Kim Seul-Ki, Kwon Yong-Jin, Seo Eun-Bi, Lee Hyun-Seung, Sohn Jie Ohn, Shin Hyun Mu, Kim Sung Joon, Ye Sang-Kyu
Department of Pharmacology and Biomedical Sciences, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Department of Cosmetic Science, Kyungsung University, Busan, 48434, Republic of Korea.
Neurochem Res. 2024 Dec 9;50(1):52. doi: 10.1007/s11064-024-04252-3.
This study investigates the neuroprotective potential of STAT3 inhibition in reducing oxidative stress-induced neuronal damage and apoptosis, a major factor contributing to the onset and progression of neurodegenerative diseases, including Alzheimer's disease (AD). Our findings demonstrate that STAT3 inhibitors significantly enhance cell survival and reduce apoptosis in SH-SY5Y cells exposed to hydrogen peroxide. These protective effects are mediated through the ERK/CREB signaling pathway rather than direct suppression of STAT3 phosphorylation. Further analysis revealed that the ERK pathway is a critical mediator of CREB activation following STAT3 inhibition. The protective effects of STAT3 inhibitors were significantly reduced in the presence of the ERK inhibitor PD98059, underscoring the importance of the ERK/CREB axis in neuroprotection. We observed that STAT3 inhibitors promote CREB phosphorylation, leading to the upregulation of immediate early genes such as c-Fos, c-Jun, Arc, Egr-1, NR4A1, and Homer1a, as well as BDNF. These genes are crucial for synaptic plasticity and long-term memory formation, suggesting that STAT3 inhibition may ameliorate cognitive impairments in neurodegenerative conditions. Our results highlight the potential of STAT3 inhibitors to counteract oxidative stress and enhance cognitive functions by modulating the ERK/CREB signaling pathway. These findings provide valuable insights into the molecular mechanisms of STAT3 inhibition and support its therapeutic potential for treating neurodegenerative diseases.
本研究调查了信号转导与转录激活因子3(STAT3)抑制在减轻氧化应激诱导的神经元损伤和凋亡方面的神经保护潜力,氧化应激是导致包括阿尔茨海默病(AD)在内的神经退行性疾病发生和进展的主要因素。我们的研究结果表明,STAT3抑制剂可显著提高暴露于过氧化氢的SH-SY5Y细胞的存活率并减少其凋亡。这些保护作用是通过细胞外信号调节激酶/环磷腺苷效应元件结合蛋白(ERK/CREB)信号通路介导的,而非直接抑制STAT3磷酸化。进一步分析显示,ERK通路是STAT3抑制后CREB激活的关键介质。在存在ERK抑制剂PD98059的情况下,STAT3抑制剂的保护作用显著降低,这突出了ERK/CREB轴在神经保护中的重要性。我们观察到,STAT3抑制剂可促进CREB磷酸化,导致即刻早期基因如c-Fos、c-Jun、Arc、Egr-1、NR4A1和Homer1a以及脑源性神经营养因子(BDNF)的上调。这些基因对于突触可塑性和长期记忆形成至关重要,表明STAT3抑制可能改善神经退行性疾病中的认知障碍。我们的结果突出了STAT3抑制剂通过调节ERK/CREB信号通路来对抗氧化应激和增强认知功能的潜力。这些发现为STAT3抑制的分子机制提供了有价值的见解,并支持其在治疗神经退行性疾病方面的治疗潜力。