, vegf receptor, VCAM,
ICAM, ELAM) are thought to be regulated by NF-kappaB or contain NF-kappaB
binding sites in their promoters. However, the vast majority of these data
have been accumulated using in vitro systems. It is well known, that in
vitro systems may not accurately portray in vivo events. In order to
investigate NF-kappaB's role in vivo, this grant proposes the following:
1) Study of the development of dermatitis in the IkappaBalpha deficient
mice. In this animal model, the IkappaBalpha gene has been deleted via
homologous recombination. These animals develop a severe wide-spread
dermatitis in the first week of life. The development of this dermatitis is
temporally predictable occurring between 3 to 6 days after birth, which will
allow for a staged study of the development of dermatitis. Specifically,
the expression of vascular endothelial growth factors and their targets will
be investigated in terms of the temporal and spatial pattern of expression.
Other genes potentially involved in dermatitis such as matrix proteases will
be investigated.
2) Develop the tetracycline inducible/repressible systems to create animal
models of dermal inflammation exploiting the genes involved in the NF-kappaB
system. It is anticipated that these models will also allow the
investigator to directly control the onset of dermatitis and other
inflammatory diseases allowing the study of spatial and temporal gene
expression as discussed above. Further, these animals may serve as resource
for drug development and screening as they will represent a more defined
experimental system. Once the tetracycline inducible/repressible systems
have been developed for cutaneous study, they can be further exploited to
develop animal models for other diseases.
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会议论文
Novel Technologies For Skin-Specific Gene Expression
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批准号:6662537
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项目类别:
-
资助金额:$7.85万
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财政年份:2002
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负责人:JOHN F KLEMENT
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依托单位:
Novel Technologies For Skin-Specific Gene Expression
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批准号:6561658
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项目类别:
-
资助金额:$7.85万
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财政年份:2002
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负责人:JOHN F KLEMENT
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依托单位:
CORE--ANIMAL MODELS OF EPIDERMOLYSIS BULLOSA
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批准号:6299823
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项目类别:
-
资助金额:$14.48万
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财政年份:1999
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负责人:JOHN F KLEMENT
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依托单位:
CORE--ANIMAL MODELS OF EPIDERMOLYSIS BULLOSA
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批准号:6100444
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项目类别:
-
资助金额:$14.48万
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财政年份:1998
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负责人:JOHN F KLEMENT
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依托单位:
NF-KAPPA BS IN VIVO ROLE IN DERMATITIS AND ANGIOGENESIS
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批准号:6055664
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项目类别:
-
资助金额:$8.04万
-
财政年份:1997
-
负责人:JOHN F KLEMENT
-
依托单位:
CORE--ANIMAL MODELS OF EPIDERMOLYSIS BULLOSA
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批准号:6268359
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项目类别:
-
资助金额:$14.09万
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财政年份:1997
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负责人:JOHN F KLEMENT
-
依托单位:
NF-KAPPA BS IN VIVO ROLE IN DERMATITIS AND ANGIOGENESIS
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批准号:2769683
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项目类别:
-
资助金额:$8.04万
-
财政年份:1997
-
负责人:JOHN F KLEMENT
-
依托单位:
CORE--ANIMAL MODELS OF EPIDERMOLYSIS BULLOSA
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批准号:6235723
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项目类别:
-
资助金额:$6.78万
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财政年份:1996
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负责人:JOHN F KLEMENT
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依托单位:
国内基金
海外基金
ROBO4对视网膜血管生成(angiogenesis)的调控及其分子机制
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批准号:81200692
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项目类别:青年科学基金项目
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资助金额:23.0万元
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批准年份:2012
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负责人:陈凌
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依托单位: