Zhang Jitai, Dai Kaicen, An Ruike, Wang Chengying, Zhou Xuanting, Tian Zhujun, Liao Zhonglu
School of Basic Medical Science, Wenzhou Medical University, Wenzhou 325035, China.
School of Public Health and Management, Wenzhou Medical University, Wenzhou 325035, China.
Antioxidants (Basel). 2025 Jan 21;14(2):120. doi: 10.3390/antiox14020120.
High doses of ionizing radiation (HDIR) are known to induce cellular damage, whereas low-dose ionizing radiation (LDIR) may trigger protective biological responses. Recent studies have explored the potential benefits of LDIR in treating diabetes and its complications. However, the direct effects of LDIR on pancreatic β-cells and the underlying mechanisms remain to be elucidated. This study aimed to evaluate the effects of LDIR on pancreatic β-cell functionality and elucidate the underlying molecular mechanisms involved. Rat RIN-m5F cells were exposed to LDIR (25 mGy) or HDIR (2.5 Gy) to examine changes in insulin mRNA expression, secretion, DNA damage, and apoptosis. The roles of reactive oxygen species (ROS) and the p38 mitogen-activated protein kinase (MAPK) pathway were assessed via the use of antioxidants and pathway inhibitors. The findings indicated that LDIR transiently increased both insulin synthesis and secretion without inducing apoptosis or affecting cell proliferation. In contrast, HDIR induced a significant increase in apoptosis and a marked inhibition of proliferation. LDIR was observed to temporarily increase ROS production, activating the p38 MAPK pathway and facilitating insulin synthesis via the upregulation of PDX-1. Notably, LDIR did not induce DNA double-strand breaks or activate the ATM-dependent DNA repair pathways, unlike HDIR, which induced apoptosis through overactivation of the ROS/p38 MAPK pathway. In conclusion, LDIR enhanced pancreatic β-cell functionality via ROS-mediated activation of the p38 MAPK pathway, highlighting its potential therapeutic applications in diabetes management.
已知高剂量电离辐射(HDIR)会导致细胞损伤,而低剂量电离辐射(LDIR)可能引发保护性生物学反应。最近的研究探讨了LDIR在治疗糖尿病及其并发症方面的潜在益处。然而,LDIR对胰腺β细胞的直接影响及其潜在机制仍有待阐明。本研究旨在评估LDIR对胰腺β细胞功能的影响,并阐明其中涉及的潜在分子机制。将大鼠RIN-m5F细胞暴露于LDIR(25 mGy)或HDIR(2.5 Gy),以检测胰岛素mRNA表达、分泌、DNA损伤和细胞凋亡的变化。通过使用抗氧化剂和信号通路抑制剂评估活性氧(ROS)和p38丝裂原活化蛋白激酶(MAPK)信号通路的作用。研究结果表明,LDIR可短暂增加胰岛素的合成和分泌,而不会诱导细胞凋亡或影响细胞增殖。相比之下,HDIR可显著增加细胞凋亡并明显抑制细胞增殖。观察到LDIR可暂时增加ROS生成,激活p38 MAPK信号通路,并通过上调PDX-1促进胰岛素合成。值得注意的是,与HDIR不同,LDIR不会诱导DNA双链断裂或激活ATM依赖性DNA修复通路,HDIR通过ROS/p38 MAPK信号通路的过度激活诱导细胞凋亡。总之,LDIR通过ROS介导的p38 MAPK信号通路激活增强了胰腺β细胞功能,突出了其在糖尿病管理中的潜在治疗应用价值。