Inhibition by heparin and derivatized dextrans of Staphylococcus epidermidis adhesion to in vitro fibronectin-coated or explanted polymer surfaces

التفاصيل البيبلوغرافية
العنوان: Inhibition by heparin and derivatized dextrans of Staphylococcus epidermidis adhesion to in vitro fibronectin-coated or explanted polymer surfaces
المؤلفون: Daniel Pablo Lew, Pierre Vaudaux, J. Jozefonwicz, Didier Letourneur, Patrice Francois
المصدر: Journal of Biomaterials Science, Polymer Edition, Vol. 10, No 12 (1999) pp. 1207-1221
بيانات النشر: Informa UK Limited, 1999.
سنة النشر: 1999
مصطلحات موضوعية: Cell Adhesion/ drug effects, Materials science, Polymers, Surface Properties, Guinea Pigs, Biomedical Engineering, Biophysics, Biocompatible Materials, Bioengineering, Extracellular Matrix Proteins/metabolism, Biomaterials, Extracellular matrix, chemistry.chemical_compound, Fibronectins/ metabolism, In vivo, Staphylococcus epidermidis, Cell Adhesion, Animals, Humans, ddc:576.5, Complement Inactivator Proteins/pharmacology, Cell adhesion, Complement Inactivator Proteins, Extracellular Matrix Proteins, biology, Heparin, Fibrinogen, Dextrans, Prostheses and Implants, Adhesion, biology.organism_classification, Fibrinogen/metabolism, Fibronectins, Dextrans/ pharmacology, Polymers/ metabolism, Bacterial adhesin, Fibronectin, Staphylococcus epidermidis/cytology/ metabolism, Dextran, chemistry, Biochemistry, Heparin/ pharmacology, biology.protein, Diffusion Chambers, Culture
الوصف: The ability of Staphylococcus aureus to recognize several extracellular matrix or plasma proteins (e.g., fibrinogen, fibronectin, and collagen) promotes bacterial attachment to artificial surfaces. Whereas most S. aureus clinical isolates elaborate a wide repertoire of bacterial surface receptors' called adhesins, exhibiting specific binding of individual host proteins, S. epidermidis is lacking most of such protein adhesins. To document the interactions between S. epidermidis and various surface-adsorbed proteins, we first compared promotion of bacterial attachment by seven purified human proteins immobilized onto poly(methyl methacrylate) (PMMA) coverslips. Only two of them, namely fibronectin and fibrinogen, exhibited adhesion-promoting activities. In the presence of native heparin or two functionalized dextrans (CMDBS for Carboxy Methyl, Benzylamide sulfonate/sulfate), a dose-dependent inhibition of S. epidermidis adhesion to fibronectin-coated, but not to fibrinogen-coated surfaces was observed. The inhibitory effects of each CMDBS were much stronger than that of native heparin. In contrast, a control highly negatively charged, dextran exclusively substituted with carboxy methyl groups exerted no inhibition on S. epidermidis adhesion. To evaluate how CMDBS could interfere with S. epidermidis attachment to coverslips coated in vivo with extracellular matrix components, we also tested PMMA surfaces retrieved from tissue cages subcutaneously implanted in guinea pigs. Each CMDBS, but not heparin, strongly inhibited S. epidermidis adhesion to explanted coverslips, even in the presence of tissue cage fluid. In conclusion, fibronectin plays an important role in promoting S. epidermidis attachment to implanted biomaterials. Furthermore, S. epidermidis adhesion to fibronectin-coated or implanted biomaterials can be efficiently blocked in vitro by CMDBS.
تدمد: 1568-5624
0920-5063
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24b85eacdea8fa94943b2d28c44d0ce3Test
https://doi.org/10.1163/156856299x00027Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....24b85eacdea8fa94943b2d28c44d0ce3
قاعدة البيانات: OpenAIRE