A comparison of the performance in vitro of precision cut tissue slices and suspensions of human spleen with special reference to immunoglobulin and cytokine production.

Human antibodies and hybridomas Pub Date : 1996-01-01
K James, G Skibinski, P Hoffman
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Abstract

During the past decade our knowledge of the cellular and molecular events associated with key immunological responses has been greatly advanced by the use of isolated subpopulations of immunocompetent cells, cloned cell lines and recombinant derived cytokines. Valuable as these studies have been they do not truly reflect the complex integrative events which take place in both primary and secondary lymphoid tissue both in vivo and in vitro. In order to address this problem we have developed a tissue culture procedure which is a modification of that previously used by others to study T cell maturation in the thymus. This involves culturing precision cut slices of human lymphoid tissue in a sponge culture system. Using this technique we have observed marked differences in both immunoglobulin and cytokine secretion between slices and suspensions of human spleen. In brief, cultured slices (mitogen stimulated or otherwise) consistently secrete higher levels of immunoglobulin, IL-1 beta, IL-6, IL-8 and IL-11 and exhibit much lower proliferation than suspensions of the same tissue. Mitogen stimulated suspensions on the other hand secrete higher levels of IL-2, IL-4, IL-10 and TNF alpha than do slices. These differences are also observed at the intracellular cytokine level. Additional studies reveal that the immunoglobulin and cytokine secretion observed is largely due to the de novo synthesis of these molecules and not as a result of spontaneous secretion of preformed products. Furthermore immunoglobulin secretion in both slices and suspensions can be inhibited by the addition of specific antibodies to IL-1 beta, IL-6 and TNF alpha while IL-6 production can be differentially modulated by a variety of substances. Preliminary studies indicate that close interaction between B cells and stromal cells within explants accounts for some of the observed differences. This review article describes the basic technique, summarises the results we have obtained in this system and outlines the possible basis of the observed differences.

人脾精切组织切片和脾悬液体外性能的比较,特别参考免疫球蛋白和细胞因子的产生。
在过去的十年中,我们对与关键免疫反应相关的细胞和分子事件的了解已经通过使用分离的免疫活性细胞亚群、克隆细胞系和重组的衍生细胞因子得到了极大的发展。尽管这些研究很有价值,但它们并没有真正反映出体内和体外发生在原发性和继发性淋巴组织中的复杂综合事件。为了解决这个问题,我们开发了一种组织培养程序,这是对其他人先前用于研究胸腺T细胞成熟的方法的修改。这包括在海绵培养系统中培养精确切割的人类淋巴组织切片。使用这种技术,我们观察到免疫球蛋白和细胞因子分泌在人脾切片和悬浮液之间的显著差异。简而言之,培养的切片(有丝分裂原刺激或其他)始终分泌更高水平的免疫球蛋白,IL-1 β, IL-6, IL-8和IL-11,并且表现出比相同组织的悬液低得多的增殖。另一方面,丝裂原刺激悬液比切片分泌更高水平的IL-2、IL-4、IL-10和TNF α。在细胞内细胞因子水平上也观察到这些差异。进一步的研究表明,观察到的免疫球蛋白和细胞因子的分泌主要是由于这些分子的重新合成,而不是由于预先形成的产物的自发分泌。此外,免疫球蛋白在切片和悬浮液中的分泌都可以通过添加针对IL-1 β、IL-6和TNF α的特异性抗体来抑制,而IL-6的产生可以通过多种物质进行差异调节。初步研究表明,外植体内B细胞和基质细胞之间的密切相互作用解释了一些观察到的差异。本文介绍了该系统的基本技术,总结了我们在该系统中获得的结果,并概述了观察到的差异的可能依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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