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牛嗜铬细胞中通过细胞内GTPγS介导氯离子电流激活的第二信使。

Second messengers mediating activation of chloride current by intracellular GTP gamma S in bovine chromaffin cells.

作者信息

Doroshenko P

机构信息

Max-Planck-Institut für biophysikalische Chemie, Göttingen, Germany.

出版信息

J Physiol. 1991 May;436:725-38. doi: 10.1113/jphysiol.1991.sp018576.

Abstract
  1. Intracellular mechanisms and second messengers involved in chloride current activation by intracellular GTP gamma S (guanosine 5'-O-(3-thiotriphosphate] in bovine chromaffin cells were studied using the whole-cell patch-clamp technique combined with measurements of intracellular calcium [Ca2+]i. 2. No correlation between the time of current activation and the appearance of [Ca2+]i transients was observed; intracellular introduction of sufficient EGTA (10 mM) to suppress the [Ca2+]i transients did not affect the current activation by GTP gamma S. 3. The cyclic nucleotides, cyclic AMP or cyclic GMP, did not activate the current when introduced intracellularly (50-250 microM). The ability of GTP gamma S to activate the current decreased when cyclic GMP (250 microM), together with MgATP (2 mM), was added to the perfusate. 4. Neomycin (0.5-1 mM), a presumed inhibitor of phospholipase C effectively prevented the current activation by GTP gamma S but it did not prevent [Ca2+]i transients. 5. Modulation of protein kinase C activity using specific inhibitors (H-7, 300 microM; polymyxin B, 400 U/ml) or activators (phorbol ester PMA, 100 nM, 20-90 min at 37 degrees C) did not affect the current activation by GTP gamma S nor did it cause current activation in the absence of GTP gamma S. 6. Activation of the current by GTP gamma S could be prevented by incubating the cells for 10-15 min with 2.5 microM p-bromophenacyl bromide (p-BPB), an inhibitor of phospholipase A2 activity. Exogenous arachidonic acid (5-10 microM), applied extracellularly or intracellularly, neither activated the current itself nor did it interfere with its activation by GTP gamma S. 7. Activation of the current by GTP gamma S could also be prevented by incubating the cells with 1 microM-nordihydroguaiaretic acid (NDGA), an inhibitor of lipoxygenase, but not with indomethacin (2 microM), an inhibitor of cyclo-oxygenase pathway of arachidonic acid metabolism. 8. It is suggested that chloride current activation by GTP gamma S in bovine chromaffin cells involves G protein-mediated stimulation of phospholipase A2 activity and subsequent formation of lipoxygenase product(s) of arachidonic acid metabolism.
摘要
  1. 运用全细胞膜片钳技术并结合细胞内钙离子浓度([Ca2+]i)的测定,研究了牛嗜铬细胞中细胞内机制以及细胞内鸟苷 5'-O-(3-硫代三磷酸)(GTPγS)激活氯离子电流所涉及的第二信使。2. 未观察到电流激活时间与[Ca2+]i 瞬变出现之间的相关性;细胞内引入足够的乙二醇双四乙酸(EGTA,10 mM)以抑制[Ca2+]i 瞬变,并不影响 GTPγS 对电流的激活。3. 细胞内引入环核苷酸、环磷酸腺苷(cAMP)或环磷酸鸟苷(cGMP)(50 - 250 μM)时,不会激活电流。当向灌流液中加入 cGMP(250 μM)和镁三磷酸腺苷(MgATP,2 mM)时,GTPγS 激活电流的能力降低。4. 新霉素(0.5 - 1 mM),一种推测的磷脂酶 C 抑制剂,有效阻止了 GTPγS 对电流的激活,但未阻止[Ca2+]i 瞬变。5. 使用特异性抑制剂(H - 7,300 μM;多粘菌素 B,400 U/ml)或激活剂(佛波酯 PMA,100 nM,37℃下 20 - 90 分钟)调节蛋白激酶 C 活性,既不影响 GTPγS 对电流的激活,在无 GTPγS 时也不会引起电流激活。6. 用 2.5 μM 对溴苯甲酰溴(p - BPB)处理细胞 10 -

15 分钟,p - BPB 是一种磷脂酶 A2 活性抑制剂,可阻止 GTPγS 对电流的激活。细胞外或细胞内施加外源性花生四烯酸(5 - 10 μM),既不会自身激活电流,也不会干扰 GTPγS 对电流的激活。7. 用 1 μM 去甲二氢愈创木酸(NDGA)处理细胞,NDGA 是一种脂氧合酶抑制剂,可阻止 GTPγS 对电流的激活,但用 2 μM 吲哚美辛处理细胞则不能,吲哚美辛是花生四烯酸代谢环氧化酶途径的抑制剂。8. 提示牛嗜铬细胞中 GTPγS 激活氯离子电流涉及 G 蛋白介导的对磷脂酶 A2 活性的刺激以及随后花生四烯酸代谢脂氧合酶产物的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a5/1181531/5fc7ceaf5cd9/jphysiol00446-0718-a.jpg

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