IMMUNOPHILINS IN PROTEIN-FOLDING AND IMMUNOSUPPRESSION

被引:231
作者
FRUMAN, DA
BURAKOFF, SJ
BIERER, BE
机构
[1] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DEPT PEDIAT ONCOL,BOSTON,MA 02115
[2] BRIGHAM & WOMENS HOSP,DIV HEMATOL ONCOL,BOSTON,MA 02215
[3] HARVARD UNIV,SCH MED,DIV MED SCI,COMM IMMUNOL,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,DEPT PEDIAT,BOSTON,MA 02115
[5] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02115
关键词
CYCLOSPORINE A; CYCLOPHILIN; FK506; RAPAMYCIN; FKBP; CALCINEURIN;
D O I
10.1096/fasebj.8.6.7513288
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lymphocyte activation requires the transmission of signals from molecules at the plasma membrane to nuclear signals that regulate gene expression. In recent years, several immunosuppressive compounds have been used as probes to identify important and potentially novel molecules involved in lymphocyte signal transduction processes. The immunosuppressants cyclosporin A (CsA), FK506, and rapamycin have been studied in particular detail. Two distinct classes of immunosuppressant binding proteins have been identified, and collectively termed immunophilins. The cyclophilin family of immunophilins binds CsA, whereas the FK506-binding protein (FKBP) family binds FK506 and rapamycin. This review will discuss both the endogenous functions of immunophilins as well as their roles in mediating immunosuppression.
引用
收藏
页码:391 / 400
页数:10
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