MOUSE EXTRACELLULAR CALCIUM SENSING RECEPTOR
MOUSE EXTRACELLULAR CALCIUM SENSING RECEPTOR
批准号:
6177924
负责人:
MARTIN R. POLLAK
金额:
$16.32万
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:
1997-09-26 至 2002-08-31
中文摘要
细胞外钙稳态是由
英文摘要
Extracellular calcium homeostasis is precisely regulated by the
interaction of several hormones with multiple target organs. In
addition, calcium itself acts upon a G-protein-coupled "calcium-
sensing" receptor (CaSR) on the he surface of parathyroid cells to
regulate the secretion of parathyroid hormone (PTH). This receptor
is also expressed in other tissues, where its precise function is less
well-defined. Humans with two copies of an inactivating mutation
in the caSR gene are severely hypercalcemic, presumably because
the normal inhibition of PTH secretion by calcium is no longer
present. CaSR is expressed by diverse cell types of the kidney,
where extracellular calcium has multiple effects. The purpose of
this proposal is to clarify the role of CaSR in mediating specific
effects of calcium on the kidney and to better define the role of
renal CaSR in regulating whole animal calcium homeostasis.
The aims of this proposal focus on the development of genetically
altered mice which will serve as models in understanding the
function of renal Car. Transgenic mice overexpressing CaSR in the
thick ascending limb of the kidney will be generated. This mouse
model should help clarify the contribution of CaSR activation to the
regulation of calcium, sodium, and water homeostasis. It will also
aid in defining which actions of calcium on the kidney are mediated
by CaSR.
In addition, the renal function of mice with a null mutation in CaSR
will be investigated by a combination of genetic and physiologic
methods. Normally these ~knockout~ mice do not live past the
neonatal period. Crossing CaSR deficient mice with other mutant
mice unable to mount a hypercalcemic response to PTH should
generate viable CaSR-deficient mice which will aid in the
investigation of CaSR function in the kidney and other tissues.
Multiple hypotheses regarding the role of CaSR in renal calcium
excretion and as well as its role in mediating renal responses to
calcium will be investigated.
Clarifying the functions of CaSR, a newly identified component of
the calcium homeostatic system, will likely have implications for
understanding and treatment of diseases of abnormal calcium
regulation, including osteoporosis, hyperparathyroidism, kidney
stones, and hypertension.
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会议论文
Biological Mechanism of FSGS-1
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批准号:9319727
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项目类别:
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资助金额:$41.39万
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财政年份:2016
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负责人:MARTIN R. POLLAK
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依托单位:
APOL1 variants: Understanding the basis of disparities in rates of kidney disease
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批准号:8282062
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项目类别:
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资助金额:$43.5万
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财政年份:2012
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负责人:MARTIN R. POLLAK
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依托单位:
APOL1 variants: Understanding the basis of disparities in rates of kidney disease
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批准号:8451330
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项目类别:
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资助金额:$40.67万
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财政年份:2012
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负责人:MARTIN R. POLLAK
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依托单位:
APOL1 variants: Understanding the basis of disparities in rates of kidney disease
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批准号:8791543
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资助金额:$43.5万
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财政年份:2012
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依托单位:
APOL1 variants: Understanding the basis of disparities in rates of kidney disease
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批准号:8607479
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资助金额:$43.5万
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财政年份:2012
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负责人:MARTIN R. POLLAK
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依托单位:
Biological Mechanism of INF2-mediated FSGS
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批准号:8517110
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项目类别:
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资助金额:$39.66万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological Mechanism of INF2-mediated FSGS
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批准号:8318904
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项目类别:
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资助金额:$41.1万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Molecular Genetics of Inherited Focal Glomerulosclerosis
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批准号:8223174
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项目类别:
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资助金额:$39.44万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological Mechanism of INF2-mediated FSGS
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批准号:8970699
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项目类别:
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资助金额:$43.65万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Molecular Genetics of Inherited Focal Glomerulosclerosis
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批准号:8287701
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项目类别:
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资助金额:$37.34万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological Mechanism of INF2-mediated FSGS
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批准号:9195717
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项目类别:
-
资助金额:$43.65万
-
财政年份:2010
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负责人:MARTIN R. POLLAK
-
依托单位:
Molecular Genetics of Inherited Focal Glomerulosclerosis
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批准号:8208917
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项目类别:
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资助金额:$40.68万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological Mechanism of INF2-mediated FSGS
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批准号:7947472
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项目类别:
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资助金额:$48.67万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological Mechanism of INF2-mediated FSGS
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批准号:9390786
-
项目类别:
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资助金额:$43.65万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological Mechanism of INF2-mediated FSGS
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批准号:8109281
-
项目类别:
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资助金额:$39.72万
-
财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological Mechanism of INF2-mediated FSGS
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批准号:8817734
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项目类别:
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资助金额:$47.34万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological mechanism of familial focal segmental glomerulosclerosis-1
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批准号:8214866
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项目类别:
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资助金额:$5.28万
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财政年份:2010
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负责人:MARTIN R. POLLAK
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依托单位:
Biological mechanism of familial focal segmental glomerulosclerosis-1
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批准号:7921105
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项目类别:
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资助金额:$4.72万
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财政年份:2009
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负责人:MARTIN R. POLLAK
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依托单位:
Molecular Genetics of Inherited Focal Glomerulosclerosis
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批准号:7625306
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项目类别:
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资助金额:$5.36万
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财政年份:2008
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负责人:MARTIN R. POLLAK
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依托单位:
Characterization of alpha-actinin-4 deficient mice
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批准号:6984831
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项目类别:
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资助金额:$29.97万
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财政年份:2004
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负责人:MARTIN R. POLLAK
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依托单位:
海外基金