The role of survivin in angiogenesis during zebrafish embryonic development
<p>Abstract</p> <p>Background</p> <p>Survivin is the smallest member of the inhibitor of apoptosis (IAP) gene family. Recently, the zebrafish <it>survivin-1 </it>gene has been cloned, showing remarkable sequence identity and similarity over the BIR domain co...
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doaj-df9e0174a08340c0aff38e47c02fa04b2020-11-25T00:13:40ZengBMCBMC Developmental Biology1471-213X2007-05-01715010.1186/1471-213X-7-50The role of survivin in angiogenesis during zebrafish embryonic developmentMeng AnmingChan Loretta YYLeung Joseph CKChan Po-KwokLin RachelMa Alvin CHVerfaillie Catherine MLiang RaymondLeung Anskar YH<p>Abstract</p> <p>Background</p> <p>Survivin is the smallest member of the inhibitor of apoptosis (IAP) gene family. Recently, the zebrafish <it>survivin-1 </it>gene has been cloned, showing remarkable sequence identity and similarity over the BIR domain compared with human and mouse <it>survivin </it>gene. Here we investigated the role of survivin in angiogenesis during zebrafish development. Morpholinos (MOs) targeting the 5' untranslated region (UTR) (Sur<sub>UTR</sub>) and sequences flanking the initiation codon (Sur<sub>ATG</sub>) of zebrafish <it>survivin-1 </it>gene were injected into embryos at 1–4 cell stage. Vasculature was examined by microangiography and GFP expression in <it>Tg(fli1:EGFP)</it><sup><it>y</it>1 </sup>embryos. Results: In embryos co-injected with Sur<sub>UTR </sub>and Sur<sub>ATG</sub>-MOs, vasculogenesis was intact but angiogenesis was markedly perturbed, especially in the inter-segmental vessels (ISV) and dorsal longitudinal anastomotic vessels (DLAV) of the trunk, the inner optic circle and optic veins of developing eyes and the sub-intestinal vessels. Apoptosis was increased, as shown by TUNEL staining and increase in caspase-3 activity. Efficacy of Sur<sub>UTR </sub>and Sur<sub>ATG</sub>-MOs was demonstrated by translation inhibition of co-injected 5'UTR survivin:GFP plasmids. The phenotypes could be recapitulated by splice-site MO targeting the exon2-intron junction of <it>survivin </it>gene and rescued by <it>survivin </it>mRNA. Injection of human vascular endothelial growth factor (VEGF) protein induced ectopic angiogenesis and increased survivin expression, whereas treatment with a VEGF receptor inhibitor markedly reduced angiogenesis and suppressed survivin expression. Conclusion: Survivin is involved in angiogenesis during zebrafish development and may be under VEGF regulation.</p> http://www.biomedcentral.com/1471-213X/7/50 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Meng Anming Chan Loretta YY Leung Joseph CK Chan Po-Kwok Lin Rachel Ma Alvin CH Verfaillie Catherine M Liang Raymond Leung Anskar YH |
spellingShingle |
Meng Anming Chan Loretta YY Leung Joseph CK Chan Po-Kwok Lin Rachel Ma Alvin CH Verfaillie Catherine M Liang Raymond Leung Anskar YH The role of survivin in angiogenesis during zebrafish embryonic development BMC Developmental Biology |
author_facet |
Meng Anming Chan Loretta YY Leung Joseph CK Chan Po-Kwok Lin Rachel Ma Alvin CH Verfaillie Catherine M Liang Raymond Leung Anskar YH |
author_sort |
Meng Anming |
title |
The role of survivin in angiogenesis during zebrafish embryonic development |
title_short |
The role of survivin in angiogenesis during zebrafish embryonic development |
title_full |
The role of survivin in angiogenesis during zebrafish embryonic development |
title_fullStr |
The role of survivin in angiogenesis during zebrafish embryonic development |
title_full_unstemmed |
The role of survivin in angiogenesis during zebrafish embryonic development |
title_sort |
role of survivin in angiogenesis during zebrafish embryonic development |
publisher |
BMC |
series |
BMC Developmental Biology |
issn |
1471-213X |
publishDate |
2007-05-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Survivin is the smallest member of the inhibitor of apoptosis (IAP) gene family. Recently, the zebrafish <it>survivin-1 </it>gene has been cloned, showing remarkable sequence identity and similarity over the BIR domain compared with human and mouse <it>survivin </it>gene. Here we investigated the role of survivin in angiogenesis during zebrafish development. Morpholinos (MOs) targeting the 5' untranslated region (UTR) (Sur<sub>UTR</sub>) and sequences flanking the initiation codon (Sur<sub>ATG</sub>) of zebrafish <it>survivin-1 </it>gene were injected into embryos at 1–4 cell stage. Vasculature was examined by microangiography and GFP expression in <it>Tg(fli1:EGFP)</it><sup><it>y</it>1 </sup>embryos. Results: In embryos co-injected with Sur<sub>UTR </sub>and Sur<sub>ATG</sub>-MOs, vasculogenesis was intact but angiogenesis was markedly perturbed, especially in the inter-segmental vessels (ISV) and dorsal longitudinal anastomotic vessels (DLAV) of the trunk, the inner optic circle and optic veins of developing eyes and the sub-intestinal vessels. Apoptosis was increased, as shown by TUNEL staining and increase in caspase-3 activity. Efficacy of Sur<sub>UTR </sub>and Sur<sub>ATG</sub>-MOs was demonstrated by translation inhibition of co-injected 5'UTR survivin:GFP plasmids. The phenotypes could be recapitulated by splice-site MO targeting the exon2-intron junction of <it>survivin </it>gene and rescued by <it>survivin </it>mRNA. Injection of human vascular endothelial growth factor (VEGF) protein induced ectopic angiogenesis and increased survivin expression, whereas treatment with a VEGF receptor inhibitor markedly reduced angiogenesis and suppressed survivin expression. Conclusion: Survivin is involved in angiogenesis during zebrafish development and may be under VEGF regulation.</p> |
url |
http://www.biomedcentral.com/1471-213X/7/50 |
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