Alcohol intoxication inhibits pulmonary S100A8 and S100A9 expression in rats challenged with intratracheal lipopolysaccharide

被引:10
作者
Zhang, Ping
Zhong, Qiu
Bagby, Gregory J.
Nelson, Steve
机构
[1] Louisiana State Univ, Ctr Hlth Sci, Dept Med, Sect Pulm CCM,Alcohol Res Ctr, New Orleans, LA 70112 USA
[2] Louisiana State Univ, Ctr Hlth Sci, Gene Therapy Program, New Orleans, LA 70112 USA
[3] Louisiana State Univ, Ctr Hlth Sci, Dept Physiol, New Orleans, LA 70112 USA
关键词
alcohol; lung; S100; proteins; neutrophils; LPS;
D O I
10.1111/j.1530-0277.2006.00269.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Alcohol is known to inhibit the recruitment of polymorphonuclear leukocytes (PMNs) into tissue sites including the lung. During infection and inflammation, recruited neutrophils (PMNs) release S100 proteins that function to promote the recruitment of additional phagocytes. Methods and Results: This study investigated the effects of alcohol intoxication on S100 protein production in the lung in response to lipopolysaccharide (LPS). Animals were administered alcohol (5.5 g/kg) or saline 30 minutes before intratracheal challenge with LPS (100 mg/rat). Alcohol suppressed PMN recruitment into the lung following intratracheal LPS, which was associated with an inhibition of increase in S100A8 levels in both the bronchoalveolar lavage (BAL) fluid and lysates of cells recovered by BAL at 90 minutes and 4 hours post-LPS challenge. S100A8 and S100A9 mRNA expression in cells recovered by BAL was significantly up-regulated at both 90 minutes and 4 hours after the LPS challenge, and alcohol also suppressed this response. In addition, intratracheal LPS caused a transient increase in S100A8 mRNA expression in circulating leukocytes at 90 minutes after the challenge. Similarly, this LPS-induced up-regulation of S100A8 mRNA expression was inhibited in rats intoxicated with alcohol. Conclusion: These data show that alcohol inhibits the S100 protein response in the lung, which may serve as a mechanism underlying alcohol-induced suppression of PMN recruitment into the terminal airways during pulmonary infection.
引用
收藏
页码:113 / 121
页数:9
相关论文
共 50 条
  • [41] Increased expression of S100A8 and S100A9 in patients with diffuse cutaneous systemic sclerosis. A correlation with organ involvement and immunological abnormalities
    Xu, Xue
    Wu, Wen-yu
    Tu, Wen-zheng
    Chu, Hai-yan
    Zhu, Xiao-xia
    Liang, Min-rui
    Xue, Yu
    Wang, Jiu-cun
    Zou, He-jian
    CLINICAL RHEUMATOLOGY, 2013, 32 (10) : 1501 - 1510
  • [42] Generation and Application of Monoclonal Antibodies against Porcine S100A8, S100A9, and S100A12 Proteins Using Hybridoma Technology
    Xia, Pengpeng
    Ma, Xin
    Yan, Li
    Lian, Siqi
    Li, Xiangyu
    Luo, Yi
    Chen, Ziyue
    Ji, Xingduo
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (02)
  • [43] Tissue mRNA for S100A4, S100A6, S100A8, S100A9, S100A11 and S100P Proteins in Colorectal Neoplasia: A Pilot Study
    Peterova, Eva
    Bures, Jan
    Moravkova, Paula
    Kohoutova, Darina
    MOLECULES, 2021, 26 (02):
  • [44] Inhibition of S100A9 expression by propofol in monocytes of rats with endotoxemia
    Li, Zhen
    Zhao, Guodong
    Zhou, Guobin
    Wang, Yan
    Wang, Qing
    Ji, Jinquan
    Wang, Zhipeng
    MOLECULAR MEDICINE REPORTS, 2012, 6 (03) : 657 - 661
  • [45] Binding of Pro-Inflammatory Proteins S100A8 or S100A9 to Amyloid-β Peptide Suppresses Its Fibrillation
    Litus, Ekaterina A.
    Shevelyova, Marina P.
    Vologzhannikova, Alisa A.
    Deryusheva, Evgenia I.
    Machulin, Andrey V.
    Nemashkalova, Ekaterina L.
    Permyakova, Maria E.
    Sokolov, Andrey S.
    Alikova, Valeria D.
    Uversky, Vladimir N.
    Permyakov, Sergei E.
    BIOMOLECULES, 2025, 15 (03)
  • [46] Expression of S100 proteins in normal human tissues and common cancers using tissue microarrays: S100A6, S100A8, S100A9 and S100A11 are all overexpressed in common cancers
    Cross, SS
    Hamdy, FC
    Deloulme, JC
    Rehman, I
    HISTOPATHOLOGY, 2005, 46 (03) : 256 - 269
  • [47] High plasma level of S100A8/S100A9 and S100A12 at admission indicates a higher risk of death in septic shock patients
    Dubois, Christelle
    Marce, Dominique
    Faivre, Valerie
    Lukaszewicz, Anne-Claire
    Junot, Christophe
    Fenaille, Francois
    Simon, Stephanie
    Becher, Francois
    Morel, Nathalie
    Payen, Didier
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [48] Hepatocyte-specific S100a8 and S100a9 transgene expression in mice causes Cxcl1 induction and systemic neutrophil enrichment
    Lars Wiechert
    Julia Németh
    Tobias Pusterla
    Christine Bauer
    Aurora De Ponti
    Sandra Manthey
    Silke Marhenke
    Arndt Vogel
    Ursula Klingmüller
    Jochen Hess
    Peter Angel
    Cell Communication and Signaling, 10
  • [49] Hepatocyte-specific S100a8 and S100a9 transgene expression in mice causes Cxcl1 induction and systemic neutrophil enrichment
    Wiechert, Lars
    Nemeth, Julia
    Pusterla, Tobias
    Bauer, Christine
    De Ponti, Aurora
    Manthey, Sandra
    Marhenke, Silke
    Vogel, Arndt
    Klingmueller, Ursula
    Hess, Jochen
    Angel, Peter
    CELL COMMUNICATION AND SIGNALING, 2012, 10
  • [50] Pro-Inflammatory S100A8 and S100A9 Proteins: Self-Assembly into Multifunctional Native and Amyloid Complexes
    Vogl, Thomas
    Gharibyan, Anna L.
    Morozova-Roche, Ludmilla A.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2012, 13 (03) : 2893 - 2917