Authors
Jhunjhunwala, SiddharthAresta-DaSilva, Stephanie
Tang, Katherine
Alvarez, David
Webber, Matthew J.
Tang, Benjamin C.
Lavin, Danya M.
Veiseh, Omid
Doloff, Joshua C.
Bose, Suman
Vegas, Arturo
Ma, Minglin
Sahay, Gaurav
Chiu, Alan
Bader, Andrew
Langan, Erin
Siebert, Sean
Li, Jie
Greiner, Dale L.
Newburger, Peter E.
von Andrian, Ulrich H.
Langer, Robert
Anderson, Daniel G.
UMass Chan Affiliations
Department of Pediatrics, Division of Hematology/OncologyDiabetes Center of Excellence
Department of Molecular Medicine
Document Type
Journal ArticlePublication Date
2015-09-10Keywords
Analytical, Diagnostic and Therapeutic Techniques and EquipmentBiotechnology
Hematology
Immunopathology
Metadata
Show full item recordAbstract
In vivo implantation of sterile materials and devices results in a foreign body immune response leading to fibrosis of implanted material. Neutrophils, one of the first immune cells to be recruited to implantation sites, have been suggested to contribute to the establishment of the inflammatory microenvironment that initiates the fibrotic response. However, the precise numbers and roles of neutrophils in response to implanted devices remains unclear. Using a mouse model of peritoneal microcapsule implantation, we show 30-500 fold increased neutrophil presence in the peritoneal exudates in response to implants. We demonstrate that these neutrophils secrete increased amounts of a variety of inflammatory cytokines and chemokines. Further, we observe that they participate in the foreign body response through the formation of neutrophil extracellular traps (NETs) on implant surfaces. Our results provide new insight into neutrophil function during a foreign body response to peritoneal implants which has implications for the development of biologically compatible medical devices.Source
PLoS One. 2015 Sep 10;10(9):e0137550. doi: 10.1371/journal.pone.0137550. eCollection 2015. Link to article on publisher's siteDOI
10.1371/journal.pone.0137550Permanent Link to this Item
http://hdl.handle.net/20.500.14038/39841PubMed ID
26355958Related Resources
Link to Article in PubMedRights
Copyright: 2015 Jhunjhunwala et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Distribution License
http://creativecommons.org/licenses/by/4.0/ae974a485f413a2113503eed53cd6c53
10.1371/journal.pone.0137550
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Except where otherwise noted, this item's license is described as <p>Copyright: 2015 Jhunjhunwala et al. This is an open access article distributed under the terms of the <a href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</a>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited</p>