دورية أكاديمية
FXII contact activation products have an inhibitory effect on αFXIIa.
العنوان: | FXII contact activation products have an inhibitory effect on αFXIIa. |
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المؤلفون: | Xu LC; Department of Surgery, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA., Siedlecki CA; Department of Surgery, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.; Department of Bioengineering, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA. |
المصدر: | Journal of biomedical materials research. Part A [J Biomed Mater Res A] 2024 Aug; Vol. 112 (8), pp. 1213-1223. Date of Electronic Publication: 2023 Sep 22. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101234237 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4965 (Electronic) Linking ISSN: 15493296 NLM ISO Abbreviation: J Biomed Mater Res A Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: Hoboken, NJ : John Wiley & Sons, c2002- |
مواضيع طبية MeSH: | Wettability*, Humans ; Hydrophobic and Hydrophilic Interactions ; Factor XIIa/metabolism ; Factor XIIa/antagonists & inhibitors ; Prekallikrein/metabolism ; Glass/chemistry ; Blood Coagulation/drug effects ; Factor XII/metabolism ; Factor XII/antagonists & inhibitors ; Silanes/chemistry ; Surface Properties |
مستخلص: | It is accepted that the contact activation complex of the intrinsic pathway of blood coagulation cascade produces active enzymes that lead to plasma coagulation following biomaterial contact. In this study, FXII was activated through contact with hydrophilic glass beads and hydrophobic octadecyltrichlorosilane-modified glass beads from neat buffer solutions. These FXII contact activation products generated from material interaction were found to suppress the procoagulant activity of exogenous αFXIIa, and this inhibition was dependent on surface wettability and the concentration of exogenous αFXIIa. Higher relative inhibition rates were generally observed at low concentrations of αFXIIa (1-2 μg/mL) while both hydrophobic and hydrophilic materials showed similar inhibition levels (~39%) at high concentrations of αFXIIa (20 μg/mL). The presence of prekallikrein in the activation system increased the amount of FXIIa produced during FXII contact activation, and also suppressed the apparent levels of inhibitors on hydrophilic surfaces, while having no effect on apparent levels of inhibitors on hydrophobic surface. The combination of FXII contact activation products and activator surfaces was found to dramatically increase inhibition of αFXIIa activity compared to the activation products alone, regardless of activator surface wettability and the presence of prekallikrein. This finding of inhibitors in the suite of proteins generated by contact activation provides additional knowledge into the complex series of interactions that occur when plasma comes into contact with material surfaces. (© 2023 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals LLC.) |
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معلومات مُعتمدة: | R01 HL069965 United States HL NHLBI NIH HHS; RO1HL069965 United States HL NHLBI NIH HHS; RO1HL069965 United States HL NHLBI NIH HHS |
فهرسة مساهمة: | Keywords: biomaterials surfaces; blood‐materials interactions; coagulation |
المشرفين على المادة: | EC 3.4.21.38 (Factor XIIa) 9055-02-1 (Prekallikrein) 9001-30-3 (Factor XII) 0 (Silanes) 112-04-9 (octadecyltrichlorosilane) |
تواريخ الأحداث: | Date Created: 20230922 Date Completed: 20240618 Latest Revision: 20240703 |
رمز التحديث: | 20240703 |
مُعرف محوري في PubMed: | PMC10957503 |
DOI: | 10.1002/jbm.a.37612 |
PMID: | 37737653 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1552-4965 |
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DOI: | 10.1002/jbm.a.37612 |