Interferon-γ Alters the Immune-related miRNA Expression of Microvesicles Derived from Mesenchymal Stem Cells

Increasing studies have demonstrated that interferon gamma(IFN-γ),which serves as a critical inflammatory cytokine,is essential to induce the immunosuppressive effects of mesenchymal stem cells(MSCs).However,the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs(γM...

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Published inJournal of Huazhong University of Science and Technology. Medical sciences Vol. 37; no. 2; pp. 179 - 184
Main Author 赵爱琪 谢慧 林生彦 雷倩 任文祥 高飞 郭豪 郭安源 陈智超 王红祥
Format Journal Article
LanguageEnglish
Published Wuhan Huazhong University of Science and Technology 01.04.2017
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China%Department of Geriatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China%Department of Hematology, Wuhan Central Hospital, Wuhan 430022, China
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ISSN1672-0733
1993-1352
1993-1352
DOI10.1007/s11596-017-1712-1

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Abstract Increasing studies have demonstrated that interferon gamma(IFN-γ),which serves as a critical inflammatory cytokine,is essential to induce the immunosuppressive effects of mesenchymal stem cells(MSCs).However,the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs(γMSCs) are not fully understood.MSC-derived microvesicles(MSC-MVs) have been viewed as potential pivotal mediators of the immunosuppressive effects of MSCs.Moreover,micro RNAs(miR NAs) are important regulators of immunological processes and can be shuttled from cell to cell by MVs.The aim of our study was to analyze the the mi RNA expression signature of MVs derived from γMSCs(γMSC-MVs),which may provide better understanding of the immunosuppressive property of their parent cells.Through mi RNA microarray and bioinformatics analysis,we found 62 significantly differentially expressed miR NAs(DEMs) in γMSC-MVs compared with MSC-MVs.And the potential target genes and signaling pathways regulated by DEMs were predicted and analyzed.Interestingly,many DEMs and predicted signaling pathways had been demonstrated to be involved in immunoregulation.Furthermore,the network between immunoregulation-related pathways and relevant DEMs was constructed.Collectively,our research on the mi RNA repertoires of γMSC-MVs not only provides new perspectives into the mechanisms underlying the enhanced immunosuppressive property of γMSCs,but also paves the way to clinical application of these potent organelles in the future.
AbstractList Increasing studies have demonstrated that interferon gamma (IFN-γ), which serves as a critical inflammatory cytokine, is essential to induce the immunosuppressive effects of mesenchymal stem cells (MSCs). However, the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs (γMSCs) are not fully understood. MSC-derived microvesicles (MSC-MVs) have been viewed as potential pivotal mediators of the immunosuppressive effects of MSCs. Moreover, microRNAs (miRNAs) are important regulators of immunological processes and can be shuttled from cell to cell by MVs. The aim of our study was to analyze the the miRNA expression signature of MVs derived from γMSCs (γMSC-MVs), which may provide better understanding of the immunosuppressive property of their parent cells. Through miRNA microarray and bioinformatics analysis, we found 62 significantly differentially expressed miRNAs (DEMs) in γMSC-MVs compared with MSC-MVs. And the potential target genes and signaling pathways regulated by DEMs were predicted and analyzed. Interestingly, many DEMs and predicted signaling pathways had been demonstrated to be involved in immunoregulation. Furthermore, the network between immunoregulation-related pathways and relevant DEMs was constructed. Collectively, our research on the miRNA repertoires of γMSC-MVs not only provides new perspectives into the mechanisms underlying the enhanced immunosuppressive property of γMSCs, but also paves the way to clinical application of these potent organelles in the future.
Increasing studies have demonstrated that interferon gamma(IFN-γ),which serves as a critical inflammatory cytokine,is essential to induce the immunosuppressive effects of mesenchymal stem cells(MSCs).However,the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs(γMSCs) are not fully understood.MSC-derived microvesicles(MSC-MVs) have been viewed as potential pivotal mediators of the immunosuppressive effects of MSCs.Moreover,micro RNAs(miR NAs) are important regulators of immunological processes and can be shuttled from cell to cell by MVs.The aim of our study was to analyze the the mi RNA expression signature of MVs derived from γMSCs(γMSC-MVs),which may provide better understanding of the immunosuppressive property of their parent cells.Through mi RNA microarray and bioinformatics analysis,we found 62 significantly differentially expressed miR NAs(DEMs) in γMSC-MVs compared with MSC-MVs.And the potential target genes and signaling pathways regulated by DEMs were predicted and analyzed.Interestingly,many DEMs and predicted signaling pathways had been demonstrated to be involved in immunoregulation.Furthermore,the network between immunoregulation-related pathways and relevant DEMs was constructed.Collectively,our research on the mi RNA repertoires of γMSC-MVs not only provides new perspectives into the mechanisms underlying the enhanced immunosuppressive property of γMSCs,but also paves the way to clinical application of these potent organelles in the future.
