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T 淋巴细胞与激活表面的早期接触。

Early contacts between T lymphocytes and activating surfaces.

机构信息

INSERM UMR 600, Laboratory Adhesion and Inflammation, Parc Scientifique de Luminy, Marseille, France.

出版信息

J Phys Condens Matter. 2010 May 19;22(19):194107. doi: 10.1088/0953-8984/22/19/194107. Epub 2010 Apr 26.

Abstract

Cells continually probe their environment to adapt their behaviour. A current challenge is to determine how they analyse nearby surfaces and how they process information to take decisions. We addressed this problem by monitoring human T lymphocyte attachment to surfaces coated with activating anti-CD3 or control anti-HLA antibodies. Interference reflection microscopy allowed us to monitor cell-to-surface apposition with a few nanometre vertical resolution during the first minutes following contact. We found that (i) when a cell fell on a surface, contact extension was preceded by a lag of several tens of seconds. (ii) During this lag, vertical membrane undulations seemed to generate transient contacts with underlying surfaces. (iii) After the lag period, the contact area started increasing linearly with a rate of about 1.5 µm(2) s(-1) on activating surfaces and about 0.2 µm(2) s(-1) on control surfaces. (iv) Concomitantly with lateral surface extension, the apparent distance between cell membranes and surfaces steadily decreased. These results are consistent with the hypothesis that the cell decision to spread rapidly on activating surfaces resulted from the integration of information yielded by transient contacts with these surfaces generated by membrane undulations during a period of about 1 min.

摘要

细胞不断探测其环境以适应其行为。目前的一个挑战是确定它们如何分析附近的表面以及它们如何处理信息以做出决策。我们通过监测人类 T 淋巴细胞附着在涂有激活型抗 CD3 或对照型抗 HLA 抗体的表面上来解决这个问题。干涉反射显微镜使我们能够在接触后的最初几分钟内以几纳米的垂直分辨率监测细胞与表面的贴合。我们发现:(i) 当一个细胞落在表面上时,接触延伸之前会有几十秒的延迟。(ii) 在这段延迟期间,垂直膜波动似乎会与下面的表面产生短暂的接触。(iii) 延迟期结束后,接触面积开始在线性增加,激活表面上的速率约为 1.5 µm(2) s(-1),对照表面上的速率约为 0.2 µm(2) s(-1)。(iv) 随着横向表面扩展,细胞膜和表面之间的表观距离稳步减小。这些结果与以下假设一致:细胞决定在激活表面上快速扩展是由于在大约 1 分钟的时间内,通过膜波动与这些表面产生的短暂接触所产生的信息的整合。

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