共 55 条
Interferon. induced compositional changes in human bone marrow derived mesenchymal stem/stromal cells
被引:31
作者:

Guan, Qingdong
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机构:
Univ Manitoba, Dept Pediat & Child Hlth, Manitoba Ctr Adv Cell & Tissue Therapy, Winnipeg, MB, Canada
CancerCare Manitoba, Cellular Therapy Lab, Winnipeg, MB, Canada Univ Manitoba, Dept Pediat & Child Hlth, Manitoba Ctr Adv Cell & Tissue Therapy, Winnipeg, MB, Canada

Ezzati, Peyman
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机构:
Univ Manitoba, Rady Fac Hlth Sci, Dept Internal Med, Manitoba Ctr Prote & Syst Biol,Sect Biomed Prote, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada
799 John Buhler Res Ctr, Hlth Sci Ctr, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada Univ Manitoba, Dept Pediat & Child Hlth, Manitoba Ctr Adv Cell & Tissue Therapy, Winnipeg, MB, Canada

Spicer, Victor
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Univ Manitoba, Rady Fac Hlth Sci, Dept Internal Med, Manitoba Ctr Prote & Syst Biol,Sect Biomed Prote, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada
799 John Buhler Res Ctr, Hlth Sci Ctr, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada Univ Manitoba, Dept Pediat & Child Hlth, Manitoba Ctr Adv Cell & Tissue Therapy, Winnipeg, MB, Canada

Krokhin, Oleg
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Univ Manitoba, Rady Fac Hlth Sci, Dept Internal Med, Manitoba Ctr Prote & Syst Biol,Sect Biomed Prote, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada
799 John Buhler Res Ctr, Hlth Sci Ctr, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada Univ Manitoba, Dept Pediat & Child Hlth, Manitoba Ctr Adv Cell & Tissue Therapy, Winnipeg, MB, Canada

Wall, Donna
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Univ Toronto, Hosp Sick Children, Dept Paediat, Div Haematol Oncol, Toronto, ON, Canada Univ Manitoba, Dept Pediat & Child Hlth, Manitoba Ctr Adv Cell & Tissue Therapy, Winnipeg, MB, Canada

Wilkins, John A.
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Univ Manitoba, Rady Fac Hlth Sci, Dept Internal Med, Manitoba Ctr Prote & Syst Biol,Sect Biomed Prote, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada
799 John Buhler Res Ctr, Hlth Sci Ctr, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada Univ Manitoba, Dept Pediat & Child Hlth, Manitoba Ctr Adv Cell & Tissue Therapy, Winnipeg, MB, Canada
机构:
[1] Univ Manitoba, Dept Pediat & Child Hlth, Manitoba Ctr Adv Cell & Tissue Therapy, Winnipeg, MB, Canada
[2] CancerCare Manitoba, Cellular Therapy Lab, Winnipeg, MB, Canada
[3] Univ Manitoba, Rady Fac Hlth Sci, Dept Internal Med, Manitoba Ctr Prote & Syst Biol,Sect Biomed Prote, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada
[4] 799 John Buhler Res Ctr, Hlth Sci Ctr, 715 McDermot Ave, Winnipeg, MB R3E 3P4, Canada
[5] Univ Toronto, Hosp Sick Children, Dept Paediat, Div Haematol Oncol, Toronto, ON, Canada
关键词:
Proteomics;
Human;
2D LC mass spectrometry;
Interferon gamma;
Mesenchymal stem/stromal cells ( MSC);
Quantitative proteome profiling;
Licensing;
Membrane;
STROMAL CELLS;
STEM-CELLS;
IFN-GAMMA;
INDOLEAMINE 2,3-DIOXYGENASE;
PROSTACYCLIN SYNTHASE;
TGF-BETA;
INDUCTION;
IMMUNOSUPPRESSION;
SUPPRESSION;
ACTIVATION;
D O I:
10.1186/s12014-017-9161-1
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Background: Mesenchymal stem/stromal cells ( MSC) display a range of immunoregulatory properties which can be enhanced by the exposure to cytokines such interferon. ( IFN-gamma).However the compositional changes associated with the 'licensing' of these cells have not been clearly defined. The present study was undertaken to provide a detailed comparative proteomic analysis of the compositional changes that occur in human bone marrow derived MSC following 20 h treatment with IFN-gamma. Methods: 2D LC MSMS analysis of control and IFN-gamma treated cells from 5 different healthy donors provided confident identification of more than 8400 proteins. Results: In total 210 proteins were shown to be significantly altered in their expression levels (>=|2SD|) following IFN-gamma treatment. The changes for several of these proteins were confirmed by flow cytometry. STRING analysis determined that approximately 30% of the altered proteins physically interacted in described interferon mediated processes. Comparison of the list of proteins that were identified as changed in the proteomic analysis with data for the same proteins in the Interferome DB indicated that similar to 35% of these proteins have not been reported to be IFN-gamma responsive in a range of cell types. Conclusions: This data provides an in depth analysis of the proteome of basal and IFN-gamma treated human mesenchymal stem cells and it identifies a number of novel proteins that may contribute to the immunoregulatory capacity if IFN-gamma licensed cells.
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Emory Univ, Winship Canc Inst, Dept Pediat, Atlanta, GA 30322 USA
Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
Emory Univ, Winship Canc Inst, Dept Hematol & Med Oncol, Atlanta, GA 30322 USA Emory Univ, Winship Canc Inst, Dept Pediat, Atlanta, GA 30322 USA