Increasing studies have demonstrated that interferon gamma (IFN-γ),which serves as a critical inflammatory cytokine,is essential to induce the immunosuppressive effects of mesenchymal stem cells (MSCs).However,the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs (γMSCs) are not fully understood.MSC-derived rnicrovesicles (MSC-MVs) have been viewed as potential pivotal mediators of the immunosuppressive effects of MSCs.Moreover,microRNAs (miRNAs) are important regulators of immunological processes and can be shuttled from cell to cell by MVs.The aim of our study was to analyze the the miRNA expression signature of MVs derived from γMSCs (γMSC-MVs),which may provide better understanding of the immunosuppressive property of their parent cells.Through miRNA microarray and bioinformatics analysis,we found 62 significantly differentially expressed miRNAs (DEMs) in γMSC-MVs compared with MSC-MVs.And the potential target genes and signaling pathways regulated by DEMs were predicted and analyzed.Interestingly,many DEMs and predicted signaling pathways had been.demonstrated to be involved in immunoregulation.Furthermore,the network between immunoregulation-related pathways and relevant DEMs was constructed.Collectively,our research on the miRNA repertoires of γMSC-MVs not only provides new perspectives into the mechanisms underlying the enhanced immunosuppressive property of γMSCs,but also paves the way to clinical application of these potent organelles in the future.
Increasing studies have demonstrated that interferon gamma (IFN-γ), which serves as a critical inflammatory cytokine, is essential to induce the immunosuppressive effects of mesenchymal stem cells (MSCs). However, the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs (γMSCs) are not fully understood. MSC-derived microvesicles (MSC-MVs) have been viewed as potential pivotal mediators of the immunosuppressive effects of MSCs. Moreover, microRNAs (miRNAs) are important regulators of immunological processes and can be shuttled from cell to cell by MVs. The aim of our study was to analyze the the miRNA expression signature of MVs derived from γMSCs (γMSC-MVs), which may provide better understanding of the immunosuppressive property of their parent cells. Through miRNA microarray and bioinformatics analysis, we found 62 significantly differentially expressed miRNAs (DEMs) in γMSC-MVs compared with MSC-MVs. And the potential target genes and signaling pathways regulated by DEMs were predicted and analyzed. Interestingly, many DEMs and predicted signaling pathways had been demonstrated to be involved in immunoregulation. Furthermore, the network between immunoregulation-related pathways and relevant DEMs was constructed. Collectively, our research on the miRNA repertoires of γMSC-MVs not only provides new perspectives into the mechanisms underlying the enhanced immunosuppressive property of γMSCs, but also paves the way to clinical application of these potent organelles in the future.Increasing studies have demonstrated that interferon gamma (IFN-γ), which serves as a critical inflammatory cytokine, is essential to induce the immunosuppressive effects of mesenchymal stem cells (MSCs). However, the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs (γMSCs) are not fully understood. MSC-derived microvesicles (MSC-MVs) have been viewed as potential pivotal mediators of the immunosuppressive effects of MSCs. Moreover, microRNAs (miRNAs) are important regulators of immunological processes and can be shuttled from cell to cell by MVs. The aim of our study was to analyze the the miRNA expression signature of MVs derived from γMSCs (γMSC-MVs), which may provide better understanding of the immunosuppressive property of their parent cells. Through miRNA microarray and bioinformatics analysis, we found 62 significantly differentially expressed miRNAs (DEMs) in γMSC-MVs compared with MSC-MVs. And the potential target genes and signaling pathways regulated by DEMs were predicted and analyzed. Interestingly, many DEMs and predicted signaling pathways had been demonstrated to be involved in immunoregulation. Furthermore, the network between immunoregulation-related pathways and relevant DEMs was constructed. Collectively, our research on the miRNA repertoires of γMSC-MVs not only provides new perspectives into the mechanisms underlying the enhanced immunosuppressive property of γMSCs, but also paves the way to clinical application of these potent organelles in the future.
