Expression Profiling of Human Basophils: Modulation by Cytokines and Secretagogues

• Published in: PloS one Vol. 10; no. 5; p. e0126435
• Main Author: MacGlashan, Donald
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 11.05.2015; Public Library of Science (PLoS)
• Subjects: Apoptosis; Asthma; Atopy; Basophils; Basophils - drug effects; Basophils - immunology; Basophils - metabolism; Cell division; Cluster Analysis; Computational Biology; Cytokines; Cytokines - metabolism; Cytokines - pharmacology; DNA microarrays; Food allergies; Gene expression; Gene Expression Profiling; Gene Expression Regulation - drug effects; Genotype & phenotype; Glucose; Health aspects; Human behavior; Humans; Hypersensitivity; Immunoglobulin E; Immunoglobulin E - immunology; Immunoglobulins; Interleukin 2; Interleukin 3; Interleukin 5; Kinases; Leukocytes (basophilic); Nerve growth factor; Phosphorylation; Physiological aspects; Signal transduction; Signaling; Signatures; Stimuli; Studies; Transcriptome; Viability; United States
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0126435

Human basophils are an accessible participant of the human allergic reaction. There is natural variation in various functional endpoints and in signaling molecule expression but there has been only a limited effort to place this information in the context of mRNA expression profiles. This study examined the hypothesis that unique mRNA signatures could be identified during the response of human basophils to several known forms of stimulation. Highly purified human basophils were cultured in vitro and exposed to IL-3, IL-5, NGF, IL-33, IL-2, anti-IgE Ab, or FMLP and the mRNA profiles examined by microarrays. The response to IL-3 and anti-IgE Ab were examined on 2-3 time frames and the response to IL-3 examined at several concentrations. In addition, the mRNA signatures of 3 different potential phenotypes were examined. These included basophils with the so-called non-releaser phenotype, and basophils from atopic and non-atopic subjects. Given the role of IL-3 in basophil maturation and the known profound effects on mature basophil function, it was not surprising that IL-3 showed the greatest influence on the basophil transcriptome. However, it also became apparent that the act of isolating and culturing basophils was sufficient to induce a large number of changes in the transcriptome, despite high viability and recovery. These "culture-effect" changes dominated the changes in mRNA profiles induced by other stimuli. Unique signatures for anti-IgE antibody and IL-33 could be identified although the number of gene transcripts (6-30) that were unique to these two stimuli was very limited. There were no apparent unique profiles for IL-5, NGF, IL-2 or FMLP. Therefore, a potential tool for screening basophil phenotypes was limited to changes that could be induced by IL-3 (or no IL-3), IL-33 and anti-IgE Ab.