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B细胞成熟与分化的调控。I. 肿瘤坏死因子(TNF)对商陆丝裂原诱导的B细胞分化的抑制作用。

Regulation of B cell maturation and differentiation. I. Suppression of pokeweed mitogen-induced B cell differentiation by tumor necrosis factor (TNF).

作者信息

Kashiwa H, Wright S C, Bonavida B

出版信息

J Immunol. 1987 Mar 1;138(5):1383-90.

PMID:2949015
Abstract

Growth and differentiation of B cells into Ig-secreting plasma cells is regulated by both T cells and macrophages and/or their secreted factors. Although the regulatory role of various cell-derived factors has been examined, the involvement of the macrophage-derived factor, TNF, in human B cell growth and differentiation has not yet been investigated. In the present study we examine the role of rTNF in polyclonal B cell response of human PBL induced by PWM. The addition of rTNF at the initiation of the culture resulted in the dose-dependent inhibition of the generation of both IgG and IgM PFC. Inhibition of PFC development followed the same dose response as rTNF-mediated cytotoxicity against a TNF-sensitive tumor target. The mechanism of rTNF-mediated suppression was examined in different experimental systems. Recombinant TNF did not affect the viability or proliferation of either the T cell or B cell subpopulations, suggesting that TNF does not mediate its suppressive effect by cytotoxic mechanisms. Kinetic studies in which rTNF was added at different times after initiation of culture indicated that inhibition can be observed as late as 4 days of culture and suggested that TNF acts at a late phase of the growth and differentiation pathway of B cells. In further studies we examined the cellular level of TNF-mediated suppression. The addition of rTNF to supernatants containing helper factors and enriched B cells resulted in no inhibition, suggesting that TNF does not act at the B cell level. This was confirmed by demonstrating that rTNF does not inhibit spontaneous PFC development by the CESS B cell line. The effect of TNF on T cell subpopulations was examined by using normal or irradiated T cells, which inactivate suppressor cells. Addition of rTNF to B cells combined with either T cell population suppressed both IgG and IgM PFC development, indicating that the target cell for suppression is the T helper cell but not ruling out an effect on macrophages or the T suppressor cells. Combined, the observed results demonstrate that rTNF suppresses PWM-induced B cell differentiation without affecting B cell proliferation. TNF appears to mediate the suppression by acting directly on T helper cells or else by regulating the production of factors controlling T cell activation and lymphokine secretion.

摘要

B细胞生长并分化为分泌免疫球蛋白(Ig)的浆细胞,这一过程受T细胞和巨噬细胞及(或)它们所分泌因子的调控。尽管已经对各种细胞衍生因子的调节作用进行了研究,但巨噬细胞衍生因子肿瘤坏死因子(TNF)在人B细胞生长和分化中的作用尚未得到研究。在本研究中,我们检测了重组TNF(rTNF)在由美洲商陆有丝分裂原(PWM)诱导的人外周血淋巴细胞(PBL)多克隆B细胞反应中的作用。在培养开始时加入rTNF导致IgG和IgM空斑形成细胞(PFC)生成呈剂量依赖性抑制。PFC发育的抑制遵循与rTNF介导的对TNF敏感肿瘤靶标的细胞毒性相同的剂量反应。在不同的实验系统中检测了rTNF介导的抑制机制。重组TNF不影响T细胞或B细胞亚群的活力或增殖,这表明TNF不是通过细胞毒性机制介导其抑制作用的。在培养开始后不同时间加入rTNF的动力学研究表明,培养4天时仍可观察到抑制作用,这表明TNF作用于B细胞生长和分化途径的晚期。在进一步的研究中,我们检测了TNF介导抑制作用的细胞水平。向含有辅助因子和富集B细胞的上清液中加入rTNF未导致抑制作用,这表明TNF不在B细胞水平发挥作用。通过证明rTNF不抑制CESS B细胞系的自发PFC发育,这一点得到了证实。通过使用正常或经辐照的T细胞(可使抑制细胞失活)检测了TNF对T细胞亚群的作用。将rTNF加入与任一T细胞群体组合的B细胞中,均抑制了IgG和IgM PFC的发育,这表明抑制作用的靶细胞是辅助性T细胞,但不排除对巨噬细胞或抑制性T细胞有影响。综合来看,观察到的结果表明rTNF抑制PWM诱导的B细胞分化而不影响B细胞增殖。TNF似乎通过直接作用于辅助性T细胞或通过调节控制T细胞活化和淋巴因子分泌的因子的产生来介导抑制作用。

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