The DOI matches its Crossref record; 86 of the 86 references it cites were found in a registry or an index.
Purinergic Signaling and Vascular Cell Proliferation and Death
Abstract
Abstract— Evidence for the role of purinergic signaling (via P1 and P2Y receptors) in the proliferation of vascular smooth muscle and endothelial cells is reviewed. The involvement of the mitogen-activated protein kinase second-messenger cascade in this action is clearly implicated, although details of the precise intracellular pathways involved still remain to be determined. Synergistic actions of purines and pyrimidines with growth factors occur in promoting cell proliferation. Interaction between purinergic signaling for vascular cell proliferation and cell death mediated by P2X 7 receptors is discussed. There is evidence of the release of ATP from endothelial cells, platelets, and sympathetic nerves as well as from damaged cells in atherosclerosis, hypertension, restenosis, and ischemia; furthermore, there is evidence that vascular smooth muscle and endothelial cells proliferate in these pathological conditions. Thus, the involvement of ATP and its breakdown product, adenosine, is implicated; it is hoped that with the development of selective P1 (A 2 ) and P2Y receptor agonists and antagonists, new therapeutic strategies will be explored.
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Cites
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The ectonucleotidases CD 39 and CD 73: Novel checkpoint inhibitor targets
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Metadata
- Authors
- Burnstock, G.
- Venue
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Published
- 2002-03
- Volume
- 22
- Issue
- 3
- Pages
- 364-373
- ISSN
- 1079-5642 (ISSN-L)
- 1524-4636
- OpenAlex
- W2117926778
- Cited by
- 414
- References
- 86
- FWCI
- 16.27
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.