Summary Increasing studies have demonstrated that interferon gamma (IFN-γ), which serves as a critical inflammatory cytokine, is essential to induce the immunosuppressive effects of mesenchymal stem cells (MSCs). However, the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs (γMSCs) are not fully understood. MSC-derived microvesicles (MSC-MVs) have been viewed as potential pivotal mediators of the immunosuppressive effects of MSCs. Moreover, microRNAs (miRNAs) are important regulators of immunological processes and can be shuttled from cell to cell by MVs. The aim of our study was to analyze the the miRNA expression signature of MVs derived from γMSCs (γMSC-MVs), which may provide better understanding of the immunosuppressive property of their parent cells. Through miRNA microarray and bioinformatics analysis, we found 62 significantly differentially expressed miRNAs (DEMs) in γMSC-MVs compared with MSC-MVs. And the potential target genes and signaling pathways regulated by DEMs were predicted and analyzed. Interestingly, many DEMs and predicted signaling pathways had been demonstrated to be involved in immunoregulation. Furthermore, the network between immunoregulation-related pathways and relevant DEMs was constructed. Collectively, our research on the miRNA repertoires of γMSC-MVs not only provides new perspectives into the mechanisms underlying the enhanced immunosuppressive property of γMSCs, but also paves the way to clinical application of these potent organelles in the future.
Author 赵爱琪 谢慧 林生彦 雷倩 任文祥 高飞 郭豪 郭安源 陈智超 王红祥
AuthorAffiliation Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China Department of Geriatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China Hubei Bioinformatics & Molecular Imaging Key Laboratory, Department of Bioinformatics and Systems Biology, Key Laboratory of Molecular Biophysics of the Min&try of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China Department of Hematology, Wuhan Central Hospital, Wuhan 430022, China
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Cites_doi 10.1038/cr.2008.80
10.1038/cr.2014.121
10.1016/j.exphem.2010.10.009
10.1038/nri2395
10.1016/j.biomaterials.2015.03.005
10.1038/embor.2008.224
10.1634/stemcells.2005-0008
10.1182/blood-2006-01-0057
10.3727/096368913X675728
10.1016/j.cell.2016.01.043
10.4049/jimmunol.1000798
10.1097/MIB.0000000000000339
10.1038/ncomms10307
10.1093/toxsci/kfu315
10.1016/S1074-7613(03)00325-X
10.1073/pnas.0811817106
10.1016/j.molimm.2011.02.001
10.1016/j.imlet.2012.06.001
10.1007/s12015-014-9545-9
10.1016/j.mcn.2015.07.004
10.1371/journal.pone.0011803
10.1002/art.34505
10.4161/onci.22245
10.1016/j.cell.2008.12.027
10.1021/cr000241p
10.1186/1742-2094-11-135
10.3727/096368911X582769b
10.2174/1381612805666230112210939
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Keywords microRNAs
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microvesicles
mesenchymal stem cells
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Notes Increasing studies have demonstrated that interferon gamma(IFN-γ),which serves as a critical inflammatory cytokine,is essential to induce the immunosuppressive effects of mesenchymal stem cells(MSCs).However,the mechanisms underlying the enhanced immunosuppressive effects of IFN-γ-stimulated MSCs(γMSCs) are not fully understood.MSC-derived microvesicles(MSC-MVs) have been viewed as potential pivotal mediators of the immunosuppressive effects of MSCs.Moreover,micro RNAs(miR NAs) are important regulators of immunological processes and can be shuttled from cell to cell by MVs.The aim of our study was to analyze the the mi RNA expression signature of MVs derived from γMSCs(γMSC-MVs),which may provide better understanding of the immunosuppressive property of their parent cells.Through mi RNA microarray and bioinformatics analysis,we found 62 significantly differentially expressed miR NAs(DEMs) in γMSC-MVs compared with MSC-MVs.And the potential target genes and signaling pathways regulated by DEMs were predicted and analyzed.Interestingly,many DEMs and predicted signaling pathways had been demonstrated to be involved in immunoregulation.Furthermore,the network between immunoregulation-related pathways and relevant DEMs was constructed.Collectively,our research on the mi RNA repertoires of γMSC-MVs not only provides new perspectives into the mechanisms underlying the enhanced immunosuppressive property of γMSCs,but also paves the way to clinical application of these potent organelles in the future.
