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Multiparametric Flow Cytometry-Based Immunophenotyping of Mouse Liver Immune Cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F22%3A00563508" target="_blank" >RIV/61388963:_____/22:00563508 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/22:10447060

  • Result on the web

    <a href="https://doi.org/10.3390/mps5050070" target="_blank" >https://doi.org/10.3390/mps5050070</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/mps5050070" target="_blank" >10.3390/mps5050070</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Multiparametric Flow Cytometry-Based Immunophenotyping of Mouse Liver Immune Cells

  • Original language description

    The liver is a complex organ that governs many types of metabolisms, including energy metabolism and other cellular processes. The liver also plays a crucial role in important functions in immunity, and the activity of liver tissue-associated immunity affects the outcome of many liver pathologies. A thorough characterization of the liver immune microenvironment may contribute to a better understanding of immune signaling, the mechanisms of specific immune responses, and even to improved predictions about therapy outcomes. In this paper, we present an optimized, simple, and rapid protocol to characterize the liver-associated immune cell milieu. We believe that the most suitable technique for obtaining a complex immune cell suspension and for removing contaminating blood cells is to perform mouse liver perfusion, using only phosphate buffer saline. Combining an enzymatic digestion and a mechanical dissociation of liver tissue, followed by cell purification, improves downstream applications. This combination is an essential prerequisite for immune cell determination and characterization. We then demonstrate a flow cytometry-based multiparametric immunophenotyping along with a gating strategy to detect and quantify liver endothelial cells, T cells (helper and cytotoxic), B cells, NK cells, NKT cells, neutrophils, monocytes (subsets included), dendritic cells (subsets included), macrophages and Kupffer cells.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    <a href="/en/project/EF16_019%2F0000729" target="_blank" >EF16_019/0000729: Chemical biology for drugging undruggable targets</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Methods and Protocols

  • ISSN

    2409-9279

  • e-ISSN

    2409-9279

  • Volume of the periodical

    5

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    15

  • Pages from-to

    70

  • UT code for WoS article

    000873086400001

  • EID of the result in the Scopus database

    2-s2.0-85140616880