• 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

高度糖酵解永生化人真皮微血管内皮细胞能够在葡萄糖饥饿条件下生长。

Highly Glycolytic Immortalized Human Dermal Microvascular Endothelial Cells are Able to Grow in Glucose-Starved Conditions.

机构信息

Universidad de Málaga, Andalucía Tech, Departamento de Biología Molecular y Bioquímica, Facultad de Ciencias, E-29071 Málaga, Spain.

IBIMA (Biomedical Research Institute of Málaga), E-29071 Málaga, Spain.

出版信息

Biomolecules. 2019 Aug 1;9(8):332. doi: 10.3390/biom9080332.

DOI:10.3390/biom9080332
PMID:31374952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6723428/
Abstract

Endothelial cells form the inner lining of blood vessels, in a process known as angiogenesis. Excessive angiogenesis is a hallmark of several diseases, including cancer. The number of studies in endothelial cell metabolism has increased in recent years, and new metabolic targets for pharmacological treatment of pathological angiogenesis are being proposed. In this work, we wanted to address experimental evidence of substrate (namely glucose, glutamine and palmitate) dependence in immortalized dermal microvascular endothelial cells in comparison to primary endothelial cells. In addition, due to the lack of information about lactate metabolism in this specific type of endothelial cells, we also checked their capability of utilizing extracellular lactate. For fulfilling these aims, proliferation, migration, Seahorse, substrate uptake/utilization, and mRNA/protein expression experiments were performed. Our results show a high glycolytic capacity of immortalized dermal microvascular endothelial cells, but an early independence of glucose for cell growth, whereas a total dependence of glutamine to proliferate was found. Additionally, in contrast with reported data in other endothelial cell lines, these cells lack monocarboxylate transporter 1 for extracellular lactate incorporation. Therefore, our results point to the change of certain metabolic features depending on the endothelial cell line.

摘要

内皮细胞形成血管的内层,这个过程被称为血管生成。血管生成过度是包括癌症在内的几种疾病的标志。近年来,内皮细胞代谢的研究数量有所增加,并且正在提出针对病理性血管生成的药理学治疗的新代谢靶标。在这项工作中,我们希望针对与原代内皮细胞相比,永生化皮肤微血管内皮细胞对基质(即葡萄糖、谷氨酰胺和棕榈酸)的依赖性的实验证据进行研究。此外,由于缺乏关于这种特定类型内皮细胞中乳酸代谢的信息,我们还检查了它们利用细胞外乳酸的能力。为了实现这些目标,进行了增殖、迁移、 Seahorse 实验、基质摄取/利用以及 mRNA/蛋白表达实验。我们的结果表明,永生化皮肤微血管内皮细胞具有很高的糖酵解能力,但对葡萄糖的早期生长独立性,而发现完全依赖谷氨酰胺来增殖。此外,与其他内皮细胞系中的报道数据相反,这些细胞缺乏用于细胞外乳酸摄取的单羧酸转运蛋白 1。因此,我们的结果表明,某些代谢特征会根据内皮细胞系而发生变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/8be16444b7fb/biomolecules-09-00332-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/f27d0b1c75ee/biomolecules-09-00332-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/c18244163e7a/biomolecules-09-00332-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/fd3a9b04298f/biomolecules-09-00332-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/69cac0407295/biomolecules-09-00332-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/5380ef99d4c3/biomolecules-09-00332-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/8ccd18afc833/biomolecules-09-00332-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/583b035675ed/biomolecules-09-00332-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/8be16444b7fb/biomolecules-09-00332-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/f27d0b1c75ee/biomolecules-09-00332-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/c18244163e7a/biomolecules-09-00332-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/fd3a9b04298f/biomolecules-09-00332-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/69cac0407295/biomolecules-09-00332-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/5380ef99d4c3/biomolecules-09-00332-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/8ccd18afc833/biomolecules-09-00332-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/583b035675ed/biomolecules-09-00332-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbd/6723428/8be16444b7fb/biomolecules-09-00332-g008.jpg