Ai-qi ZHAO 1, Hui XIE2, Sheng-yan LIN3, Qian LEI 1, Wen-xiang REN1, Fei GAO 1, Hao GUO 1, An-yuan GUO 3, Zhi-chao CHEN 1, Hong-xiang WANG 4( 1Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China 2Department of Geriatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China 3Hubei Bioinformatics & Molecular Imaging Key Laboratory, Department of Bioinformatics and Systems Biology, Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China 4Department of Hematology, Wuhan Central Hospital, Wuhan 430022, China)
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mesenchymal stem cells interferon gamma microvesicles microRNAs
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Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China%Department of Geriatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China%Department of Hematology, Wuhan Central Hospital, Wuhan 430022, China
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References Hofbauer, Kaye, Kapiotis (CR25) 1999; 5
Uccelli, Moretta, Pistoia (CR1) 2008; 8
Fierabracci, Del, Luciano (CR6) 2015; 24
Budoni, Fierabracci, Luciano (CR7) 2013; 22
Tsukerman, Enk, Mandelboim (CR15) 2013; 2
Mokarizadeh, Delirezh, Morshedi (CR8) 2012; 147
Chan, Tang, Patel (CR2) 2006; 107
Liu, Zhang, Yan (CR23) 2014; 11
Chen, Gibson, Robinson (CR22) 2001; 101
Shi, Liao, Zhang (CR28) 2011; 39
Zhu, Yang, Tang (CR24) 2015; 53
Ueda, Kohanbash, Sasaki (CR12) 2009; 106
Sheng, Wang, Jin (CR4) 2008; 18
Collino, Deregibus, Bruno (CR11) 2010; 5
Guo, Kong, Liu (CR26) 2016; 7
Koukos, Polytarchou, Kaplan (CR16) 2015; 21
Xiao, Rajewsky (CR10) 2009; 136
Tkach, Thery (CR5) 2016; 164
Zhu, Liu, Chen (CR21) 2010; 185
Akyurekli, Le, Richardson (CR9) 2015; 11
Rao, Nagarkatti, Nagarkatti (CR13) 2015; 144
Liu, Wang, Jiang (CR18) 2011; 48
Ding, Liang, Zhao (CR20) 2012; 64
Huang, Zhao, Lei (CR19) 2009; 10
Krampera, Cosmi, Angeli (CR3) 2006; 24
Cho, Song, Oh (CR17) 2015; 68
Yin, Cai, Chen (CR14) 2014; 24
Maillard, Adler, Pear (CR27) 2003; 19
R Rao (1712_CR13) 2015; 144
I Maillard (1712_CR27) 2003; 19
JL Chan (1712_CR2) 2006; 107
H Zhu (1712_CR24) 2015; 53
M Tkach (1712_CR5) 2016; 164
Y Liu (1712_CR18) 2011; 48
QY Zhu (1712_CR21) 2010; 185
C Akyurekli (1712_CR9) 2015; 11
R Hofbauer (1712_CR25) 1999; 5
H Sheng (1712_CR4) 2008; 18
C Xiao (1712_CR10) 2009; 136
G Koukos (1712_CR16) 2015; 21
Y Yin (1712_CR14) 2014; 24
P Tsukerman (1712_CR15) 2013; 2
Z Chen (1712_CR22) 2001; 101
M Krampera (1712_CR3) 2006; 24
A Uccelli (1712_CR1) 2008; 8
D Shi (1712_CR28) 2011; 39
Z Guo (1712_CR26) 2016; 7
A Fierabracci (1712_CR6) 2015; 24
R Ueda (1712_CR12) 2009; 106
KJ Cho (1712_CR17) 2015; 68
A Mokarizadeh (1712_CR8) 2012; 147
S Ding (1712_CR20) 2012; 64
Y Liu (1712_CR23) 2014; 11
M Budoni (1712_CR7) 2013; 22
F Collino (1712_CR11) 2010; 5
B Huang (1712_CR19) 2009; 10
21078360 - Exp Hematol. 2011 Feb;39(2):214-224.e1
19098714 - EMBO Rep. 2009 Feb;10(2):180-5
22549634 - Arthritis Rheum. 2012 Sep;64(9):2953-63
23479551 - Oncoimmunology. 2013 Jan 1;2(1):e22245
26221772 - Mol Cell Neurosci. 2015 Sep;68:167-76
16123384 - Stem Cells. 2006 Feb;24(2):386-98
14670296 - Immunity. 2003 Dec;19(6):781-91
21367459 - Mol Immunol. 2011 May;48(9-10):1084-90
16493000 - Blood. 2006 Jun 15;107(12):4817-24
25088370 - J Neuroinflammation. 2014 Aug 04;11:135
19135886 - Cell. 2009 Jan 9;136(1):26-36
18607390 - Cell Res. 2008 Aug;18(8):846-57
26728942 - Nat Commun. 2016 Jan 05;7:10307
24268069 - Cell Transplant. 2015;24(2):133-49
10607859 - Curr Pharm Des. 1999 Dec;5(12):1015-27
25564423 - Toxicol Sci. 2015 Apr;144(2):284-97
25223704 - Cell Res. 2014 Oct;24(10):1164-80
21068409 - J Immunol. 2010 Dec 15;185(12):7435-42
20668554 - PLoS One. 2010 Jul 27;5(7):e11803
26967288 - Cell. 2016 Mar 10;164(6):1226-1232
25738378 - Inflamm Bowel Dis. 2015 May;21(5):996-1005
23433427 - Cell Transplant. 2013;22(2):369-79
