TY - JOUR
T1 - Cutting edge
T2 - A double-mutant knockin of the CD28 YMNM and PYAP motifs reveals a critical role for the YMNM motif in regulation of T cell proliferation and Bcl-xL expression
AU - Boomer, Jonathan S.
AU - Deppong, Christine M.
AU - Shah, Dulari D.
AU - Bricker, Traci L.
AU - Green, Jonathan M.
PY - 2014/4/15
Y1 - 2014/4/15
N2 - CD28 is a critical regulator of T cell function, augmenting proliferation, cytokine secretion, and cell survival. Our previous work using knockin mice expressing point mutations in CD28 demonstrated that the distal proline motif was primarily responsible for much of CD28 function, whereas in marked contrast to prior studies, mutation of the PI3K-binding motif had little discernible effect. In this study, we examined the phenotype of mice in which both motifs are simultaneously mutated. We found that mutation of the PYAP motif unmasks a critical role for the proximal tyrosine motif in regulating T cell proliferation and expression of Bcl-xL but not cytokine secretion. In addition, we demonstrated that, although function is more severely impaired in the double mutant than in either single mutant, there remained residual CD28- dependent responses, definitively establishing that additional motifs can partially mediate CD28 function.
AB - CD28 is a critical regulator of T cell function, augmenting proliferation, cytokine secretion, and cell survival. Our previous work using knockin mice expressing point mutations in CD28 demonstrated that the distal proline motif was primarily responsible for much of CD28 function, whereas in marked contrast to prior studies, mutation of the PI3K-binding motif had little discernible effect. In this study, we examined the phenotype of mice in which both motifs are simultaneously mutated. We found that mutation of the PYAP motif unmasks a critical role for the proximal tyrosine motif in regulating T cell proliferation and expression of Bcl-xL but not cytokine secretion. In addition, we demonstrated that, although function is more severely impaired in the double mutant than in either single mutant, there remained residual CD28- dependent responses, definitively establishing that additional motifs can partially mediate CD28 function.
UR - http://www.scopus.com/inward/record.url?scp=84898652112&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.1301240
DO - 10.4049/jimmunol.1301240
M3 - Article
C2 - 24639356
AN - SCOPUS:84898652112
SN - 0022-1767
VL - 192
SP - 3465
EP - 3469
JO - Journal of Immunology
JF - Journal of Immunology
IS - 8
ER -