相似文献

1
Highly Glycolytic Immortalized Human Dermal Microvascular Endothelial Cells are Able to Grow in Glucose-Starved Conditions.高度糖酵解永生化人真皮微血管内皮细胞能够在葡萄糖饥饿条件下生长。
Biomolecules. 2019 Aug 1;9(8):332. doi: 10.3390/biom9080332.
2
Monocarboxylate transporter 1 is a key player in glioma-endothelial cell crosstalk.单羧酸转运蛋白1是胶质瘤-内皮细胞相互作用中的关键因子。
Mol Carcinog. 2017 Dec;56(12):2630-2642. doi: 10.1002/mc.22707. Epub 2017 Aug 25.
3
Lactate promotes glutamine uptake and metabolism in oxidative cancer cells.乳酸促进氧化性癌细胞对谷氨酰胺的摄取和代谢。
Cell Cycle. 2016;15(1):72-83. doi: 10.1080/15384101.2015.1120930.
4
Targeting the lactate transporter MCT1 in endothelial cells inhibits lactate-induced HIF-1 activation and tumor angiogenesis.靶向内皮细胞中的乳酸转运蛋白 MCT1 可抑制乳酸诱导的 HIF-1 激活和肿瘤血管生成。
PLoS One. 2012;7(3):e33418. doi: 10.1371/journal.pone.0033418. Epub 2012 Mar 13.
5
A CD147-targeting siRNA inhibits the proliferation, invasiveness, and VEGF production of human malignant melanoma cells by down-regulating glycolysis.一种靶向CD147的小干扰RNA通过下调糖酵解来抑制人恶性黑色素瘤细胞的增殖、侵袭及血管内皮生长因子的产生。
Cancer Lett. 2009 Jan 8;273(1):140-7. doi: 10.1016/j.canlet.2008.07.034. Epub 2008 Sep 7.
6
Lactate as substrate for mitochondrial respiration in alveolar epithelial type II cells.乳酸作为肺泡II型上皮细胞线粒体呼吸的底物。
Am J Physiol Lung Cell Mol Physiol. 2015 May 1;308(9):L953-61. doi: 10.1152/ajplung.00335.2014. Epub 2015 Mar 6.
7
Glucose deprivation increases monocarboxylate transporter 1 (MCT1) expression and MCT1-dependent tumor cell migration.葡萄糖剥夺会增加单羧酸转运蛋白 1(MCT1)的表达和依赖 MCT1 的肿瘤细胞迁移。
Oncogene. 2014 Jul 31;33(31):4060-8. doi: 10.1038/onc.2013.454. Epub 2013 Oct 28.
8
Androgens enhance the glycolytic metabolism and lactate export in prostate cancer cells by modulating the expression of GLUT1, GLUT3, PFK, LDH and MCT4 genes.雄激素通过调节葡萄糖转运蛋白1(GLUT1)、葡萄糖转运蛋白3(GLUT3)、磷酸果糖激酶(PFK)、乳酸脱氢酶(LDH)和单羧酸转运蛋白4(MCT4)基因的表达,增强前列腺癌细胞的糖酵解代谢和乳酸输出。
J Cancer Res Clin Oncol. 2016 Jan;142(1):5-16. doi: 10.1007/s00432-015-1992-4. Epub 2015 Jun 6.
9
miR-124 Suppresses Pancreatic Ductal Adenocarcinoma Growth by Regulating Monocarboxylate Transporter 1-Mediated Cancer Lactate Metabolism.微小RNA-124通过调控单羧酸转运蛋白1介导的癌症乳酸代谢抑制胰腺导管腺癌生长。
Cell Physiol Biochem. 2018;50(3):924-935. doi: 10.1159/000494477. Epub 2018 Oct 24.
10
Monocarboxylate transport inhibition potentiates the cytotoxic effect of 5-fluorouracil in colorectal cancer cells.单羧酸转运抑制增强5-氟尿嘧啶对结肠癌细胞的细胞毒性作用。
Cancer Lett. 2015 Aug 28;365(1):68-78. doi: 10.1016/j.canlet.2015.05.015. Epub 2015 May 25.

引用本文的文献

1
Aerobic glycolysis of vascular endothelial cells: a novel perspective in cancer therapy.血管内皮细胞的有氧糖酵解:癌症治疗的新视角。
Mol Biol Rep. 2024 Jun 1;51(1):717. doi: 10.1007/s11033-024-09588-1.
2
New insights in the targets of action of dimethyl fumarate in endothelial cells: effects on energetic metabolism and serine synthesis in vitro and in vivo.二甲基富马酸在血管内皮细胞中作用靶点的新见解:对体外和体内能量代谢和丝氨酸合成的影响。
Commun Biol. 2023 Oct 25;6(1):1084. doi: 10.1038/s42003-023-05443-4.
3
Arterial Blood Pressure Features of Hypertensive Patients with Typical and Atypical 460 nm Skin Fluorescence Response to Transient Ischaemia.

