Linalool inhibits the angiogenic activity of endothelial cells by downregulating intracellular ATP levels and activating TRPM8.
Vivien BeckerXin HuiLisa NalbachEmmanuel AmpofoPeter LippMichael D MengerMatthias W LaschkeYuan GuPublished in: Angiogenesis (2021)
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.
Keyphrases
- endothelial cells
- high glucose
- signaling pathway
- diabetic retinopathy
- cell proliferation
- protein kinase
- vascular endothelial growth factor
- poor prognosis
- mesenchymal stem cells
- heart failure
- mass spectrometry
- type diabetes
- anti inflammatory
- optical coherence tomography
- pulmonary artery
- escherichia coli
- risk assessment
- drug induced
- reactive oxygen species
- wound healing
- left ventricular
- aortic valve
- cell migration
- climate change
- bone marrow
- staphylococcus aureus
- pulmonary arterial hypertension
- biofilm formation
- atomic force microscopy
- long non coding rna
- ionic liquid