Activation of the innate immune receptor Dectin-1 upon formation of a ‘phagocytic synapse’

被引:0
作者
Helen S. Goodridge
Christopher N. Reyes
Courtney A. Becker
Tamiko R. Katsumoto
Jun Ma
Andrea J. Wolf
Nandita Bose
Anissa S. H. Chan
Andrew S. Magee
Michael E. Danielson
Arthur Weiss
John P. Vasilakos
David M. Underhill
机构
[1] IBD and Immunobiology Research Institute,Department of Medicine
[2] 8700 Beverly Boulevard,undefined
[3] Cedars-Sinai Medical Center,undefined
[4] Regenerative Medicine Institute,undefined
[5] Cedars-Sinai Medical Center,undefined
[6] 8700 Beverly Boulevard,undefined
[7] David Geffen School of Medicine at UCLA,undefined
[8] 10833 Le Conte Avenue,undefined
[9] University of California,undefined
[10] Rosalind Russell Medical Research Center for Arthritis,undefined
[11] 513 Parnassus,undefined
[12] University of California,undefined
[13] Biothera,undefined
[14] 3388 Mike Collins Drive,undefined
[15] Howard Hughes Medical Institute,undefined
[16] University of California,undefined
来源
Nature | 2011年 / 472卷
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摘要
Invading microbes are detected and ingested by white blood cells known as phagocytes. To do this they must distinguish between soluble microbe-derived components, such as pieces of cell wall, and the particulate microbes themselves. A study of the action of Dectin-1, an innate immune receptor that detects invading fungal pathogens, shows that although the receptor binds to both soluble and particulate cell-wall β-glucans, its activation is restricted to sites of contact with fungal cell walls by the formation of 'phagocytic synapses'. The phagocytic synapse provides a mechanistic model for the specific detection of ligands associated with a microbial surface, as opposed to those released from microbes at a distance.
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页码:471 / 475
页数:4
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