25091427 - Stem Cell Rev. 2015 Feb;11(1):150-60
22705267 - Immunol Lett. 2012 Sep;147(1-2):47-54
19172693 - Nat Rev Immunol. 2008 Sep;8(9):726-36
11749383 - Chem Rev. 2001 Aug;101(8):2449-76
19520829 - Proc Natl Acad Sci U S A. 2009 Jun 30;106(26):10746-51
25890764 - Biomaterials. 2015;53:688-98
References_xml – volume: 18
  start-page: 846
  issue: 8
  year: 2008
  end-page: 857
  ident: CR4
  article-title: A critical role of IFNgamma in priming MSC-mediated suppression of T cell proliferation through up-regulation of B7-H1
  publication-title: Cell Res
  doi: 10.1038/cr.2008.80
– volume: 24
  start-page: 1164
  issue: 10
  year: 2014
  end-page: 1180
  ident: CR14
  article-title: Tumor-secreted miR-214 induces regulatory T cells: a major link between immune evasion and tumor growth
  publication-title: Cell Res
  doi: 10.1038/cr.2014.121
– volume: 39
  start-page: 214
  issue: 2
  year: 2011
  end-page: 224
  ident: CR28
  article-title: Human adipose tissue-derived mesenchymal stem cells facilitate the immunosuppressive effect of cyclosporin A on T lymphocytes through Jagged-1-mediated inhibition of NF-kappaB signaling
  publication-title: Exp Hematol
  doi: 10.1016/j.exphem.2010.10.009
– volume: 8
  start-page: 726
  issue: 9
  year: 2008
  end-page: 736
  ident: CR1
  article-title: Mesenchymal stem cells in health and disease
  publication-title: Nat Rev Immunol
  doi: 10.1038/nri2395
– volume: 53
  start-page: 688
  year: 2015
  end-page: 698
  ident: CR24
  article-title: Mesenchymal stem cells attenuated PLGA-induced inflammatory responses by inhibiting host DC maturation and function
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2015.03.005
– volume: 10
  start-page: 180
  issue: 2
  year: 2009
  end-page: 185
  ident: CR19
  article-title: miR-142-3p restricts cAMP production in CD4+CD25-T cells and CD4+CD25+ TREG cells by targeting AC9 mRNA
  publication-title: EMBO Rep
  doi: 10.1038/embor.2008.224
– volume: 24
  start-page: 386
  issue: 2
  year: 2006
  end-page: 398
  ident: CR3
  article-title: Role for interferon-gamma in the immunomodulatory activity of human bone marrow mesenchymal stem cells
  publication-title: Stem Cells
  doi: 10.1634/stemcells.2005-0008
– volume: 107
  start-page: 4817
  issue: 12
  year: 2006
  end-page: 4824
  ident: CR2
  article-title: Antigen-presenting property of mesenchymal stem cells occurs during a narrow window at low levels of interferon-gamma
  publication-title: Blood
  doi: 10.1182/blood-2006-01-0057
– volume: 24
  start-page: 133
  issue: 2
  year: 2015
  end-page: 149
  ident: CR6
  article-title: Recent advances in mesenchymal stem cell immunomodulation: the role of microvesicles
  publication-title: Cell Transplant
  doi: 10.3727/096368913X675728
– volume: 164
  start-page: 1226
  issue: 6
  year: 2016
  end-page: 1232
  ident: CR5
  article-title: Communication by extracellular vesicles: where we are and where we need to go
  publication-title: Cell
  doi: 10.1016/j.cell.2016.01.043
– volume: 185
  start-page: 7435
  issue: 12
  year: 2010
  end-page: 7442
  ident: CR21
  article-title: MicroRNA-101 targets MAPK phosphatase-1 to regulate the activation of MAPKs in macrophages
  publication-title: J Immunol
  doi: 10.4049/jimmunol.1000798
– volume: 21
  start-page: 996
  issue: 5
  year: 2015
  end-page: 1005
  ident: CR16
  article-title: A microRNA signature in pediatric ulcerative colitis: deregulation of the miR-4284/CXCL5 pathway in the intestinal epithelium
  publication-title: Inflamm Bowel Dis
  doi: 10.1097/MIB.0000000000000339
– volume: 7
  start-page: 10307
  year: 2016
  ident: CR26
  article-title: DCAF1 controls T-cell function via p53-dependent and -independent mechanisms
  publication-title: Nat Commun
  doi: 10.1038/ncomms10307
– volume: 5
  start-page: 1015
  issue: 12
  year: 1999
