|本期目录/Table of Contents|

[1]樊亚童,郑鉴,肖俊,等.炎症反应中巨噬细胞的Siglec-G分子对DAMPs和PAMPs的识别及调节作用[J].天津医科大学学报,2018,24(02):93-96.
 FAN Ya-tong,ZHENG Jian,XIAO Jun,et al.Identification of DAMPs and PAMPs by Siglec-G in macrophages and its regulatory effect on DAMPs and PAMPs in inflammatory response[J].Journal of Tianjin Medical University,2018,24(02):93-96.
点击复制

炎症反应中巨噬细胞的Siglec-G分子对DAMPs和PAMPs的识别及调节作用(PDF)
分享到:

《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
24卷
期数:
2018年02期
页码:
93-96
栏目:
出版日期:
2018-03-20

文章信息/Info

Title:
Identification of DAMPs and PAMPs by Siglec-G in macrophages and its regulatory effect on DAMPs and PAMPs in inflammatory response
作者:
樊亚童郑鉴肖俊张学军
天津医科大学免疫学系,天津300070
Author(s):
FAN Ya-tong ZHENG Jian XIAO Jun ZHANG Xue-jun
Department of Immunology, Tianjin Medical University, Tianjin 300070, China
关键词:
DAMPsPAMPs巨噬细胞Siglec-G
Keywords:
PAMPs DAMPs macrophage Siglec-G
分类号:
R392.1
DOI:
-
文献标志码:
A
摘要:
目的:探究巨噬细胞中唾液酸结合性免疫球蛋白样凝集素(Siglecs)家族的成员Siglec-G参与损伤相关分子模式(DAMPs)和病原相关分子模式(PAMPs)识别及其在炎症反应中的调节作用。方法:提取并纯化野生型小鼠腹腔巨噬细胞, 用DAMPs中的高迁移率族蛋白Bl(HMGB1)和PAMPs中的脂多糖(LPS)分别刺激24 h,Real-time PCR方法检测细胞中Siglec-G基因的表达,ELISA方法检测野生型和Siglec-G基因敲除小鼠腹腔巨噬细胞培养上清中肿瘤坏死因子α (TNF-α)和白细胞介素6(IL-6)的分泌情况。结果:HMGB1能够使巨噬细胞中Siglec-G的表达明显升高,而LPS作用后Siglec-G的表达没有明显改变,同时发现,HMGB1作用于Siglec-G敲除小鼠的巨噬细胞后,TNF-α和IL-6的分泌明显增加,而LPS刺激后炎症因子的分泌没有明显改变。结论:巨噬细胞通过表达Siglec-G来识别DAMPs并发挥免疫抑制作用,而其对于PAMPs缺乏识别及调控作用。
Abstract:
Objective: To identify the PAMPs and DAMPs by Siglec-G, a member of the Sialic acid-binding immunoglobulin-like lectin (Siglecs) family, in macrophages and to explore its regulatory effect on PAMPs and DAMPs in inflammatory response. Methods: Peritoneal macrophages harvested and purified from wild type mice were stimulated with high mobility group protein Bl (HMGB1) in DAMPs and lipopolysaccharide (LPS) in PAMPs for 24 h, respectively. Real-time PCR was performed to analyze the Siglec-G mRNA expression in macrophages. ELISA was used to detect the secretion of TNF-α and IL-6 in the culture supernatants of peritoneal macrophages in wild type and Siglec-G knockout mice. Results: HMGB1 could significantly increase the expression of Siglec-G in macrophages, while the expression of Siglec-G was not altered after the stimulation of LPS. And it was found that the secretion of TNF-α and IL-6 increased significantly after HMGB1 acted on macrophages of Siglec-G knockout mice, but the secretion of inflammatory factors did not change markedly after LPS stimulation. Conclusion: Macrophages could recognize DAMPs by Siglec-G , and play a critical role in immune suppression, but it may not recognise or regulate PAMPs.

