Central Laboratory of Yong-Chuan Hospital, Chongqing Medical University, Chongqing, 402160, China; Key Laboratory of Laboratory Medical Diagnostics, Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, China.
Key Laboratory of Laboratory Medical Diagnostics, Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, China.
Biochem Biophys Res Commun. 2020 Jul 23;528(2):276-284. doi: 10.1016/j.bbrc.2020.05.076. Epub 2020 May 29.
A majority of acute promyelocytic leukaemia (APL) cases are characterized by the PML-RARα fusion gene. Previous studies have shown that neutrophil elastase (NE) can cleave PML-RARα and is important for the development of APL. Here, we demonstrate that one of the cleavage products of PML-RARα, NLS-RARα, can block cell differentiation by repressing the expression of the target genes within the retinoic acid signalling pathway. The results of reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot analysis showed that NLS-RARα depressed the expression of the cell differentiation marker protein, CD11b and CEBPβ, as well as the retinoic acid signalling pathway target genes, RARβ and CEBPε. Studies have shown that NLS-RARα forms heterodimers with retinoid X receptor α(RXRα) and interacts with SMRT. When treated with all-trans retinoic acid (ATRA), NLS-RARα exhibits diminished transcriptional activity compared to RARα. Moreover, in the presence of high doses of ATRA, NLS-RARα could be degraded along with the consequent transactivation of retinoic acid signalling pathway target genes and cell differentiation induction in a dose- and time-dependent manner. Together, these results indicate that NLS-RARα blocks cell differentiation by inhibiting the retinoic acid signalling pathway.
大多数急性早幼粒细胞白血病 (APL) 病例的特征是存在 PML-RARα 融合基因。先前的研究表明,中性粒细胞弹性蛋白酶 (NE) 可以切割 PML-RARα,对 APL 的发展很重要。在这里,我们证明 PML-RARα 的一种裂解产物 NLS-RARα 可以通过抑制视黄酸信号通路内的靶基因的表达来阻断细胞分化。逆转录聚合酶链反应 (RT-PCR) 和 Western blot 分析的结果表明,NLS-RARα 抑制了细胞分化标志物蛋白 CD11b 和 CEBPβ 以及视黄酸信号通路靶基因 RARβ 和 CEBPε 的表达。研究表明,NLS-RARα 与视黄酸受体 X 受体 α (RXRα) 形成异二聚体并与 SMRT 相互作用。用全反式维甲酸 (ATRA) 处理时,与 RARα 相比,NLS-RARα 的转录活性降低。此外,在存在高剂量 ATRA 的情况下,NLS-RARα 可以与随之而来的视黄酸信号通路靶基因的反式激活以及细胞分化诱导一起被降解,呈剂量和时间依赖性。综上所述,这些结果表明 NLS-RARα 通过抑制视黄酸信号通路来阻断细胞分化。