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dc.contributor.authorClancy, Lauren
dc.contributor.authorFreedman, Jane E.
dc.date2022-08-11T08:09:20.000
dc.date.accessioned2022-08-23T16:27:01Z
dc.date.available2022-08-23T16:27:01Z
dc.date.issued2016-02-05
dc.date.submitted2017-04-20
dc.identifier.citationCirc Res. 2016 Feb 5;118(3):374-6. doi: 10.1161/CIRCRESAHA.115.308190. <a href="https://doi.org/10.1161/CIRCRESAHA.115.308190">Link to article on publisher's site</a>
dc.identifier.issn0009-7330 (Linking)
dc.identifier.doi10.1161/CIRCRESAHA.115.308190
dc.identifier.pmid26846635
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36687
dc.description.abstractThe interaction between blood cells and disease has continued to grow both more complex and increasingly intriguing. Once thought to be static populations, circulating blood cells are now known to interact and communicate in ways far beyond the singular processes historically attributed to each population. A primary example is the platelet, an anucleate cell with a traditional role in hemostasis and thrombosis. The platelets’ defined biological roles have expanded exponentially over the last decade to include immunity, inflammation and mediation of oncogenesis. Platelets, although anucleate, contain a wealth of transcriptomic information. When viewed from the perspective of a large population analysis, platelets demonstrate wide diversity, important patterns, including association with obesity and diabetes, and distinct expression profiles as compared to white cells. Platelets' ability to participate in diverse systemic responses has been elucidated by our growing understanding of their contents and the revelation of their capacity to share these contents. Platelets are now known to horizontally transfer RNA, traffic pathogens and regulate physiological and pathophysiological processes far beyond hemostasis.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26846635&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745999/
dc.subjectEditorial
dc.subjectdiabetes mellitus
dc.subjectmicroRNA
dc.subjectplatelet
dc.subjectthrombosis
dc.subjecttranscriptomics
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.titleBlood-Derived Extracellular RNA and Platelet Pathobiology: Adding Pieces to a Complex Circulating Puzzle
dc.typeEditorial
dc.source.journaltitleCirculation research
dc.source.volume118
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/metnet_pubs/55
dc.identifier.contextkey10048076
html.description.abstract<p>The interaction between blood cells and disease has continued to grow both more complex and increasingly intriguing. Once thought to be static populations, circulating blood cells are now known to interact and communicate in ways far beyond the singular processes historically attributed to each population. A primary example is the platelet, an anucleate cell with a traditional role in hemostasis and thrombosis. The platelets’ defined biological roles have expanded exponentially over the last decade to include immunity, inflammation and mediation of oncogenesis. Platelets, although anucleate, contain a wealth of transcriptomic information. When viewed from the perspective of a large population analysis, platelets demonstrate wide diversity, important patterns, including association with obesity and diabetes, and distinct expression profiles as compared to white cells. Platelets' ability to participate in diverse systemic responses has been elucidated by our growing understanding of their contents and the revelation of their capacity to share these contents. Platelets are now known to horizontally transfer RNA, traffic pathogens and regulate physiological and pathophysiological processes far beyond hemostasis.</p>
dc.identifier.submissionpathmetnet_pubs/55
dc.contributor.departmentUMass Metabolic Network
dc.contributor.departmentDepartment of Medicine, Division of Cardiovascular Medicine
dc.source.pages374-6


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