Functionalized Bead Assay to Measure Three-dimensional Traction Forces during T-cell Activation

被引:30
作者
Aramesh, Morteza [1 ]
Mergenthal, Simon [2 ]
Issler, Marcel [2 ]
Plochberger, Birgit [3 ]
Weber, Florian [3 ]
Qin, Xiao-Hua [4 ]
Liska, Robert [5 ]
Duda, Georg N. [6 ]
Huppa, Johannes B. [7 ]
Ries, Jonas [8 ]
Schuetz, Gerhard J. [9 ]
Klotzsch, Enrico [1 ,2 ]
机构
[1] Swiss Fed Inst Technol, Lab Appl Mechanobiol, Dept Hlth Sci & Technol, CH-8093 Zurich, Switzerland
[2] Humboldt Univ, Inst Biol Expt Biophys Mechanobiol, D-10115 Berlin, Germany
[3] Upper Austria Univ Appl Sci, A-4020 Linz, Austria
[4] Swiss Fed Inst Technol, Dept Hlth Sci & Technol, Inst Biomech, CH-8093 Zurich, Switzerland
[5] TU Wien, Inst Appl Synthet Chem, A-1060 Vienna, Austria
[6] Charite, BIH Ctr Regenerat Therapies, Julius Wolff Inst Biomech & Musculoskeletal Regen, Berlin Inst Hlth, D-13353 Berlin, Germany
[7] Med Univ Vienna, Ctr Pathophysiol Infectiol & Immunol, Inst Hyg & Appl Immunol, A-1090 Vienna, Austria
[8] EMBL Heidelberg, D-69117 Heidelberg, Germany
[9] TU Wien, Inst Appl Phys, A-1040 Vienna, Austria
基金
澳大利亚研究理事会;
关键词
traction force microscopy; T-cell activation; microvilli; actin dynamics; TCR; KINETICS; SUPERRESOLUTION; RECOGNITION; MICROSCOPY; RECEPTOR; CD28; CD3;
D O I
10.1021/acs.nanolett.0c03964
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
When T-cells probe their environment for antigens, the bond between the T-cell receptor (TCR) and the peptide-loaded major histocompatibility complex (MHC) is put under tension, thereby influencing the antigen discrimination. Yet, the quantification of such forces in the context of T-cell signaling is technically challenging. Here, we developed a traction force microscopy platform which allows for quantifying the pulls and pushes exerted via T-cell microvilli, in both tangential and normal directions, during T-cell activation. We immobilized specific T-cell activating antibodies on the marker beads used to read out the hydrogel deformation. Microvilli targeted the functionalized beads, as confirmed by superresolution microscopy of the local actin organization. Moreover, we found that cellular components, such as actin, TCR, and CD45 reorganize upon interaction with the beads, such that actin forms a vortex-like ring structure around the beads and TCR is enriched at the bead surface, whereas CD45 is excluded from bead-microvilli contacts.
引用
收藏
页码:507 / 514
页数:8
相关论文
共 44 条
[1]   Mechanical Modulation of Receptor-Ligand Interactions at Cell-Cell Interfaces [J].
Allard, Jun F. ;
Dushek, Omer ;
Coombs, Daniel ;
van der Merwe, P. Anton .
BIOPHYSICAL JOURNAL, 2012, 102 (06) :1265-1273
[2]   Determination of Interaction Kinetics between the T Cell Receptor and Peptide-Loaded MHC Class II via Single-Molecule Diffusion Measurements [J].
Axmann, Markus ;
Huppa, Johannes B. ;
Davis, Mark M. ;
Schuetz, Gerhard J. .
BIOPHYSICAL JOURNAL, 2012, 103 (02) :L17-L19
[3]   Cross Talk between CD3 and CD28 Is Spatially Modulated by Protein Lateral Mobility [J].
Bashour, Keenan T. ;
Tsai, Jones ;
Shen, Keyue ;
Lee, Joung-Hyun ;
Sun, Eileen ;
Milone, Michael C. ;
Dustin, Michael L. ;
Kam, Lance C. .
MOLECULAR AND CELLULAR BIOLOGY, 2014, 34 (06) :955-964
[4]   CD28 and CD3 have complementary roles in T-cell traction forces [J].
Bashour, Keenan T. ;
Gondarenko, Alexander ;
Chen, Haoqian ;
Shen, Keyue ;
Liu, Xin ;
Huse, Morgan ;
Hone, James C. ;
Kam, Lance C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (06) :2241-2246
[5]   How T Cells Do the "Search for the Needle in the Haystack" [J].
Baumgart, Florian ;
Schneider, Magdalena ;
Schuetz, Gerhard J. .
FRONTIERS IN PHYSICS, 2019, 7 (FEB)
[6]   Visualizing dynamic microvillar search and stabilization during ligand detection by T cells [J].
Cai, En ;
Marchuk, Kyle ;
Beemiller, Peter ;
Beppler, Casey ;
Rubashkin, Matthew G. ;
Weaver, Valerie M. ;
Gerard, Audrey ;
Liu, Tsung-Li ;
Chen, Bi-Chang ;
Betzig, Eric ;
Bartumeus, Frederic ;
Krummel, Matthew F. .
SCIENCE, 2017, 356 (6338)
[7]   Full control of ligand positioning reveals spatial thresholds for T cell receptor triggering [J].
Cai, Haogang ;
Muller, James ;
Depoil, David ;
Mayya, Viveka ;
Sheetz, Michael P. ;
Dustin, Michael L. ;
Wind, Shalom J. .
NATURE NANOTECHNOLOGY, 2018, 13 (07) :610-+
[8]   A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo [J].
Chu, Jun ;
Oh, Younghee ;
Sens, Alex ;
Ataie, Niloufar ;
Dana, Hod ;
Macklin, John J. ;
Laviv, Tal ;
Welf, Erik S. ;
Dean, Kevin M. ;
Zhang, Feijie ;
Kim, Benjamin B. ;
Tang, Clement Tran ;
Hu, Michelle ;
Baird, Michelle A. ;
Davidson, Michael W. ;
Kay, Mark A. ;
Fiolka, Reto ;
Yasuda, Ryohei ;
Kim, Douglas S. ;
Ng, Ho-Leung ;
Lin, Michael Z. .
NATURE BIOTECHNOLOGY, 2016, 34 (07) :760-+
[9]   Cytoskeletal Control of Antigen-Dependent T Cell Activation [J].
Colin-York, Huw ;
Javanmardi, Yousef ;
Skamrahl, Mark ;
Kumari, Sudha ;
Chang, Veronica T. ;
Khuon, Satya ;
Taylor, Aaron ;
Chew, Teng-Leong ;
Betzig, Eric ;
Moeendarbary, Emad ;
Cerundolo, Vincenzo ;
Eggeling, Christian ;
Fritzsche, Marco .
CELL REPORTS, 2019, 26 (12) :3369-+
[10]  
Dey A, 2014, NANOINDENTATION OF BRITTLE SOLIDS, P1, DOI 10.1201/b17110