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低氯刺激小鼠致密斑细胞系中前列腺素E2释放及环氧化酶-2表达

Low chloride stimulation of prostaglandin E2 release and cyclooxygenase-2 expression in a mouse macula densa cell line.

作者信息

Yang T, Park J M, Arend L, Huang Y, Topaloglu R, Pasumarthy A, Praetorius H, Spring K, Briggs J P, Schnermann J

机构信息

NIDDK and NHLBI, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

J Biol Chem. 2000 Dec 1;275(48):37922-9. doi: 10.1074/jbc.M006218200.

Abstract

Reducing luminal NaCl concentration in the macula densa region of the nephron stimulates renin secretion, and this response is blocked by a specific inhibitor of cyclooxygenase-2 (COX-2) (Traynor, T. R., Smart, A., Briggs, J. P., and Schnermann, J. (1999) Am. J. Physiol. Renal Physiol. 277, F706-710). To study whether low NaCl activates COX-2 activity or expression we clonally derived a macula densa cell line (MMDD1 cells) from SV-40 transgenic mice using fluorescence-activated cell sorting of renal tubular cells labeled with segment-specific fluorescent lectins. MMDD1 cells express COX-2, bNOS, NKCC2, and ROMK, but not Tamm-Horsfall protein, and showed rapid (86)Rb(+) uptake that was inhibited by a reduction in NaCl concentration and by bumetanide or furosemide. Isosmotic exposure of MMDD1 cells to low NaCl (60 mm) caused a prompt and time-dependent stimulation of prostaglandin E(2) (PGE(2)) release that was prevented by the COX-2 specific inhibitor NS-398 (10 microm). Reducing NaCl to 60 and 6 mm for 16 h increased COX-2 expression in a chloride-dependent fashion. Low NaCl phosphorylated p38 kinase within 30 min and ERK1/2 kinases within 15 min without changing total MAP kinase levels. Low NaCl-stimulated PGE(2) release and COX-2 expression was inhibited by SB 203580 and PD 98059 (10 microm), inhibitors of p38 and ERK kinase pathways. We conclude that low chloride stimulates PGE(2) release and COX-2 expression in MMDD1 cells through activation of MAP kinases.

摘要

降低肾单位致密斑区域的管腔氯化钠浓度可刺激肾素分泌,而这种反应可被环氧化酶-2(COX-2)的特异性抑制剂阻断(特雷纳,T.R.,斯马特,A.,布里格斯,J.P.,和施内曼,J.(1999年)《美国生理学杂志:肾脏生理学》277卷,F706 - 710页)。为了研究低氯化钠是否激活COX-2活性或表达,我们使用经节段特异性荧光凝集素标记的肾小管细胞进行荧光激活细胞分选,从SV - 40转基因小鼠中克隆得到了一种致密斑细胞系(MMDD1细胞)。MMDD1细胞表达COX-2、bNOS、NKCC2和ROMK,但不表达Tamm - Horsfall蛋白,并且表现出快速的(86)Rb(+)摄取,这种摄取可被氯化钠浓度降低以及布美他尼或呋塞米抑制。MMDD1细胞等渗暴露于低氯化钠(60 mM)会导致前列腺素E2(PGE2)释放迅速且呈时间依赖性增加,而COX-2特异性抑制剂NS - 398(10 μM)可阻止这种增加。将氯化钠浓度分别降至60 mM和6 mM持续16小时,会以氯离子依赖的方式增加COX-2表达。低氯化钠在30分钟内使p38激酶磷酸化,在15分钟内使ERK1/2激酶磷酸化,而总丝裂原活化蛋白激酶水平不变。低氯化钠刺激的PGE2释放和COX-2表达被p38和ERK激酶途径的抑制剂SB 203580和PD 98059(10 μM)抑制。我们得出结论,低氯离子通过激活丝裂原活化蛋白激酶刺激MMDD1细胞中PGE2释放和COX-2表达。

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