  end-page: 1027
  ident: CR25
  article-title: The immune system and the effects of non-volatile anesthetics on neutrophil transmigration through endothelial cell monolayers
  publication-title: Curr Pharm Des
– volume: 144
  start-page: 284
  issue: 2
  year: 2015
  end-page: 297
  ident: CR13
  article-title: Role of miRNA in the regulation of inflammatory genes in staphylococcal enterotoxin B-induced acute inflammatory lung injury and mortality
  publication-title: Toxicol Sci
  doi: 10.1093/toxsci/kfu315
– volume: 19
  start-page: 781
  issue: 6
  year: 2003
  end-page: 791
  ident: CR27
  article-title: Notch and the immune system
  publication-title: Immunity
  doi: 10.1016/S1074-7613(03)00325-X
– volume: 106
  start-page: 10746
  issue: 26
  year: 2009
  end-page: 10751
  ident: CR12
  article-title: Dicer-regulated microRNAs 222 and 339 promote resistance of cancer cells to cytotoxic T-lymphocytes by down-regulation of ICAM-1
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.0811817106
– volume: 48
  start-page: 1084
  issue: 9-10
  year: 2011
  end-page: 1090
  ident: CR18
  article-title: Modulation of T cell cytokine production by miR-144* with elevated expression in patients with pulmonary tuberculosis
  publication-title: Mol Immunol
  doi: 10.1016/j.molimm.2011.02.001
– volume: 147
  start-page: 47
  issue: 1-2
  year: 2012
  end-page: 54
  ident: CR8
  article-title: Microvesicles derived from mesenchymal stem cells: potent organelles for induction of tolerogenic signaling
  publication-title: Immunol Lett
  doi: 10.1016/j.imlet.2012.06.001
– volume: 11
  start-page: 150
  issue: 1
  year: 2015
  end-page: 160
  ident: CR9
  article-title: A systematic review of preclinical studies on the therapeutic potential of mesenchymal stromal cell-derived microvesicles
  publication-title: Stem Cell Rev
  doi: 10.1007/s12015-014-9545-9
– volume: 68
  start-page: 167
  year: 2015
  end-page: 176
  ident: CR17
  article-title: MicroRNA-Let-7a regulates the function of microglia in inflammation
  publication-title: Mol Cell Neurosci
  doi: 10.1016/j.mcn.2015.07.004
– volume: 5
  start-page: e11803
  issue: 7
  year: 2010
  ident: CR11
  article-title: Microvesicles derived from adult human bone marrow and tissue specific mesenchymal stem cells shuttle selected pattern of miRNAs
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0011803
– volume: 64
  start-page: 2953
  issue: 9
  year: 2012
  end-page: 2963
  ident: CR20
  article-title: Decreased microRNA-142-3p/5p expression causes CD4+ T cell activation and B cell hyperstimulation in systemic lupus erythematosus
  publication-title: Arthritis Rheum
  doi: 10.1002/art.34505
– volume: 2
  start-page: e22245
  issue: 1
  year: 2013
  ident: CR15
  article-title: Metastamir-mediated immune evasion: miR-10b downregulates the stress-induced molecule MICB, hence avoid recognition by NKG2D receptor
  publication-title: Oncoimmunology
  doi: 10.4161/onci.22245
– volume: 136
  start-page: 26
  issue: 1
  year: 2009
  end-page: 36
  ident: CR10
  article-title: MicroRNA control in the immune system: basic principles
  publication-title: Cell
  doi: 10.1016/j.cell.2008.12.027
– volume: 22
  start-page: 369
  issue: 2
  year: 2013
  end-page: 379
  ident: CR7
  article-title: The immunosuppressive effect of mesenchymal stromal cells on B lymphocytes is mediated by membrane vesicles
  publication-title: Cell Transplant
– volume: 101
  start-page: 2449
  issue: 8
  year: 2001
  end-page: 2476
  ident: CR22
  article-title: MAP kinases
  publication-title: Chem Rev
  doi: 10.1021/cr000241p
– volume: 11
  start-page: 135
  year: 2014
  ident: CR23
  article-title: Mesenchymal stem cells inhibit lipopolysaccharide-induced inflammatory responses of BV2 microglial cells through TSG-6
  publication-title: J Neuroinflammation.
