College of Pharmacy and Medical Research Center, Chungbuk National University, 194-31, Osongsaengmyeong 1-ro, Heungdeok-gu, Cheongju, Chungbuk, 361-951, Republic of Korea.
Mol Neurobiol. 2019 May;56(5):3132-3144. doi: 10.1007/s12035-018-1287-2. Epub 2018 Aug 10.
Impaired neurogenesis has been associated with several brain disorders, such as Alzheimer's disease (AD) and Parkinson's disease (PD). The role of peroxiredoxin 6 (PRDX6) in neurodegenerative diseases is very controversial. To demonstrate the role of PRDX6 in neurogenesis, we compared the neurogenesis ability of PRDX6-overexpressing transgenic (Tg) mice and wild-type mice and studied the involved molecular mechanisms. We showed that the neurogenesis of neural stem cells (NSCs) and the expression of the marker protein were lower in PRDX6 Tg-mice than in wild-type mice. To determine the factors involved in PRDX6-related neural stem cell impairment, we performed a microarray experiment. We showed that the expression of WDFY1 was dramatically decreased in PRDX6-Tg mice. Moreover, WDFY1 siRNA decreases the differentiation ability of primary neural stem cells. Interestingly, WDFY1 reportedly recruits the signaling adaptor TIR-domain-containing adapter-inducing interferon-β (TRIF) to toll-like receptors (TLRs); thus, we showed the relationship among TLRs, PRDX6, and WDFY1. We showed that TLR4 was dramatically reduced in PRDX6 Tg mice, and reduced TLR4 expression and neurogenesis was reversed by the introduction of WDFY1 plasmid in the neural stem cells from PRDX6 Tg mice. This study indicated that PRDX6 inhibits the neurogenesis of neural precursor cells through TLR4-dependent downregulation of WDFY1 and suggested that the inhibitory effect of PRDX6 on neurogenesis play a role in the development of neurodegenerative diseases in the PRDX6 overexpressing transgenic mice.
神经发生受损与多种脑部疾病有关,如阿尔茨海默病(AD)和帕金森病(PD)。过氧化物还原酶 6(PRDX6)在神经退行性疾病中的作用存在很大争议。为了证明 PRDX6 在神经发生中的作用,我们比较了 PRDX6 过表达转基因(Tg)小鼠和野生型小鼠的神经发生能力,并研究了涉及的分子机制。我们表明,PRDX6 Tg 小鼠的神经干细胞(NSCs)的神经发生和标记蛋白的表达均低于野生型小鼠。为了确定与 PRDX6 相关的神经干细胞损伤涉及的因素,我们进行了微阵列实验。我们表明,PRDX6-Tg 小鼠中 WDFY1 的表达明显降低。此外,WDFY1 siRNA 降低了原代神经干细胞的分化能力。有趣的是,据报道 WDFY1 招募信号适配器 TIR 结构域包含衔接诱导干扰素-β(TRIF)到 Toll 样受体(TLR);因此,我们显示了 TLRs、PRDX6 和 WDFY1 之间的关系。我们表明,PRDX6 Tg 小鼠中的 TLR4 明显减少,并且通过在 PRDX6 Tg 小鼠的神经干细胞中引入 WDFY1 质粒,降低 TLR4 表达和神经发生得到逆转。这项研究表明,PRDX6 通过 TLR4 依赖性下调 WDFY1 抑制神经前体细胞的神经发生,并表明 PRDX6 对神经发生的抑制作用在 PRDX6 过表达转基因小鼠的神经退行性疾病发展中起作用。