Proteomic alterations associated with the formation of monocyte extracellular trap induced by Candida albicans hyphae

被引:0
|
作者
Wu, Xian [1 ]
Sun, Liying [1 ]
Huang, Lei [1 ]
Huang, Chenwei [1 ]
Sun, Kuixia [1 ]
Li, Haixia [1 ]
机构
[1] Peking Univ First Hosp, Dept Clin Lab, Beijing, Peoples R China
关键词
Candida albicans; extracellular trap; hyphae; monocyte; proteome; TLR4;
D O I
10.2217/fmb-2023-0029
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: The interaction between the host and Candida albicans is dynamic and intricate. We performed proteomic analysis to explore monocyte-C. albicans hyphae interaction. Materials & methods: Primary human monocytes were stimulated by heat-killed C. albicans hyphae and their proteins were profiled by tandem liquid chromatography with mass spectrometry (LC-MS/MS). Results: Based on the protein database of different species for analysis, we found that stimulation of monocytes by hyphae was accompanied by upregulation of histones and activation of extracellular traps (ETs) formation pathway. Meanwhile, monocyte ETs (MoETs) were evoked by synthesis or alteration of C. albicans cell wall proteins expression during the morphological switch to hyphal. Conclusion: MoETs formation is linked to cell wall proteins of C. albicans hyphae.
引用
收藏
页码:307 / 316
页数:10
相关论文
共 50 条
  • [31] Extracellular DNA release confers heterogeneity in Candida albicans biofilm formation
    Ranjith Rajendran
    Leighann Sherry
    David F Lappin
    Chris J Nile
    Karen Smith
    Craig Williams
    Carol A Munro
    Gordon Ramage
    BMC Microbiology, 14
  • [32] Components of Candida albicans cell wall involved in mast cell degranulation and extracellular-trap formation in response to fungal infection
    Ostrowska, Dominika
    Zawrotniak, Marcin
    Proba, Adrianna
    Karkowska-Kuleta, Justyna
    Bochenska, Oliwia
    Aoki, Wataru
    Ueda, Mitsuyoshi
    Kozik, Andrzej
    Rapala-Kozik, Maria
    NEW BIOTECHNOLOGY, 2016, 33 : S209 - S209
  • [33] FUNGICIDAL ACTIVITY OF CANDIDA-ALBICANS-INDUCED MURINE LYMPHOKINE-ACTIVATED KILLER-CELLS AGAINST CANDIDA-ALBICANS HYPHAE INVITRO
    SCARINGI, L
    BLASI, E
    ROSATI, E
    MARCONI, P
    BISTONI, F
    JOURNAL OF GENERAL MICROBIOLOGY, 1991, 137 : 2851 - 2856
  • [34] 2-Alkyl-anthraquinones inhibit Candida albicans biofilm via inhibiting the formation of matrix and hyphae
    Song, Yuanyuan
    Wang, Ziqi
    Long, Yijing
    Mao, Yang
    Jiang, Feng
    Lu, Yuanyuan
    RESEARCH IN MICROBIOLOGY, 2022, 173 (6-7)
  • [35] Histatin-induced alterations in Candida albicans:: A microscopic and submicroscopic comparison
    Isola, Raffaella
    Isola, Michela
    Conti, Gabriele
    Lantini, Maria Serenella
    Riva, Alessandro
    MICROSCOPY RESEARCH AND TECHNIQUE, 2007, 70 (07) : 607 - 616
  • [36] Proteomic analysis of Candida albicans yeast and hyphal cell wall and associated proteins
    Ebanks, RO
    Chisholm, K
    McKinnon, S
    Whiteway, M
    Pinto, DM
    PROTEOMICS, 2006, 6 (07) : 2147 - 2156
  • [37] Hydroquinones Including Tetrachlorohydroquinone Inhibit Candida albicans Biofilm Formation by Repressing Hyphae-Related Genes
    Kim, Yong-Guy
    Lee, Jin-Hyung
    Park, Sunyoung
    Khadke, Sagar Kiran
    Shim, Jae-Jin
    Lee, Jintae
    MICROBIOLOGY SPECTRUM, 2022, 10 (05):
  • [38] Activation of MAPK/c-Fos induced responses in oral epithelial cells is specific to Candida albicans and Candida dubliniensis hyphae
    David L. Moyes
    Celia Murciano
    Manohursingh Runglall
    Arinder Kohli
    Ayesha Islam
    Julian R. Naglik
    Medical Microbiology and Immunology, 2012, 201 : 93 - 101
  • [39] Lfc controls the formation of neutrophil extracellular traps against Candida albicans infection
    Weng, Chen-Min
    Chiang, Hao-Sen
    CYTOKINE, 2017, 100 : 39 - 39
  • [40] Activation of MAPK/c-Fos induced responses in oral epithelial cells is specific to Candida albicans and Candida dubliniensis hyphae
    Moyes, David L.
    Murciano, Celia
    Runglall, Manohursingh
    Kohli, Arinder
    Islam, Ayesha
    Naglik, Julian R.
    MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 2012, 201 (01) : 93 - 101