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细胞在抛物线飞行中的交替重力下的流动和免疫细胞的启动。

Cells´ Flow and Immune Cell Priming under alternating g-forces in Parabolic Flight.

机构信息

Laboratory of Translational Research "Stress and Immunity", Department of Anaesthesiology, University Hospital, LMU Munich, Munich, Germany.

Key Laboratory of Microgravity (National Microgravity Laboratory), Center of Biomechanics and Bioengineering, and Beijing Key Laboratory of Engineered Construction and Mechanobiology, Institute of Mechanics, Chinese Academy of Sciences, Beijing, 100190, China.

出版信息

Sci Rep. 2019 Aug 2;9(1):11276. doi: 10.1038/s41598-019-47655-x.

DOI:10.1038/s41598-019-47655-x
PMID:31375732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6677797/
Abstract

Gravitational stress in general and microgravity (µg) in particular are regarded as major stress factors responsible for immune system dysfunction in space. To assess the effects of alternating µg and hypergravity (hyper-g) on immune cells, the attachment of peripheral blood mononuclear cells (PBMCs) to adhesion molecules under flow conditions and the antigen-induced immune activation in whole blood were investigated in parabolic flight (PF). In contrast to hyper-g (1.8 g) and control conditions (1 g), flow and rolling speed of PBMCs were moderately accelerated during µg-periods which were accompanied by a clear reduction in rolling rate. Whole blood analyses revealed a "primed" state of monocytes after PF with potentiated antigen-induced pro-inflammatory cytokine responses. At the same time, concentrations of anti-inflammatory cytokines were increased and monocytes displayed a surface molecule pattern that indicated immunosuppression. The results suggest an immunologic counterbalance to avoid disproportionate immune responses. Understanding the interrelation of immune system impairing and enhancing effects under different gravitational conditions may support the design of countermeasures to mitigate immune deficiencies in space.

摘要

重力应激,特别是微重力(µg),被认为是导致空间免疫系统功能障碍的主要应激因素。为了评估交替µg 和超重力(hyper-g)对免疫细胞的影响,在抛物线飞行(PF)中研究了外周血单核细胞(PBMCs)在流动条件下与粘附分子的附着和全血中的抗原诱导免疫激活。与 hyper-g(1.8g)和对照条件(1g)相比,µg 期间 PBMCs 的流动和滚动速度被适度加速,同时滚动速度明显降低。全血分析显示,PF 后单核细胞处于“启动”状态,抗原诱导的促炎细胞因子反应增强。与此同时,抗炎细胞因子的浓度增加,单核细胞显示出表明免疫抑制的表面分子模式。结果表明存在免疫平衡以避免不成比例的免疫反应。了解不同重力条件下免疫系统损伤和增强效应的相互关系,可能有助于设计减轻太空免疫缺陷的对策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/a23601c87729/41598_2019_47655_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/63b5bc966086/41598_2019_47655_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/7da2a306b3dc/41598_2019_47655_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/b1ad11aa1f65/41598_2019_47655_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/1cb6e9eae93a/41598_2019_47655_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/2e904837fbc1/41598_2019_47655_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/a23601c87729/41598_2019_47655_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/63b5bc966086/41598_2019_47655_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/7da2a306b3dc/41598_2019_47655_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/b1ad11aa1f65/41598_2019_47655_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/1cb6e9eae93a/41598_2019_47655_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/2e904837fbc1/41598_2019_47655_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0e4/6677797/a23601c87729/41598_2019_47655_Fig6_HTML.jpg

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