Profiling of the human monocytic cell secretome by quantitative label-free mass spectrometry identifies stimulus-specific cytokines and proinflammatory proteins

被引:13
作者
Groessl, M. [1 ]
Luksch, H. [2 ]
Roesen-Wolff, A. [2 ]
Shevchenko, A. [1 ]
Gentzel, M. [1 ]
机构
[1] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[2] Univ Med Ctr Carl Gustav Carus, Dept Pediat, Dresden, Germany
关键词
Cell biology; Cytokines; Immune response; Protein marker discovery; Quantitative proteomics; Secretome profiling; INTRACELLULAR SENSORS; PROTEOMICS; INFLAMMATION; MICROBES;
D O I
10.1002/pmic.201200108
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The immune response to pathogens or injury relies on the concerted release of cytokines and proteins with biological activity important for host protection, host defense, and wound healing. Consequently, the secretome of immune cells provides a promising resource for discovery of specific molecular markers and targets for pharmacological intervention. Here, we employ label-free MS for unbiased, quantitative profiling of the human monocytic cell secretome under different proinflammatory stimuli. The quantitative secretome profiles reveal the highly stimulus-dependent cellular response and differential, specific secretion of more than 200 proteins, including important proinflammatory proteins and cytokines.
引用
收藏
页码:2833 / 2842
页数:10
相关论文
共 35 条
  • [1] Feature-based prediction of non-classical and leaderless protein secretion
    Bendtsen, JD
    Jensen, LJ
    Blom, N
    von Heijne, G
    Brunak, S
    [J]. PROTEIN ENGINEERING DESIGN & SELECTION, 2004, 17 (04) : 349 - 356
  • [2] Normalization approaches for removing systematic biases associated with mass spectrometry and label-free proteomics
    Callister, SJ
    Barry, RC
    Adkins, JN
    Johnson, ET
    Qian, WJ
    Webb-Robertson, BJM
    Smith, RD
    Lipton, MS
    [J]. JOURNAL OF PROTEOME RESEARCH, 2006, 5 (02) : 277 - 286
  • [3] AmiGO: online access to ontology and annotation data
    Carbon, Seth
    Ireland, Amelia
    Mungall, Christopher J.
    Shu, ShengQiang
    Marshall, Brad
    Lewis, Suzanna
    [J]. BIOINFORMATICS, 2009, 25 (02) : 288 - 289
  • [4] Intracellular sensors of extracellular bacteria
    Clarke, Thomas B.
    Weiser, Jeffrey N.
    [J]. IMMUNOLOGICAL REVIEWS, 2011, 243 : 9 - 25
  • [5] Copy number variation in chemokine superfamily: the complex scene of CCL3L-CCL4L genes in health and disease
    Colobran, R.
    Pedrosa, E.
    Carretero-Iglesia, L.
    Juan, M.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2010, 162 (01) : 41 - 52
  • [6] Advances in immunology - Autoimmune diseases
    Davidson, A
    Diamond, B
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (05) : 340 - 350
  • [7] Inflammasome activation and IL-1β and IL-18 processing during infection
    de Veerdonk, Frank L. van
    Netea, Mihai G.
    Dinarello, Charles A.
    Joosten, Leo A. B.
    [J]. TRENDS IN IMMUNOLOGY, 2011, 32 (03) : 110 - 116
  • [8] A guided tour of the Trans-Proteomic Pipeline
    Deutsch, Eric W.
    Mendoza, Luis
    Shteynberg, David
    Farrah, Terry
    Lam, Henry
    Tasman, Natalie
    Sun, Zhi
    Nilsson, Erik
    Pratt, Brian
    Prazen, Bryan
    Eng, Jimmy K.
    Martin, Daniel B.
    Nesvizhskii, Alexey I.
    Aebersold, Ruedi
    [J]. PROTEOMICS, 2010, 10 (06) : 1150 - 1159
  • [9] Conserved gene structure and genomic linkage for D-dopachrome tautomerase (DDT) and MIF
    Esumi, N
    Budarf, M
    Ciccarelli, L
    Sellinger, B
    Kozak, CA
    Wistow, G
    [J]. MAMMALIAN GENOME, 1998, 9 (09) : 753 - 757
  • [10] Immunity, Inflammation, and Cancer
    Grivennikov, Sergei I.
    Greten, Florian R.
    Karin, Michael
    [J]. CELL, 2010, 140 (06) : 883 - 899