TY - JOUR
T1 - Blood eosinophils from atopic donors express messenger RNA for the α, β, and γ subunits of the high-affinity IgE receptor (FcεRI) and intracellular, but not cell surface, α subunit protein
AU - Smith, Susan J.
AU - Ying, Sun
AU - Meng, Qui
AU - Sullivan, Mark H.F.
AU - Barkans, Julia
AU - Kon, Onn Min
AU - Sihra, Bhupinder
AU - Larché, Mark
AU - Levi-Schaffer, Francesca
AU - Kay, A. Barry
N1 - Funding Information:
Supported by the Aimwell Charitable Trust. S. J. S. is a recipient of the Isaac and Myrna Kaye Travelling Fellowship (Imperial College School of Medicine, London, United Kingdom, and the Hebrew University, Jerusalem, Israel).
PY - 2000
Y1 - 2000
N2 - Background: Blood eosinophils from hypereosinophilic donors were previously reported to possess the functional high-affinity IgE receptor (FcεRI), so providing a potential mechanism to account for eosinophil degranulation in atopic allergic disease. Furthermore, tissue eosinophils from allergic tissue reactions were shown to be mRNA+ for the α, β, and γ subunits of FcεRI and gave positive immunostaining with an anti-FcεRI-α anti-body. Recent studies, however, revealed negative surface staining on peripheral blood eosinophils, but intracellular FcεRI-α protein was identified by Western blot analysis. Objective: Our purpose was to examine on peripheral blood eosinophils from atopic subjects (1) surface expression and mRNA for FcεRI-α, (2) up-regulation of FcεRI-α by allergy-associated tissue factors, and (3) FcεRI-α-dependent release of eosinophil peroxidase (EPO). Methods: We measured (1) FcεRI mRNA expression by in situ hybridization, (2) FcεRI-α by flow cytometry and immunocytochemistry (with use of nonpermeabilized and permeabilized cells), and (3) FcεRI-α-dependent release of EPO. Results: Eosinophils from atopic donors had negligible surface expression of FcεRI-α, which was not enhanced by culture with IgE, IL-3, IL-4, IL-5, GM-CSF, or fibronectin or coculture with fibroblasts. Permeabilization, however, revealed appreciable intracellular staining for FcεRI-α. The majority of eosinophils were mRNA+ for the α, β, and γ subunits of FcεRI. Small but significant (P = .03) increases in a chain mRNA expression were observed after coculture of eosinophils with fibroblasts but not with IgE, IL-4, or fibronectin. Cross-linking of FcεRI on the surface of eosinophils from atopic donors did not lead to detectable EPO release. Conclusion: Human blood eosinophils express negligible, non-functional membrane FcεRI-α but have intracellular FcεRI-α protein and mRNA expression for the α, β, and γ subunits.
AB - Background: Blood eosinophils from hypereosinophilic donors were previously reported to possess the functional high-affinity IgE receptor (FcεRI), so providing a potential mechanism to account for eosinophil degranulation in atopic allergic disease. Furthermore, tissue eosinophils from allergic tissue reactions were shown to be mRNA+ for the α, β, and γ subunits of FcεRI and gave positive immunostaining with an anti-FcεRI-α anti-body. Recent studies, however, revealed negative surface staining on peripheral blood eosinophils, but intracellular FcεRI-α protein was identified by Western blot analysis. Objective: Our purpose was to examine on peripheral blood eosinophils from atopic subjects (1) surface expression and mRNA for FcεRI-α, (2) up-regulation of FcεRI-α by allergy-associated tissue factors, and (3) FcεRI-α-dependent release of eosinophil peroxidase (EPO). Methods: We measured (1) FcεRI mRNA expression by in situ hybridization, (2) FcεRI-α by flow cytometry and immunocytochemistry (with use of nonpermeabilized and permeabilized cells), and (3) FcεRI-α-dependent release of EPO. Results: Eosinophils from atopic donors had negligible surface expression of FcεRI-α, which was not enhanced by culture with IgE, IL-3, IL-4, IL-5, GM-CSF, or fibronectin or coculture with fibroblasts. Permeabilization, however, revealed appreciable intracellular staining for FcεRI-α. The majority of eosinophils were mRNA+ for the α, β, and γ subunits of FcεRI. Small but significant (P = .03) increases in a chain mRNA expression were observed after coculture of eosinophils with fibroblasts but not with IgE, IL-4, or fibronectin. Cross-linking of FcεRI on the surface of eosinophils from atopic donors did not lead to detectable EPO release. Conclusion: Human blood eosinophils express negligible, non-functional membrane FcεRI-α but have intracellular FcεRI-α protein and mRNA expression for the α, β, and γ subunits.
KW - Allergy
KW - Atopy
KW - Eosinophils
KW - High-affinity IgE receptor (FcεRI)
UR - http://www.scopus.com/inward/record.url?scp=0033952492&partnerID=8YFLogxK
U2 - 10.1016/s0091-6749(00)90081-2
DO - 10.1016/s0091-6749(00)90081-2
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C2 - 10669852
AN - SCOPUS:0033952492
SN - 0091-6749
VL - 105
SP - 309
EP - 317
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 2 II
ER -