• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

过量葡萄糖会阻碍贴壁培养条件下骨骼肌卫星细胞的增殖。

Excess Glucose Impedes the Proliferation of Skeletal Muscle Satellite Cells Under Adherent Culture Conditions.

作者信息

Furuichi Yasuro, Kawabata Yuki, Aoki Miho, Mita Yoshitaka, Fujii Nobuharu L, Manabe Yasuko

机构信息

Department of Health Promotion Sciences, Graduate School of Human Health Sciences, Tokyo Metropolitan University, Tokyo, Japan.

出版信息

Front Cell Dev Biol. 2021 Mar 1;9:640399. doi: 10.3389/fcell.2021.640399. eCollection 2021.

DOI:10.3389/fcell.2021.640399
PMID:33732705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7957019/
Abstract

Glucose is a major energy source consumed by proliferating mammalian cells. Therefore, in general, proliferating cells have the preference of high glucose contents in extracellular environment. Here, we showed that high glucose concentrations impede the proliferation of satellite cells, which are muscle-specific stem cells, under adherent culture conditions. We found that the proliferation activity of satellite cells was higher in glucose-free DMEM growth medium (low-glucose medium with a glucose concentration of 2 mM) than in standard glucose DMEM (high-glucose medium with a glucose concentration of 19 mM). Satellite cells cultured in the high-glucose medium showed a decreased population of reserve cells, identified by staining for Pax7 expression, suggesting that glucose concentration affects cell fate determination. In conclusion, glucose is a factor that decides the cell fate of skeletal muscle-specific stem cells. Due to this unique feature of satellite cells, hyperglycemia may negatively affect the regenerative capability of skeletal muscle myofibers and thus facilitate sarcopenia.

摘要

葡萄糖是增殖中的哺乳动物细胞消耗的主要能量来源。因此,一般来说,增殖细胞倾向于细胞外环境中高葡萄糖含量。在此,我们表明,在贴壁培养条件下,高葡萄糖浓度会阻碍卫星细胞(肌肉特异性干细胞)的增殖。我们发现,无葡萄糖的DMEM生长培养基(葡萄糖浓度为2 mM的低葡萄糖培养基)中卫星细胞的增殖活性高于标准葡萄糖DMEM(葡萄糖浓度为19 mM的高葡萄糖培养基)。在高葡萄糖培养基中培养的卫星细胞显示,通过Pax7表达染色鉴定的储备细胞数量减少,这表明葡萄糖浓度会影响细胞命运的决定。总之,葡萄糖是决定骨骼肌特异性干细胞细胞命运的一个因素。由于卫星细胞的这一独特特性,高血糖可能会对骨骼肌肌纤维的再生能力产生负面影响,从而促进肌肉减少症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/002cd38d6530/fcell-09-640399-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/ab789ca5e04c/fcell-09-640399-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/3187b1453250/fcell-09-640399-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/2a32cb55f0f0/fcell-09-640399-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/03617ec292fe/fcell-09-640399-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/002cd38d6530/fcell-09-640399-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/ab789ca5e04c/fcell-09-640399-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/3187b1453250/fcell-09-640399-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/2a32cb55f0f0/fcell-09-640399-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/03617ec292fe/fcell-09-640399-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ee/7957019/002cd38d6530/fcell-09-640399-g005.jpg

