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人类单核细胞亚群在促进B细胞集落形成中的异质性及白细胞介素1的作用

Heterogeneity of human monocyte subsets in the promotion of B cell colonies and the role of interleukin 1.

作者信息

Whisler R L, Newhouse Y G, Lachman L B

出版信息

J Immunol. 1982 Aug;129(2):455-60.

PMID:6806370
Abstract

The abilities of human peripheral blood mononuclear-phagocyte (M phi) subpopulations and of interleukin 1 (IL 1) to support human B cell colony formation in semisolid cultures stimulated by staph protein A were analyzed. Human M phi subsets enriched for complement receptors (CR) effectively functioned as accessory cells supporting colony growth, whereas the responses obtained with CR-depleted M phi were 4.6-fold less. In experiments analyzing IL 1 production, CR-enriched M phi secreted four to 12 fold greater amounts of basal and stimulated IL 1 than CR-depleted M phi. Also, the addition of IL 1 to CR-depleted M phi resulted in a fourfold increase of colony numbers. The responses of cultures containing CR-depleted M phi plus IL 1, however, remained 30% less than those observed for cultures supplemented with CR-enriched M phi. Other studies showed that IL 1 was unable to substitute for M phi; the responses of cultures containing IL 1 and B cells were reduced 10-fold compared to cultures supplemented with autologous M phi. These findings indicate that human M phi subsets exist that differ in their ability to function as accessory cells. Although IL 1 can collaborate with certain M phi subsets to restore their accessory cell function, it cannot replace intact M phi. Thus, it is possible that other monokines or lymphokines play a role in M phi accessory cell function.

摘要

分析了人类外周血单核吞噬细胞(M phi)亚群以及白细胞介素1(IL 1)在葡萄球菌蛋白A刺激的半固体培养物中支持人类B细胞集落形成的能力。富含补体受体(CR)的人类M phi亚群有效地发挥辅助细胞的作用,支持集落生长,而用去除CR的M phi获得的反应则减少了4.6倍。在分析IL 1产生的实验中,富含CR的M phi分泌的基础和刺激的IL 1量比去除CR的M phi多4至12倍。此外,向去除CR的M phi中添加IL 1导致集落数量增加四倍。然而,含有去除CR的M phi加IL 1的培养物的反应仍比补充富含CR的M phi的培养物观察到的反应少30%。其他研究表明,IL 1不能替代M phi;与补充自体M phi的培养物相比,含有IL 1和B细胞的培养物的反应降低了10倍。这些发现表明,存在功能作为辅助细胞的能力不同的人类M phi亚群。虽然IL 1可以与某些M phi亚群协作以恢复其辅助细胞功能,但它不能替代完整的M phi。因此,其他单核因子或淋巴细胞因子可能在M phi辅助细胞功能中起作用。

相似文献

1
Heterogeneity of human monocyte subsets in the promotion of B cell colonies and the role of interleukin 1.人类单核细胞亚群在促进B细胞集落形成中的异质性及白细胞介素1的作用
J Immunol. 1982 Aug;129(2):455-60.
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引用本文的文献

1
Quantification of interleukin-1 in nasal polyps from patients with chronic sinusitis.慢性鼻窦炎患者鼻息肉中白细胞介素-1的定量分析。
Eur Arch Otorhinolaryngol. 1993;250(2):123-5. doi: 10.1007/BF00179312.
2
Long-term growth of human B cells and their use in a microassay for B-cell growth factor.人B细胞的长期生长及其在B细胞生长因子微量测定中的应用。
Proc Natl Acad Sci U S A. 1983 Aug;80(16):5047-51. doi: 10.1073/pnas.80.16.5047.
3
The role of complement in the induction and regulation of immune responses.补体在免疫反应的诱导和调节中的作用。
Immunology. 1984 Feb;51(2):207-24.
4
Normal human alveolar macrophages obtained by bronchoalveolar lavage have a limited capacity to release interleukin-1.通过支气管肺泡灌洗获得的正常人肺泡巨噬细胞释放白细胞介素-1的能力有限。
J Clin Invest. 1984 Dec;74(6):2208-18. doi: 10.1172/JCI111647.
5
Characterization of a human blood monocyte subset with low peroxidase activity.具有低过氧化物酶活性的人血单核细胞亚群的特征分析。
J Clin Invest. 1983 Sep;72(3):1093-105. doi: 10.1172/JCI111034.
6
Ia antigen expression and IL-1 activity in murine tumour-associated macrophages.小鼠肿瘤相关巨噬细胞中的Ia抗原表达及白细胞介素-1活性
Immunology. 1986 Dec;59(4):527-33.
7
Comparison of human monocytes isolated by elutriation and adherence suggests that heterogeneity may reflect a continuum of maturation/activation states.通过淘析法和贴壁法分离的人单核细胞的比较表明,异质性可能反映了成熟/激活状态的连续统一体。
Immunology. 1988 Mar;63(3):491-8.
8
Receptors for the third component of complement: their association with maturation stage in non-Hodgkin lymphomas (NHL) and their possible implication with the development of follicular structures.补体第三成分的受体:它们与非霍奇金淋巴瘤(NHL)成熟阶段的关联及其与滤泡结构形成的可能关系。
Clin Exp Immunol. 1986 May;64(2):423-31.
9
Interleukin-2 and interferon-gamma recruit different subsets of human peripheral blood monocytes to secrete interleukin-1 beta and tumour necrosis factor-alpha.白细胞介素-2和干扰素-γ募集人外周血单核细胞的不同亚群以分泌白细胞介素-1β和肿瘤坏死因子-α。
Clin Exp Immunol. 1989 Jul;77(1):97-100.