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Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system.

Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system. Research Abstract Details 

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  • Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system. Abstract Text:

    yoshinobu murakamiYoshinobu Murakami,hiroo iwataHiroo Iwata,etsuko kitanoEtsuko Kitano,hajime kitamuraHajime Kitamura,yoshito ikadaYoshito Ikada,

    Bioartificial pancreas, in which the islets of Langerhans (islets) are enclosed in artificial membrane to be protected from the host immune system, is expected to be a promising medical device to treat patients who suffer from insulin-dependent diabetes. Our strategy for the preparation of a bioartificial pancreas involves utilizing a membrane including polymeric materials that can inhibit the complement. When we examined a membrane containing poly(styrene sulfonic acid), long survival of islets enclosed in the membrane was observed in recipients carrying antibodies against islet cells. This fact stimulated us to start examinations of effects of PSSa on the complement system. In this study, we examined effects of PSSa on the classical pathway (CP) of the serum complement system to identify the mechanism(s) involved. The electric static interaction between cationic C1q (pI 9.3) and anionic PSSa induces PSSa-C1q complex formation. The dissociation of C1q(r2s2) complex by PSSa results inactivation of the CP activity. Those results indicate that PSSa was not an activator of the CP, but an inhibitor of CP activation. This study clarifies the mechanism by which PSSa protects islets in a microcapsule from the humoral immunity of the recipient carrying anti-islet antibodies. A microcapsule containing PSSa seems to effectively protect the islet from attacks of the host immune system after transplantation carrying antibodies against islet cells.

    Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system. Publishing Authors By Initials

    y murakamiY Murakami,h iwataH Iwata,e kitanoE Kitano,h kitamuraH Kitamura,y ikadaY Ikada,

    For similar biochemical phenomena, metabolism, and nutrition: biochemical phenomena: protein binding research abstracts see: biochemical phenomena, metabolism, and nutrition: biochemical phenomena: protein binding research

    PUBMED ID PMID:

    MEDLINE DATE:

    Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of biomaterials science. Polymer edition

    VOLUME: 16

    Page Numbers: 685-97

    Journal Abbreviation:

    ISSN: 0920-5063

    DAY: 20

    MONTH: 02

    YEAR: 2005

    Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9007393

    Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system. Keywords Mesh Terms:

    KEYWORDS: Protein Binding

    MESH TERMS: pharmacology

    Chemical & Substance for Abstract: Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system. Information

    Substance Name: Complement C1q

    Registry Number: 80295-33-6

    Grant and Affiliation Information for Interaction of poly(styrene sulfonic acid) with the classical pathway of the serum complement system.

    AFFILIATION: Institute for Frontier Medical Sciences, Kyoto University, 53 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: J Biomater Sci Polym Ed

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