STRUCTURE AND REGULATION OF OSTEOBLAST CALCIUM CHANNELS
STRUCTURE AND REGULATION OF OSTEOBLAST CALCIUM CHANNELS
批准号:
6177547
负责人:
ELIZABETH L BARRY
金额:
$11.88万
依托单位:
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:
1997-05-01 至 2002-04-30
关键词:
RNase protection assay bone metabolism calcium channel calcium channel blockers cell differentiation clone cells fluorescent dye /probe gel electrophoresis gene expression hormone regulation /control mechanism human subject messenger RNA molecular cloning northern blottings nucleic acid sequence osteoblasts parathyroid hormones physiologic bone resorption polymerase chain reaction protein isoforms protein kinase protein structure function scintillation counter statistics /biometry tissue /cell culture
中文摘要
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英文摘要
DESCRIPTION (Adapted from the Applicant's Abstract): The long-term goal of
this research proposal is to understand how changes in the expression, or
regulation of calcium channels in osteoblasts affect bone metabolism.
Recent research indicating that the activation of calcium channels in
osteoblasts is a common feature of many bone regulatory factors suggests a
significant role for intracellular calcium signalling in the control of bone
remodeling. However, the molecular structure and cellular regulation of
osteoblast calcium channels remain largely undefined. Previous studies have
demonstrated that three isoforms of calcium channels are expressed in
osteoblast-like osteosarcoma cells (alpha1S, alpha1C and alpha1D), and that
parathyroid hormone selectively activates the alpha1D isoform. The
objective of this study is to more fully characterize the structure,
function and regulation of the calcium channel alpha1D isoform in
osteoblasts. The Specific Aims are to: 1) determine the molecular
structure of the alpha1D isoform; 2) examine the temporal and hormonal
regulation of alpha1D gene expression during osteoblast differentiation; 3)
define the mechanism of alpha1D activation by parathyroid hormone; 4)
determine the specific functional effects mediated by the alpha1D signaling
pathway; and 5) examine the regulation of alpha1D activity by other hormones
and drugs. Calcium channel cDNA clones will be isolated, sequenced and used
for the quantitative analysis of mRNA levels. Calcium channel activity will
be assessed (using a fluorescent probe) to measure the level of
intracellular calcium, as well as a radioisotope uptake assay to measure
calcium influx. Specific calcium channel antagonists, as well as antisense
techniques, will be used to examine the functional roles and hormonal
regulation of osteoblast calcium channels. It is suggested that the results
of the proposed research study will provide novel and important information
about the molecular structure and cellular regulation of osteoblast calcium
channels and their role in bone metabolism, as well as providing insight
into the cellular mechanisms of action of bone regulatory hormones. These
insights are critical to an understanding of the events that regulate bone
remodeling and, ultimately, for the development of effective therapeutic
approaches for the treatment of bone diseases, including osteoporosis.
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海外基金