参考文献/References:

[1] Chen G Y, Tang J, Zheng P, et al. CD24 and Siglec-10 selectively repress tissue damage-Induced immune responses[J]. Science (New York, NY), 2009, 323(5922):1722
[2] Cao H, Crocker P R. Evolution of CD33-related siglecs: regulating host immune functions and escaping pathogen exploitation[J]. Immunology, 2011, 132(1):18
[3] Zelenay S, Reise Sousa C. Adaptive immunity after cell death[J]. Trends immunol, 2013, 34(7):329
[4] Segonzac C, Zipfel C. Activation of plant pattern-recognition receptors by bacteria[J]. Curr Opini Microbiol, 2011, 14(1):54
[5] Chaochao Q, Lou G, Yang Y, et al. Macrophage inflammatory protein-2 in high mobility group box 1 secretion of macrophage cells exposed to lipopolysaccharide[J]. Cell Physiol Biochem, 2017, 42(3):913
[6] Wang X, Sun R, Wei H, et al. High-mobility group box 1 (HMGB1)-Toll-like receptor (TLR)4-interleukin (IL)-23-IL-17A axis in drug-induced damage-associated lethal hepatitis: Interaction of gammadelta T cells with macrophages[J]. Hepatology, 2013, 57(1):373
[7] Scrima R, Menqa M, Pacelli C, et al. Para-hydroxyphenylpyruvate inhibits the pro-inflammatory stimulation of macrophage preventing LPS-mediated nitro-oxidative unbalance and immunometabolic shift[J]. PloS One, 2017,12(11):e0188683
[8] He X, Liu W, Shi M, et al . Docosahexaenoic acid attenuates LPS-stimulated inflammatory response by regulating the PPARγ/NF-κB pathways in primary bovine mammary epithelial cells[J]. Res Vet Sci, 2017,112:7
[9] Lin S Y, Hsieh S Y, Fan Y T, et al. Necroptosis promotes autophagy-dependent upregulation of DAMP and results in immunosurveillance[J]. Autophagy, 2017[Epub ahead of print]
[10] Zhu J, Wang F L, Wang H B, et al. TNF-alpha mRNA is negatively regulated by microRNA-181a-5p in maturation of dendritic cells induced by high mobility group box-1 protein[J]. Sci Rep, 2017, 7(1):12239
[11] Pillai S, Netravali I A, Cariappa A, et al. Siglecs and immune regulation[J]. Annu Rev Immunol, 2012, 30:357
[12] O’Keefe T L, Williams G T, Davies S L, et al. Hyperresponsive B cells in CD22-deficient mice[J]. Science (New York, NY), 1996, 274(5288):798
[13] Nitschke L. CD22 and Siglec-G: B-cell inhibitory receptors with distinct functions[J]. Immunol Rev, 2009, 230(1):128
[14] Poe J C, Tedder T F. CD22 and Siglec-G in B cell function and tolerance[J]. Trends Immunol, 2012, 33(8):413
[15] Macauley M S, Crocker P R, Paulson J C. Siglec-mediated regulation of immune cell function in disease[J]. Nat Rev Immunol, 2014, 14(10):653
[16] Toubai T, Hou G, Mathewson N, et al. Siglec-G-CD24 axis controls the severity of graft-versus-host disease in mice[J]. Blood, 2014, 123(22):3512
[17] Ding Y, Guo Z, Liu Y, et al. The lectin Siglec-G inhibits dendritic cell cross-presentation by impairing MHC class I-peptide complex formation[J]. Nat Immunol, 2016, 17(10):1167
[18] Gruber S, Hendrikx T, Tsiantoulas D, et al. Sialic acid-binding immunoglobulin-like lectin G promotes atherosclerosis and liver inflammation by suppressing the protective functions of B-1 cells[J]. Cell Rep, 2016, 14(10):2348
[19] Toubai T, Rossi C, Oravecz-Wilson K, et al. Siglec-G represses DAMP-mediated effects on T cells[J]. JCI Insight, 2017, 2(14): pii: 92293

相似文献/References:

备注/Memo

备注/Memo:
文章编号 1006-8147(2018)02-0093-04
基金项目 国家自然科学基金资助项目(31370891,31240036);天津市自然科学基金重点项目(13JCZDJC30000)
作者简介 樊亚童(1990-),女,硕士在读,研究方向:免疫学;通信作者:张学军,E-mail:xjzhimmunology@163.com。
更新日期/Last Update: 2018-03-20