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The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

VEGF-B inhibits apoptosis via VEGFR-1–mediated suppression of the expression of BH3-only protein genes in mice and rats

Open access
Li, Yang, Zhang, Fan, Nagai, Nobuo, Tang, Zhongshu, Zhang, Shuihua, Scotney, Pierre, Lennartsson, Johan, Zhu, Chaoyong, Qu, Yi, Fang, Changge, Hua, Jianyuan, Matsuo, Osamu, Fong, Guo-Hua, Ding, Hao, Cao, Yihai, Becker, Kevin G., Nash, Andrew, Heldin, Carl-Henrik, Li, Xuri·2008·Journal of Clinical Investigation

Abstract

Despite its early discovery and high sequence homology to the other VEGF family members, the biological functions of VEGF-B remain poorly understood. We revealed here a novel function for VEGF-B as a potent inhibitor of apoptosis. Using gene expression profiling of mouse primary aortic smooth muscle cells, and confirming the results by real-time PCR using mouse and rat cell lines, we showed that VEGF-B inhibited the expression of genes encoding the proapoptotic BH3-only proteins and other apoptosis- and cell death-related proteins, including p53 and members of the caspase family, via activation of VEGFR-1. Consistent with this, VEGF-B treatment rescued neurons from apoptosis in the retina and brain in mouse models of ocular neurodegenerative disorders and stroke, respectively. Interestingly, VEGF-B treatment at the dose effective for neuronal survival did not cause retinal neovascularization, suggesting that VEGF-B is the first member of the VEGF family that has a potent antiapoptotic effect while lacking a general angiogenic activity. These findings indicate that VEGF-B may potentially offer a new therapeutic option for the treatment of neurodegenerative diseases.

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Crossref · 10.1172/jci33673

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Metadata

Authors
Li, Y., Zhang, F., Nagai, N., Tang, Z., Zhang, S., Scotney, P., Lennartsson, J., Zhu, C., Qu, Y., Fang, C., Hua, J., Matsuo, O., Fong, G.-H., Ding, H., Cao, Y., Becker, K. G., Nash, A., Heldin, C.-H., & Li, X.
Venue
Journal of Clinical Investigation
Published
2008-02-01
Volume
118
Issue
3
Pages
913-23
ISSN
0021-9738 (ISSN-L)
OpenAlex
W2056110140
Cited by
194
References
4
FWCI
5.58
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: VEGF-B inhibits apoptosis via VEGFR-1–mediated suppression of the expression of BH3-only protein genes in mice and rats. https://app.cochat.ai/papers/10.1172/jci33673
The paper
Li, Y., Zhang, F., Nagai, N., Tang, Z., Zhang, S., Scotney, P., Lennartsson, J., Zhu, C., Qu, Y., Fang, C., Hua, J., Matsuo, O., Fong, G.-H., Ding, H., Cao, Y., Becker, K. G., Nash, A., Heldin, C.-H., & Li, X. (2008). VEGF-B inhibits apoptosis via VEGFR-1–mediated suppression of the expression of BH3-only protein genes in mice and rats. Journal of Clinical Investigation. https://doi.org/10.1172/jci33673

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.