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甘草酸抑制中性粒细胞相关的交替活化巨噬细胞生成。

Glycyrrhizin inhibits neutrophil-associated generation of alternatively activated macrophages.

作者信息

Yoshida Tsuyoshi, Tsuda Yasuhiro, Takeuchi Dan, Kobayashi Makiko, Pollard Richard B, Suzuki Fujio

机构信息

Department of Internal Medicine, The University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-0435, USA.

出版信息

Cytokine. 2006 Mar 21;33(6):317-22. doi: 10.1016/j.cyto.2006.03.001. Epub 2006 Apr 21.

DOI:10.1016/j.cyto.2006.03.001
PMID:16631375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7128827/
Abstract

Patients with severe burn injuries are extremely susceptible to infection, and the host's antibacterial responses are frequently suppressed by alternatively activated macrophages (M2Mphi), commonly demonstrated in these patients. An immunosuppressive subset of neutrophils (PMN-II), demonstrated in the peripheral blood of thermally injured patients, has been described as an inducer of M2Mphi. In the present studies, the inhibitory effect of glycyrrhizin (GL) on M2Mphi generation stimulated by PMN-II was examined. M2Mphi were generated from resident Mphi (R-Mphi, lower chamber) after cultivation with PMN-II (upper chamber) in a dual-chamber transwell. However, M2Mphi were not generated from R-Mphi when the same transwell cultures were performed in the presence of GL. M2Mphi were not generated from R-Mphi after cultivation with PMN-II previously treated with GL, while R-Mphi previously treated with GL converted to M2Mphi after they were cultured with PMN-II in transwells. Interleukin-10 and CCL2 released from PMN-II were shown to be effector molecules responsible for the generation of M2Mphi. However, these soluble factors were not produced by PMN-II treated with GL. These results indicate that GL inhibits PMN-II-stimulated M2Mphi generation through the inhibition of CCL2/interleukin-10 production by PMN-II.

摘要

严重烧伤患者极易受到感染,且在这些患者中常见的替代性活化巨噬细胞(M2Mphi)常常会抑制宿主的抗菌反应。热损伤患者外周血中存在一种免疫抑制性中性粒细胞亚群(PMN-II),已被描述为M2Mphi的诱导剂。在本研究中,检测了甘草酸(GL)对PMN-II刺激产生M2Mphi的抑制作用。在双室Transwell中,将常驻巨噬细胞(R-Mphi,下室)与PMN-II(上室)共培养后可产生M2Mphi。然而,在GL存在的情况下进行相同的Transwell培养时,R-Mphi不会产生M2Mphi。用GL预处理PMN-II后再与R-Mphi共培养,R-Mphi不会产生M2Mphi,而预先用GL处理过的R-Mphi在Transwell中与PMN-II共培养后会转变为M2Mphi。PMN-II释放的白细胞介素-10和CCL2被证明是负责产生M2Mphi的效应分子。然而,用GL处理的PMN-II不会产生这些可溶性因子。这些结果表明,GL通过抑制PMN-II产生CCL2/白细胞介素-10来抑制PMN-II刺激的M2Mphi生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/c6d27e894c91/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/d350b8c308f5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/bab6e71f1aea/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/f87ad06fce3b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/c6d27e894c91/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/d350b8c308f5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/bab6e71f1aea/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/f87ad06fce3b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0564/7128827/c6d27e894c91/gr4.jpg

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Enhanced TLR4 reactivity following injury is mediated by increased p38 activation.损伤后增强的Toll样受体4(TLR4)反应性由p38激活增加介导。
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