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Inflammation-Stimulated Mesenchymal Stromal Cell-Derived Extracellular Vesicles Attenuate Inflammation.
Harting, Matthew T; Srivastava, Amit K; Zhaorigetu, Siqin; Bair, Henry; Prabhakara, Karthik S; Toledano Furman, Naama E; Vykoukal, Jody V; Ruppert, Katherine A; Cox, Charles S; Olson, Scott D.
Afiliación
  • Harting MT; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
  • Srivastava AK; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
  • Zhaorigetu S; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
  • Bair H; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
  • Prabhakara KS; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
  • Toledano Furman NE; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
  • Vykoukal JV; McCombs Institute for the Early Detection and Treatment of Cancer, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Ruppert KA; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
  • Cox CS; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
  • Olson SD; Department of Pediatric Surgery, University of Texas McGovern Medical School, Houston, Texas, USA.
Stem Cells ; 36(1): 79-90, 2018 01.
Article en En | MEDLINE | ID: mdl-29076623
ABSTRACT
Extracellular vesicles (EVs) secreted by mesenchymal stromal cells (MSCs) have been proposed to be a key mechanistic link in the therapeutic efficacy of cells in response to cellular injuries through paracrine effects. We hypothesize that inflammatory stimulation of MSCs results in the release of EVs that have greater anti-inflammatory effects. The present study evaluates the immunomodulatory abilities of EVs derived from inflammation-stimulated and naive MSCs (MSCEv+ and MSCEv, respectively) isolated using a current Good Manufacturing Practice-compliant tangential flow filtration system. Detailed characterization of both EVs revealed differences in protein composition, cytokine profiles, and RNA content, despite similarities in size and expression of common surface markers. MSCEv+ further attenuated release of pro-inflammatory cytokines in vitro when compared to MSCEv, with a distinctly different pattern of EV-uptake by activated primary leukocyte subpopulations. The efficacy of EVs was partially attributed to COX2/PGE2 expression. The present study demonstrates that inflammatory stimulation of MSCs renders release of EVs that have enhanced anti-inflammatory properties partially due to COX2/PGE2 pathway alteration. Stem Cells 2018;3679-90.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Microscopía Electrónica de Transmisión / Células Madre Mesenquimatosas / Vesículas Extracelulares / Inflamación Límite: Humans Idioma: En Revista: Stem Cells Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Microscopía Electrónica de Transmisión / Células Madre Mesenquimatosas / Vesículas Extracelulares / Inflamación Límite: Humans Idioma: En Revista: Stem Cells Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos