Singh Dinesh Kumar, Kumar Dhiraj, Siddiqui Zaved, Basu Sandip Kumar, Kumar Vikas, Rao Kanury V S
Immunology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Dehli, India.
Cell. 2005 Apr 22;121(2):281-93. doi: 10.1016/j.cell.2005.02.036.
Activation of cell-surface receptors stimulates generation of intracellular signals that, in turn, direct the cellular response. However, mechanisms that ensure combinatorial control of these signaling events are not well understood. We show here that the Ca2+ and reactive oxygen intermediates generated upon BCR activation rapidly engage in a cooperative interaction that acts in a feedback manner to amplify the early signal generated. This cooperativity acts by regulating the concentration of the oxidant produced. The latter exerts its influence through a pulsed inactivation of receptor-coupled phosphatases, where the amplitude of this pulse is determined by oxidant concentration. The extent of phosphatase inhibition, in turn, dictates what proportion of receptor-proximal kinases are activated and, as a result, the net strength of the initial signal. It is the strength of this initial signal that finally determines the eventual duration of BCR signaling and the rate of its transmission through downstream pathways.
细胞表面受体的激活会刺激细胞内信号的产生,这些信号进而指导细胞反应。然而,确保对这些信号事件进行组合控制的机制尚未得到充分理解。我们在此表明,BCR激活时产生的Ca2+和活性氧中间体迅速进行协同相互作用,以反馈方式作用于放大早期产生的信号。这种协同作用通过调节所产生氧化剂的浓度来发挥作用。后者通过受体偶联磷酸酶的脉冲失活发挥其影响,该脉冲的幅度由氧化剂浓度决定。磷酸酶抑制的程度反过来又决定了受体近端激酶被激活的比例,从而决定了初始信号的净强度。正是这个初始信号的强度最终决定了BCR信号传导的最终持续时间及其通过下游途径的传递速率。