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1000 Titel
  • Linalool inhibits the angiogenic activity of endothelial cells by downregulating intracellular ATP levels and activating TRPM8
1000 Autor/in
  1. Becker, Vivien |
  2. Hui, Xin |
  3. Nalbach, Lisa |
  4. Ampofo, Emmanuel |
  5. Lipp, Peter |
  6. Menger, Michael D. |
  7. Laschke, Matthias W. |
  8. Gu, Yuan |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-03-02
1000 Erschienen in
1000 Quellenangabe
  • 24(3):613-630
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s10456-021-09772-y |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292279/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Angiogenesis crucially contributes to various diseases, such as cancer and diabetic retinopathy. Hence, anti-angiogenic therapy is considered as a powerful strategy against these diseases. Previous studies reported that the acyclic monoterpene linalool exhibits anticancer, anti-inflammatory and anti-oxidative activity. However, the effects of linalool on angiogenesis still remain elusive. Therefore, we investigated the action of (3R)-(-)-linalool, a main enantiomer of linalool, on the angiogenic activity of human dermal microvascular endothelial cells (HDMECs) by a panel of angiogenesis assays. Non-cytotoxic doses of linalool significantly inhibited HDMEC proliferation, migration, tube formation and spheroid sprouting. Linalool also suppressed the vascular sprouting from rat aortic rings. In addition, Matrigel plugs containing linalool exhibited a significantly reduced microvessel density 7 days after implantation into BALB/c mice. Mechanistic analyses revealed that linalool promotes the phosphorylation of extracellular signal-regulated kinase (ERK), downregulates the intracellular level of adenosine triphosphate (ATP) and activates the transient receptor potential cation channel subfamily M (melastatin) member (TRPM)8 in HDMECs. Inhibition of ERK signaling, supplementation of ATP and blockade of TRPM8 significantly counteracted linalool-suppressed HDMEC spheroid sprouting. Moreover, ATP supplementation completely reversed linalool-induced ERK phosphorylation. In addition, linalool-induced ERK phosphorylation inhibited the expression of bone morphogenetic protein (BMP)-2 and linalool-induced TRPM8 activation caused the inhibition of β1 integrin/focal adhesion kinase (FAK) signaling. These findings indicate an anti-angiogenic effect of linalool, which is mediated by downregulating intracellular ATP levels and activating TRPM8.
1000 Sacherschließung
lokal Endothelial Cells/metabolism [MeSH]
lokal Down-Regulation/drug effects [MeSH]
lokal Mice, Inbred BALB C [MeSH]
lokal TRPM Cation Channels/metabolism [MeSH]
lokal Humans [MeSH]
lokal MAP Kinase Signaling System/drug effects [MeSH]
lokal Cell Line [MeSH]
lokal TRPM Cation Channels/antagonists
lokal Neovascularization, Physiologic/drug effects [MeSH]
lokal Adenosine Triphosphate/metabolism [MeSH]
lokal Heterografts [MeSH]
lokal Animals [MeSH]
lokal Dermis/blood supply [MeSH]
lokal Vascularization
lokal Endothelial cells
lokal Microvessels/metabolism [MeSH]
lokal Original Paper
lokal TRPM8
lokal Acyclic Monoterpenes/pharmacology [MeSH]
lokal Endothelial Cells/transplantation [MeSH]
lokal Angiogenesis
lokal ATP
lokal Dermis/metabolism [MeSH]
lokal Linalool
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/QmVja2VyLCBWaXZpZW4=|https://frl.publisso.de/adhoc/uri/SHVpLCBYaW4=|https://frl.publisso.de/adhoc/uri/TmFsYmFjaCwgTGlzYQ==|https://frl.publisso.de/adhoc/uri/QW1wb2ZvLCBFbW1hbnVlbA==|https://frl.publisso.de/adhoc/uri/TGlwcCwgUGV0ZXI=|https://frl.publisso.de/adhoc/uri/TWVuZ2VyLCBNaWNoYWVsIEQu|https://frl.publisso.de/adhoc/uri/TGFzY2hrZSwgTWF0dGhpYXMgVy4=|https://orcid.org/0000-0003-1401-6233
1000 Hinweis
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1000 @id frl:6446173.rdf
1000 Erstellt am 2023-04-28T12:24:24.265+0200
1000 Erstellt von 322
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1000 Zuletzt bearbeitet 2023-10-20T17:43:24.623+0200
1000 Objekt bearb. Fri Oct 20 17:43:24 CEST 2023
1000 Vgl. frl:6446173
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