Identification of DC-SIGN as the receptor during the interaction of Lactobacillus plantarum CGMCC 1258 and dendritic cells

Identification of DC-SIGN as the receptor during the interaction of Lactobacillus plantarum CGMCC 1258 and dendritic cells
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DOI:
10.1007/s11274-010-0495-3
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发表时间:
2011-03
影响因子:
4.1
通讯作者:
Zhihua Liu;Yanlei Ma;T. Shen;Hong-Qi Chen;Yu‐kun Zhou;P. Zhang;Ming Zhang;Zhao-xin Chu;H. Qin-H
Zhihua Liu;Yanlei Ma;T. Shen;Hong-Qi Chen;Yu‐kun Zhou;P. Zhang;Ming Zhang;Zhao-xin Chu;H. Qin-H
中科院分区:
工程技术3区
文献类型:
--
作者:
Zhihua Liu;Yanlei Ma;T. Shen;Hong-Qi Chen;Yu‐kun Zhou;P. Zhang;Ming Zhang;Zhao-xin Chu;H. Qin-H

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Lactobacillus plantarumcan exert additional probiotic effects via regulation of human immune system. However, the direct interaction between probiotics and the receptors of immune cells still needs to be further studied. To identify the receptor of dendritic cells during the interaction withL. plantarum. Dendritic cells were pretreated withL. plantarumand the antibody to dendritic cells specific intercellular adhesion molecule-grabbing nonintegrin (DC-SIGN), toll like receptor (TLR)-2 and TLR-4. The maturation of immature dendritic cells, cytokine production, and modulation of T cells were studied by flow cytometry. Adherence betweenL. plantarumand dendritic cells were studied by ELISA, flow cytometry, and Western blot.L. plantarumcould mature dendritic cells by up-regulating MHC-II and CD80 and CD86. Anti-inflammatory interlectin (IL)-10 and IL-6 was up-regulated and pro-inflammatory IL-12p70 was retro-regulated byL. plantarum.L. plantarummay interact with DC-SIGN and modulate of T to differentiate into IL-4 producing T cells. The interaction ofL. plantarumand DC-SIGN and the biological effects could be blocked by EDTA and antibody to DC-SIGN. Effects ofL. plantarumwere concentration-dependent.L. plantarumcould bind to DC-SIGN to improve DC maturation at different ratios, regulate the secretion of anti-inflammatory and pro-inflammatory cytokines, and induce the polarization of interlectin-4-producing T cells.