Chen Guoqing, Sun Wenhua, Liang Yan, Chen Tian, Guo Weihua, Tian Weidong
State Key Laboratory of Oral Diseases, West China College of Stomatology, Sichuan University, Chengdu, China.
National Engineering Laboratory for Oral Regenerative Medicine, West China College of Stomatology, Sichuan University, Chengdu, China.
Cell Prolif. 2017 Jun;50(3). doi: 10.1111/cpr.12324. Epub 2016 Dec 16.
OBJECTIVES: Maternal gestational diabetes leads to an adverse in utero environment and increases the risk of malformations during embryo organogenesis. In the present study, we analysed the effects of maternal diabetes on tooth germ cell proliferation and apoptosis in offspring, and investigated their underlying mechanisms. MATERIALS AND METHODS: A rat model of maternal diabetes was induced by intraperitoneal injection of streptozotocin and the pregnant rats were divided into three groups: controls, the diabetic group and diabetic group with insulin treatment. Offspring of the three groups were collected and cell proliferation and apoptosis in tooth germs were analysed. Primary dental papilla cells and dental epithelial stem cells were isolated and treated with high glucose in vitro, in an attempt to simulate maternal diabetes-induced hyperglycaemia in vivo. RESULTS: Maternal diabetes significantly affected cell proliferation and apoptosis in offspring tooth germs. The TLR4/NF-ĸB signalling pathway was activated in the tooth germs of offspring of diabetic dams. High glucose treatment activated the TLR4/NF-ĸB signalling pathway in primary dental papilla cells and dental epithelial stem cells in vitro, resulting in suppression of cell proliferation and enhancement of apoptosis. TLR4 knockdown significantly reduced adverse effects induced by high glucose treatment. CONCLUSIONS: Maternal gestational diabetes significantly impaired dental epithelial and mesenchymal cell proliferation and apoptosis in offspring, possibly by activation of the TLR4/NF-ĸB signalling pathway.
目的:母体妊娠期糖尿病会导致子宫内环境不良,并增加胚胎器官形成期间出现畸形的风险。在本研究中,我们分析了母体糖尿病对后代牙胚细胞增殖和凋亡的影响,并探究其潜在机制。 材料与方法:通过腹腔注射链脲佐菌素诱导建立母体糖尿病大鼠模型,将怀孕大鼠分为三组:对照组、糖尿病组和胰岛素治疗糖尿病组。收集三组的后代,分析牙胚中的细胞增殖和凋亡情况。分离原代牙乳头细胞和牙上皮干细胞,并在体外给予高糖处理,以模拟母体糖尿病在体内诱导的高血糖状态。 结果:母体糖尿病显著影响后代牙胚中的细胞增殖和凋亡。糖尿病母鼠后代的牙胚中TLR4/NF-κB信号通路被激活。高糖处理在体外激活了原代牙乳头细胞和牙上皮干细胞中的TLR4/NF-κB信号通路,导致细胞增殖受抑制和凋亡增强。TLR4基因敲低显著降低了高糖处理诱导的不良影响。 结论:母体妊娠期糖尿病可能通过激活TLR4/NF-κB信号通路,显著损害后代的牙上皮和间充质细胞增殖及凋亡。
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