Mesenchymal Stem Cells Modulate Differentiation of Myeloid Progenitor Cells During Inflammation

被引:31
作者
Amouzegar, Afsaneh [1 ,2 ]
Mittal, Sharad K. [1 ,2 ]
Sahu, Anuradha [1 ]
Sahu, Srikant K. [1 ,3 ]
Chauhan, Sunil K. [1 ,2 ]
机构
[1] Schepens Eye Res Inst, Massachusetts Eye & Ear, Boston, MA 02114 USA
[2] Harvard Med Sch, Dept Ophthalmol, Boston, MA 02114 USA
[3] LV Prasad Eye Inst, Bhubaneswar 751024, Odisha, India
关键词
Mesenchymal stem cells; Myeloid progenitor cells; Immunoregulation; Differentiation; Inflammation; STROMAL CELLS; CORD BLOOD; FAMILY; CD200; TSG-6; IDENTIFICATION; MACROPHAGES; MONOCYTES; INFECTION; RECEPTOR;
D O I
10.1002/stem.2611
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem cells (MSCs) possess distinct immunomodulatory properties and have tremendous potential for use in therapeutic applications in various inflammatory diseases. MSCs have been shown to regulate pathogenic functions of mature myeloid inflammatory cells, such as macrophages and neutrophils. Intriguingly, the capacity of MSCs to modulate differentiation of myeloid progenitors (MPs) to mature inflammatory cells remains unknown to date. Here, we report the novel finding that MSCs inhibit the expression of differentiation markers on MPs under inflammatory conditions. We demonstrate that the inhibitory effect of MSCs is dependent on direct cell-cell contact and that this intercellular contact is mediated through interaction of CD200 expressed by MSCs and CD200R1 expressed by MPs. Furthermore, using an injury model of sterile inflammation, we show that MSCs promote MP frequencies and suppress infiltration of inflammatory cells in the inflamed tissue. We also find that downregulation of CD200 in MSCs correlates with abrogation of their immunoregulatory function. Collectively, our study provides unequivocal evidence that MSCs inhibit differentiation of MPs in the inflammatory environment via CD200-CD200R1 interaction.
引用
收藏
页码:1532 / 1541
页数:10
相关论文
共 42 条
[1]   A clonogenic common myeloid progenitor that gives rise to all myeloid lineages [J].
Akashi, K ;
Traver, D ;
Miyamoto, T ;
Weissman, IL .
NATURE, 2000, 404 (6774) :193-197
[2]   Human limbal biopsy-derived stromal stem cells prevent corneal scarring [J].
Basu, Sayan ;
Hertsenberg, Andrew J. ;
Funderburgh, Martha L. ;
Burrow, Michael K. ;
Mann, Mary M. ;
Du, Yiqin ;
Lathrop, Kira L. ;
Syed-Picard, Fatima N. ;
Adams, Sheila M. ;
Birk, David E. ;
Funderburgh, James L. .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (266)
[3]   Mesenchymal Stromal Cells: Sensors and Switchers of Inflammation [J].
Bernardo, Maria Ester ;
Fibbe, Willem E. .
CELL STEM CELL, 2013, 13 (04) :392-402
[4]   B7 family checkpoint regulators in immune regulation and disease [J].
Ceeraz, Sabrina ;
Nowak, Elizabeth C. ;
Noelle, Randolph J. .
TRENDS IN IMMUNOLOGY, 2013, 34 (11) :556-563
[5]   Mesenchymal stem cells in immunoregulation [J].
Chen, Xi ;
Armstrong, Marilyn Ann ;
Li, Gang .
IMMUNOLOGY AND CELL BIOLOGY, 2006, 84 (05) :413-421
[6]   Anti-inflammatory protein TSG-6 secreted by activated MSCs attenuates zymosan-induced mouse peritonitis by decreasing TLR2/NF-κB signaling in resident macrophages [J].
Choi, Hosoon ;
Lee, Ryang Hwa ;
Bazhanov, Nikolay ;
Oh, Joo Youn ;
Prockop, Darwin J. .
BLOOD, 2011, 118 (02) :330-338
[7]   Dynamic cell-cell interactions between cord blood haematopoietic progenitors and the cellular niche are essential for the expansion of CD34+, CD34+CD38- and early lymphoid CD7+ cells [J].
da Silva, Claudia Lobato ;
Goncalves, Raquel ;
dos Santos, Francisco ;
Andrade, Pedro Z. ;
Almeida-Porada, Graca ;
Cabral, Joaquim M. S. .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2010, 4 (02) :149-158
[8]   Impact of interferon-γ on hematopoiesis [J].
de Bruin, Alexander M. ;
Voermans, Carlijn ;
Nolte, Martijn A. .
BLOOD, 2014, 124 (16) :2479-2486
[9]   Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[10]   CD200 is a ligand for all members of the CD200R family of immunoregulatory molecules [J].
Gorczynski, R ;
Chen, ZQ ;
Kai, Y ;
Lee, L ;
Wong, S ;
Marsden, PA .
JOURNAL OF IMMUNOLOGY, 2004, 172 (12) :7744-7749