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人单核细胞系U937的Fcγ受体表达及吞噬作用的调节。环磷酸腺苷(cAMP)和蛋白激酶C在γ干扰素(IFN-γ)和佛波酯作用中的参与情况。

Regulation of Fc gamma receptor expression and phagocytosis of a human monoblast cell line U937. Participation of cAMP and protein kinase C in the effects of IFN-gamma and phorbol ester.

作者信息

Nambu M, Morita M, Watanabe H, Uenoyama Y, Kim K M, Tanaka M, Iwai Y, Kimata H, Mayumi M, Mikawa H

机构信息

Department of Pediatrics, Faculty of Medicine, Kyoto University, Japan.

出版信息

J Immunol. 1989 Dec 15;143(12):4158-65.

PMID:2556478
Abstract

We investigated the positive and negative effects of IFN-gamma, PMA, dibutyryl cAMP (Bt2cAMP), dexamethasone and transforming growth factor-beta (TGF-beta) on Fc gamma R subtype expression and phagocytosis of a human monoblast cell line, U937. IFN-gamma increased and Bt2cAMP decreased Fc gamma RI expression determined by a mAb 32.2, whereas PMA and Bt2cAMP increased Fc gamma RII expression determined by a mAb IV-3. Phagocytosis was measured microscopically by counting ingested aggregated human IgG- or BSA-treated ox E (Eo'-IgG or Eo'-BSA). IFN-gamma increased the phagocytosis of Eo'-IgG but not that of Eo'-BSA, and PMA increased the phagocytosis of both Eo'-IgG and Eo'-BSA. Bt2cAMP decreased both basal and IFN-gamma- and PMA-augmented phagocytosis of U937 cells. Dexamethasone also inhibited both basal and IFN-gamma-augmented Fc gamma RI expression and PMA-augmented Fc gamma RII expression and phagocytosis, but did not affect IFN-gamma-augmented phagocytosis of Eo'-IgG. The augmentation of phagocytosis of Eo'-IgG by IFN-gamma thus seems to be due mainly to the increased internalizing process rather than to increased Fc gamma RI expression. TGF-beta slightly decreased Fc gamma R expression. In a study of the participation of protein kinase C (PK-C), it was found that H-7, a PK-C inhibitor, did not inhibit either IFN-gamma- or PMA-enhanced Fc gamma RI and Fc gamma RII expression, respectively, and 1-oleoyl-2-acetylglycerol and N-(6-phenylhexyl)-5-chloro-1-naphthalenesulfonamide, both PK-C activators, did not show any apparent increase in Fc gamma R expression and phagocytosis. These results show that Fc gamma RI and Fc gamma RII expression on U937 cells is regulated by different mechanisms and that IFN-gamma and PMA play their roles in Fc gamma R expression and phagocytosis by different pathways. It is possible that cAMP but not PK-C plays an important role in the regulation of Fc gamma R expression and phagocytosis.

摘要

我们研究了干扰素-γ(IFN-γ)、佛波酯(PMA)、二丁酰环磷腺苷(Bt2cAMP)、地塞米松和转化生长因子-β(TGF-β)对人单核细胞系U937的FcγR亚型表达及吞噬作用的正负效应。通过单克隆抗体32.2测定,IFN-γ使FcγRI表达增加,Bt2cAMP使其降低;而通过单克隆抗体IV-3测定,PMA和Bt2cAMP使FcγRII表达增加。通过显微镜计数摄入的聚集人IgG或牛血清白蛋白处理的氧化型红细胞(Eo'-IgG或Eo'-BSA)来测量吞噬作用。IFN-γ增加了Eo'-IgG的吞噬作用,但未增加Eo'-BSA的吞噬作用;PMA增加了Eo'-IgG和Eo'-BSA两者的吞噬作用。Bt2cAMP降低了U937细胞的基础吞噬作用以及IFN-γ和PMA增强的吞噬作用。地塞米松也抑制基础及IFN-γ增强的FcγRI表达、PMA增强的FcγRII表达和吞噬作用,但不影响IFN-γ增强的Eo'-IgG吞噬作用。因此,IFN-γ增强Eo'-IgG的吞噬作用似乎主要是由于内化过程增加,而非FcγRI表达增加。TGF-β使FcγR表达略有降低。在一项关于蛋白激酶C(PK-C)参与情况的研究中,发现PK-C抑制剂H-7分别不抑制IFN-γ或PMA增强的FcγRI和FcγRII表达,并且PK-C激活剂1-油酰-2-乙酰甘油和N-(6-苯基己基)-5-氯-1-萘磺酰胺均未使FcγR表达和吞噬作用出现明显增加。这些结果表明,U937细胞上的FcγRI和FcγRII表达受不同机制调控,且IFN-γ和PMA通过不同途径在FcγR表达和吞噬作用中发挥作用。cAMP而非PK-C可能在FcγR表达和吞噬作用的调控中起重要作用。

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