相似文献

1
Excess Glucose Impedes the Proliferation of Skeletal Muscle Satellite Cells Under Adherent Culture Conditions.过量葡萄糖会阻碍贴壁培养条件下骨骼肌卫星细胞的增殖。
Front Cell Dev Biol. 2021 Mar 1;9:640399. doi: 10.3389/fcell.2021.640399. eCollection 2021.
2
Myostatin signals through Pax7 to regulate satellite cell self-renewal.肌肉生长抑制素通过PAX7发出信号来调节卫星细胞的自我更新。
Exp Cell Res. 2008 Jan 15;314(2):317-29. doi: 10.1016/j.yexcr.2007.09.012. Epub 2007 Sep 22.
3
beta-Catenin promotes self-renewal of skeletal-muscle satellite cells.β-连环蛋白促进骨骼肌卫星细胞的自我更新。
J Cell Sci. 2008 May 1;121(Pt 9):1373-82. doi: 10.1242/jcs.024885. Epub 2008 Apr 8.
4
Satellite-like cells contribute to pax7-dependent skeletal muscle repair in adult zebrafish.卫星样细胞有助于成年斑马鱼中依赖于PAX7的骨骼肌修复。
Dev Biol. 2017 Apr 15;424(2):162-180. doi: 10.1016/j.ydbio.2017.03.004. Epub 2017 Mar 7.
5
Pattern of Pax7 expression during myogenesis in the posthatch chicken establishes a model for satellite cell differentiation and renewal.孵化后鸡的成肌过程中Pax7表达模式建立了卫星细胞分化和更新的模型。
Dev Dyn. 2004 Nov;231(3):489-502. doi: 10.1002/dvdy.20151.
6
Defining the transcriptional signature of skeletal muscle stem cells.定义骨骼肌干细胞的转录特征。
J Anim Sci. 2008 Apr;86(14 Suppl):E207-16. doi: 10.2527/jas.2007-0473. Epub 2007 Sep 18.
7
Neuromuscular electrical stimulation improves skeletal muscle regeneration through satellite cell fusion with myofibers in healthy elderly subjects.神经肌肉电刺激通过与健康老年受试者的肌纤维融合来改善骨骼肌再生。
J Appl Physiol (1985). 2017 Sep 1;123(3):501-512. doi: 10.1152/japplphysiol.00855.2016. Epub 2017 Jun 1.
8
Plasticity and physiological role of stem cells derived from skeletal muscle interstitium: contribution to muscle fiber hyperplasia and therapeutic use.源自骨骼肌间质的干细胞的可塑性和生理作用:对肌纤维增生的贡献和治疗用途。
Curr Pharm Des. 2010;16(8):956-67. doi: 10.2174/138161210790883408.
9
CCAAT/enhancer binding protein β is required for satellite cell self-renewal.CCAAT/增强子结合蛋白β对于卫星细胞自我更新是必需的。
Skelet Muscle. 2016 Dec 7;6(1):40. doi: 10.1186/s13395-016-0112-8.
10
mTOR is necessary for proper satellite cell activity and skeletal muscle regeneration.mTOR对于卫星细胞的正常活动和骨骼肌再生是必需的。
Biochem Biophys Res Commun. 2015;463(1-2):102-8. doi: 10.1016/j.bbrc.2015.05.032. Epub 2015 May 18.

引用本文的文献

1
Transplantation of Cultured Myoblasts Into Intact Skeletal Muscle and Analysis of Muscle Contraction Force in Mice Model.将培养的成肌细胞移植到完整骨骼肌中并对小鼠模型的肌肉收缩力进行分析
Bio Protoc. 2025 Aug 20;15(16):e5413. doi: 10.21769/BioProtoc.5413.
2
Oxaloacetate and Ketone Bodies Synergistically Promote Myoblast Differentiation in L6 Cells.草酰乙酸和酮体协同促进L6细胞中的成肌细胞分化。
Molecules. 2025 May 9;30(10):2101. doi: 10.3390/molecules30102101.
3
Dnmt3a overexpression disrupts skeletal muscle homeostasis, promotes an aging-like phenotype, and reduces metabolic elasticity.

