Involvement of a transporter in an autocrine / paracrine release of ATP.
转运蛋白参与 ATP 的自分泌/旁分泌释放。
基本信息
- 批准号:15590243
- 负责人:
- 金额:$ 2.18万
- 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:2003
- 资助国家:日本
- 起止时间:2003 至 2004
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Bradykinin induces the release of ATP from cultured taenia coli smooth muscle cells from guinea pigs. The evoked release was prohibited by a B2-receptor antagonist (HOE-140) and (inhibitors (U-73122 and thapsigargin) for the phospholipase C - inositol (1,4,5) P_3 signal pathway. The release of ATP was interfered, with MRP inhibitors (NM-571 and benzbromarone). However, hemichann el blockers (gap26) and the blockers (glybemclamid and Gd^<3+>) of Cl channels coupled with activation of CFTR failed to attenuate the evoked release. The release of ATP by hadykinin was also inhibited by cytochalasin D, staurosporine and NEM, but not by inhibitors for Golgi body (brefeldin A) and mitochondria (oligomycin). Therefore, we conclude that the bradykinini-evoked release of ATP may be mediated by the membrane MRP transporter activated by intracellular ATP released from endoplasmic reticulum,
Bradyinin诱导从豚鼠中培养的Taenia大肠杆菌平滑肌细胞中释放ATP。 B2受体拮抗剂(HOE-140)和(抑制剂(U-73122和Thapsigargin)禁止磷脂酶C-肌醇(1,4,5)P_3 P_3信号途径。 (GAP26)和CL通道的阻滞剂(Glybemclamid和Gd^<3+>)与CFTR的激活结合使用,无法减轻诱发的释放,而Hadykinin也被CytoChalasin d,Staurosporine and Nem和bygion Brodiry(bref and bregi)抑制了Hadykinin。 (寡霉素)。
项目成果
期刊论文数量(46)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Adenosine induces ATP release via an inositol 1,4,5-trisphosphate signaling pathway in MDCK cells
腺苷通过 MDCK 细胞中的肌醇 1,4,5-三磷酸信号通路诱导 ATP 释放
- DOI:
- 发表时间:2005
- 期刊:
- 影响因子:0
- 作者:K.Migita et al.;K.Migita et al.
- 通讯作者:K.Migita et al.
Induction of leukotriene C_4 synthase after the differentiation of rat basophillic leukemia cells with retinoic acid and a low dose of actinomycin D and its suppression with methylprednisolone.
视黄酸和低剂量放线菌素 D 诱导大鼠嗜碱性白血病细胞分化后白三烯 C_4 合酶的诱导及其甲基强的松龙的抑制。
- DOI:
- 发表时间:2003
- 期刊:
- 影响因子:0
- 作者:T.Iwamoto;S.Kita;S.Ueno et al.;M.Abe et al.
- 通讯作者:M.Abe et al.
Harada, N. et al.: "Contribution of capsaicin-sensitive sensory neurons to stress-induced increase in gastric tissue levels of prostaglandins in rats."Am J Physiol (Gastrointest Liver Physiol). 285. G1214-G1224 (2003)
Harada, N. 等人:“辣椒素敏感的感觉神经元对压力诱导的大鼠胃组织前列腺素水平增加的贡献。”Am J Physiol(胃肠测试肝脏生理学)。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Extracellular Nucleotides and Nucleosides: Release, Receptor, and Physiological and Pathophysiological effects: Relating the structur of the ATP-gated ion channel-receptors to their function
细胞外核苷酸和核苷:释放、受体以及生理和病理生理效应:ATP 门控离子通道受体的结构与其功能的关系
- DOI:
- 发表时间:2003
- 期刊:
- 影响因子:0
- 作者:T.Iwamoto;S.Kita;S.Ueno et al.;M.Abe et al.;S.Ueno et al.;M.Abe et al.;T.M.Eagan et al.;T.M.Eagan et al.
- 通讯作者:T.M.Eagan et al.
Induction of leukotriene C_4 synthase after the differentiation of rat basophillic leukemia cells with retinoic acid and a low dose of actinomycin D and its suppression with methylprednisolone
视黄酸和低剂量放线菌素D诱导大鼠嗜碱性白血病细胞分化后白三烯C_4合酶的诱导及其甲泼尼龙的抑制
- DOI:
- 发表时间:2003
- 期刊:
- 影响因子:0
- 作者:T.Iwamoto;S.Kita;S.Ueno et al.;M.Abe et al.;S.Ueno et al.;M.Abe et al.
- 通讯作者:M.Abe et al.
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
KATSURAGI Takeshi其他文献
KATSURAGI Takeshi的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('KATSURAGI Takeshi', 18)}}的其他基金
Identification of a specific transporter on extracellular release of ATP
细胞外释放 ATP 的特定转运蛋白的鉴定
- 批准号:
17590234 - 财政年份:2005
- 资助金额:
$ 2.18万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
ATP-autocrine/paracrine release and its intracellular Ca^<2+> signals
ATP-自分泌/旁分泌释放及其胞内Ca^2信号
- 批准号:
13670107 - 财政年份:2001
- 资助金额:
$ 2.18万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Possible involvement of CaィイD12+ィエD1-signaling transferred to mitochondria in release of ATP as an autacoid
CaD12+D1 信号可能参与转移至线粒体并作为自体物质释放 ATP
- 批准号:
10670102 - 财政年份:1998
- 资助金额:
$ 2.18万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Intracellular signalling pathway involved in ATP release from isolated smooth muscle cells.
细胞内信号通路参与分离的平滑肌细胞释放 ATP。
- 批准号:
07670127 - 财政年份:1995
- 资助金额:
$ 2.18万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Involvement of ATP released from non-neuronal tlssues in presynaptic neuromodulation.
非神经元组织释放的 ATP 参与突触前神经调节。
- 批准号:
04670132 - 财政年份:1992
- 资助金额:
$ 2.18万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
A possible role as a neuromodulator of extraneuronally released-ATP.
可能作为神经元外释放的 ATP 的神经调节剂。
- 批准号:
02670102 - 财政年份:1990
- 资助金额:
$ 2.18万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
Novel characteristics of ATP as a potential neuro-co-transmitter.
ATP 作为潜在神经递质的新特征。
- 批准号:
61570114 - 财政年份:1986
- 资助金额:
$ 2.18万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
相似海外基金
Potential of tissue kallikreins as therapeutic targets for neuropsychiatric lupus
组织激肽释放酶作为神经精神狼疮治疗靶点的潜力
- 批准号:
10667764 - 财政年份:2023
- 资助金额:
$ 2.18万 - 项目类别:
Negative allosteric modulators for bradykinin B1 receptors
缓激肽 B1 受体的负变构调节剂
- 批准号:
10680762 - 财政年份:2023
- 资助金额:
$ 2.18万 - 项目类别:
NOS3 and p38 MAP kinase - is the interaction between them a mechanism of p38 regulation?
NOS3 和 p38 MAP 激酶 - 它们之间的相互作用是 p38 调节机制吗?
- 批准号:
10653595 - 财政年份:2023
- 资助金额:
$ 2.18万 - 项目类别:
Proteomic signatures to identify pathways underlying the progression to heart failure
蛋白质组学特征可识别心力衰竭进展的潜在途径
- 批准号:
10895160 - 财政年份:2023
- 资助金额:
$ 2.18万 - 项目类别:
Piezo2-mediated neuroplasticity in osteoarthritis
Piezo2 介导的骨关节炎神经可塑性
- 批准号:
10752471 - 财政年份:2023
- 资助金额:
$ 2.18万 - 项目类别: