TY - JOUR
T1 - Ligation of Siglec-8
T2 - A selective mechanism for induction of human eosinophil apoptosis
AU - Nutku, Esra
AU - Aizawa, Hideyuki
AU - Hudson, Sherry A.
AU - Bochner, Bruce S.
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China (No. 21373253, 20903114) and the Youth Innovation Promotion Association CAS (No. 2014155).
PY - 2003/6/15
Y1 - 2003/6/15
N2 - Sialic acid binding immunoglobulin-like lectin 8 (Siglec-8), which exists in 2 isoforms including one possessing cytoplasmic tyrosine motifs, is expressed only on human eosinophils, basophils, and mast cells. Until now, its function was unknown. Here we define a novel function of Siglec-8 on eosinophils. Siglec-8 crosslinking with antibodies rapidly generated caspase-3-like activity and reduced eosinophil viability through induction of apoptosis. The pancaspase inhibitor benzyloxycarbonyl (Cbz)-Val-Ala-Asp-(Ome)-fluoromethyl ketone (zVAD-FMK) completely blocked this response, implicating caspases in Siglec-8 cross-linking-induced apoptosis. Eosinophil survival-promoting cytokines such as interleukin 5 (IL-5) and granulocyte-macrophage colonystimulating factor (GM-CSF) failed to block apoptosis and instead enhanced the sensitivity of eosinophils to undergo apoptosis in response to Siglec-8 antibody. Siglec-8 activation may provide a useful therapeutic approach to reduce numbers of eosinophils (and perhaps basophils and mast cells) in disease states where these cells are important.
AB - Sialic acid binding immunoglobulin-like lectin 8 (Siglec-8), which exists in 2 isoforms including one possessing cytoplasmic tyrosine motifs, is expressed only on human eosinophils, basophils, and mast cells. Until now, its function was unknown. Here we define a novel function of Siglec-8 on eosinophils. Siglec-8 crosslinking with antibodies rapidly generated caspase-3-like activity and reduced eosinophil viability through induction of apoptosis. The pancaspase inhibitor benzyloxycarbonyl (Cbz)-Val-Ala-Asp-(Ome)-fluoromethyl ketone (zVAD-FMK) completely blocked this response, implicating caspases in Siglec-8 cross-linking-induced apoptosis. Eosinophil survival-promoting cytokines such as interleukin 5 (IL-5) and granulocyte-macrophage colonystimulating factor (GM-CSF) failed to block apoptosis and instead enhanced the sensitivity of eosinophils to undergo apoptosis in response to Siglec-8 antibody. Siglec-8 activation may provide a useful therapeutic approach to reduce numbers of eosinophils (and perhaps basophils and mast cells) in disease states where these cells are important.
UR - http://www.scopus.com/inward/record.url?scp=0038044928&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0038044928&partnerID=8YFLogxK
U2 - 10.1182/blood-2002-10-3058
DO - 10.1182/blood-2002-10-3058
M3 - Article
C2 - 12609831
AN - SCOPUS:0038044928
SN - 0006-4971
VL - 101
SP - 5014
EP - 5020
JO - Blood
JF - Blood
IS - 12
ER -