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Bacterial infection-mimicking three-dimensional phagocytosis and chemotaxis in electrospun poly(ε-caprolactone) nanofibrous membrane

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dc.contributor.authorLee, SJ-
dc.contributor.authorMaza, PAMA-
dc.contributor.authorSun, GM-
dc.contributor.authorSlama, P-
dc.contributor.authorLee, IJ-
dc.contributor.authorKwak, JY-
dc.date.accessioned2022-12-26T00:39:14Z-
dc.date.available2022-12-26T00:39:14Z-
dc.date.issued2021-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/23507-
dc.description.abstractIn this study, we developed a three-dimensional (3D) in vitro infection model to investigate the crosstalk between phagocytes and microbes in inflammation using a nanofibrous membrane (NM). Poly(ε-caprolactone) (PCL)-NMs (PCL-NMs) were generated via electrospinning of PCL in chloroform. Staphylococcus aureus and phagocytes were able to adhere to the nanofibers and phagocytes engulfed S. aureus in the PCL-NM. The migration of phagocytes to S. aureus was evaluated in a two-layer co-culture system using PCL-NM. Neutrophils, macrophages and dendritic cells (DCs) cultured in the upper PCL-NM layer migrated to the lower PCL-NM layer containing bacteria. DCs migrated to neutrophils that cultured with bacteria and then engulfed neutrophils in two-layer system. In addition, phagocytes in the upper PCL-NM layer migrated to bacteria-infected MLE-12 lung epithelial cells in the lower PCL-NM layer. S. aureus-infected MLE-12 cells stimulated the secretion of tumor necrosis factor-α and IL-1α in 3D culture conditions, but not in 2D culture conditions. Therefore, the PCL-NM-based 3D culture system with phagocytes and bacteria mimics the inflammatory response to microbes in vivo and is applicable to the biomimetic study of various microbe infections.-
dc.language.isoen-
dc.titleBacterial infection-mimicking three-dimensional phagocytosis and chemotaxis in electrospun poly(ε-caprolactone) nanofibrous membrane-
dc.typeArticle-
dc.identifier.pmid34436332-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8399938/-
dc.subject.keyword3D culture-
dc.subject.keywordDendritic cell-
dc.subject.keywordInflammation-
dc.subject.keywordNanofiber-
dc.subject.keywordNeutrophil-
dc.subject.keywordPoly(caprolactone)-
dc.subject.keywordStaphylococcus aureus-
dc.contributor.affiliatedAuthorLee, IJ-
dc.contributor.affiliatedAuthorKwak, JY-
dc.type.localJournal Papers-
dc.identifier.doi10.3390/membranes11080569-
dc.citation.titleMembranes-
dc.citation.volume11-
dc.citation.number8-
dc.citation.date2021-
dc.citation.startPage569-
dc.citation.endPage569-
dc.identifier.bibliographicCitationMembranes, 11(8). : 569-569, 2021-
dc.identifier.eissn2077-0375-
dc.relation.journalidJ020770375-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Biochemistry & Molecular Biology
Journal Papers > School of Medicine / Graduate School of Medicine > Pharmacology
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