REGULATION OF NEURAL PRECURSORS: ROLE OF NEUROPEPTIDES
REGULATION OF NEURAL PRECURSORS: ROLE OF NEUROPEPTIDES
批准号:
2889295
负责人:
JAMES A WASCHEK
金额:
$22.49万
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:
1997-09-01 至 2001-08-31
关键词:
adenylate cyclase animal genetic material tag developmental neurobiology embryo /fetus embryogenesis enzyme activity gene induction /repression laboratory mouse mammalian embryology microglia neurogenesis neurogenetics neuropeptides neuropharmacology pharmacogenetics pituitary gland vasoactive intestinal peptide
中文摘要
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英文摘要
DESCRIPTION: Vasoactive intestinal peptide (VIP) is a potent regulator of
neuroblast proliferation and survival in vitro. Administration of VIP
antagonist to pregnant mice produced a pronounced microcephaly condition in
offspring, providing a new model for human brain disease. VIP effects in
tissue culture can also be brought about by the structurally-related
neuropeptide pituitary adenylate cyclase activating peptide (PACAP).
Despite the demonstrated capacity of these peptides to regulate CNS
development, investigators have been unable to show that VIP or PACAP is
expressed in embryonic CNS of mice at early stages. Thus, the current model
contends that VIP is derived transplacentally from the mother, and thereby
acts as a global regulator of embryonic CNS development.
To challenge this model , sensitive in situ hybridization protocols to
detect mRNA for these ligands and their receptors was developed. This
combined with data obtained by Northern analyses suggest that the VIP/PACAP
ligand/receptor system may be operational within the embryo at the earliest
stages of neurogenesis. It is thus proposed that VIP and PACAP are derived
from the embryo and act in local domains to regulate CNS development.
Two novel potential target populations for VIP and PACAP were identified by
this analysis, neuroepithelial cells and microglia. It is proposed that VIP
and PACAP regulate the proliferation of these cells. This will be tested
using dispersed cell and short-term cultures of intact embryos. In
addition, the unexplained ability of these peptides to induce proliferation
in some cell populations and cell cycle withdrawal in others will be
examined. It is hypothesized that the differences are due to G-protein
coupling of receptors to different signal transduction pathways. This will
be tested using a combination of pharmacological, molecular, and biochemical
approaches, including analysis of the Rs/Raf/MAP kinase pathway. The
results are expected to provide important mechanistic information on how
these neuropeptides play important roles in CNS development, as well as in
nerve injury, neurological tumors, and degenerative diseases of the nervous
system.
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财政年份:2005
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MR STUDIES OF A PACAP MOUSE MODEL
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财政年份:2002
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资助金额:$15.26万
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财政年份:2002
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依托单位:
VIP AND PACP ACTION IN CNS DEVELOPMENT AND INJURY
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资助金额:$24.28万
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财政年份:2000
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依托单位:
VIP AND PACP ACTION IN CNS DEVELOPMENT AND INJURY
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项目类别:
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资助金额:$17.71万
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财政年份:1999
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依托单位:
VIP AND PACP ACTION IN CNS DEVELOPMENT AND INJURY
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项目类别:
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资助金额:$17.71万
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财政年份:1998
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依托单位:
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项目类别:
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财政年份:1997
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负责人:JAMES A WASCHEK
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依托单位:
Regulation of Neural Precursors: Role of Neuropeptides
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负责人:JAMES A WASCHEK
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依托单位:
REGULATION OF NEURAL PRECURSORS: ROLE OF NEUROPEPTIDES
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依托单位: