Tsang Jennifer Ly, Jia Song Hui, Parodo Jean, Plant Pamela, Lodyga Monika, Charbonney Emmanuel, Szaszi Katalin, Kapus Andras, Marshall John C
Division of Critical Care, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Division of Critical Care, Department of Medicine, Niagara Health System, Niagara, Ontario, Canada.
PLoS One. 2016 Apr 21;11(4):e0153946. doi: 10.1371/journal.pone.0153946. eCollection 2016.
Src family tyrosine kinases (SFKs) phosphorylate caspase-8A at tyrosine (Y) 397 resulting in suppression of apoptosis. In addition, the phosphorylation of caspase-8A at other sites including Y465 has been implicated in the regulation of caspase-8 activity. However, the functional consequences of these modifications on caspase-8 processing/activity have not been elucidated. Moreover, various Src substrates are known to act as potent Src regulators, but no such role has been explored for caspase-8. We asked whether the newly identified caspase-8 phosphorylation sites might regulate caspase-8 activation and conversely, whether caspase-8 phosphorylation might affect Src activity. Here we show that Src phosphorylates caspase-8A at multiple tyrosine sites; of these, we have focused on Y397 within the linker region and Y465 within the p12 subunit of caspase-8A. We show that phosphomimetic mutation of caspase-8A at Y465 prevents its cleavage and the subsequent activation of caspase-3 and suppresses apoptosis. Furthermore, simultaneous phosphomimetic mutation of caspase-8A at Y397 and Y465 promotes the phosphorylation of c-Src at Y416 and increases c-Src activity. Finally, we demonstrate that caspase-8 activity prevents its own tyrosine phosphorylation by Src. Together these data reveal that dual phosphorylation converts caspase-8 from a pro-apoptotic to a pro-survival mediator. Specifically, tyrosine phosphorylation by Src renders caspase-8 uncleavable and thereby inactive, and at the same time converts it to a Src activator. This novel dynamic interplay between Src and caspase-8 likely acts as a potent signal-integrating switch directing the cell towards apoptosis or survival.
Src家族酪氨酸激酶(SFKs)使半胱天冬酶-8A在酪氨酸(Y)397处磷酸化,从而抑制细胞凋亡。此外,半胱天冬酶-8A在包括Y465在内的其他位点的磷酸化与半胱天冬酶-8活性的调节有关。然而,这些修饰对半胱天冬酶-8加工/活性的功能后果尚未阐明。此外,已知各种Src底物可作为有效的Src调节剂,但尚未对半胱天冬酶-8进行此类作用的探索。我们询问新发现的半胱天冬酶-8磷酸化位点是否可能调节半胱天冬酶-8的激活,反之,半胱天冬酶-8磷酸化是否可能影响Src活性。在这里,我们表明Src在多个酪氨酸位点使半胱天冬酶-8A磷酸化;其中,我们重点关注了半胱天冬酶-8A连接区的Y397和p12亚基内的Y465。我们表明,半胱天冬酶-8A在Y465处的磷酸模拟突变可阻止其切割以及随后半胱天冬酶-3的激活,并抑制细胞凋亡。此外,半胱天冬酶-8A在Y397和Y465处同时进行的磷酸模拟突变促进了c-Src在Y416处的磷酸化并增加了c-Src活性。最后,我们证明半胱天冬酶-8活性可阻止其自身被Src酪氨酸磷酸化。这些数据共同表明,双重磷酸化将半胱天冬酶-8从促凋亡介质转变为促生存介质。具体而言,Src介导的酪氨酸磷酸化使半胱天冬酶-8无法切割从而无活性,同时将其转变为Src激活剂。Src与半胱天冬酶-8之间这种新的动态相互作用可能作为一种强大的信号整合开关,引导细胞走向凋亡或生存。