The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
Pericyte-endothelial crosstalk: implications and opportunities for advanced cellular therapies
Open accessAbstract
Pericytes are mural cells of the microcirculation, which have been shown to play key roles in regulating microvascular morphogenesis and stability, throughout each tissue bed and organ system assessed. Importantly, recent work has revealed that pericytes share several characteristics with mesenchymally- and adipose-derived stem cells suggesting that there may be lineage-related connections amongst bonafide pericytes and these vascular ‘progenitors,’ which can assume a perivascular position in association with endothelial cells. Hence, pericyte identity as a mediator of vascular remodeling may be confounded by its close relationships with its progenitors or pluripotent cell counterparts and yet demonstrates their potential utility as cell-based therapies for unmet clinical needs. Crucial to the development of such therapies will be a comprehensive understanding of the origin and fate regulating these related cell types as well as the unveiling of the molecular mechanisms by which pericytes and endothelial cells communicate. Such mechanistic inputs, which disrupt normal cellular ‘cross-talk’ during disease inception and progression, offer opportunities for intervention and will be discussed in the context of the vasculopathies accompanying tumor growth, diabetes, and fibrosis.
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Cites
A perivascular origin for mesenchymal stem cells in multiple human organs
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“The authors identified a population of CD31−CD73+CD90+CD105+ cells that expressed pericyte markers such as NG2, CD146, and PDGFR-β but did not express α-SMA.”
BackgroundInfluentialHepatic Stellate Cells: Protean, Multifunctional, and Enigmatic Cells of the Liver
Friedman, S. L. (2008) · Physiological Reviews · doi:10.1152/physrev.00013.2007 · Cited by 2,842
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Adipose-derived stem cells for regenerative medicine
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Endothelial/Pericyte Interactions
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Cited by
Mesenchymal Stem Cells: Time to Change the Name!
Caplan, A. I. (2017) · Stem Cells Translational Medicine · doi:10.1002/sctm.17-0051 · Cited by 1,119
Targeting and Crossing the Blood-Brain Barrier with Extracellular Vesicles
Saint-Pol, J., Gosselet, F., Duban-Deweer, S., Pottiez, G., & Karamanos, Y. (2020) · Cells · doi:10.3390/cells9040851 · Cited by 503
Bioprinting for vascular and vascularized tissue biofabrication
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Type-1 pericytes accumulate after tissue injury and produce collagen in an organ-dependent manner
Birbrair, A., Zhang, T., Files, D. C., Mannava, S., Smith, T., Wang, Z.-M., Messi, M. L., Mintz, A., & Delbono, O. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt512 · Cited by 282
Bernstein, D. L., Zuluaga-Ramirez, V., Gajghate, S., Reichenbach, N. L., Polyak, B., Persidsky, Y., & Rom, S. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x19882264 · Cited by 120
Metadata
- Authors
- Geevarghese, A., & Herman, I. M.
- Venue
- Translational Research
- Publisher
- Elsevier BV
- Published
- 2014-04
- Volume
- 163
- Issue
- 4
- Pages
- 296-306
- ISSN
- 1878-1810 (ISSN-L)
- 1931-5244
- OpenAlex
- W2050497029
- Cited by
- 249
- References
- 9
- FWCI
- 6.81
- Type
- journal article
- Language
- en
- Open access
- green
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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.