TY - JOUR
T1 - A comprehensive guide to study the immunological synapse using imaging flow cytometry
AU - Biolato, Andrea Michela
AU - Filali, Liza
AU - Krecke, Max
AU - Thomas, Clément
AU - Hoffmann, Céline
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2025/2/5
Y1 - 2025/2/5
N2 - Cytotoxic lymphocytes, such as cytotoxic T cells and natural killer (NK) cells, are instrumental in the recognition and eradication of pathogenic cells, notably those undergoing malignant transformation. Cytotoxic lymphocytes establish direct contact with cancer cells via the formation of a specialized cell-cell junction known as the lytic immunological synapse. This structure serves as a critical platform for lymphocytes to integrate surface signals from potential cancer cells and to direct their cytolytic apparatus toward the confirmed targets. Conversely, cancer cells evolve synaptic defense strategies to evade lymphocyte cytotoxicity. This chapter delineates protocols using imaging flow cytometry to examine and quantify important subcellular processes occurring within cytotoxic lymphocytes and cancer cells engaged into an immunological synapse. These processes encompass the spatial redistribution of cytoskeletal components, vesicles, organelles and cell surface molecules. We specifically describe methods to generate and select conjugates between MDA-MB-231 breast cancer cells or K-562 leukemic cells and either the NK-92MI cell line or primary human NK cells. In addition, we detail procedures to evaluate the synaptic polarization of the actin cytoskeleton, CD63-positive vesicular compartments, MHC class I molecules, as well as the microtubule-organizing center in effector cells.
AB - Cytotoxic lymphocytes, such as cytotoxic T cells and natural killer (NK) cells, are instrumental in the recognition and eradication of pathogenic cells, notably those undergoing malignant transformation. Cytotoxic lymphocytes establish direct contact with cancer cells via the formation of a specialized cell-cell junction known as the lytic immunological synapse. This structure serves as a critical platform for lymphocytes to integrate surface signals from potential cancer cells and to direct their cytolytic apparatus toward the confirmed targets. Conversely, cancer cells evolve synaptic defense strategies to evade lymphocyte cytotoxicity. This chapter delineates protocols using imaging flow cytometry to examine and quantify important subcellular processes occurring within cytotoxic lymphocytes and cancer cells engaged into an immunological synapse. These processes encompass the spatial redistribution of cytoskeletal components, vesicles, organelles and cell surface molecules. We specifically describe methods to generate and select conjugates between MDA-MB-231 breast cancer cells or K-562 leukemic cells and either the NK-92MI cell line or primary human NK cells. In addition, we detail procedures to evaluate the synaptic polarization of the actin cytoskeleton, CD63-positive vesicular compartments, MHC class I molecules, as well as the microtubule-organizing center in effector cells.
KW - Cancer cell
KW - Cytoskeleton
KW - Imaging flow cytometry
KW - Immunological synapse
KW - Lymphocytes
KW - Surface molecules
KW - Vesicles
UR - http://www.scopus.com/inward/record.url?scp=85189658809&partnerID=8YFLogxK
UR - https://pubmed.ncbi.nlm.nih.gov/39919848/
U2 - 10.1016/bs.mcb.2024.03.001
DO - 10.1016/bs.mcb.2024.03.001
M3 - Article
C2 - 39919848
AN - SCOPUS:85189658809
SN - 0091-679X
VL - 193
SP - 69
EP - 97
JO - Methods in Cell Biology
JF - Methods in Cell Biology
ER -