  doi: 10.1186/1742-2094-11-135
– volume: 22
  start-page: 369
  issue: 2
  year: 2013
  ident: 1712_CR7
  publication-title: Cell Transplant
  doi: 10.3727/096368911X582769b
– volume: 48
  start-page: 1084
  issue: 9-10
  year: 2011
  ident: 1712_CR18
  publication-title: Mol Immunol
  doi: 10.1016/j.molimm.2011.02.001
– volume: 7
  start-page: 10307
  year: 2016
  ident: 1712_CR26
  publication-title: Nat Commun
  doi: 10.1038/ncomms10307
– volume: 53
  start-page: 688
  year: 2015
  ident: 1712_CR24
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2015.03.005
– volume: 24
  start-page: 386
  issue: 2
  year: 2006
  ident: 1712_CR3
  publication-title: Stem Cells
  doi: 10.1634/stemcells.2005-0008
– volume: 144
  start-page: 284
  issue: 2
  year: 2015
  ident: 1712_CR13
  publication-title: Toxicol Sci
  doi: 10.1093/toxsci/kfu315
– volume: 24
  start-page: 133
  issue: 2
  year: 2015
  ident: 1712_CR6
  publication-title: Cell Transplant
  doi: 10.3727/096368913X675728
– volume: 101
  start-page: 2449
  issue: 8
  year: 2001
  ident: 1712_CR22
  publication-title: Chem Rev
  doi: 10.1021/cr000241p
– volume: 2
  start-page: e22245
  issue: 1
  year: 2013
  ident: 1712_CR15
  publication-title: Oncoimmunology
  doi: 10.4161/onci.22245
– volume: 136
  start-page: 26
  issue: 1
  year: 2009
  ident: 1712_CR10
  publication-title: Cell
  doi: 10.1016/j.cell.2008.12.027
– volume: 185
  start-page: 7435
  issue: 12
  year: 2010
  ident: 1712_CR21
  publication-title: J Immunol
  doi: 10.4049/jimmunol.1000798
– volume: 21
  start-page: 996
  issue: 5
  year: 2015
  ident: 1712_CR16
  publication-title: Inflamm Bowel Dis
  doi: 10.1097/MIB.0000000000000339
– volume: 18
  start-page: 846
  issue: 8
  year: 2008
  ident: 1712_CR4
  publication-title: Cell Res
  doi: 10.1038/cr.2008.80
– volume: 24
  start-page: 1164
  issue: 10
  year: 2014
  ident: 1712_CR14
  publication-title: Cell Res
  doi: 10.1038/cr.2014.121
– volume: 11
  start-page: 150
  issue: 1
  year: 2015
  ident: 1712_CR9
  publication-title: Stem Cell Rev
  doi: 10.1007/s12015-014-9545-9
– volume: 68
  start-page: 167
  year: 2015
  ident: 1712_CR17
  publication-title: Mol Cell Neurosci
  doi: 10.1016/j.mcn.2015.07.004
– volume: 11
  start-page: 135
  year: 2014
  ident: 1712_CR23
  publication-title: J Neuroinflammation.
  doi: 10.1186/1742-2094-11-135
– volume: 147
  start-page: 47
  issue: 1-2
  year: 2012
  ident: 1712_CR8
  publication-title: Immunol Lett
  doi: 10.1016/j.imlet.2012.06.001
– volume: 19
  start-page: 781
  issue: 6
  year: 2003
  ident: 1712_CR27
  publication-title: Immunity
  doi: 10.1016/S1074-7613(03)00325-X
– volume: 64
  start-page: 2953
  issue: 9
  year: 2012
  ident: 1712_CR20
  publication-title: Arthritis Rheum
  doi: 10.1002/art.34505
– volume: 39
  start-page: 214
  issue: 2
  year: 2011
  ident: 1712_CR28
  publication-title: Exp Hematol
  doi: 10.1016/j.exphem.2010.10.009
– volume: 107
  start-page: 4817
  issue: 12
  year: 2006
  ident: 1712_CR2
  publication-title: Blood
  doi: 10.1182/blood-2006-01-0057
– volume: 106
  start-page: 10746
  issue: 26
  year: 2009
  ident: 1712_CR12
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.0811817106
– volume: 5
  start-page: 1015
  issue: 12
  year: 1999
  ident: 1712_CR25
  publication-title: Curr Pharm Des
  doi: 10.2174/1381612805666230112210939
– volume: 8
  start-page: 726
  issue: 9
  year: 2008
  ident: 1712_CR1
  publication-title: Nat Rev Immunol
  doi: 10.1038/nri2395
– volume: 5
  start-page: e11803
  issue: 7
  year: 2010
  ident: 1712_CR11