本文引用的文献

1
Metabolism within the tumor microenvironment and its implication on cancer progression: An ongoing therapeutic target.肿瘤微环境中的代谢及其对癌症进展的影响:一个持续的治疗靶点。
Med Res Rev. 2019 Jan;39(1):70-113. doi: 10.1002/med.21511. Epub 2018 May 22.
2
Consensus guidelines for the use and interpretation of angiogenesis assays.血管生成分析检测应用和解释的共识指南。
Angiogenesis. 2018 Aug;21(3):425-532. doi: 10.1007/s10456-018-9613-x.
3
Monocarboxylate transporter 1 (MCT1), a tool to stratify acute myeloid leukemia (AML) patients and a vehicle to kill cancer cells.
对短暂性缺血具有典型和非典型460nm皮肤荧光反应的高血压患者的动脉血压特征
J Clin Med. 2023 Sep 10;12(18):5886. doi: 10.3390/jcm12185886.
4
Glutamate dehydrogenase 1 mediated glutaminolysis sustains HCC cells survival under glucose deprivation.谷氨酸脱氢酶1介导的谷氨酰胺分解代谢在葡萄糖剥夺条件下维持肝癌细胞存活。
J Cancer. 2022 Jan 4;13(3):1061-1072. doi: 10.7150/jca.64195. eCollection 2022.
5
Glucose Favors Lipid Anabolic Metabolism in the Invasive Breast Cancer Cell Line MDA-MB-231.葡萄糖有利于侵袭性乳腺癌细胞系MDA-MB-231中的脂质合成代谢。
Biology (Basel). 2020 Jan 10;9(1):16. doi: 10.3390/biology9010016.
单羧酸转运蛋白1(MCT1),一种对急性髓系白血病(AML)患者进行分层的工具以及一种杀死癌细胞的载体。
Oncotarget. 2017 Aug 16;8(47):82803-82823. doi: 10.18632/oncotarget.20294. eCollection 2017 Oct 10.
4
Monocarboxylate transporter 1 is a key player in glioma-endothelial cell crosstalk.单羧酸转运蛋白1是胶质瘤-内皮细胞相互作用中的关键因子。
Mol Carcinog. 2017 Dec;56(12):2630-2642. doi: 10.1002/mc.22707. Epub 2017 Aug 25.
5
Short-term starvation is a strategy to unravel the cellular capacity of oxidizing specific exogenous/endogenous substrates in mitochondria.短期饥饿是一种用于揭示线粒体中氧化特定外源性/内源性底物的细胞能力的策略。
J Biol Chem. 2017 Aug 25;292(34):14176-14187. doi: 10.1074/jbc.M117.786582. Epub 2017 Jun 29.
6
Glutamine fuels proliferation but not migration of endothelial cells.谷氨酰胺为内皮细胞的增殖提供能量,但不支持其迁移。
EMBO J. 2017 Aug 15;36(16):2321-2333. doi: 10.15252/embj.201796436. Epub 2017 Jun 28.
7
Role of glutamine and interlinked asparagine metabolism in vessel formation.谷氨酰胺和相互关联的天冬酰胺代谢在血管形成中的作用。
EMBO J. 2017 Aug 15;36(16):2334-2352. doi: 10.15252/embj.201695518. Epub 2017 Jun 28.
8
Oleate protects macrophages from palmitate-induced apoptosis through the downregulation of CD36 expression.油酸通过下调CD36表达保护巨噬细胞免受棕榈酸诱导的凋亡。
Biochem Biophys Res Commun. 2017 Jul 1;488(3):477-482. doi: 10.1016/j.bbrc.2017.05.066. Epub 2017 May 15.
9
Palmitate impairs angiogenesis via suppression of cathepsin activity.棕榈酸盐通过抑制组织蛋白酶活性损害血管生成。
Mol Med Rep. 2017 Jun;15(6):3644-3650. doi: 10.3892/mmr.2017.6463. Epub 2017 Apr 12.
10
Metformin represses glucose starvation induced autophagic response in microvascular endothelial cells and promotes cell death.二甲双胍可抑制微血管内皮细胞中葡萄糖饥饿诱导的自噬反应,并促进细胞死亡。
Biochem Pharmacol. 2017 May 15;132:118-132. doi: 10.1016/j.bcp.2017.03.001. Epub 2017 Mar 6.