Imaging Spatiotemporal Activities of ZAP-70 in Live T Cells Using a FRET-Based Biosensor

被引:0
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作者
Kaitao Li
Xue Xiang
Jie Sun
Hai-Tao He
Jianhua Wu
Yingxiao Wang
Cheng Zhu
机构
[1] Georgia Institute of Technology,Coulter Department of Biomedical Engineering
[2] SUN YAT-SEN University,School of Life Sciences
[3] University of Illinois,Department of Bioengineering and Beckman Institute for Advanced Science and Technology
[4] Urbana-Champaign,Center for Cell Engineering
[5] Centre d’Immunologie de Marseille-Luminy,School of Bioscience
[6] Aix Marseille Université UM2,Department of Bioengineering
[7] Inserm,undefined
[8] U1104,undefined
[9] CNRS UMR7280,undefined
[10] UnionPay Smart Co.,undefined
[11] Ltd,undefined
[12] Memorial Sloan Kettering Cancer Center,undefined
[13] South China University of Technology,undefined
[14] University of California,undefined
[15] San Diego,undefined
来源
关键词
TCR signaling; Syk family kinase; Immunological synapse; Membrane microdomains;
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学科分类号
摘要
The zeta-chain-associated protein kinase 70 kDa (ZAP-70), a member of the spleen tyrosine kinase (Syk) family, plays an essential role in early T cell receptor (TCR) signaling. Defects in ZAP-70 lead to impaired thymocyte development and peripheral T cell activation. To better understand its activation dynamics and regulation, we visualized ZAP-70 activities in single live T cells with a Förster resonance energy transfer (FRET)‐based biosensor, which was designed for probing kinase activities of the Syk family. We observed in Jurkat E6.1 T cells rapid and specific FRET changes following anti-CD3 stimulation and subsequent piceatannol inhibition. The initiation of ZAP-70 activation was prompt (within 10 s) and correlates with the accompanied intracellular calcium elevation, as revealed by simultaneous imaging of the biosensor and calcium. Different from the previously reported ZAP-70 activation in the immunological synapse and the opposite pole (anti-synapse), we have observed rapid and sustained ZAP-70 activation only at the synapse with superantigen-pulsed Raji B cells. Furthermore, ZAP-70 signaling was impaired by cholesterol depletion, further supporting the importance of membrane organization in TCR signaling. Together our results provide a direct characterization of the spatiotemporal features of ZAP-70 activity in real time at subcellular levels.
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页码:3510 / 3521
页数:11
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