VIP AND PACP ACTION IN CNS DEVELOPMENT AND INJURY
VIP AND PACP ACTION IN CNS DEVELOPMENT AND INJURY
批准号:
6108238
负责人:
JAMES A WASCHEK
金额:
$17.71万
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:
1998-12-01 至 1999-11-30
关键词:
biological signal transduction cell proliferation developmental neurobiology disease /disorder model genetic regulatory element genetically modified animals glia in situ hybridization laboratory mouse laboratory rat mental retardation nerve injury neuropeptide receptor neuropeptides neurotrophic factors receptor expression reporter genes tissue /cell culture vasoactive intestinal peptide
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Vasoactive intestinal peptide (VIP) and the related neuropeptide
pituitary adenylate cyclase activating peptide (PACAP) are potent
regulators of neuroblast proliferation and survival in vitro.
Administration of a VIP antagonist to pregnant mice produced a
microcephaly condition in offspring, providing a new model for a human
disease that is nearly always associated with mental retardation. In
addition, VIP has been found to be highly upregulated in nerve injury
models, and PACAP has been found to reduce the degree of cell death in
the hippocampus following experimental forebrain ischemia. Thus, the
VIP/PACAP ligand/receptor system may be important in CNS morphogenesis
and injury. With respect to development, the current model contends that
VIP is derived transplacentally from the mother, and thereby acts as a
global regulator of embryonic CNS growth. However, key data from this
laboratory indicate that the VIP gene is expressed in the mouse
hindbrain as early as embryonic day 11, suggesting that the peptides are
derived from the embryo and act in local domains (rather than globally)
to regulate CNS development.
In this proposal, the temporal and spatial expression patterns of VIP
and PACAP, and their receptors during normal development will be
determined using in situ hybridization and immunohistochemistry. The
phenotype of potential target cell types will be identified by
colocalizing receptors with markers for various developing neural
lineages. It will also be determined if the VIP/PACAP ligand/receptor
system is upregulated in an injury model. Based on the patterns of
expression of peptide and receptor during development and after injury,
in vitro model will be established to study the growth- or injury-
related actions of these peptides on relevant cell populations Signal
transduction pathways leading to these actions will be examined using
pharmacological, biochemical, an molecular approaches. The results are
expected to provide important mechanistic information on the role of
peptides such as VIP and PACAP in normal and abnormal CNS development
and after injury to the developing brain.
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海外基金