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Bcl-2基因受白细胞介素-2和白细胞介素-4的差异调节:转录因子NF-AT的作用。

The Bcl-2 gene is differentially regulated by IL-2 and IL-4: role of the transcription factor NF-AT.

作者信息

Gómez J, Martínez-A C, González A, García A, Rebollo A

机构信息

Department of Immunology and Oncology, Centro Nacional de Biotecnología, Universidad Autónoma, Madrid, Spain.

出版信息

Oncogene. 1998 Sep 10;17(10):1235-43. doi: 10.1038/sj.onc.1202049.

Abstract

The murine TS1alphabeta T cell line expresses the anti-apoptotic protein Bcl-2 upon IL-2 stimulation, whereas IL-4-mediated growth of this cell line proceeds in the absence of Bcl-2 expression. In addition, IL-4 stimulation inhibits Bcl-2 expression and modulates its mRNA level. IL-2-induced DNA binding activity for these transcription factors is sensitive to phosphatidylinositol 3 kinase inhibitor wortmannin and to Rho inhibitor Clostridium difficile toxin B, which inhibit IL-2-induced Bcl-2 expression. NF-AT transcription factor appears to be the most important in the control Bcl-2 expression, since inhibition of the calcium-calmodulin-dependent phosphatase calcineurin, which regulates NF-AT activity, downregulates Bcl-2 expression in IL-2-stimulated cells. Constitutive expression of this phosphatase also upregulates Bcl-2 expression in IL-4-stimulated cells. In addition, a dominant negative NF-AT expression vector downregulates Bcl-2 expression in IL-2-stimulated cells. These results suggest that IL-2 induction of Bcl-2 expression may be directly or indirectly mediated by NF-AT.

摘要

鼠源TS1αβ T细胞系在白细胞介素-2(IL-2)刺激下表达抗凋亡蛋白Bcl-2,而该细胞系在白细胞介素-4(IL-4)介导下生长时,其生长过程中不存在Bcl-2表达。此外,IL-4刺激会抑制Bcl-2表达并调节其mRNA水平。这些转录因子的IL-2诱导的DNA结合活性对磷脂酰肌醇3激酶抑制剂渥曼青霉素和Rho抑制剂艰难梭菌毒素B敏感,这两种抑制剂会抑制IL-2诱导的Bcl-2表达。核因子活化T细胞(NF-AT)转录因子似乎在控制Bcl-2表达中最为重要,因为抑制调节NF-AT活性的钙调神经磷酸酶会下调IL-2刺激细胞中的Bcl-2表达。该磷酸酶的组成型表达也会上调IL-4刺激细胞中的Bcl-2表达。此外,显性负性NF-AT表达载体可下调IL-2刺激细胞中的Bcl-2表达。这些结果表明,IL-2诱导的Bcl-2表达可能直接或间接由NF-AT介导。

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