RECEPTOR TYROSINE PHOSPHATASES IN THE GROWTH OF AXONS
RECEPTOR TYROSINE PHOSPHATASES IN THE GROWTH OF AXONS
批准号:
6394174
负责人:
John L Bixby
金额:
$27.24万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-07-15 至 2003-06-30
关键词:
Escherichia coli affinity chromatography axon binding sites biological signal transduction cell adhesion molecules cell line chimeric proteins expression cloning genetically modified animals growth cones immunoprecipitation laboratory mouse ligands neurogenesis neuronal guidance neuroregulation protein protein interaction protein tyrosine phosphatase receptor receptor binding receptor expression
中文摘要
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英文摘要
DESCRIPTION (Verbatim from the Applicant's Abstract): The regulation of
tyrosine kinase phosphorylation is critical for the growth and guidance of
axons. Evidence suggests that the CAM-like receptor-tyrosine phosphatases
(RPTPs) play key roles in the signaling processes underlying axon growth. This
project tests the hypothesis that RPTPs, expressed on the surface of developing
neurons regulate axon growth during embryogenesis, through the binding of
specific ligands to their extracellular domains. The focus here is on 2
specific RPTPs -- CRYP-2 and PTP-deltadelta -- that are excellent candidates
for involvement in the regulation of axon growth. Evidence implicating these
two RPTPs includes structure, expression pattern, and preliminary analysis of
function in vitro. The major questions concerning these RPTPs are: What are the
regulatory ligands for CRYP-2 and PTP-delta?, and How are CRYP-2 and PTP-delta
involved in axon growth? These questions will be addressed through correlation
of expression of ligands for CRYP-2 and PTP-delta with expression of the RPTPs
themselves, characterization of these ligands, and examination of the function
of CRYP-2 and PTP-delta in axon growth, both in vitro and in vivo. There are
three specific aims. First, potential regulatory ligands for the RPTPs will be
localized, and identified through immunoprecipitation, affinity chromatography
and expression cloning. Identification of ligands will allow key biochemical
experiments on adhesive and signaling functions of these RPTPs. Second, the
extracellular domains of the RPTPs will be used as regulators of axon growth
and guidance in vitro, in an analysis of the mechanisms involved in this
regulation. These results will provide detailed mechanistic evidence concerning
how these RPTPs function. Finally, two different in vivo assay systems
(retroviral expression of mutants and gene knockout) will be employed to assess
the role of these RPTPs in neuronal development during embryogenesis. These
assays will provide direct tests of the hypothesis that the specific PTPs under
study are functionally linked to axon growth and guidance in vivo. The proposed
experiments will move the field closer to a molecular understanding of the
regulation of vertebrate axon growth. This understanding is critical for
rational approaches to developmental disorders of the nervous system, as well
as the problem of spinal cord regeneration.
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会议论文
Targeting Multiple Kinases to Treat Experimental Spinal Cord Injury.
-
批准号:10393353
-
项目类别:
-
资助金额:$1.68万
-
财政年份:2017
-
负责人:John L Bixby
-
依托单位:
Targeting Multiple Kinases to Treat Experimental Spinal Cord Injury
-
批准号:9917854
-
项目类别:
-
资助金额:$46.55万
-
财政年份:2017
-
负责人:John L Bixby
-
依托单位:
Targeting Multiple Kinases to Treat Experimental Spinal Cord Injury
-
批准号:10160972
-
项目类别:
-
资助金额:$46.55万
-
财政年份:2017
-
负责人:John L Bixby
-
依托单位:
Regenbase: A Searchable Database to Organize Regeneration Knowledge via Ontologie
-
批准号:8465934
-
项目类别:
-
资助金额:$55.02万
-
财政年份:2012
-
负责人:John L Bixby
-
依托单位:
Regenbase: A Searchable Database to Organize Regeneration Knowledge via Ontologie
-
批准号:8653627
-
项目类别:
-
资助金额:$56.44万
-
财政年份:2012
-
负责人:John L Bixby
-
依托单位:
Regenbase: A Searchable Database to Organize Regeneration Knowledge via Ontologie
-
批准号:8365739
-
项目类别:
-
资助金额:$60.38万
-
财政年份:2012
-
负责人:John L Bixby
-
依托单位:
Regenbase: A Searchable Database to Organize Regeneration Knowledge via Ontologie
-
批准号:8839677
-
项目类别:
-
资助金额:$57.01万
-
财政年份:2012
-
负责人:John L Bixby
-
依托单位:
Triazine-based compounds to promote regeneration in optic neuropathies
-
批准号:8284307
-
项目类别:
-
资助金额:$3.28万
-
财政年份:2011
-
负责人:John L Bixby
-
依托单位:
Triazine-based compounds to promote regeneration in optic neuropathies
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批准号:8128170
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项目类别:
-
资助金额:$19.68万
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财政年份:2011
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负责人:John L Bixby
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依托单位:
Novel Compounds That Overcome Glial Inhibition of Axonal Regeneration
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批准号:8394926
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项目类别:
-
资助金额:$31.65万
-
财政年份:2009
-
负责人:John L Bixby
-
依托单位:
Novel Compounds That Overcome Glial Inhibition of Axonal Regeneration
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批准号:7582047
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项目类别:
-
资助金额:$33.07万
-
财政年份:2009
-
负责人:John L Bixby
-
依托单位:
Novel Compounds That Overcome Glial Inhibition of Axonal Regeneration
-
批准号:7848703
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项目类别:
-
资助金额:$4.46万
-
财政年份:2009
-
负责人:John L Bixby
-
依托单位:
Novel Compounds That Overcome Glial Inhibition of Axonal Regeneration
-
批准号:7752485
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项目类别:
-
资助金额:$33.13万
-
财政年份:2009
-
负责人:John L Bixby
-
依托单位:
Novel Compounds That Overcome Glial Inhibition of Axonal Regeneration
-
批准号:7991788
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项目类别:
-
资助金额:$32.8万
-
财政年份:2009
-
负责人:John L Bixby
-
依托单位:
Novel Compounds That Overcome Glial Inhibition of Axonal Regeneration
-
批准号:8065240
-
项目类别:
-
资助金额:$6.89万
-
财政年份:2009
-
负责人:John L Bixby
-
依托单位:
Novel Compounds That Overcome Glial Inhibition of Axonal Regeneration
-
批准号:8204614
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项目类别:
-
资助金额:$32.8万
-
财政年份:2009
-
负责人:John L Bixby
-
依托单位:
Novel Gene Targets for CNS Axonal Regeneration
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批准号:9093811
-
项目类别:
-
资助金额:$46.58万
-
财政年份:2007
-
负责人:John L Bixby
-
依托单位:
Novel Gene Targets for CNS Axonal Regeneration
-
批准号:8827566
-
项目类别:
-
资助金额:$47.05万
-
财政年份:2007
-
负责人:John L Bixby
-
依托单位:
Novel Gene Targets for CNS Axonal Regeneration
-
批准号:8931007
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项目类别:
-
资助金额:$45.88万
-
财政年份:2007
-
负责人:John L Bixby
-
依托单位:
PREDOCTORAL TRAINING PROGRAM IN THE NEUROSCIENCES
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批准号:6313974
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项目类别:
-
资助金额:$14.9万
-
财政年份:2001
-
负责人:John L Bixby
-
依托单位:
海外基金