CHROMOGRANINS IN NEUROENDOCRINE TUMOR CELLS
CHROMOGRANINS IN NEUROENDOCRINE TUMOR CELLS
批准号:
2141407
负责人:
JONATHAN G SCAMMELL
金额:
$16.03万
依托单位国家:
美国
项目类别:
财政年份:
1988
资助国家:
美国
项目状态:
已结题
起止时间:
1988-09-30 至 1998-06-30
关键词:
PC12 cells biomarker cell type clone cells cyclic AMP developmental genetics embryo /fetus cell /tissue gel mobility shift assay gene expression gene induction /repression genetic promoter element genetic regulation genetic transcription histogenesis immunocytochemistry in situ hybridization laboratory rat messenger RNA neuroendocrine system nuclear runoff assay nucleic acid sequence pituitary gland reporter genes secretory protein transcription factor
中文摘要
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英文摘要
The granins are a family of immunologically distinct, secretory proteins
that are expressed only in endocrine and neuronal cells that concentrate
their secretory products in storage granules and release it upon
stimulation. In these cells the granins are integral to the formation of
the dense-core matrix which forms in the Golgi prior to packaging of the
secretory products. The granins also possess a number of proteolytic
processing sites and peptides derived from granin precursors have been
shown to have important autocrine regulatory activity. The granins are
secreted at high rates by endocrine neoplasms and their immunocytochemical
detection in tumoral tissue is considered diagnostic of the presence of
tissue of neuroendocrine origin. Despite these and other studies on granin
structure and function, the molecular basis for tissue-specific expression
of the granins has yet to be studied. The present study is designed to
investigate in detail the expression of a single member of the granin
family, secretogranin II (SgII), in the rat anterior pituitary gland and
to use the rat PC12 and GH4C1 neuroendocrine cell lines as models to study
the molecular basis of SgII expression. These results of these studies
will establish where, when and how SgII is expressed in neuroendocrine
cells.
The following specific questions will be answered by these studies:
1. Which cells in the anterior pituitary gland express SgII?
2. Is SgII a marker for early pituitary differentiation or granulation in
the developing pituitary gland?
3. Which cis-acting elements in the SgII promoter mediate tissue-specific
expression of SgII in neuroendocrine cells and can specific trans-acting
factors be identified which mediate neuroendocrine-specific expression?
4. Which cis-acting elements mediate negative regulation of SgII
expression by cyclic AMP in PC12 cells and can specific trans-acting
factors be identified which mediate this regulation?
The results of these studies will provide the first analysis of the
molecular mechanism for expression of SgII in neuroendocrine cells.
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