Intravascular Leukocyte Labeling Refines the Distribution of Myeloid Cells in the Lung in Models of Allergen-induced Airway Inflammation.

Immunohorizons

Division of Pulmonary, Critical Care, and Sleep Medicine and Center for Lung Biology, Department of Medicine, University of Washington, Seattle, WA 98109.

Published: December 2023

AI Article Synopsis

  • Innate immune cell populations play a vital role in asthma, with unique functions depending on their location in the body, prompting research on their distribution in mouse models.
  • This study used intravascular (IV) labeling to differentiate between innate immune cells in the bloodstream and those in lung tissue or airway fluid in two asthma models.
  • Results showed that IV labeled leukocytes did not interfere with bronchoalveolar lavage analysis, and excluding them improved the assessment accuracy of myeloid cells in lung tissue, enhancing understanding of immune cell movement in asthma.

Article Abstract

Innate immune cell populations are critical in asthma with different functional characteristics based on tissue location, which has amplified the importance of characterizing the precise number and location of innate immune populations in murine models of asthma. In this study, we performed premortem intravascular (IV) labeling of leukocytes in mice in two models of asthma to differentiate innate immune cell populations within the IV compartment versus those residing in the lung tissue or airway lumen. We performed spectral flow cytometry analysis of the blood, suspensions of digested lung tissue, and bronchoalveolar lavage fluid. We discovered that IV labeled leukocytes do not contaminate analysis of bronchoalveolar lavage fluid but represent a significant proportion of cells in digested lung tissue. Exclusion of IV leukocytes significantly improved the accuracy of the assessments of myeloid cells in the lung tissue and provided important insights into ongoing trafficking in both eosinophilic and neutrophilic asthma models.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10759158PMC
http://dx.doi.org/10.4049/immunohorizons.2300059DOI Listing

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