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与人类单核细胞体外发育为活化巨噬细胞相关的功能和表型变化。

Functional and phenotypic changes associated with the in vitro development of human monocytes into activated macrophages.

作者信息

Cottrell B, Jones D

机构信息

University Department of Pathology, Southampton General Hospital, U.K.

出版信息

FEMS Microbiol Immunol. 1990 Dec;2(5-6):333-7. doi: 10.1111/j.1574-6968.1990.tb03537.x.

Abstract

Freshly isolated human peripheral blood monocytes had minimal cytotoxic effect in vitro on the schistosomula of Schistosoma mansoni. However, stimulation of the cells with either interferon gamma (IFN) or specific anti-parasite antiserum caused an increase in cytotoxicity. Additionally, the normal development of monocytes into macrophages over 7 days was associated with a sharp increase in cytotoxicity. The non-cytotoxic monocytes were compared with activated macrophages to assess whether cytotoxicity was associated with changes in immunophenotype. As monocytes developed into macrophages there were marked increases in transferrin receptors (HB21), macrophage cellular integrin (3.9), and Fc receptors (KB61). A further three markers showed increased expression in 7-day-old macrophages stimulated by IFN, namely a high affinity Fc gamma receptor (10.1), MHC Class II (1B5) and tumour necrosis factor (TNF).

摘要

新鲜分离的人外周血单核细胞在体外对曼氏血吸虫的童虫细胞毒性作用极小。然而,用γ干扰素(IFN)或特异性抗寄生虫抗血清刺激这些细胞会导致细胞毒性增加。此外,单核细胞在7天内正常发育为巨噬细胞与细胞毒性的急剧增加有关。将无细胞毒性的单核细胞与活化的巨噬细胞进行比较,以评估细胞毒性是否与免疫表型的变化有关。随着单核细胞发育为巨噬细胞,转铁蛋白受体(HB21)、巨噬细胞细胞整合素(3.9)和Fc受体(KB61)显著增加。另外三个标志物在经IFN刺激的7日龄巨噬细胞中表达增加,即高亲和力Fcγ受体(10.1)、MHCⅡ类分子(1B5)和肿瘤坏死因子(TNF)。

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