本文引用的文献

1
High glucose alters the DNA methylation pattern of neurodevelopment associated genes in human neural progenitor cells in vitro.高葡萄糖在体外改变人神经祖细胞中与神经发育相关的基因的 DNA 甲基化模式。
Sci Rep. 2020 Sep 24;10(1):15676. doi: 10.1038/s41598-020-72485-7.
2
Myomaker, and Myomixer-Myomerger-Minion modulate the efficiency of skeletal muscle development with melatonin supplementation through Wnt/β-catenin pathway.肌生成素、肌融合素和肌生成素调节剂通过 Wnt/β-连环蛋白通路调节褪黑素补充对骨骼肌发育的效率。
Exp Cell Res. 2019 Dec 15;385(2):111705. doi: 10.1016/j.yexcr.2019.111705. Epub 2019 Nov 1.
3
Glucose Metabolism Drives Histone Acetylation Landscape Transitions that Dictate Muscle Stem Cell Function.
Dnmt3a过表达会破坏骨骼肌稳态,促进衰老样表型,并降低代谢弹性。
iScience. 2025 Mar 3;28(4):112144. doi: 10.1016/j.isci.2025.112144. eCollection 2025 Apr 18.
4
Glucose modulates IRF6 transcription factor dimerization to enable epidermal differentiation.葡萄糖调节IRF6转录因子二聚化以促进表皮分化。
Cell Stem Cell. 2025 May 1;32(5):795-810.e10. doi: 10.1016/j.stem.2025.02.017. Epub 2025 Mar 21.
5
Achieving myoblast engraftment into intact skeletal muscle via extracellular matrix.通过细胞外基质实现成肌细胞植入完整的骨骼肌。
Front Cell Dev Biol. 2025 Jan 14;12:1502332. doi: 10.3389/fcell.2024.1502332. eCollection 2024.
6
Myokine BDNF highly expressed in Type I fibers inhibits the differentiation of myotubes into Type II fibers.Ⅰ型纤维中高度表达的肌肉因子脑源性神经营养因子抑制肌管向Ⅱ型纤维分化。
Mol Biol Rep. 2024 Nov 12;51(1):1143. doi: 10.1007/s11033-024-10044-3.
7
Effect of glucose and lysine supplementation on myogenic and adipogenic gene expression in muscle satellite cells isolated from Hanwoo with different genotypes of PLAG1: Implications for cell-based food production.补充葡萄糖和赖氨酸对不同PLAG1基因型韩牛分离的肌肉卫星细胞中肌源性和成脂性基因表达的影响:对基于细胞的食品生产的启示
Curr Res Food Sci. 2024 Oct 10;9:100879. doi: 10.1016/j.crfs.2024.100879. eCollection 2024.
8
Protocol for cell proliferation and cell death analysis of primary muscle stem cell culture using flow cytometry.使用流式细胞术对原代肌肉干细胞培养物进行细胞增殖和细胞死亡分析的实验方案。
STAR Protoc. 2024 Dec 20;5(4):103411. doi: 10.1016/j.xpro.2024.103411. Epub 2024 Oct 23.
9
Sympathetic Activation Promotes Sodium Glucose Co-Transporter-1 Protein Expression in Rodent Skeletal Muscle.交感神经激活促进啮齿动物骨骼肌中钠葡萄糖协同转运蛋白1的蛋白表达。
Biomedicines. 2024 Jul 1;12(7):1456. doi: 10.3390/biomedicines12071456.
10
Mechanism of muscle atrophy in a normal-weight rat model of type 2 diabetes established by using a soft-pellet diet.2 型糖尿病正常体重大鼠模型中肌肉萎缩的机制:采用软饲料喂养。
Sci Rep. 2024 Apr 1;14(1):7670. doi: 10.1038/s41598-024-57727-2.
葡萄糖代谢驱动组蛋白乙酰化景观转变,从而决定肌肉干细胞功能。
Cell Rep. 2019 Jun 25;27(13):3939-3955.e6. doi: 10.1016/j.celrep.2019.05.092.
4
Hyperglycemia induces skeletal muscle atrophy via a WWP1/KLF15 axis.高血糖通过 WWP1/KLF15 轴诱导骨骼肌萎缩。
JCI Insight. 2019 Feb 21;4(4). doi: 10.1172/jci.insight.124952.
5
High Glucose-Induced ROS Production Stimulates Proliferation of Pancreatic Cancer via Inactivating the JNK Pathway.高糖诱导的 ROS 产生通过使 JNK 通路失活来刺激胰腺癌的增殖。
Oxid Med Cell Longev. 2018 Nov 21;2018:6917206. doi: 10.1155/2018/6917206. eCollection 2018.
6
AMP-activated protein kinase stabilizes FOXO3 in primary myotubes.AMP 激活的蛋白激酶稳定原代肌管中的 FOXO3。
Biochem Biophys Res Commun. 2018 May 15;499(3):493-498. doi: 10.1016/j.bbrc.2018.03.176. Epub 2018 Mar 30.
7
In Situ Fixation Redefines Quiescence and Early Activation of Skeletal Muscle Stem Cells.原位固定重新定义了骨骼肌干细胞的静息和早期激活。
Cell Rep. 2017 Nov 14;21(7):1982-1993. doi: 10.1016/j.celrep.2017.10.080.
8
Glucose stimulates intestinal epithelial crypt proliferation by modulating cellular energy metabolism.葡萄糖通过调节细胞能量代谢刺激肠道上皮隐窝增殖。
J Cell Physiol. 2018 Apr;233(4):3465-3475. doi: 10.1002/jcp.26199. Epub 2017 Nov 1.
9
AMPKα1-LDH pathway regulates muscle stem cell self-renewal by controlling metabolic homeostasis.AMPKα1-LDH 通路通过控制代谢稳态来调节肌肉干细胞的自我更新。
EMBO J. 2017 Jul 3;36(13):1946-1962. doi: 10.15252/embj.201695273. Epub 2017 May 17.
10
High Glucose Accelerates Cell Proliferation and Increases the Secretion and mRNA Expression of Osteopontin in Human Pancreatic Duct Epithelial Cells.高糖加速人胰腺导管上皮细胞的增殖并增加骨桥蛋白的分泌及mRNA表达。
Int J Mol Sci. 2017 Apr 12;18(4):807. doi: 10.3390/ijms18040807.