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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Raghunath, Michael | - |
dc.contributor.author | Wong, Yuan Sy | - |
dc.contributor.author | Farooq, Muhammad | - |
dc.contributor.author | Gee, Ruowen | - |
dc.date.accessioned | 2018-10-26T14:44:50Z | - |
dc.date.available | 2018-10-26T14:44:50Z | - |
dc.date.issued | 2009 | - |
dc.identifier.issn | 0006-291X | de_CH |
dc.identifier.issn | 1090-2104 | de_CH |
dc.identifier.uri | https://digitalcollection.zhaw.ch/handle/11475/12206 | - |
dc.description.abstract | The rapid vascularisation of biomaterials and engineered tissue after implantation is a current unmet need. To this end, we explored the pharmacological option of inducing neovascularisation using compounds that inhibit hypoxia-induced factor-1α prolyl hydroxylase. This stabilises hypoxia inducible factor-1α and therefore de-repress the transcription of various angiogenic genes. In the quest for a small vertebrate model allowing for in vivo screening we exposed transgenic zebrafish embryos exhibiting fluorescent blood vessels to hydralazine hydrochloride and 2,4-pyridine dicarboxylic acid from 6 hpf to 72 hpf by immersion. Live observation of embryos revealed that the substances induced formation of ectopic blood vessels in the subintestinal vessel basket. We confirmed the HIF-stabilising effects biochemically in human fibroblasts and with an in vitro angiogenesis fibroblast/HUVEC co-culture model. Cross-inhibition of collagen prolyl hydroxylase was confirmed by reduced collagen secretion by fibroblasts and reduced collagen content of zebrafish embryos. | de_CH |
dc.language.iso | en | de_CH |
dc.publisher | Elsevier | de_CH |
dc.relation.ispartof | Biochemical and Biophysical Research Communications | de_CH |
dc.rights | Licence according to publishing contract | de_CH |
dc.subject.ddc | 571: Physiologie und verwandte Themen | de_CH |
dc.subject.ddc | 572: Biochemie | de_CH |
dc.title | Pharmacologically induced angiogenesis in transgenic zebrafish | de_CH |
dc.type | Beitrag in wissenschaftlicher Zeitschrift | de_CH |
dcterms.type | Text | de_CH |
zhaw.departement | Life Sciences und Facility Management | de_CH |
zhaw.organisationalunit | Institut für Chemie und Biotechnologie (ICBT) | de_CH |
dc.identifier.doi | 10.1016/j.bbrc.2008.11.127 | de_CH |
zhaw.funding.eu | No | de_CH |
zhaw.issue | 4 | de_CH |
zhaw.originated.zhaw | No | de_CH |
zhaw.pages.end | 771 | de_CH |
zhaw.pages.start | 766 | de_CH |
zhaw.publication.status | publishedVersion | de_CH |
zhaw.volume | 378 | de_CH |
zhaw.publication.review | Peer review (Publikation) | de_CH |
zhaw.webfeed | Metabolic Tissue Engineering | de_CH |
Appears in collections: | Publikationen Life Sciences und Facility Management |
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Raghunath, M., Wong, Y. S., Farooq, M., & Gee, R. (2009). Pharmacologically induced angiogenesis in transgenic zebrafish. Biochemical and Biophysical Research Communications, 378(4), 766–771. https://doi.org/10.1016/j.bbrc.2008.11.127
Raghunath, M. et al. (2009) ‘Pharmacologically induced angiogenesis in transgenic zebrafish’, Biochemical and Biophysical Research Communications, 378(4), pp. 766–771. Available at: https://doi.org/10.1016/j.bbrc.2008.11.127.
M. Raghunath, Y. S. Wong, M. Farooq, and R. Gee, “Pharmacologically induced angiogenesis in transgenic zebrafish,” Biochemical and Biophysical Research Communications, vol. 378, no. 4, pp. 766–771, 2009, doi: 10.1016/j.bbrc.2008.11.127.
RAGHUNATH, Michael, Yuan Sy WONG, Muhammad FAROOQ und Ruowen GEE, 2009. Pharmacologically induced angiogenesis in transgenic zebrafish. Biochemical and Biophysical Research Communications. 2009. Bd. 378, Nr. 4, S. 766–771. DOI 10.1016/j.bbrc.2008.11.127
Raghunath, Michael, Yuan Sy Wong, Muhammad Farooq, and Ruowen Gee. 2009. “Pharmacologically Induced Angiogenesis in Transgenic Zebrafish.” Biochemical and Biophysical Research Communications 378 (4): 766–71. https://doi.org/10.1016/j.bbrc.2008.11.127.
Raghunath, Michael, et al. “Pharmacologically Induced Angiogenesis in Transgenic Zebrafish.” Biochemical and Biophysical Research Communications, vol. 378, no. 4, 2009, pp. 766–71, https://doi.org/10.1016/j.bbrc.2008.11.127.
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