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Fas诱导的肺泡上皮细胞凋亡需要血管紧张素II的生成及受体相互作用。

Fas-induced apoptosis of alveolar epithelial cells requires ANG II generation and receptor interaction.

作者信息

Wang R, Zagariya A, Ang E, Ibarra-Sunga O, Uhal B D

机构信息

The Cardiovascular Institute, Michael Reese Hospital and Medical Center, Chicago, Illinois 60616, USA.

出版信息

Am J Physiol. 1999 Dec;277(6):L1245-50. doi: 10.1152/ajplung.1999.277.6.L1245.

Abstract

Recent works from this laboratory demonstrated potent inhibition of Fas-induced apoptosis in alveolar epithelial cells (AECs) by the angiotensin-converting enzyme (ACE) inhibitor captopril [B. D. Uhal, C. Gidea, R. Bargout, A. Bifero, O. Ibarra-Sunga, M. Papp, K. Flynn, and G. Filippatos. Am. J. Physiol. 275 (Lung Cell. Mol. Physiol. 19): L1013-L1017, 1998] and induction of dose-dependent apoptosis in AECs by purified angiotensin (ANG) II [R. Wang, A. Zagariya, O. Ibarra-Sunga, C. Gidea, E. Ang, S. Deshmukh, G. Chaudhary, J. Baraboutis, G. Filippatos and B. D. Uhal. Am. J. Physiol. 276 (Lung Cell. Mol. Physiol. 20): L885-L889, 1999]. These findings led us to hypothesize that the synthesis and binding of ANG II to its receptor might be involved in the induction of AEC apoptosis by Fas. Apoptosis was induced in the AEC-derived human lung carcinoma cell line A549 or in primary AECs isolated from adult rats with receptor-activating anti-Fas antibodies or purified recombinant Fas ligand, respectively. Apoptosis in response to either Fas activator was inhibited in a dose-dependent manner by the nonthiol ACE inhibitor lisinopril or the nonselective ANG II receptor antagonist saralasin, with maximal inhibitions of 82 and 93% at doses of 0.5 and 5 microg/ml, respectively. In both cell types, activation of Fas caused a significant increase in the abundance of mRNA for angiotensinogen (ANGEN) that was unaffected by saralasin. Transfection with antisense oligonucleotides against ANGEN mRNA inhibited the subsequent induction of Fas-stimulated apoptosis by 70% in A549 cells and 87% in primary AECs (both P < 0.01). Activation of Fas increased the concentration of ANG II in the serum-free extracellular medium 3-fold in primary AECs and 10-fold in A549 cells. Apoptosis in response to either Fas activator was completely abrogated by neutralizing antibodies specific for ANG II (P < 0.01), but isotype-matched nonimmune immunoglobulins had no significant effect. These data indicate that the induction of AEC apoptosis by Fas requires a functional renin-angiotensin system in the target cell. They also suggest that therapeutic control of AEC apoptosis is feasible through pharmacological manipulation of the local renin-angiotensin system.

摘要

该实验室近期的研究表明,血管紧张素转换酶(ACE)抑制剂卡托普利可有效抑制Fas诱导的肺泡上皮细胞(AECs)凋亡[B.D. 乌哈尔、C. 吉迪亚、R. 巴尔古特、A. 比费罗、O. 伊瓦拉 - 桑加、M. 帕普、K. 弗林和G. 菲利帕托斯。《美国生理学杂志》275卷(肺细胞与分子生理学19):L1013 - L1017,1998年],而纯化的血管紧张素(ANG)II可诱导AECs发生剂量依赖性凋亡[R. 王、A. 扎加里亚、O. 伊瓦拉 - 桑加、C. 吉迪亚、E. 安、S. 德什穆克、G. 乔杜里、J. 巴拉博蒂斯、G. 菲利帕托斯和B.D. 乌哈尔。《美国生理学杂志》276卷(肺细胞与分子生理学20):L885 - L889,1999年]。这些发现使我们推测,ANG II的合成及其与受体的结合可能参与了Fas诱导的AEC凋亡过程。分别用受体激活型抗Fas抗体或纯化的重组Fas配体诱导源自AECs的人肺癌细胞系A549或从成年大鼠分离的原代AECs发生凋亡。非巯基ACE抑制剂赖诺普利或非选择性ANG II受体拮抗剂沙拉新可剂量依赖性地抑制对任一Fas激活剂产生的凋亡反应,在剂量分别为0.5和5微克/毫升时,最大抑制率分别为82%和93%。在这两种细胞类型中,Fas激活均导致血管紧张素原(ANGEN)mRNA丰度显著增加,而沙拉新对此无影响。用针对ANGEN mRNA的反义寡核苷酸转染可使A549细胞中Fas刺激诱导的后续凋亡减少70%,在原代AECs中减少87%(两者P < 0.01)。Fas激活使原代AECs无血清细胞外培养基中ANG II浓度增加3倍,在A549细胞中增加10倍。针对ANG II的中和抗体可完全消除对任一Fas激活剂产生的凋亡反应(P < 0.01),但同型匹配的非免疫球蛋白无显著影响。这些数据表明,Fas诱导AEC凋亡需要靶细胞中功能性肾素 - 血管紧张素系统。它们还提示,通过对局部肾素 - 血管紧张素系统进行药理学调控来治疗性控制AEC凋亡是可行的。

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