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Bacterial infection-mimicking three-dimensional phagocytosis and chemotaxis in electrospun poly(ε-caprolactone) nanofibrous membrane
DC Field | Value | Language |
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dc.contributor.author | Lee, SJ | - |
dc.contributor.author | Maza, PAMA | - |
dc.contributor.author | Sun, GM | - |
dc.contributor.author | Slama, P | - |
dc.contributor.author | Lee, IJ | - |
dc.contributor.author | Kwak, JY | - |
dc.date.accessioned | 2022-12-26T00:39:14Z | - |
dc.date.available | 2022-12-26T00:39:14Z | - |
dc.date.issued | 2021 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/23507 | - |
dc.description.abstract | In 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.iso | en | - |
dc.title | Bacterial infection-mimicking three-dimensional phagocytosis and chemotaxis in electrospun poly(ε-caprolactone) nanofibrous membrane | - |
dc.type | Article | - |
dc.identifier.pmid | 34436332 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8399938/ | - |
dc.subject.keyword | 3D culture | - |
dc.subject.keyword | Dendritic cell | - |
dc.subject.keyword | Inflammation | - |
dc.subject.keyword | Nanofiber | - |
dc.subject.keyword | Neutrophil | - |
dc.subject.keyword | Poly(caprolactone) | - |
dc.subject.keyword | Staphylococcus aureus | - |
dc.contributor.affiliatedAuthor | Lee, IJ | - |
dc.contributor.affiliatedAuthor | Kwak, JY | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.3390/membranes11080569 | - |
dc.citation.title | Membranes | - |
dc.citation.volume | 11 | - |
dc.citation.number | 8 | - |
dc.citation.date | 2021 | - |
dc.citation.startPage | 569 | - |
dc.citation.endPage | 569 | - |
dc.identifier.bibliographicCitation | Membranes, 11(8). : 569-569, 2021 | - |
dc.identifier.eissn | 2077-0375 | - |
dc.relation.journalid | J020770375 | - |
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