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首页> 外文期刊>Cytokine >Interferon-gamma and interleukin 4 inhibit interleukin 1beta-induced delayed prostaglandin E(2)generation through suppression of cyclooxygenase-2 expression in human fibroblasts.
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Interferon-gamma and interleukin 4 inhibit interleukin 1beta-induced delayed prostaglandin E(2)generation through suppression of cyclooxygenase-2 expression in human fibroblasts.

机译:干扰素-γ和白介素4抑制白介素1β诱导的延迟前列腺素E(2)生成通过抑制人类成纤维细胞中环氧合酶2表达。

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摘要

Interleukin (IL-)1 stimulates prostaglandin E(2)(PGE(2)) generation in fibroblasts, and preferential couplings between particular phospholipase A(2)(PLA(2)) and cyclooxygenase (COX) isozymes are implicated with IL-1-induced delayed PGE(2)generation. The regulatory effects of interferon (IFN)-gamma and IL-4 on IL-1beta-induced COX, PLA(2)isoforms expression and terminal delayed PGE(2)generation were examined in three types of human fibroblasts. These human fibroblasts constitutively expressed cytosolic PLA(2)(cPLA(2)) and COX-1 enzymes, and exhibited delayed PGE(2)generation in response to IL-1beta. IL-1beta also stimulated expression of cPLA(2)and COX-2 only, while constitutive and IL-1beta-induced type IIA and type V secretory PLA(2)s (sPLA(2)s) expression could not be detected. A COX-2 inhibitor and cPLA(2)inhibitor markedly suppressed the IL-1beta-induced delayed PGE(2)generation, while a type IIA sPLA(2)inhibitor failed to affect it. IFN-gamma and IL-4 dramatically inhibited the IL-1beta-induced delayed PGE(2)generation; these cytokines apparently suppressed IL-1beta-stimulated COX-2 expression and only weakly suppressed cPLA(2)expression in response to IL-1beta. These results indicate that IL-1beta-induced delayed PGE(2)generation in these human fibroblasts mainly depends on de novo induction of COX-2 and cPLA(2), irrespective of the constitutive presence of COX-1, and that IFN-gamma and IL-4 inhibit IL-1beta-induced delayed PGE(2)generation by suppressing, predominantly, COX-2 expression. Copyright 2000 Academic Press.
机译:白介素(IL-)1刺激成纤维细胞中的前列腺素E(2)(PGE(2))生成,并且特定磷脂酶A(2)(PLA(2))和环氧合酶(COX)同工酶之间的优先偶联与IL-1有关-诱导的延迟PGE(2)生成。在三种类型的人类成纤维细胞中检查了干扰素(IFN)-γ和IL-4对IL-1β诱导的COX,PLA(2)异构体表达和终末延迟PGE(2)生成的调节作用。这些人类成纤维细胞组成性表达胞质PLA(2)(cPLA(2))和COX-1酶,并表现出对IL-1beta的延迟PGE(2)生成。 IL-1beta也仅刺激cPLA(2)和COX-2的表达,而无法检测到组成型和IL-1beta诱导的IIA型和V型分泌PLA(2)s(sPLA(2)s)表达。一个COX-2抑制剂和cPLA(2)抑制剂显着抑制了IL-1beta诱导的延迟PGE(2)生成,而IIA sPLA(2)抑制剂未能对其产生影响。 IFN-γ和IL-4显着抑制IL-1beta诱导的延迟PGE(2)生成;这些细胞因子显然抑制了IL-1beta刺激的COX-2表达,并且仅弱抑制了响应IL-1beta的cPLA(2)表达。这些结果表明,IL-1β诱导的这些人成纤维细胞中延迟的PGE(2)生成主要取决于从头诱导产生COX-2和cPLA(2),而与COX-1的组成性存在无关,并且IFN-γ IL-4和IL-4通过抑制COX-2表达来抑制IL-1beta诱导的PGE(2)延迟生成。版权所有2000学术出版社。

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