Department of Pharmacology, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, 755-8505, Japan.
YIC Rehabilitation College, 4-11-1 Nishiube-Minami, Ube, Yamaguchi, 759-0208, Japan.
Sci Rep. 2020 Jan 24;10(1):1140. doi: 10.1038/s41598-020-58116-1.
PDZRN3 is a PDZ domain-containing RING-finger family protein that functions in various developmental processes. We previously showed that expression of PDZRN3 is induced together with that of MyoD during the early phase of skeletal muscle regeneration in vivo. We here show that PDZRN3 suppresses apoptosis and promotes proliferation in myoblasts in a manner dependent on cyclin A2. Depletion of PDZRN3 in mouse C2C12 myoblasts by RNA interference reduced the proportion of Ki-67-positive cells and the level of Akt phosphorylation, implicating PDZRN3 in regulation of both cell proliferation and apoptosis. Exposure of C2C12 cells as well as of C3H10T1/2 mesenchymal stem cells and NIH-3T3 fibroblasts to various inducers of apoptosis including serum deprivation resulted in a greater increase in the amount of cleaved caspase-3 in PDZRN3-depleted cells than in control cells. The abundance of cyclin A2 was reduced in PDZRN3-depleted C2C12 myoblasts, as was that of Mre11, which contributes to the repair of DNA damage. Overexpression of cyclin A2 restored the expression of Mre11 and Ki-67 as well as attenuated caspase-3 cleavage in PDZRN3-depleted cells deprived of serum. These results indicate that PDZRN3 suppresses apoptosis and promotes proliferation in myoblasts and other cell types by maintaining cyclin A2 expression.
PDZRN3 是一个 PDZ 结构域包含的 RING 指家族蛋白,在多种发育过程中发挥作用。我们之前曾表明,在体内骨骼肌再生的早期阶段,PDZRN3 的表达与 MyoD 的表达一起被诱导。我们在这里表明,PDZRN3 通过依赖于细胞周期蛋白 A2 的方式抑制成肌细胞的凋亡并促进其增殖。RNA 干扰使小鼠 C2C12 成肌细胞中的 PDZRN3 耗竭,减少了 Ki-67 阳性细胞的比例和 Akt 磷酸化水平,表明 PDZRN3 参与了细胞增殖和凋亡的调节。暴露于各种凋亡诱导剂(包括血清剥夺)的 C2C12 细胞、C3H10T1/2 间充质干细胞和 NIH-3T3 成纤维细胞中,PDZRN3 耗竭细胞中 cleaved caspase-3 的量增加比对照细胞更大。PDZRN3 耗竭的 C2C12 成肌细胞中细胞周期蛋白 A2 的丰度降低,Mre11 的丰度也降低,Mre11 有助于 DNA 损伤的修复。过表达细胞周期蛋白 A2 恢复了 PDZRN3 耗竭的细胞中 Mre11 和 Ki-67 的表达,并减轻了血清剥夺后 caspase-3 的切割。这些结果表明,PDZRN3 通过维持细胞周期蛋白 A2 的表达来抑制成肌细胞和其他细胞类型的凋亡并促进其增殖。