Cyclic Nucleotides and the Response to Sonic Hedgehog
Cyclic Nucleotides and the Response to Sonic Hedgehog
批准号:
6501181
负责人:
HENK ROELINK
金额:
$15.18万
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
项目状态:
已结题
起止时间:
2002-03-15 至 2004-01-31
关键词:
biological signal transduction chick embryo congenital brain disorder cyclic AMP cyclic GMP developmental neurobiology embryo /fetus disorder embryo /fetus toxicology environmental exposure forskolin gene environment interaction immunocytochemistry neural plate /tube neurotoxicology neurotoxins nucleotides phosphodiesterases protein kinase A tissue /cell culture veratrum alkaloid
中文摘要
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英文摘要
Description:
The Sonic Hedgehog is a signaling molecule that is required for normal
development of the central nervous system. The response to Shh is complex,
and can be changed by environmental compounds like cyclopamine. Changes in
the Shh response result in a specific type of embryo malformations
characterized by defects of the neural midline, like holoprosencephaly, which
can be reflected in the face as cyclopia or hypotelorism. All cell types in
the ventral neural tube develop as a consequence of Shh signaling, and it is
likely that small changes in the Shh response has subtle effects on the
formation of ventral cell types. This in turn might result in congenital
neurological defects. It has been determined that the Shh response is
influenced by the cyclic nucleotide concentration within the responding cells.
Increasing the camp concentration attenuates the Shh response, while loss of
the camp dependent kinase (PKA) activates the Shh response. These authors
showed that increasing the cGMP concentration also enhances the response to
Shh, suggesting a model in which the Shh response is dependent on the cyclic
nucleotide concentration within the responsive cells, and that camp and cGMP
have opposite effects on the Shh response. Several compounds present in the
environment can alter the intracellular cyclic nucleotide concentration,
either by activating GTP/ATP cyclases, enzymes that generate cyclic
nucleotides, or by blocking phosphodiesterases, enzymes that degrade cyclic
nucleotides. It is hypothesized that environmental compounds that change the
cyclic nucleotide complement of a cell, alter Shh response in such cells,
resulting in embryo malformations and thus birth defects. The hypothesis will
be tested using sensitive assays of the Shh response in the chick embryo. It
will be determined if environmental compounds that change the cyclic
nucleotide complement of a cell interfere with normal Shh signaling in the
developing neural tube in vivo, or in neural explants in vitro. In humans,
exposure to the compounds that will be tested is either voluntary, like
forskolin, or involuntary, like bacterial enterotoxins, but in either case
little is known about their possible adverse effects on early embryos and thus
as a cause of birth defects.
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海外基金