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FAN可刺激肿瘤坏死因子(α)诱导的基因表达、白细胞募集和体液反应。

FAN stimulates TNF(alpha)-induced gene expression, leukocyte recruitment, and humoral response.

作者信息

Montfort Anne, de Badts Bénédicte, Douin-Echinard Victorine, Martin Pascal G P, Iacovoni Jason, Nevoit Caroline, Therville Nicole, Garcia Virginie, Bertrand Marie-Antoinette, Bessières Marie-Hélène, Trombe Marie-Claude, Levade Thierry, Benoist Hervé, Ségui Bruno

机构信息

U858 INSERM, Toulouse, France.

出版信息

J Immunol. 2009 Oct 15;183(8):5369-78. doi: 10.4049/jimmunol.0803384. Epub 2009 Sep 28.

Abstract

Factor associated with neutral sphingomyelinase activation (FAN) is an adaptor protein that constitutively binds to TNF-R1. Microarray analysis was performed in fibroblasts derived from wild-type or FAN knockout mouse embryos to evaluate the role of FAN in TNF-induced gene expression. Approximately 70% of TNF-induced genes exhibited lower expression levels in FAN-deficient than in wild-type fibroblasts. Of particular interest, TNF-induced expression of cytokines/chemokines, such as IL-6 and CXCL-2, was impaired in FAN-deficient cells. This was confirmed by real time RT-PCR and ELISA. Upon i.p. TNF or thioglycollate injection, neutrophil recruitment into the peritoneal cavity was reduced by more than 50% in FAN-deficient mice. Nevertheless, FAN-deficient animals did not exhibit an increased susceptibility to different microorganisms including bacteria and parasites, indicating that FAN is not essential for pathogen clearance. Specific Ab response to BSA was substantially impaired in FAN-deficient mice and this was associated with a reduced content of leukocytes in the spleen of BSA-challenged FAN-deficient mice as compared with their wild-type counterparts. Altogether, our results indicate the involvement of FAN in TNF-induced gene expression and leukocyte recruitment, contributing to the establishment of the specific immune response.

摘要

与中性鞘磷脂酶激活相关的因子(FAN)是一种衔接蛋白,可组成性地与TNF-R1结合。在源自野生型或FAN基因敲除小鼠胚胎的成纤维细胞中进行微阵列分析,以评估FAN在TNF诱导的基因表达中的作用。大约70%的TNF诱导基因在FAN缺陷型成纤维细胞中的表达水平低于野生型。特别值得关注的是,TNF诱导的细胞因子/趋化因子(如IL-6和CXCL-2)的表达在FAN缺陷型细胞中受损。这通过实时RT-PCR和ELISA得到了证实。腹腔注射TNF或巯基乙酸盐后,FAN缺陷型小鼠腹腔内中性粒细胞的募集减少了50%以上。然而,FAN缺陷型动物对包括细菌和寄生虫在内的不同微生物并未表现出易感性增加,这表明FAN对于病原体清除并非必不可少。FAN缺陷型小鼠对BSA的特异性抗体反应明显受损,这与BSA刺激的FAN缺陷型小鼠脾脏中白细胞含量低于野生型小鼠有关。总之,我们的结果表明FAN参与了TNF诱导的基因表达和白细胞募集,有助于特异性免疫反应的建立。

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