Department of Dermatology, Taipei Tzuchi Hospital, Buddhist Tzuchi Medical Foundation, 231, New Taipei City, Taiwan.
School of Medicine, Tzu Chi University, 970, Hualien, Taiwan.
Cell Biochem Biophys. 2019 Sep;77(3):253-260. doi: 10.1007/s12013-019-00876-3. Epub 2019 May 26.
Phospholipase A and acyltransferase 4 (PLAAT4) is a member of the HREV107 tumor suppressor gene family. The expression of PLAAT4 has been shown to induce cell death; however, the underlying mechanism remains unknown. Here, we found that RPLP0, a ribosomal protein, can interact with PLAAT4, as determined by yeast two-hybrid screening, coimmunoprecipitation, and colocalization. The level of RPLP0 was suppressed in HtTA cervical cancer cells expressing PLAAT4. In PLAAT4-expressing or RPLP0-silenced cells, decreased cell viability and cell proliferation combined with increased cell death were observed. Furthermore, the levels of cell cycle-associated proteins and anti-apoptotic proteins decreased in PLAAT4-expressing or RPLP0-silenced cells. Similar patterns of cell viability and expression levels of cell-cycle-associated proteins and apoptosis-related proteins were observed in PLAAT4-expressing and RPLP0-knockdown cells, indicating that RPLP0 deficiency might be involved in PLAAT4-mediated growth inhibition and cellular apoptosis.
磷酸酶 A 和酰基转移酶 4(PLAAT4)是 HREV107 肿瘤抑制基因家族的成员。已经表明 PLAAT4 的表达可诱导细胞死亡;然而,其潜在机制尚不清楚。在这里,我们发现核糖体蛋白 RPLP0 可以与 PLAAT4 相互作用,这是通过酵母双杂交筛选、共免疫沉淀和共定位确定的。在表达 PLAAT4 的 HtTA 宫颈癌细胞中,RPLP0 的水平受到抑制。在表达 PLAAT4 或沉默 RPLP0 的细胞中,观察到细胞活力和增殖降低,同时细胞死亡增加。此外,细胞周期相关蛋白和抗凋亡蛋白的水平在表达 PLAAT4 或沉默 RPLP0 的细胞中降低。在表达 PLAAT4 和敲低 RPLP0 的细胞中观察到类似的细胞活力模式和细胞周期相关蛋白及凋亡相关蛋白的表达水平,表明 RPLP0 缺乏可能参与 PLAAT4 介导的生长抑制和细胞凋亡。