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0011803
– volume: 164
  start-page: 1226
  issue: 6
  year: 2016
  ident: 1712_CR5
  publication-title: Cell
  doi: 10.1016/j.cell.2016.01.043
– volume: 10
  start-page: 180
  issue: 2
  year: 2009
  ident: 1712_CR19
  publication-title: EMBO Rep
  doi: 10.1038/embor.2008.224
– reference: 23433427 - Cell Transplant. 2013;22(2):369-79
– reference: 21367459 - Mol Immunol. 2011 May;48(9-10):1084-90
– reference: 19172693 - Nat Rev Immunol. 2008 Sep;8(9):726-36
– reference: 21068409 - J Immunol. 2010 Dec 15;185(12):7435-42
– reference: 14670296 - Immunity. 2003 Dec;19(6):781-91
– reference: 26967288 - Cell. 2016 Mar 10;164(6):1226-1232
– reference: 25223704 - Cell Res. 2014 Oct;24(10):1164-80
– reference: 22705267 - Immunol Lett. 2012 Sep;147(1-2):47-54
– reference: 16493000 - Blood. 2006 Jun 15;107(12):4817-24
– reference: 20668554 - PLoS One. 2010 Jul 27;5(7):e11803
– reference: 21078360 - Exp Hematol. 2011 Feb;39(2):214-224.e1
– reference: 26728942 - Nat Commun. 2016 Jan 05;7:10307
– reference: 18607390 - Cell Res. 2008 Aug;18(8):846-57
– reference: 26221772 - Mol Cell Neurosci. 2015 Sep;68:167-76
– reference: 23479551 - Oncoimmunology. 2013 Jan 1;2(1):e22245
– reference: 25088370 - J Neuroinflammation. 2014 Aug 04;11:135
– reference: 11749383 - Chem Rev. 2001 Aug;101(8):2449-76
– reference: 25890764 - Biomaterials. 2015;53:688-98
– reference: 19098714 - EMBO Rep. 2009 Feb;10(2):180-5
– reference: 22549634 - Arthritis Rheum. 2012 Sep;64(9):2953-63
– reference: 25738378 - Inflamm Bowel Dis. 2015 May;21(5):996-1005
– reference: 10607859 - Curr Pharm Des. 1999 Dec;5(12):1015-27
– reference: 24268069 - Cell Transplant. 2015;24(2):133-49
– reference: 25564423 - Toxicol Sci. 2015 Apr;144(2):284-97
– reference: 19135886 - Cell. 2009 Jan 9;136(1):26-36
– reference: 19520829 - Proc Natl Acad Sci U S A. 2009 Jun 30;106(26):10746-51
– reference: 25091427 - Stem Cell Rev. 2015 Feb;11(1):150-60
– reference: 16123384 - Stem Cells. 2006 Feb;24(2):386-98
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Snippet Increasing studies have demonstrated that interferon gamma(IFN-γ),which serves as a critical inflammatory cytokine,is essential to induce the...
Summary Increasing studies have demonstrated that interferon gamma (IFN-γ), which serves as a critical inflammatory cytokine, is essential to induce the...
Increasing studies have demonstrated that interferon gamma (IFN-γ), which serves as a critical inflammatory cytokine, is essential to induce the...
Increasing studies have demonstrated that interferon gamma (IFN-γ),which serves as a critical inflammatory cytokine,is essential to induce the...
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SubjectTerms Cell-Derived Microparticles - drug effects
Cell-Derived Microparticles - genetics
Cells, Cultured
Computational Biology - methods
Gene Expression Regulation - drug effects
Gene Regulatory Networks
Humans
IFN-γ
Interferon-gamma - pharmacology
Medicine
Medicine & Public Health
Mesenchymal Stromal Cells - drug effects
Mesenchymal Stromal Cells - immunology
MicroRNAs - genetics
miRNA
MSCs
Oligonucleotide Array Sequence Analysis
Signal Transduction
免疫抑制作用
免疫相关
干扰素-γ
微泡
骨髓间充质干细胞
Title Interferon-γ Alters the Immune-related miRNA Expression of Microvesicles Derived from Mesenchymal Stem Cells
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https://www.ncbi.nlm.nih.gov/pubmed/28397044
https://www.proquest.com/docview/1886752515
https://d.wanfangdata.com.cn/periodical/tjykdxxb-e201702004
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