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Total Flavones of Abelmoschus manihot Exhibits Pro-Angiogenic Activity by Activating the VEGF-A/VEGFR2-PI3K/Akt Signaling Axis

Intensive Care Unit, The Third Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210001, P. R. China

Nanjing University of Chinese Medicine, Nanjing 210029, P. R. China

These authors contributed equally to this work.

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Ling-Yi Tang

Nanjing University of Chinese Medicine, Nanjing 210029, P. R. China

These authors contributed equally to this work.

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Dong-Ling Lv

Department of Outpatient, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210029, P. R. China

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, and

Meng Jiang

Good Clinical Practice, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210029, P. R. China

E-mail Address: [email protected]

Correspondence to: Prof. Meng Jiang, Good Clinical Practice, Affiliated Hospital of Nanjing University of Chinese Medicine, No. 155, Hanzhong Road, Nanjing 210029, P. R. China. Tel: (+86) 25-8655-9331, Fax: (+86) 25-8661-8472.

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https://doi.org/10.1142/S0192415X18500295Cited by:28 (Source: Crossref)

Abstract

Angiogenesis is a process of new blood vessel formation from pre-existing vessels. Vascular endothelial growth factor-A (VEGF-A) binds to VEGF receptor-2 (VEGFR2) and thus activation of phosphatidylinositol 3-kinase (PI3K)/Akt pathway play a central role in angiogenesis. Total flavones of Abelmoschus manihot (TFA), the major active component of the traditional Chinese herb Abelmoschus manihot, display novel pro-angiogenic activity. However, little information concerning its underlying mechanism is available. Here we investigate the pro-angiogenesis of TFA with the aim of understanding its mechanism of action. Human umbilical vein endothelial cells (HUVECs) and the chick chorioallantoic membrane (CAM) model were used to evaluate pro-angiogenesis of TFA using cell viability, wounding healing, transwell invasion, tube formation, RT-qPCR and Western blot methods. LY294002, a PI3K inhibitor, was used to interfere with PI3K/Akt pathway signal for assessing the underlying mechanism. Results in vitro indicated TFA obviously promoted HUVECs proliferation, migration, invasion and tube formation. Furthermore, TFA markedly augmented PI3K and Akt phosphorylation and up-regulated VEGF-A and VEGFR2 expression in HUVECs. However, pre-treatment with LY294002 not only markedly attenuated TFA-induced cells proliferation, migration, invasion and tube formation, but also significantly abolished TFA-induced VEGF-A and VEGFR2 over-expression as well as PI3K and Akt phosphorylation. Experiments in CAM model showed TFA significantly promoted the formation of branched blood vessels and was dramatically suppressed by LY294002. Taken together, TFA promoted angiogenesis both in vitro and in vivo which, however, were counteracted by LY294002, suggesting at least in part, TFA exhibits pro-angiogenic activity by activating the VEGF-A/VEGFR2-PI3K/Akt signaling axis.

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References

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