Tsai Fu-Ming, Chen Mao-Liang, Wang Lu-Kai, Lee Ming-Cheng
Department of Research, Taipei Tzuchi Hospital, The Buddhist Tzuchi Medical Foundation, New Taipei City, Taiwan.
Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
PLoS One. 2015 Sep 18;10(9):e0138586. doi: 10.1371/journal.pone.0138586. eCollection 2015.
H-rev107 is a member of the HREV107 type II tumor suppressor gene family and acts as a phospholipase to catalyze the release of fatty acids from glycerophospholipid. H-rev107 has been shown to play an important role in fat metabolism in adipocytes through the PGE2/cAMP pathway, but the detailed molecular mechanism underlying H-rev107-mediated lipid degradation has not been studied. In this study, the interaction between H-rev107 and cytochrome P450 reductase (POR), which is involved in hepatic lipid content regulation, was determined by yeast two-hybrid screen and confirmed by using in vitro pull down assays and immunofluorescent staining. The expression of POR in H-rev107-expressing cells enhanced the H-rev107-mediated release of arachidonic acid. However, H-rev107 inhibited POR activity and relieved POR-mediated decreased triglyceride content in HtTA and HeLa cervical cells. The inhibitory effect of H-rev107 will be abolished when POR-expressing cells transfected with PLA2-lacking pH-rev107 or treated with PLA2 inhibitor. Silencing of H-rev107 using siRNA resulted in increased glycerol production and reversion of free fatty acid-mediated growth suppression in Huh7 hepatic cells. In summary, our results revealed that H-rev107 is also involved in lipid accumulation in liver cells through the POR pathway via its PLA2 activity.
H-rev107是II型肿瘤抑制基因家族HREV107的成员,作为一种磷脂酶催化从甘油磷脂中释放脂肪酸。H-rev107已被证明通过PGE2/cAMP途径在脂肪细胞的脂肪代谢中发挥重要作用,但H-rev107介导的脂质降解的详细分子机制尚未得到研究。在本研究中,通过酵母双杂交筛选确定了H-rev107与参与肝脏脂质含量调节的细胞色素P450还原酶(POR)之间的相互作用,并通过体外下拉试验和免疫荧光染色进行了证实。在表达H-rev107的细胞中POR的表达增强了H-rev107介导的花生四烯酸释放。然而,H-rev107抑制了POR活性,并缓解了POR介导的HtTA和HeLa宫颈细胞中甘油三酯含量的降低。当用缺乏PLA2的pH-rev107转染表达POR的细胞或用PLA2抑制剂处理时,H-rev107的抑制作用将被消除。使用siRNA沉默H-rev107导致Huh7肝细胞中甘油生成增加以及游离脂肪酸介导的生长抑制的逆转。总之,我们的结果表明,H-rev107还通过其PLA2活性通过POR途径参与肝细胞中的脂质积累。