Magnesium ions regulate the Warburg effect to promote the differentiation of enteric neural crest cells into neurons.

IF 7.3 2区 医学 Q1 CELL & TISSUE ENGINEERING Stem Cell Research & Therapy Pub Date : 2025-01-23 DOI:10.1186/s13287-024-04121-4
Qiongqian Xu, Xixi He, Yaru Mou, Dong Sun, Xintao Zhang, Jichang Han, Xiaoyang Liu, Xingjian Liu, Xue Ren, Dongming Wang, Jian Wang, Chuncan Ma, Qiangye Zhang, Aiwu Li
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Abstract

Background: Understanding how enteric neural crest cells (ENCCs) differentiate into neurons is crucial for neurogenesis therapy and gastrointestinal disease research. This study explores how magnesium ions regulate the glycolytic pathway to enhance ENCCs differentiation into neurons.

Materials and methods: We used polymerase chain reaction, western blot, immunofluorescence, and multielectrode array techniques to assess magnesium ions' impact on ENCCs differentiation. Non-targeted metabolomic sequencing, cellular acidification rate, oxygen consumption, and western blot analyzed sugar metabolism changes. D-glucose-13C6 isotope tracing identified key glucose flux changes. Surface plasmon resonance was used to detect the binding affinity of magnesium ions with key glycolysis genes. The elastic modulus of the hydrogel was measured using a universal testing machine, while pore size and porosity were assessed with scanning electron microscopy. Swelling ratios were determined using gravimetric analysis. In vivo, ENCCs in hydrogels were transplanted into renal capsule and subcutaneously, and magnesium ions' effects on ENCCs differentiation were evaluated.

Results: Magnesium ions increased glycolysis levels during ENCCs differentiation into neurons, along with significant upregulation of neuronal markers β-Tubulin and ubiquitin C-terminal hydrolase L1, and enhanced functional neuronal properties. D-glucose-13C6 tracing results showed increased carbon flux in the glycolytic pathway after magnesium supplementation. The binding affinity of magnesium ions with the glycolytic key enzyme 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 was found to be 1.08 μM. Inhibiting glycolysis suppressed ENCCs differentiation into neurons, emphasizing its crucial role. The double-cross-linked hydrogel gelatin methacryloyl-alginate (gelMA-ALMA), cross-linked with magnesium ions, showed promise in enhancing ENCCs differentiation in vivo without causing systemic hypermagnesemia.

Conclusion: Magnesium ions promote ENCCs differentiation into neurons by activating the Warburg effect. The GelMA-ALMA hydrogel serves as an effective localized magnesium delivery system, supporting neuronal differentiation in vivo.

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镁离子通过调节Warburg效应促进肠神经嵴细胞向神经元的分化。
背景:了解肠神经嵴细胞(enteric neural crest cells, ENCCs)如何分化为神经元对于神经发生治疗和胃肠道疾病的研究至关重要。本研究探讨镁离子如何调节糖酵解通路,促进ENCCs向神经元分化。材料和方法:我们使用聚合酶链反应、免疫印迹、免疫荧光和多电极阵列技术来评估镁离子对ENCCs分化的影响。非靶向代谢组学测序、细胞酸化率、耗氧量和western blot分析糖代谢变化。d -葡萄糖- 13c6同位素示踪确定了关键的葡萄糖通量变化。利用表面等离子体共振检测镁离子与糖酵解关键基因的结合亲和力。水凝胶的弹性模量采用万能试验机测量,孔径和孔隙率采用扫描电子显微镜评估。用重量分析法测定溶胀率。在体内,将水凝胶中的ENCCs移植到肾包膜和皮下,观察镁离子对ENCCs分化的影响。结果:在ENCCs向神经元分化过程中,镁离子增加了糖酵解水平,同时显著上调神经元标志物β-微管蛋白和泛素c端水解酶L1,增强了神经元的功能特性。d -葡萄糖- 13c6示踪结果显示,补充镁后糖酵解途径中的碳通量增加。镁离子与糖酵解关键酶6-磷酸果糖-2-激酶/果糖-2,6-双磷酸酶3的结合亲和力为1.08 μM。抑制糖酵解抑制ENCCs向神经元分化,强调其重要作用。与镁离子交联的双交联水凝胶明胶甲基丙烯酰海藻酸盐(gelMA-ALMA)有望增强ENCCs在体内的分化,而不会引起全身高镁血症。结论:镁离子通过激活Warburg效应促进ENCCs向神经元分化。GelMA-ALMA水凝胶作为一种有效的局部镁递送系统,在体内支持神经元分化。
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来源期刊
Stem Cell Research & Therapy
Stem Cell Research & Therapy CELL BIOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
13.20
自引率
8.00%
发文量
525
审稿时长
1 months
期刊介绍: Stem Cell Research & Therapy serves as a leading platform for translational research in stem cell therapies. This international, peer-reviewed journal publishes high-quality open-access research articles, with a focus on basic, translational, and clinical research in stem cell therapeutics and regenerative therapies. Coverage includes animal models and clinical trials. Additionally, the journal offers reviews, viewpoints, commentaries, and reports.
期刊最新文献
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