Biomaterial-induced alterations of human neutrophils under fluid shear stress: scanning electron microscopical study in vitro
Morphological changes of human polymorphonuclear neutrophils (PMN) adhering to hydrophilic (glass) and hydrophobic (FEP-Teflon, polyethylene, polypropylene) surfaces were studied in a parallel-plate flow chamber at the light and scanning electron microscopical levels. The PMN were exposed to a shear...
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Veröffentlicht in: | Biomaterials 1996-07, Vol.17 (14), p.1359-1367 |
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description | Morphological changes of human polymorphonuclear neutrophils (PMN) adhering to hydrophilic (glass) and hydrophobic (FEP-Teflon, polyethylene, polypropylene) surfaces were studied in a parallel-plate flow chamber at the light and scanning electron microscopical levels. The PMN were exposed to a shear stress of 0.19Pa (1.9 dynes cm−2) or were allowed to adhere without the stress component (static control) during 30 min for all four biomaterials. Observation by light microscopy was performed in situ in the flow chamber at 1,5,10,15,20,25 and 30 min. The total number of adherent cells as a function of time and the activation status of the population on the basis of morphological criteria were determined. On the hydrophilic material adhesion of activated PMN was significantly higher (P < 0.05) than on the more hydrophobic surfaces. This effect was most pronounced for the adhesion of neutrophils to glass and polypropylene (PP). Polyethylene (PE) showed only minor adhesion rates. Scanning electron microscopy revealed details of cell shape changes and permitted a more precise classification of populations of neutrophils based on distinctive shapes. As PMN were exposed to shear stress on glass, the majority of cells exhibited surface veils, ridges and ruffles, suggesting a high level of cell migration. In this case, on polymeric surfaces the presence of filopodial networks (FEP-Teflon) and ameoboid cell shapes (PP and PE) was noted. The results suggest that a low shear stress, as well as various chemical and physical properties of biomaterial surfaces, are together responsible for differentiation of PMN populations on solid substrata. |
doi_str_mv | 10.1016/0142-9612(96)87275-9 |
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The PMN were exposed to a shear stress of 0.19Pa (1.9 dynes cm−2) or were allowed to adhere without the stress component (static control) during 30 min for all four biomaterials. Observation by light microscopy was performed in situ in the flow chamber at 1,5,10,15,20,25 and 30 min. The total number of adherent cells as a function of time and the activation status of the population on the basis of morphological criteria were determined. On the hydrophilic material adhesion of activated PMN was significantly higher (P < 0.05) than on the more hydrophobic surfaces. This effect was most pronounced for the adhesion of neutrophils to glass and polypropylene (PP). Polyethylene (PE) showed only minor adhesion rates. Scanning electron microscopy revealed details of cell shape changes and permitted a more precise classification of populations of neutrophils based on distinctive shapes. As PMN were exposed to shear stress on glass, the majority of cells exhibited surface veils, ridges and ruffles, suggesting a high level of cell migration. In this case, on polymeric surfaces the presence of filopodial networks (FEP-Teflon) and ameoboid cell shapes (PP and PE) was noted. The results suggest that a low shear stress, as well as various chemical and physical properties of biomaterial surfaces, are together responsible for differentiation of PMN populations on solid substrata.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/0142-9612(96)87275-9</identifier><identifier>PMID: 8830960</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Biocompatible Materials ; Biological and medical sciences ; Cell Adhesion ; Cell Membrane ; Cell Size ; flow chamber ; Glass ; Humans ; Image Processing, Computer-Assisted ; Medical sciences ; Microscopy, Electron, Scanning ; Microscopy, Phase-Contrast ; Neutrophil-biomaterial interactions ; neutrophils ; Neutrophils - cytology ; Polyethylenes ; Polymers ; Polypropylenes ; Polytetrafluoroethylene ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; scanning electron microscope ; shear stress ; Stress, Mechanical ; Technology. Biomaterials. Equipments. Material. 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The PMN were exposed to a shear stress of 0.19Pa (1.9 dynes cm−2) or were allowed to adhere without the stress component (static control) during 30 min for all four biomaterials. Observation by light microscopy was performed in situ in the flow chamber at 1,5,10,15,20,25 and 30 min. The total number of adherent cells as a function of time and the activation status of the population on the basis of morphological criteria were determined. On the hydrophilic material adhesion of activated PMN was significantly higher (P < 0.05) than on the more hydrophobic surfaces. This effect was most pronounced for the adhesion of neutrophils to glass and polypropylene (PP). Polyethylene (PE) showed only minor adhesion rates. Scanning electron microscopy revealed details of cell shape changes and permitted a more precise classification of populations of neutrophils based on distinctive shapes. As PMN were exposed to shear stress on glass, the majority of cells exhibited surface veils, ridges and ruffles, suggesting a high level of cell migration. In this case, on polymeric surfaces the presence of filopodial networks (FEP-Teflon) and ameoboid cell shapes (PP and PE) was noted. The results suggest that a low shear stress, as well as various chemical and physical properties of biomaterial surfaces, are together responsible for differentiation of PMN populations on solid substrata.