Herbal Research Laboratory, CSIR-Indian Institute of Toxicology Research (CSIR-IITR), Vishvigyan Bhawan 31, Mahatma Gandhi Marg, Lucknow 226001, India; Academy of Scientific and Innovative Research, CSIR-IITR, Lucknow, India.
Herbal Research Laboratory, CSIR-Indian Institute of Toxicology Research (CSIR-IITR), Vishvigyan Bhawan 31, Mahatma Gandhi Marg, Lucknow 226001, India.
Toxicol Appl Pharmacol. 2018 May 15;347:92-103. doi: 10.1016/j.taap.2018.03.033. Epub 2018 Apr 4.
Pleckstrin homology domain leucine-rich repeat protein phosphatase 2 (PHLPP2) has been known to exert tumor suppressive activity for long without much knowledge about its regulation and implications. Protein kinase B (Akt), Protein kinase C (PKC) and Ribosomal protein S6 Kinase (S6K) are known downtargets of PHLPP2, regulating a plethora of life processes viz. cell growth, survival and evasion from apoptosis. Present study decoded the crucial role of PHLPP2 in inducing apoptosis by its interaction with the newly found binding partner Mammalian sterile 20-like kinase 1 (Mst1) in berberine (BBR)-treated human hepatoma cells. HepG2 cells were exposed to (50 μM, 100 μM) berberine for different time intervals (18 h, 24 h). The results showed enhanced expression of PHLPP2 at transcriptional (2.13 fold, P < 0.01) and translational level (4 fold, P < 0.001), but not of PHLPP1, in berberine-treated HepG2 cells. Elevated expression of PHLPP2 was reported to inactivate Akt by dephosphorylating it on Ser473 (P < 0.001). As Akt is known to inhibit apoptotic effect of Mst1, we found that PHLPP2 mediated inactivation of Akt releases its repression from Mst1 leading to heightened phosphorylation of Mst1 on its activating site Thr183 (1.5 fold, P < 0.001). Consequently, coordination between PHLPP2, Akt and Mst1 stimulated downstream targets c-jun N-terminal kinase (JNK), Bim and Bak which are direct activators of pro-apoptotic proteins leading to cell death. Further, PHLPP2/Mst1 knock-down efficiently curtailed anti-proliferative effect of berberine by restoring the basal level of downstream anti-apoptotic proteins. In addition, pre-treatment of NAC (5 mM) showed that ROS generation was a primitive event to initiate activation of stress kinases. Thus, our findings suggest that PHLPP2, Akt and Mst1 constitute an autoinhibitory triangle which may be partly responsible for antiproliferative effect of berberine.
PHLPP2 结构域亮氨酸丰富重复蛋白磷酸酶 2(PHLPP2)长期以来一直具有肿瘤抑制活性,但对其调节和影响知之甚少。蛋白激酶 B(Akt)、蛋白激酶 C(PKC)和核糖体蛋白 S6 激酶(S6K)是 PHLPP2 的已知靶点,调节着细胞生长、存活和逃避凋亡等众多生命过程。本研究通过 PHLPP2 与新发现的结合伴侣哺乳动物不育 20 样激酶 1(Mst1)在小檗碱(BBR)处理的人肝癌细胞中的相互作用,解析了 PHLPP2 在诱导细胞凋亡中的关键作用。用不同浓度(50 μM、100 μM)的小檗碱处理 HepG2 细胞不同时间间隔(18 h、24 h)。结果表明,在小檗碱处理的 HepG2 细胞中,PHLPP2 在转录(2.13 倍,P<0.01)和翻译水平(4 倍,P<0.001)上的表达增强,但 PHLPP1 没有表达增强。已有报道称,PHLPP2 通过磷酸化 Akt 的 Ser473 使其去磷酸化来使 Akt 失活(P<0.001)。由于 Akt 已知能抑制 Mst1 的凋亡作用,我们发现 PHLPP2 介导的 Akt 失活释放了其对 Mst1 的抑制作用,导致 Mst1 在其激活位点 Thr183 上的磷酸化增加(1.5 倍,P<0.001)。因此,PHLPP2、Akt 和 Mst1 之间的协调作用刺激了下游靶点 c-jun N 末端激酶(JNK)、Bim 和 Bak 的磷酸化,它们是促凋亡蛋白的直接激活剂,导致细胞死亡。此外,PHLPP2/Mst1 敲低通过恢复下游抗凋亡蛋白的基础水平,有效地抑制了小檗碱的抗增殖作用。此外,NAC(5 mM)预处理表明 ROS 的产生是激活应激激酶的初始事件。因此,我们的研究结果表明,PHLPP2、Akt 和 Mst1 构成一个自动抑制三角形,这可能是小檗碱的抗增殖作用的部分原因。