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Mass Separation and in vitro Immunological Activity of Membrane-fractionated Polysaccharides from Fruiting Body and Mycelium of Agaricus subrufescens
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  • Mass Separation and in vitro Immunological Activity of Membrane-fractionated Polysaccharides from Fruiting Body and Mycelium of Agaricus subrufescens
  • Mass Separation and in vitro Immunological Activity of Membrane-fractionated Polysaccharides from Fruiting Body and Mycelium of Agaricus subrufescens
저자명
Silveira. Douglas Bardini,Celmer. Alvaro Jose,Camelini. Carla Maisa,Rossi. Marcio Jose,Petrus. Jose Carlos Cunha,de Mendonca. Ma
간행물명
Biotechnology and bioprocess engineering
권/호정보
2012년|17권 4호|pp.804-811 (8 pages)
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한국생물공학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Membrane technology has been applied to separate polysaccharides from Agaricus subrufescens (ASPs). The membrane-retained fractions and unfractionated preparations have been tested for in vitro immunological activity. Both the microfiltration (MF) and ultrafiltration (UF1) membranes were able to separate high-molecular weight polysaccharides from fruiting body (ASP-FB) and submerge-fermented mycelium (ASP-SmF) extracts. All fractions showed immunostimulatory effects on RAW 264.7 macrophages, measured by TNF-${alpha}$, iNOs gene expression, and NO production. In contrast, antibody and proliferation levels in B lymphoblastoid SKW 6.4 cells were significantly increased after treatment with ASP-FB, but did not with ASP-SmF preparations. The ASPs- and LPS-induced stimulation could be differentiated by the finding that polymyxin B, a specific inhibitor of LPS, did not significantly affect the immunoactivating response and proliferation activity of ASPs on macrophages and B cells, respectively. Furthermore, the ASP-FB treatment was unable to induce IL-6 production by B cells unlike LPS activation, sustaining distinct signaling pathways for ASP-FB and LPS. The overall results provided additional information about the action of ASPs on the immune system and support the membrane method to separate and concentrate high-molecular weight ASPs for immunopharmacological and biotechnological applications.