</description><subject>Biocompatible Materials</subject><subject>Biological and medical sciences</subject><subject>Cell Adhesion</subject><subject>Cell Membrane</subject><subject>Cell Size</subject><subject>flow chamber</subject><subject>Glass</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Scanning</subject><subject>Microscopy, Phase-Contrast</subject><subject>Neutrophil-biomaterial interactions</subject><subject>neutrophils</subject><subject>Neutrophils - cytology</subject><subject>Polyethylenes</subject><subject>Polymers</subject><subject>Polypropylenes</subject><subject>Polytetrafluoroethylene</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>scanning electron microscope</subject><subject>shear stress</subject><subject>Stress, Mechanical</subject><subject>Technology. Biomaterials. Equipments. Material. 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Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>scanning electron microscope</topic><topic>shear stress</topic><topic>Stress, Mechanical</topic><topic>Technology. Biomaterials. Equipments. Material. Instrumentation</topic><topic>Vinyl Compounds</topic><topic>Wettability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tomczok, J.</creatorcontrib><creatorcontrib>Sliwa-tomczok, W.</creatorcontrib><creatorcontrib>Klein, C.L.</creatorcontrib><creatorcontrib>Van Kooten, T.G.</creatorcontrib><creatorcontrib>Kirkpatrick, C.J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tomczok, J.</au><au>Sliwa-tomczok, W.</au><au>Klein, C.L.</au><au>Van Kooten, T.G.</au><au>Kirkpatrick, C.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biomaterial-induced alterations of human neutrophils under fluid shear stress: scanning electron microscopical study in vitro</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>1996-07-01</date><risdate>1996</risdate><volume>17</volume><issue>14</issue><spage>1359</spage><epage>1367</epage><pages>1359-1367</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Morphological changes of human polymorphonuclear neutrophils (PMN) adhering to hydrophilic (glass) and hydrophobic (FEP-Teflon, polyethylene, polypropylene) surfaces were studied in a parallel-plate flow chamber at the light and scanning electron microscopical levels. The PMN were exposed to a shear stress of 0.19Pa (1.9 dynes cm−2) or were allowed to adhere without the stress component (static control) during 30 min for all four biomaterials. Observation by light microscopy was performed in situ in the flow chamber at 1,5,10,15,20,25 and 30 min. The total number of adherent cells as a function of time and the activation status of the population on the basis of morphological criteria were determined. On the hydrophilic material adhesion of activated PMN was significantly higher (P < 0.05) than on the more hydrophobic surfaces. This effect was most pronounced for the adhesion of neutrophils to glass and polypropylene (PP). Polyethylene (PE) showed only minor adhesion rates. Scanning electron microscopy revealed details of cell shape changes and permitted a more precise classification of populations of neutrophils based on distinctive shapes. As PMN were exposed to shear stress on glass, the majority of cells exhibited surface veils, ridges and ruffles, suggesting a high level of cell migration. In this case, on polymeric surfaces the presence of filopodial networks (FEP-Teflon) and ameoboid cell shapes (PP and PE) was noted. The results suggest that a low shear stress, as well as various chemical and physical properties of biomaterial surfaces, are together responsible for differentiation of PMN populations on solid substrata.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>8830960</pmid><doi>10.1016/0142-9612(96)87275-9</doi><tpages>9</tpages></addata></record> |
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subjects | Biocompatible Materials Biological and medical sciences Cell Adhesion Cell Membrane Cell Size flow chamber Glass Humans Image Processing, Computer-Assisted Medical sciences Microscopy, Electron, Scanning Microscopy, Phase-Contrast Neutrophil-biomaterial interactions neutrophils Neutrophils - cytology Polyethylenes Polymers Polypropylenes Polytetrafluoroethylene Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) scanning electron microscope shear stress Stress, Mechanical Technology. Biomaterials. Equipments. Material. Instrumentation Vinyl Compounds Wettability |
title | Biomaterial-induced alterations of human neutrophils under fluid shear stress: scanning electron microscopical study in vitro |
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