Studies on the requlatory mechanisms of renal glomerular and tubular functions.
Studies on the requlatory mechanisms of renal glomerular and tubular functions.
批准号:
02404036
负责人:
KUROKAWA Kiyoshi
金额:
$20.99万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (A)
财政年份:
1990
资助国家:
日本
项目状态:
已结题
起止时间:
1990 至 1992
中文摘要
我们在这项研究项目中获得的主要发现如下。1)肾小球系膜细胞表达TGF-β mRNA,其表达受胎牛血清和蛋白激酶C的刺激。几乎所有由系膜细胞产生并释放到条件培养基中的TGF-β都是以潜伏形式存在的。外源性TGF-β抑制系膜细胞生长。2)3)克隆的肾小管细胞LLC-PK 1表达单一的PAF受体mRNA,PAF可诱导LLC-PK 1细胞产生浓度依赖性的钙瞬变。4)内皮素-1剂量依赖性地增加皮质和髓质集合管中的[Ca^++]i。内皮素-1 mRNA被发现只表达在皮质和髓质集合管,除了肾小球和内皮素-1结合发生显着的肾小球和集合管。5)我们根据在培养的系膜细胞中所获得的观察结果,提出了我们关于肾小管-肾小球反馈中跨细胞信号转导的假说。
英文摘要
The major findings we obtained in this research project are as follows. 1) Mesangial cell expressed TGF-beta mRNA and its expression is stimulated by the addition of fetal calf serum and protein kinase C.Almost all the TGF-beta produced by mesangial cell and released into condition medium is in a latent form. Exogenously added TGF-beta inhibited mesangial cell growth. 2) A single class of PAF receptor is present in the quinea pig kidney which is most abundant in the cortex 3) Cloned renal tubule cells, LLC-PK1 cells, express a single entity of PAF receptor mRNA and PAF induced a dose-dependent calcium transients in LLC-PK1 cells. 4) Endothelin-1 dose-dependently increased [Ca^<++>]i both in cortical and medullary collecting duct. Endothelin-1 mRNA was found to be expressed only in cortical and medullary collecting ducts in addition to glomeruli and endothelin-1 binding occurs significantly in glomeruli and collecting tubules. 5) We proposed our hypothesis concerning the transcellular signal transduction in tubulo-glomerular feedback based on the observations we obtained in cultured mesangial cells.
期刊论文(20)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
S.Taniguchi: "Nephron distribution of platelet activating factor(PAF)reseptor mRNA detected by plymerase chain reaction(PCR)." J.Am.Sci.Nephrol.2(3). 465 (1991)
S.Taniguchi:“通过聚合酶链式反应 (PCR) 检测血小板激活因子 (PAF) 受体 mRNA 的肾单位分布。”
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
K.M, Asef Jamil: "Expression of platetet activating factor receptor in renal tubular cell line (LLC-PK1)" Biochem.Biophys.Res.Comm.187. 767-772 (1992)
K.M、Asef Jamil:“肾小管细胞系 (LLC-PK1) 中血小板激活因子受体的表达”Biochem.Biophys.Res.Comm.187。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
T.Okuda他: "Demononstration of platelet actviating factor recepttor in guinea pig kidney." Biochem Biophys Res Comm.177. 54-60 (1991)
T. Okuda 等人:“豚鼠肾脏中血小板激活因子受体的演示。”Biochem Biophys Res Comm.177 (1991)。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
H.Mathunaga,T.Okuda,K.Kurokawa: "Ionic cannel analysis of cultured rat mesangial cells.The Frontiers of Nephrology." edited by R.W.Berliner,N.Honda,K.J.Ullrich.Elsevier Science Publishers B.V., (1992)
H.Mathunaga、T.Okuda、K.Kurokawa:“培养的大鼠系膜细胞的离子通道分析。肾病学前沿”。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
K.Kurkawa: "Cholride conductance of mesangial cells." Contrib.Nephrol.95. 76-81 (1991)
K.Kurkawa:“系膜细胞的氯离子电导。”
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
共 20 条
Post genome study for mesangium-predominant functional genes
-
批准号:13307032
-
项目类别:Grant-in-Aid for Scientific Research (A)
-
资助金额:$35.53万
-
财政年份:2001
-
负责人:KUROKAWA Kiyoshi
-
依托单位:
Functional genomics for renal diseases
-
批准号:11307016
-
项目类别:Grant-in-Aid for Scientific Research (A).
-
资助金额:$24.45万
-
财政年份:1999
-
负责人:KUROKAWA Kiyoshi
-
依托单位:
Molecular Cell Biological Analysis on Renal Structure and Function
-
批准号:05404041
-
项目类别:Grant-in-Aid for General Scientific Research (A)
-
资助金额:$24.32万
-
财政年份:1993
-
负责人:KUROKAWA Kiyoshi
-
依托单位:
海外基金