Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
基本信息
- 批准号:7079414
- 负责人:
- 金额:$ 12.59万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2002
- 资助国家:美国
- 起止时间:2002-07-19 至 2008-06-30
- 项目状态:已结题
- 来源:
- 关键词:animal genetic material tagbiological signal transductioncaveolinscell growth regulationcell linecholesterolconfocal scanning microscopydevelopmental geneticsgene targetinggenetic regulationgenetically modified animalshuman genetic material tagimmunoprecipitationintermolecular interactionlaboratory mouseneoplasm /cancer geneticsprotein localizationprotein structure functionprotein transportreceptorreceptor bindingtissue /cell culture
项目摘要
DESCRIPTION (provided by applicant): As a first year Assistant Professor of
Pediatrics, the applicant is interested in developmental genetics and refining
the skills needed to achieve success as an independent researcher in academic
medicine. The focus of this research proposal involves exploring the Hedgehog
(Hh) pathway, a fundamental signaling cascade responsible for early embryonic
patterning of nearly every organ system in the developing fetus. The Hh also
pathway also plays a role in control of cell growth and proliferation in
mature organisms, and mutations in this pathway cause cancer in susceptible
tissues. Little is known about regulation of the subcellular localization,
trafficking or function of the Hh receptor complex. Of particular interest is
the fact that the Hh receptor Patched (Ptc), and the Hh ligand itself, seem to
be modified, and potentially regulated not only by other proteins, but also by
lipids, particularly cholesterol. This five-year award will provide enrichment
of the applicant's research career development through investigating the
regulation of Hedgehog receptor trafficking and function development through
investigating the regulation of Hedgehog receptor trafficking and function by
cholesterol and caveolin-l. Initially, confocal imaging studies will be
employed to assess trafficking/subcellular localization of the receptor
complex, including the ability of the receptor to internalize the Hh ligand.
Mutant constructs of caveline-1 and cholesterol blocking agents will be used
to identify the individual roles played by each of these components in Hh
receptor trafficking and ligand internalization. A luciferase reporter
construct, comprised of a Hh downstream target gene, Gli, will be used to
assay function of the Hh receptor. This will help determine the regions of Ptc
and caveolin that are critical for Hh receptor function and better define the
role of cholesterol in this process. Caveolin-l null cell lines and caveolin-l
adenoviral vectors will be generated for dynamic studies of the role of
caveolin-l in trafficking and function. This work will be integrated with
ongoing work in the mentor's lab on a caveolin-l knockout mouse, which will be
examined for developmental defects and cancer formation. Dr. Timothy
Thompson's lab, whose primary focus is the role of caveolin-l in control of
cell growth, differentiation and tumorigenesis, is an excellent environment to
aid in the development of this proposal. Because of the ubiquitous role of
the Hh pathway, and its link to cancer predisposition, this project may
provide clinical application to the understanding of aberrant human fetal
development and control of cell growth and differentiation. Understanding the
regulation of this pathway may suggest targets for gene therapy in the
developing fetus or therapeutic agents for certain Hh-related cancers.
描述(申请人提供):作为一年级助理教授
项目成果
期刊论文数量(0)
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{{ truncateString('HEIDI Eigenrauch KARPEN', 18)}}的其他基金
Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
- 批准号:
6613777 - 财政年份:2002
- 资助金额:
$ 12.59万 - 项目类别:
Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
- 批准号:
6901835 - 财政年份:2002
- 资助金额:
$ 12.59万 - 项目类别:
Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
- 批准号:
6752501 - 财政年份:2002
- 资助金额:
$ 12.59万 - 项目类别:
Regulation of Hedgehog Receptor Trafficking and Function
Hedgehog受体运输和功能的调控
- 批准号:
6460054 - 财政年份:2002
- 资助金额:
$ 12.59万 - 项目类别:
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