Activation and proliferation of lymphocytes and other mammalian cells in microgravity.

A Cogoli, M Cogoli-Greuter
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引用次数: 111

Abstract

The experimental findings reviewed in this chapter support the following conclusions: Proliferation. Human T-lymphocytes, associated with monocytes as accessory cells, show dramatic changes in the centrifuge, in the clinostat and in space. In free-floating cells the mitogenic response is depressed by 90% in microgravity, whereas in cells attached to a substratum activation is enhanced by 100% compared to 1-G ground and inflight controls. The duration of phase G1 of the mitotic cycle of HeLa cells is reduced in hypergravity, resulting in an increased proliferation rate. Other systems like Friend cells and WI38 human embryonic lung cells do not show significant changes. Genetic expression and signal transduction. T-lymphocytes and monocytes show important changes in the expression of cytokines like interleukin-1, interleukin-2, interferon-gamma and tumor necrosis factor. The data from space experiments in Spacelab, Space Shuttle mid-deck, and Biokosmos have helped to clarify certain aspects of the mechanism of T-cell activation. Epidermoid A431 cells show changes in the genetic expression of the proto-oncogenes c-fos and c-jun in the clinostat and in sounding rockets. Membrane function, in particular the binding of ligates as first messengers of a signal, is not changed in most of the cell systems in microgravity. Morphology and Mortility. Free cells, lymphocytes in particular, are able to move and form aggregates in microgravity, indicating that cell-cell contacts and cell communications do take place in microgravity. Dramatic morphological and ultrastructural changes are not detected in cells cultured in microgravity. Important experiments with single mammalian cells, including immune cells, were carried out recently in three Spacelab flights, (SL-J, D-2, and IML-2 in 1992, 1993, and 1994, respectively). The results of the D-2 mission have been published in ref. 75; those of the IML-2 mission in ref. 76. Finally, many cell biology experiments in space have suffered in the past from a lack of adequate controls (like 1-G centrifuges) and of proper experimental conditions (like well-controlled temperature). In this respect the availability of Biorack, outfitted with proper incubators with 1-G control centrifuge as well as a glovebox with a microscope, is a great advantage. It is also desirable that cell biology experiments in space are accompanied or even preceded by a program of ground-based investigations in the fast rotating clinostat and in the centrifuge, and that preparatory experiments be done in parabolic flights and sounding rockets, whenever possible. Proper publication of the results of space experiments is another important need. A great number of data have been published in proceedings and reports that are not available to the broad scientific community. To guarantee the credibility and the international recognition of space biology it is important that the results be published in international, peer reviewed journals.

淋巴细胞和其他哺乳动物细胞在微重力下的活化和增殖。
本章回顾的实验结果支持以下结论:人类t淋巴细胞与单核细胞为辅,在离心机、恒温器和空间中表现出巨大的变化。在自由漂浮的细胞中,有丝分裂反应在微重力下被抑制了90%,而在附着于基质的细胞中,与1-G地面和飞行控制相比,有丝分裂反应被增强了100%。在超重力环境下,HeLa细胞有丝分裂周期G1期持续时间缩短,导致增殖速率增加。其他系统如Friend细胞和WI38人胚胎肺细胞没有明显变化。基因表达和信号转导。t淋巴细胞和单核细胞在白细胞介素-1、白细胞介素-2、干扰素- γ和肿瘤坏死因子等细胞因子的表达方面发生重要变化。来自太空实验室、航天飞机中层甲板和生物宇宙的空间实验数据有助于阐明t细胞活化机制的某些方面。表皮样A431细胞中原癌基因c-fos和c-jun的基因表达在旋转器和探空火箭中发生变化。在微重力条件下,大多数细胞系统的膜功能,特别是作为信号第一信使的结扎体的结合,并没有改变。形态学和死亡率。游离细胞,特别是淋巴细胞,能够在微重力下移动并形成聚集体,这表明细胞间接触和细胞通讯确实发生在微重力下。在微重力环境下培养的细胞未见明显的形态和超微结构变化。最近在三次空间实验室飞行(分别于1992年、1993年和1994年进行SL-J、D-2和IML-2)中对包括免疫细胞在内的单个哺乳动物细胞进行了重要实验。D-2任务的结果已发表在参考文献75;参考文献76中的IML-2任务。最后,由于缺乏足够的控制(如1-G离心机)和适当的实验条件(如控制良好的温度),过去在太空进行的许多细胞生物学实验都受到了影响。在这方面,Biorack的可用性是一个很大的优势,配备了适当的孵化器和1-G控制离心机以及一个带显微镜的手套箱。在太空中进行细胞生物学实验时,最好在快速旋转的陀螺和离心机中进行地面研究,并尽可能在抛物线飞行和探空火箭中进行预备实验。适当公布空间实验的结果是另一个重要的需要。在会议记录和报告中发表的大量数据是广大科学界无法获得的。为了保证空间生物学的可信性和国际认可,重要的是将结果发表在国际同行评议的期刊上。
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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