Investigating T‐Cell Receptor Dynamics Under <i>In Vitro</i> Antibody‐Based Stimulation Using Imaging Flow Cytometry

T cells play a pivotal role in the immune system's response to various conditions. They are activated by antigen-presenting cells (APCs) via T-cell surface receptors, resulting in cytokine production and T-cell proliferation. These interactions occur through the formation of immunological synapses. The advent of imaging flow cytometry has enabled detailed statistical analyses of these cellular interactions. However, the dynamics of T-cell receptors in response to in vitro stimulation are yet to receive attention, despite it being a crucial aspect of understanding T-cell behavior. In this article, we explore the responses of T cells to in vitro antibody-based stimulation without APCs. Specifically, we established a Th1 cell clone, subjected it to a combination of centrifugation-induced mechanical stress and anti-human CD3 and anti-human CD28 antibody stimulation as the in vitro antibody-based stimulation, and captured and analyzed bright-field and fluorescence images of single cells various hours after stimulation using an imaging flow cytometer. Our results indicate distinct temporal dynamics of CD3 and CD28. Notably, CD3 and CD28 relocated on the T-cell surface immediately after stimulation, with CD3 receptors dispersing after 3.5 h, whereas CD28 remained clustered for 7.5 h. These receptor morphological changes precede cytokine production, suggesting their potential as early indicators of T-cell activation.

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Publication Details

Journal
Cytometry Part A
Published
2025-02-01
DOI
https://doi.org/10.1002/cyto.a.24916
Citations
1
Primary Topic
T-cell and B-cell Immunology
Type
article
Field-Weighted Citation Impact
0.80

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article

Investigating T‐Cell Receptor Dynamics Under In Vitro Antibody‐Based Stimulation Using Imaging Flow Cytometry

Natsumi Tiffany Ishii, Jeffrey Harmon, Keisuke Goda, Yuma Oka et al.
1 citations
Cytometry Part A
T-cell and B-cell Immunology
0.80
article

Investigating T‐Cell Receptor Dynamics Under In Vitro Antibody‐Based Stimulation Using Imaging Flow Cytometry

Natsumi Tiffany Ishii, Jeffrey Harmon, Keisuke Goda, Yuma Oka, Tianben Ding, Tsubasa Wakamiya, Yoshitaka Shirasaki, Mika Hayashi, Ayuko Kishimoto, Kangrui Huang, Dan Yuan, Akihiro Isozaki, Hiroki Matsumura, Masatoshi Yanagida, Maik Herbig, Masaru Ishii, Yuji Okamoto, Mai Yamagishi, Kazuma Kita, Yaqi Zhao, Tsuneji Araki
article en
1 citations

Abstract

T cells play a pivotal role in the immune system's response to various conditions. They are activated by antigen-presenting cells (APCs) via T-cell surface receptors, resulting in cytokine production and T-cell proliferation. These interactions occur through the formation of immunological synapses. The advent of imaging flow cytometry has enabled detailed statistical analyses of these cellular interactions. However, the dynamics of T-cell receptors in response to in vitro stimulation are yet to receive attention, despite it being a crucial aspect of understanding T-cell behavior. In this article, we explore the responses of T cells to in vitro antibody-based stimulation without APCs. Specifically, we established a Th1 cell clone, subjected it to a combination of centrifugation-induced mechanical stress and anti-human CD3 and anti-human CD28 antibody stimulation as the in vitro antibody-based stimulation, and captured and analyzed bright-field and fluorescence images of single cells various hours after stimulation using an imaging flow cytometer. Our results indicate distinct temporal dynamics of CD3 and CD28. Notably, CD3 and CD28 relocated on the T-cell surface immediately after stimulation, with CD3 receptors dispersing after 3.5 h, whereas CD28 remained clustered for 7.5 h. These receptor morphological changes precede cytokine production, suggesting their potential as early indicators of T-cell activation.

Cytometry Part AVol. 107(2)
Ritsumeikan University (JP), University of California, Los Angeles (US), Wuhan University of Technology (CN), CYBO (Japan) (JP), Sysmex (Japan) (JP), The University of Tokyo (JP), The University of Osaka (JP)
Nakatani Foundation for Advancement of Measuring Technologies in Biomedical Engineering, Japan Society for the Promotion of Science, Japan Science and Technology Agency
Openalex Percentile: Top 31%
T-cell and B-cell Immunology
0.80
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