The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.
Mesenchymal stem cells and neovascularization: role of platelet‐derived growth factor receptors
Open accessAbstract
Introduction The vascular endothelial growth factor/platelet‐derived growth factor super‐family of ligands and receptors Role of platelet‐derived growth factor receptors in regulating the MSC fate MSCs and the vasculature Summary There is now accumulating evidence that bone marrow‐derived mesenchymal stem cells (MSCs) make an important contribution to postnatal vasculogenesis, especially during tissue ischaemia and tumour vascularization. Identifying mechanisms which regulate the role of MSCs in vasculogenesis is a key therapeutic objective, since while increased neovascularization can be advantageous during tissue ischaemia, it is deleterious during tumourigenesis. The potent angiogenic stimulant vascular endothelial growth factor (VEGF) is known to regulate MSC mobilization and recruitment to sites of neovascularization, as well as directing the differentiation of MSCs to a vascular cell fate. Despite the fact that MSCs did not express VEGF receptors, we have recently identified that VEGF‐A can stimulate platelet‐derived growth factor (PDGF) receptors, which regulates MSC migration and proliferation. This review focuses on the role of PDGF receptors in regulating the vascular cell fate of MSCs, with emphasis on the function of the novel VEGF‐A/PDGF receptor signalling mechanism.
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Cites
The biology of VEGF and its receptors
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Isolation of Putative Progenitor Endothelial Cells for Angiogenesis
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Tumors: Wounds That Do Not Heal
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“Tumour stroma is similar to the provisional matrix deposited during wound healing, however, due to the constant high levels of VEGF-A expression, tumours have been compared to wounds that do not heal [117].”
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PDGF-A signaling is a critical event in lung alveolar myofibroblast development and alveogenesis
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“MSCs systemically administered into a murine tumour model, were shown to localize and engraft into tumour lesions, where they proliferated, differentiated into vWF- and CD31-positive endothelial-like cells and formed a significant fraction of the tumour stroma [121].”
BackgroundTargeted Delivery of CX3CL1 to Multiple Lung Tumors by Mesenchymal Stem Cells
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Cited by
Type H blood vessels in bone modeling and remodeling
Peng, Y., Wu, S., Li, Y., & Crane, J. L. (2020) · Theranostics · doi:10.7150/thno.34126 · Cited by 599
Oh, J. Y., Kim, M. K., Shin, M. S., Lee, H. J., Ko, J. H., Wee, W. R., & Lee, J. H. (2008) · Stem Cells · doi:10.1634/stemcells.2007-0737 · Cited by 400
Growth factor regulation of proliferation and survival of multipotential stromal cells
Rodrigues, M., Griffith, L. G., & Wells, A. (2010) · Stem Cell Research & Therapy · doi:10.1186/scrt32 · Cited by 301
Culture media for the differentiation of mesenchymal stromal cells
Vater, C., Kasten, P., & Stiehler, M. (2011) · Acta Biomaterialia · doi:10.1016/j.actbio.2010.07.037 · Cited by 279
Adipose-derived stem cells secretome and its potential application in “stem cell-free therapy”
Trzyna, A., & Banaś-Ząbczyk, A. (2021) · Biomolecules · doi:10.3390/biom11060878 · Cited by 201
Metadata
- Authors
- Ball, S. G., Shuttleworth, C. A., & Kielty, C. M.
- Venue
- Journal of Cellular and Molecular Medicine
- Publisher
- Wiley
- Published
- 2007-09
- Volume
- 11
- Issue
- 5
- Pages
- 1012-1030
- ISSN
- 1582-1838 (ISSN-L)
- 1582-4934
- OpenAlex
- W2045705524
- Cited by
- 178
- References
- 10
- FWCI
- 6.35
- Type
- journal article
- Language
- en
- Open access
- bronze
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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