TY - JOUR
T1 - Thymocyte Sensitivity and Supramolecular Activation Cluster Formation Are Developmentally Regulated
T2 - A Partial Role for Sialylation
AU - Starr, Timothy K.
AU - Daniels, Mark A.
AU - Lucido, Michelle M.
AU - Jameson, Stephen C.
AU - Hogquist, Kristin A.
PY - 2003/10/1
Y1 - 2003/10/1
N2 - TCR reactivity is tuned during thymic development. Immature thymocytes respond to low-affinity self-ligands resulting in positive selection. Following differentiation, T cells no longer respond to low-affinity ligands, but respond well to high-affinity (foreign) ligands. We show in this study that this response includes integrin activation, supramolecular activation cluster formation, Ca2+ flux, and CD69 expression. Because glycosylation patterns are known to change during T cell development, we tested whether alterations in sialylation influence CD8 T cell sensitivity to low affinity TCR ligands. Using neuraminidase treatment or genetic deficiency in the ST3Gal-I sialyltransferase, we show that desialylation of mature CD8 T cells enhances their sensitivity to low-affinity ligands, although these treatments do not completely recapitulate the dynamic range of immature T cells. These studies identify sialylation as one of the factors that regulate CD8 T cell tuning during development.
AB - TCR reactivity is tuned during thymic development. Immature thymocytes respond to low-affinity self-ligands resulting in positive selection. Following differentiation, T cells no longer respond to low-affinity ligands, but respond well to high-affinity (foreign) ligands. We show in this study that this response includes integrin activation, supramolecular activation cluster formation, Ca2+ flux, and CD69 expression. Because glycosylation patterns are known to change during T cell development, we tested whether alterations in sialylation influence CD8 T cell sensitivity to low affinity TCR ligands. Using neuraminidase treatment or genetic deficiency in the ST3Gal-I sialyltransferase, we show that desialylation of mature CD8 T cells enhances their sensitivity to low-affinity ligands, although these treatments do not completely recapitulate the dynamic range of immature T cells. These studies identify sialylation as one of the factors that regulate CD8 T cell tuning during development.
UR - http://www.scopus.com/inward/record.url?scp=0142149044&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0142149044&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.171.9.4512
DO - 10.4049/jimmunol.171.9.4512
M3 - Article
C2 - 14568924
AN - SCOPUS:0142149044
SN - 0022-1767
VL - 171
SP - 4512
EP - 4520
JO - Journal of Immunology
JF - Journal of Immunology
IS - 9
ER -