In:
European Journal of Immunology, Wiley, Vol. 47, No. 5 ( 2017-05), p. 848-859
Abstract:
Dectin‐1 is recognized as a major receptor for fungal ß‐glucans and contributes to anti‐fungal immunity. Human monocyte populations express Dectin‐1 isoforms A and B, which differ by the presence of a stalk region and its N‐linked glycosylation site. Here, we analyzed the expression of both isoforms in human monocyte‐derived cells. The cellular localization on cell lines stably expressing either Dectin‐1 isoform A or B was studied by flow cytometry and confocal laser scanning microscopy. Intracellular protein signaling and cytokine production were analyzed by immunoblotting and cytometric bead array, respectively. Monocyte‐derived cells showed cell type‐specific expression of the two isoforms. Glycosylated Dectin‐1 isoform A was predominantly localized at the cell surface, non‐glycosylated isoform B was retained intracellularly. Inhibition of glycosylation resulted in efficient abrogation of cell surface expression of isoform A. Signaling quality following Dectin‐1 stimulation was reduced in isoform B cells. Differential isoform specific cytokine secretion was observed by cytometric bead array. We show here that n‐glycosylation of Dectin‐1 is crucial for its cell surface expression and consequently signal transduction. Taken together, unique cytokine secretion and varying expression levels of human Dectin‐1 isoforms on monocyte‐derived cells may indicate distinct isoform usage as a cell type‐specific mechanism of regulating anti‐fungal immunity.
Type of Medium:
Online Resource
ISSN:
0014-2980
,
1521-4141
DOI:
10.1002/eji.201646849
Language:
English
Publisher:
Wiley
Publication Date:
2017
detail.hit.zdb_id:
1491907-2
