4.8 Article

Immunoprofiling Reveals Novel Mast Cell Receptors and the Continuous Nature of Human Lung Mast Cell Heterogeneity

Journal

FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.804812

Keywords

human lung mast cells; heterogenity; chymase (CMA1); carboxypeptidase A3 (CPA3); SUSD2; CD38; Fc epsilon RI

Categories

Funding

  1. Swedish Research Council [2018-02070, 2020-01693]
  2. Heart-Lung Foundation
  3. Swedish Cancer Society
  4. Ellen, Walter and Lennart Hesselman Foundation
  5. Tore Nilsson Foundation
  6. Lars Hierta Memorial Foundation
  7. Konsul Th C Bergh Foundation
  8. Tornspiran Foundation
  9. O. E. and Edla Johanssons Foundation
  10. Swedish Society for Medical Research
  11. Centre for Allergy Research Highlights Asthma Markers of Phenotype (ChAMP) consortium
  12. Swedish Foundation for Strategic Research
  13. AstraZeneca & Science for Life Laboratory Joint Research Collaboration
  14. Karolinska Institutet
  15. Swedish Research Council [2020-01693, 2018-02070] Funding Source: Swedish Research Council

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A comprehensive analysis of cell-surface markers on human lung mast cells revealed the expression of more than 100 markers, including 23 previously undescribed ones. However, no distinct mast cell subpopulations were identified, indicating the continuous nature of human lung mast cell heterogeneity.
Background: Immunohistochemical analysis of granule-associated proteases has revealed that human lung mast cells constitute a heterogeneous population of cells, with distinct subpopulations identified. However, a systematic and comprehensive analysis of cell-surface markers to study human lung mast cell heterogeneity has yet to be performed.Methods: Human lung mast cells were obtained from lung lobectomies, and the expression of 332 cell-surface markers was analyzed using flow cytometry and the LEGENDScreen (TM) kit. Markers that exhibited high variance were selected for additional analyses to reveal whether they were correlated and whether discrete mast cell subpopulations were discernable.Results: We identified the expression of 102 surface markers on human lung mast cells, 23 previously not described on mast cells, of which several showed high continuous variation in their expression. Six of these markers were correlated: SUSD2, CD49a, CD326, CD34, CD66 and HLA-DR. The expression of these markers was also correlated with the size and granularity of mast cells. However, no marker produced an expression profile consistent with a bi- or multimodal distribution.Conclusions: LEGENDScreen analysis identified more than 100 cell-surface markers on mast cells, including 23 that, to the best of our knowledge, have not been previously described on human mast cells. The comprehensive expression profiling of the 332 surface markers did not identify distinct mast cell subpopulations. Instead, we demonstrate the continuous nature of human lung mast cell heterogeneity.

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