Elucidation of the mechanisms underlying the angiogenic effects of ginsenoside Rg1
in vivo and in vitro |
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Authors: | Patrick Y.K. Yue Daisy Y.L. Wong W.Y. Ha M.C. Fung N.K. Mak H.W. Yeung H.W. Leung Kelvin Chan L. Liu T.P.D. Fan Ricky N.S. Wong |
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Affiliation: | (1) Hung Lai Ching Laboratory of Biomedical Science, Research and Development Division, School of Chinese Medicine, Hong Kong Baptist University, Kowloon, Hong Kong;(2) Department of Biology, Science Faculty, Chinese University of Hong Kong, Shatin, Hong Kong;(3) Department of Biology, Hong Kong Baptist University, Kowloon Tong, Kowloon, Hong Kong;(4) Angiogenesis & TCM Laboratory, Department of Pharmacology, University of Cambridge, Cambridge, UK |
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Abstract: | The major active constituents of ginseng are ginsenosides, and Rg1 is a predominant compound of the total extract. Recent studies have demonstrated that Rg1 can promote angiogenesis in vivo and in vitro. In this study, we used a DNA microarray technology to elucidate the mechanisms of action of Rg1. We report that Rg1 induces the proliferation of HUVECs, monitored using [3H]-thymidine incorporation and Trypan blue exclusion assays. Furthermore, Rg1 (150–600 nM) also showed an enhanced tube forming inducing effect on the HUVEC. Rg1 was also demonstrated to promote angiogenesis in an in vivo Matrigel plug assay, and increase endothelial sprouting in the ex vivo rat aorta ring assay. Differential gene expression profile of HUVEC following treatment with Rg1 revealed the expression of genes related to cell adhesion, migration and cytoskeleton, including RhoA, RhoB, IQGAP1, CALM2, Vav2 and LAMA4. Our results suggest that Rg1 can promote angiogenesis in multiple models, and this effect is partly due to the modulation of genes that are involved in
the cytoskeletal dynamics, cell–cell adhesion and migration.
Electronic Supplementary Material
An erratum to this article can be found at |
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Keywords: | angiogenesis gene expression profiling ginsenosides HUVEC microarray Rg1 |
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