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      A versatile system to record cell-cell interactions

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          Abstract

          Cell-cell interactions influence all aspects of development, homeostasis, and disease. In cancer, interactions between cancer cells and stromal cells play a major role in nearly every step of carcinogenesis. Thus, the ability to record cell-cell interactions would facilitate mechanistic delineation of the role of the cancer microenvironment. Here, we describe GFP-based Touching Nexus (G-baToN) which relies upon nanobody-directed fluorescent protein transfer to enable sensitive and specific labeling of cells after cell-cell interactions. G-baToN is a generalizable system that enables physical contact-based labeling between various human and mouse cell types, including endothelial cell-pericyte, neuron-astrocyte, and diverse cancer-stromal cell pairs. A suite of orthogonal baToN tools enables reciprocal cell-cell labeling, interaction-dependent cargo transfer, and the identification of higher order cell-cell interactions across a wide range of cell types. The ability to track physically interacting cells with these simple and sensitive systems will greatly accelerate our understanding of the outputs of cell-cell interactions in cancer as well as across many biological processes.

          eLife digest

          It takes the coordinated effort of more than 40 trillion cells to build and maintain a human body. This intricate process relies on cells being able to communicate across long distances, but also with their immediate neighbors. Interactions between cells in close contact are key in both health and disease, yet tracing these connections efficiently and accurately remains challenging.

          The surface of a cell is studded with proteins that interact with the environment, including with the proteins on neighboring cells. Using genetic engineering, it is possible to construct surface proteins that carry a fluorescent tag called green fluorescent protein (or GFP), which could help to track physical interactions between cells.

          Here, Tang et al. test this idea by developing a new technology named GFP-based Touching Nexus, or G-baToN for short. Sender cells carry a GFP protein tethered to their surface, while receiver cells present a synthetic element that recognizes that GFP. When the cells touch, the sender passes its GFP to the receiver, and these labelled receiver cells become ‘green’.

          Using this system, Tang et al. recorded physical contacts between a variety of human and mouse cells. Interactions involving more than two cells could also be detected by using different colors of fluorescent tags. Furthermore, Tang et al. showed that, alongside GFP, G-baToN could pass molecular cargo such as proteins, DNA, and other chemicals to receiver cells.

          This new system could help to study interactions among many different cell types. Changes in cell-to-cell contacts are a feature of diverse human diseases, including cancer. Tracking these interactions therefore could unravel new information about how cancer cells interact with their environment.

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          Most cited references33

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          Chemokines in the cancer microenvironment and their relevance in cancer immunotherapy

          This Review details how chemokines shape immune responses in the tumour microenvironment through their effects on immune cells, stromal cells and the tumour cells themselves. The authors discuss the potential of targeting chemokine networks for cancer therapy.
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            T cell exclusion, immune privilege, and the tumor microenvironment.

            Effective immunotherapy promotes the killing of cancer cells by cytotoxic T cells. This requires not only that cancer-specific T cells be generated, but also that these T cells physically contact cancer cells. The coexistence in some patients of cancer cells and T cells that recognize them indicates that tumors may exhibit the phenomenon of immune privilege, in which immunogenic tissue is protected from immune attack. Here, we review the evidence that stromal cells of the tumor microenvironment mediate this restriction by excluding T cells from the vicinity of cancer cells. Overcoming this T cell checkpoint may thus enable optimal immunotherapy.
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              HaloTag: a novel protein labeling technology for cell imaging and protein analysis.

              We have designed a modular protein tagging system that allows different functionalities to be linked onto a single genetic fusion, either in solution, in living cells, or in chemically fixed cells. The protein tag (HaloTag) is a modified haloalkane dehalogenase designed to covalently bind to synthetic ligands (HaloTag ligands). The synthetic ligands comprise a chloroalkane linker attached to a variety of useful molecules, such as fluorescent dyes, affinity handles, or solid surfaces. Covalent bond formation between the protein tag and the chloroalkane linker is highly specific, occurs rapidly under physiological conditions, and is essentially irreversible. We demonstrate the utility of this system for cellular imaging and protein immobilization by analyzing multiple molecular processes associated with NF-kappaB-mediated cellular physiology, including imaging of subcellular protein translocation and capture of protein--protein and protein--DNA complexes.
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                Author and article information

                Contributors
                Role: Senior Editor
                Role: Reviewing Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                07 October 2020
                2020
                : 9
                : e61080
                Affiliations
                [1 ]Department of Genetics, Stanford University School of Medicine StanfordUnited States
                [2 ]Cancer Biology Program, Stanford University School of Medicine StanfordUnited States
                [3 ]Immunology Program, Stanford University School of Medicine StanfordUnited States
                [4 ]Neuroscience Program, Stanford University School of Medicine StanfordUnited States
                [5 ]Department of Neurosurgery, Stanford University School of Medicine StanfordUnited States
                [6 ]Department of Pathology, Stanford University School of Medicine StanfordUnited States
                Memorial Sloan Kettering Cancer Center United States
                Massachusetts Institute of Technology United States
                Massachusetts Institute of Technology United States
                Salk Institute for Biological Studies United States
                Harvard University United States
                Author information
                https://orcid.org/0000-0002-6950-9580
                https://orcid.org/0000-0002-6551-2053
                http://orcid.org/0000-0003-4557-8343
                http://orcid.org/0000-0002-4950-0757
                http://orcid.org/0000-0001-8603-1526
                http://orcid.org/0000-0002-2096-9279
                https://orcid.org/0000-0002-5730-9573
                Article
                61080
                10.7554/eLife.61080
                7682987
                33025906
                caac2a91-7de1-4f41-8134-1ab74c58e751
                © 2020, Tang et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 15 July 2020
                : 06 October 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000054, National Cancer Institute;
                Award ID: R01-CA175336
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000054, National Cancer Institute;
                Award ID: R01-CA207133
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000054, National Cancer Institute;
                Award ID: R01-CA230919
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100005188, Tobacco-Related Disease Research Program;
                Award ID: 27FT-0044
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: Graduate Research Fellowship Program
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100005492, Stanford University;
                Award ID: Anne T. and Robert M. Bass Fellowship
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: CA196029
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000054, National Cancer Institute;
                Award ID: K25-CA201545
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100006521, Stanford University School of Medicine;
                Award ID: Dean’s Postdoctoral Fellowship
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Tools and Resources
                Cancer Biology
                Cell Biology
                Custom metadata
                A novel reporter system that employs cell surface antigen-nanobody pairing enables physical interaction-dependent labeling and functional modification between diverse cell types.

                Life sciences
                cell-cell interaction,cancer-stromal,nanobody,tumor microenvironment,human,mouse
                Life sciences
                cell-cell interaction, cancer-stromal, nanobody, tumor microenvironment, human, mouse

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