Schubert K M, Duronio V
Department of Medicine, University of British Columbia and Vancouver Hospital, Jack Bell Research Centre, 2660 Oak St. Vancouver, BC, Canada V6H 3Z6.
Biochem J. 2001 Jun 1;356(Pt 2):473-80. doi: 10.1042/0264-6021:3560473.
Alterations in the expression of various Bcl-2 family members may act as one means by which a cell's survival may be regulated. The mechanism by which cytokines regulate expression of Bcl-2 family members was examined in the haemopoietic cell line TF-1. Cytokine-induced Mcl-1 protein expression was shown to be controlled through a pathway dependent upon phosphatidylinositol 3-kinase (PI 3-kinase). The cytokine-induced increase in mRNA transcription was not dependent upon PI 3-kinase, thus dissociating the immediate-early transcription factors responsible for Mcl-1 transcription from the PI 3-kinase signalling pathway. In contrast, Mcl-1 mRNA levels were dependent upon MEK [mitogen-activated protein kinase (MAPK)/extracellular-signal-regulated protein kinase kinase] activation, suggesting a role for the Ras/MEK/MAPK pathway in Mcl-1 transcription. Activation of PI 3-kinase was shown to be necessary to stimulate Mcl-1 protein translation. This was not due to any effect on prolonging the half-life of the protein. Finally, the lipid second messenger ceramide was shown to cause a reduction in Mcl-1 protein translation, probably via its ability to inhibit protein kinase B activation, providing further clues regarding the death-inducing effect of this lipid.
各种Bcl-2家族成员表达的改变可能是调节细胞存活的一种方式。在造血细胞系TF-1中研究了细胞因子调节Bcl-2家族成员表达的机制。细胞因子诱导的Mcl-1蛋白表达显示是通过依赖磷脂酰肌醇3激酶(PI 3激酶)的途径来控制的。细胞因子诱导的mRNA转录增加不依赖于PI 3激酶,因此将负责Mcl-1转录的早期转录因子与PI 3激酶信号通路分开。相反,Mcl-1 mRNA水平依赖于MEK [丝裂原活化蛋白激酶(MAPK)/细胞外信号调节蛋白激酶激酶]的激活,表明Ras/MEK/MAPK途径在Mcl-1转录中起作用。PI 3激酶的激活被证明是刺激Mcl-1蛋白翻译所必需的。这不是由于对延长蛋白质半衰期有任何影响。最后,脂质第二信使神经酰胺被证明可导致Mcl-1蛋白翻译减少,可能是通过其抑制蛋白激酶B激活的能力,为这种脂质的诱导死亡作用提供了进一步线索。