Menstrual blood-derived stromal stem cells inhibit optimal generation and maturation of human monocyte-derived dendritic cells

被引:29
作者
Bozorgmehr, Mahmood [1 ]
Moazzeni, Seyed Mohammad [1 ]
Salehnia, Mojdeh [2 ]
Sheikhian, Ali [3 ]
Nikoo, Shohreh [4 ]
Zarnani, Amir-Hassan [5 ]
机构
[1] Tarbiat Modares Univ, Fac Med Sci, Dept Immunol, Tehran, Iran
[2] ACECR, Avicenna Res Inst, Nanobiotechnol Res Ctr, Tehran, Iran
[3] Lorestan Univ Med Sci, Fac Med, Dept Immunol, Khorramabad, Iran
[4] ACECR, Avicenna Res Inst, Reprod Immunol Res Ctr, Tehran, Iran
[5] Iran Univ Med Sci, Immunol Res Ctr, Tehran, Iran
关键词
Menstrual blood stromal stem cell; Dendritic cell; Monocyte; IL-6; IL-10; ENDOMETRIAL REGENERATIVE CELLS; CHONDROGENIC DIFFERENTIATION; MESENCHYMAL CELLS; MEDICINE; PROLIFERATION; MACROPHAGES; LYMPHOCYTE; CULTURE;
D O I
10.1016/j.imlet.2014.10.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Menstrual blood stromal stem Cells (MenSCs) have shown promising potential for future clinical settings. Nonetheless, data regarding their interaction with immune cells is still scarce. Here, we investigated whether MenSCs could affect the generation and/or maturation of human blood monocyte-derived dendritic cells (DCs). Materials and methods: MenSCs were isolated from menstrual blood of normal women through culture of adherent mononuclear cells. Magnetically-isolated peripheral blood monocytes were differentiated toward immature DCs (iDC) and mature DCs (mDCs) in the presence or absence of MenSCs. Monocyte-derived cells were assessed for the percentage of monocyte-, iDC-, and mDC-specific markers as well as the expression of costimulatory molecules. IL-6 and IL-10 levels were also determined in supernatants of MenSC-monocytes cocultures. Results: Optimal phenotypic differentiation of monocytes into iDCs was inhibited upon coculture with MenSCs. Moreover, higher levels of IL-6 and IL-10 were detected in these settings. Even though addition of MenSCs to iDC cultures could not prevent iDC maturation, coculture of MenSCs with monocytes from the beginning of differentiation process could effectively hinder generation of fully mature DCs. Conclusion: This is the first study to address the inhibitory impact of MenSCs on generation and maturation of DCs. IL-6 and IL-10 could be partly held responsible for this effect. Given the central roles of DCs in regulation of immune responses, these results highlight the importance of further research on the potential modulatory impacts of MenSCs, as rather easily accessible and expandable stem cells, on the immune system-related cells. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 246
页数:8
相关论文
共 35 条
[1]  
Allavena P, 1998, EUR J IMMUNOL, V28, P359, DOI 10.1002/(SICI)1521-4141(199801)28:01<359::AID-IMMU359>3.0.CO
[2]  
2-4
[3]  
Allickson Julie G, 2011, Open Stem Cell J, V3, P4
[4]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[5]   IL-6 switches the differentiation of monocytes from dendritic cells to macrophages [J].
Chomarat, P ;
Banchereau, J ;
Davoust, J ;
Palucka, AK .
NATURE IMMUNOLOGY, 2000, 1 (06) :510-514
[6]   Lessons from human teratomas to guide development of safe stem cell therapies [J].
Cunningham, Justine J. ;
Ulbright, Thomas M. ;
Pera, Martin F. ;
Looijenga, Leendert H. J. .
NATURE BIOTECHNOLOGY, 2012, 30 (09) :849-857
[7]   Mesenchymal stem cells inhibit the differentiation of dendritic cells through an interleukin-6-dependent mechanism [J].
Djouad, Farida ;
Charbonnier, Louis-Marie ;
Bouffi, Carine ;
Louis-Plence, Pascale ;
Bony, Claire ;
Apparailly, Florence ;
Cantos, Celine ;
Jorgensen, Christian ;
Noel, Daniele .
STEM CELLS, 2007, 25 (08) :2025-2032
[8]   Stem cells today: B1. Bone marrow stem cells [J].
Edwards, RG .
REPRODUCTIVE BIOMEDICINE ONLINE, 2004, 9 (05) :541-583
[9]   The potential of cord blood stem cells for use in regenerative medicine [J].
Harris, David T. ;
Badowski, Michael ;
Ahmad, Nafees ;
Gaballa, Mohamed A. .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2007, 7 (09) :1311-1322
[10]   Novel cardiac precursor-like cells from human menstrual blood-derived mesenchymal cells [J].
Hida, Naoko ;
Nishiyama, Nobuhiro ;
Miyoshi, Shunichiro ;
Kira, Shinichiro ;
Segawa, Kaoru ;
Uyama, Taro ;
Mori, Taisuke ;
Miyado, Kenji ;
Ikegami, Yukinori ;
Cui, Changhao ;
Kiyono, Tohru ;
Kyo, Satoru ;
Shimizu, Tatsuya ;
Okano, Teruo ;
Sakamoto, Michiie ;
Ogawa, Satoshi ;
Umezawa, Akihiro .
STEM CELLS, 2008, 26 (07) :1695-1704