Selected Stro‐1‐enriched bone marrow stromal cells display a major suppressive effect on lymphocyte proliferation

International Journal of Laboratory Hematology - Tập 31 Số 1 - Trang 9-19 - 2009
Aisha Nasef1, Y. Z. ZHANG1, Christelle Mazurier2, Sandrine Bouchet2, Morad Bensidhoum2, Sabine François2, N C Gorin2, M López2, Dominique Thierry2, L Fouillard2, Alain Chapel2
1EA 1638 Laboratoire de Thérapie Cellulaire et Radioprotection Accidentelle (LTCRA), Faculté de médecine Saint Antoine, Université Paris VI, Paris, France.
2Universite Pierre et Marie Curie

Tóm tắt

Summary

Mesenchymal stem cells (MSCs) have an immunosuppressive effect and can inhibit the proliferation of alloreactive T cells in vitro and in vivo. Cotransplantation of MSCs and hematopoietic stem cells (HSCs) from HLA‐identical siblings has been shown to reduce the incidence of acute graft‐vs.‐host disease. MSCs are heterogeneous and data on the inhibitory effects of different MSC subsets are lacking. The antigen Stro1 is a marker for a pure primitive MSC subset. We investigated whether Stro‐1‐enriched induce a more significant suppressive effect on lymphocytes in a mixed lymphocyte reaction (MLR), and whether this action is related to a specific gene expression profile in Stro‐1‐enriched compared to other MSCs. We demonstrated that the Stro‐1‐enriched population elicits a significantly more profound dose‐dependent inhibition of lymphocyte proliferation in a MLR than MSCs. One thousand expanded Stro‐1‐enriched induced an inhibitory effect comparable to that of 10 times as many MSCs. Inhibition by Stro‐1‐enriched was more significant in contact‐dependent cultures than in noncontact‐dependant cultures at higher ratio. The Stro‐1‐enriched inhibitory effect in both culture types was linked to increased gene expression for soluble inhibitory factors such as interleukin‐8 (IL‐8), leukemia inhibitory factor (LIF), indoleamine oxidase (IDO), human leukocyte antigen‐G (HLA‐G), and vascular cell adhesion molecule (VCAM1). However, tumor growth factor‐β1 (TGF‐β) and IL‐10 were only up‐regulated in contact‐dependant cultures. These results may support using a purified Stro‐1‐enriched population to augment the suppressive effect in allogeneic transplantation.

Từ khóa


Tài liệu tham khảo

10.1182/blood-2004-04-1559

10.1016/S1074-7613(00)80131-4

10.1016/S0301-472X(01)00769-X

10.1182/blood-2003-04-1121

10.1182/blood-2004-07-2921

Bol S.J., 1990, Selection of two human bone marrow stromal cell subpopulations with different effects on the maintenance and differentiation of myeloid progenitor cells, Experimental Hematology, 18, 764

10.1089/152581600319388

10.1182/blood.V56.2.289.289

10.1634/stemcells.2006-0174

10.1159/000046182

10.1182/blood.V99.10.3838

10.1182/blood-2003-04-1193

10.1182/blood-2005-03-1004

10.1634/stemcells.2005-0260

Friedenstein A.J., 1970, The development of fibroblast colonies in monolayer cultures of guinea‐pig bone marrow and spleen cells, Cell and Tissue Kinetica, 3, 393

10.1016/j.jtcvs.2003.07.037

10.1242/jcs.00369

10.1182/blood-2004-02-0586

10.1002/cyto.b.20118

Kenneth J.L., 2001, Analysis of relative gene expression data using relative time quantitative PCR and 2DDCt, Methods, 25, 402, 10.1006/meth.2001.1262

10.1182/blood-2002-07-2104

10.1016/j.bbmt.2005.02.001

10.1046/j.1365-3083.2003.01176.x

10.1111/j.0300-9475.2004.01483.x

10.1016/S0140-6736(04)16104-7

10.1016/j.jim.2005.10.015

Maccario R., 2005, Interaction of human mesenchymal stem cells with cells involved in alloantigen‐specific immune response favors the differentiation of CD4 +  T‐cell subsets expressing a regulatory/suppressive phenotype, Haematologica, 90, 516

10.1038/sj.bmt.1704400

10.1182/blood-2003-11-3909

10.3727/000000006780666957

10.4049/jimmunol.171.7.3426

10.1084/jem.184.2.539

10.1073/pnas.94.21.11520

10.1182/blood.V78.1.55.55

10.1046/j.1365-3083.2003.01212.x

10.1007/s00441-003-0762-9

10.1080/14653240410004943

10.1097/01.TP.0000045055.63901.A9

10.1182/blood.V92.8.2609

10.1089/154732804323099190