Article: Transcriptional profiling of angiogenesis activities of calycosin in zebrafish

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TitleTranscriptional profiling of angiogenesis activities of calycosin in zebrafish
AuthorsLi, S2
Lou, S4
Lei, BUW2
Chan, TF4
Kwan, YW4
Chan, SW3
Leung, GPH1
Tsui, SKW4
Lee, SMY2
Issue Date2011
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/is/journals/current/mbs/mbspub.htm
CitationMolecular Biosystems, 2011, v. 7 n. 11, p. 3112-3121 [How to Cite?]
DOI: http://dx.doi.org/10.1039/c1mb05206c
AbstractAngiogenesis plays an important role in a wide range of physiological processes and many diseases are associated with the dysregulation of angiogenesis. The commonly used Chinese herbal medicine Radix Astragali (known as Huang qi in Chinese) is a potential candidate for treating this type of disease. Calycosin, a major isoflavonoid in Radix Astragali, was identified in our earlier study and shown to induce angiogenesis in human umbilical vein endothelial cells (HUVEC) in vitro and in zebrafish embryos in vivo. Using zebrafish as a testing model, we investigated the angiogenic effect of calycosin on the subintestinal vessels (SIVs) in zebrafish embryos. Our findings using transcriptional profiling by deep sequencing, and confirmed by quantitative real-time PCR (qPCR), demonstrate that calycosin modulated vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF) and ErbB signaling pathways. The inhibitory effects of calycosin-induced phenotypic responses by several pathway-specific inhibitors (VRI, SU5402, MEK1/2 Inhibitor, Wortmannin and LY294002) further identified the potential involvement of VEGF(R) and FGF(R) signaling pathways in the angiogenic activities of calycosin. We present a comprehensive framework of study using fluorescence microscopy, transcriptomics and qPCR to demonstrate the proangiogenic effects of calycosin in vivo. The data have elucidated the connection between morphological observations and genomic evidence, indicating the potential roles of several key signaling pathways in angiogenesis. This journal is © The Royal Society of Chemistry.
ISSN1742-206X
2011 Impact Factor: 3.534
2011 SCImago Journal Rankings: 0.522
DOIhttp://dx.doi.org/10.1039/c1mb05206c
ReferencesReferences in Scopus
DC Field
Value
dc.contributor.authorLi, S
dc.contributor.authorLou, S
dc.contributor.authorLei, BUW
dc.contributor.authorChan, TF
dc.contributor.authorKwan, YW
dc.contributor.authorChan, SW
dc.contributor.authorLeung, GPH
dc.contributor.authorTsui, SKW
dc.contributor.authorLee, SMY
dc.date.accessioned2012-08-16T05:56:13Z
dc.date.available2012-08-16T05:56:13Z
dc.date.issued2011
dc.description.abstractAngiogenesis plays an important role in a wide range of physiological processes and many diseases are associated with the dysregulation of angiogenesis. The commonly used Chinese herbal medicine Radix Astragali (known as Huang qi in Chinese) is a potential candidate for treating this type of disease. Calycosin, a major isoflavonoid in Radix Astragali, was identified in our earlier study and shown to induce angiogenesis in human umbilical vein endothelial cells (HUVEC) in vitro and in zebrafish embryos in vivo. Using zebrafish as a testing model, we investigated the angiogenic effect of calycosin on the subintestinal vessels (SIVs) in zebrafish embryos. Our findings using transcriptional profiling by deep sequencing, and confirmed by quantitative real-time PCR (qPCR), demonstrate that calycosin modulated vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF) and ErbB signaling pathways. The inhibitory effects of calycosin-induced phenotypic responses by several pathway-specific inhibitors (VRI, SU5402, MEK1/2 Inhibitor, Wortmannin and LY294002) further identified the potential involvement of VEGF(R) and FGF(R) signaling pathways in the angiogenic activities of calycosin. We present a comprehensive framework of study using fluorescence microscopy, transcriptomics and qPCR to demonstrate the proangiogenic effects of calycosin in vivo. The data have elucidated the connection between morphological observations and genomic evidence, indicating the potential roles of several key signaling pathways in angiogenesis. This journal is © The Royal Society of Chemistry.
dc.description.natureLink_to_subscribed_fulltext
dc.identifier.citationMolecular Biosystems, 2011, v. 7 n. 11, p. 3112-3121 [How to Cite?]
DOI: http://dx.doi.org/10.1039/c1mb05206c
dc.identifier.doihttp://dx.doi.org/10.1039/c1mb05206c
dc.identifier.epage3121
dc.identifier.hkuros203459
dc.identifier.issn1742-206X
2011 Impact Factor: 3.534
2011 SCImago Journal Rankings: 0.522
dc.identifier.issue11
dc.identifier.pmid21909574
dc.identifier.scopuseid_2-s2.0-80054026500
dc.identifier.spage3112
dc.identifier.urihttp://hdl.handle.net/10722/159767
dc.identifier.volume7
dc.languageeng
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/is/journals/current/mbs/mbspub.htm
dc.publisher.placeUnited Kingdom
dc.relation.ispartofMolecular BioSystems
dc.relation.referencesReferences in Scopus
dc.titleTranscriptional profiling of angiogenesis activities of calycosin in zebrafish
dc.typeArticle
Author Affiliations
  1. The University of Hong Kong
  2. University of Macau
  3. Hong Kong Polytechnic University
  4. Chinese University of Hong Kong