Relationship between transport mode and molecular structure in Na-HCO3 cotransporter
Relationship between transport mode and molecular structure in Na-HCO3 cotransporter
批准号:
14571013
负责人:
SEKI George
金额:
$2.24万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2003
中文摘要
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英文摘要
We tried to clarify the physiological and pathological significance of Na-11C03 cotransporter, NBC-1 Firstly, we identified several new NBC-1 mutations by screening cDNAs of patients having proximal renal tubular acidosis (pRTA). The data incated that NBC1 mutations identified so far locate in different regions in the NBC1 gene, and did not accumulate in the particular hot spots. By functional analysis on Xenopus oocytes, we showed that NBC1 function should be severely reduced (at least less than half of the wild-type activity) in order to induce proximal type acidosis. By immunohistochemical analysis using the vaiant specific antibodies, we showed that pancreatic variant (pNBC1) mediates bicarbonate secretion from pancreatic duct cells in both human and rat pancreas. It is suggested that functional loss of pNTBC1 may, via a similar mechanism as in cystic fibrosis, lead to pancreatic dysfunction. This hypothesis may be supported by high serum amylase levels found I pRTA patients. We also showed that kidney type variant (kNBC1) is expressed not only in the basolateral membrane of normal human kidney proximal tubules, but also in renal carcinoma tissues. NBC1 may be involved in metastasis of renal cell carcinoma (RCC). Since the prognosis of metastatic RCC is very poor, the future studies will be required to further clarify the roles of NBC1 in RCC.
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Sun D, Seki G, Uwatoko S, Nakao A, Taniguchi S et al.: "Quantitying porphobilinogen deaminase mRNA in microdissected nephron sogments by a modified RT-PCR"Kidney Int. 61. 336-341 (2002)
Sun D、Seki G、Uwatoko S、Nakao A、Taniguchi S 等人:“通过改良的 RT-PCR 定量显微解剖肾单位片段中的胆色素原脱氨酶 mRNA”Kidney Int。
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Horita S, Zheng Y, Yamada H, Fujita T, Seki G et al.: "Biphasic regulation of Na^+-HCO_3^- cotransporter by angiotensin II type 1A receptor."Hypertension. 40. 707-712 (2002)
Horita S、Zheng Y、Yamada H、Fujita T、Seki G 等:“血管紧张素 II 1A 型受体对 Na^-HCO_3^- 协同转运蛋白的双相调节。”高血压。
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Satoh H, Moriyama N, Fujita T, Seki G et al.: "Localization of Na^+-HCO_3^- cotransporter (NBC-1) variants in rat and human pancreas."Am J Physiol Cell Physiol. 284. C729-C737 (2003)
Satoh H、Moriyama N、Fujita T、Seki G 等人:“大鼠和人胰腺中 Na^ -HCO_3^- 协同转运蛋白 (NBC-1) 变体的定位。”Am J Physiol Cell Physiol。
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Satoh H, Moriyama N, Fujita T, Seki G et al.: "Localization on Na^+-HCO_3^- cotransporter (NBC-1) variants in rat and human pancreas."Am J Physiol Cell Physiol. 284. C729-C737 (2003)
Satoh H、Moriyama N、Fujita T、Seki G 等人:“大鼠和人胰腺中 Na^-HCO_3^- 协同转运蛋白 (NBC-1) 变体的定位。”Am J Physiol Cell Physiol。
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Zheng Y, Horita S, Hara C, Fujita T, Seki G et al.: "Biphasic Regulation of Renal Proximal Bicarbonate Absorption by Luminal AT_<1A> Receptor."J Am Soc Nephrol. 14. 1116-1122 (2003)
Cheng Y、Horita S、Hara C、Fujita T、Seki G 等人:“管腔 AT_<1A> 受体对肾近端碳酸氢盐吸收的双相调节”。J Am Soc Nephrol。
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共 16 条
Development of new medication against proximal renal tubular acidosis
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批准号:21591051
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.0万
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财政年份:2009
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负责人:SEKI George
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依托单位:
Role of cytosolic phospholipase A2 in intrarenalrenin-angiotensin system
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批准号:19590934
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.0万
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财政年份:2007
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负责人:SEKI George
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依托单位:
Phypiology and pathophysiology of Na-HCO3 cotransporter
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批准号:12671024
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.66万
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财政年份:2000
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负责人:SEKI George
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依托单位:
海外基金