Generation of mesenchymal stromal cells in the presence of platelet lysate: a phenotypic and functional comparison of umbilical cord blood- and bone marrow-derived progenitors

被引:99
作者
Avanzini, Maria Antonietta [1 ]
Bernardo, Maria Ester [1 ]
Cometa, Angela Maria [1 ]
Perotti, Cesare [2 ]
Zaffaroni, Nadia [3 ]
Novara, Francesca [4 ]
Visai, Livia [5 ,6 ]
Moretta, Antonia [1 ]
Del Fante, Claudia [2 ]
Villa, Raffaella [3 ]
Ball, Lynne M. [7 ]
Fibbe, Willem E. [8 ]
Maccario, Rita [1 ,9 ]
Locatelli, Franco [1 ]
机构
[1] Univ Pavia, Fdn IRCCS Policlin San Matteo, I-27100 Pavia, Italy
[2] Fdn IRCCS Policlin San Matteo, Serv Immunoematol & Med Trasfus, Pavia, Italy
[3] Fdn IRCCS Ist Nazl Tumori, Dipartimento Oncol Sperimentale, I-20133 Milan, Italy
[4] Univ Pavia, Sez Biol Gen & Genet Med, Dipartimento Patol Umana & Ereditaria, I-27100 Pavia, Italy
[5] Univ Pavia, Dipartimento Biochim, I-27100 Pavia, Italy
[6] Univ Pavia, Ctr Tissue Engn CIT, I-27100 Pavia, Italy
[7] Leiden Univ, Dept Pediat, Med Ctr, Leiden, Netherlands
[8] Leiden Univ, Med Ctr, Ctr Stem Cell Therapy, Dept Immunohematol & Blood Transfus, Leiden, Netherlands
[9] Fdn IRCCS Policlin San Matteo, Pavia, Italy
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2009年 / 94卷 / 12期
关键词
mesenchymal stromal cells; umbilical cord blood; platelet lysate; immunomodulatory properties; cell therapy; STEM-CELLS; INDOLEAMINE 2,3-DIOXYGENASE; SERUM; FETAL; EXPANSION; CULTURE; HOST; VIVO; TRANSFORMATION; LYMPHOCYTE;
D O I
10.3324/haematol.2009.006171
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Mesenchymal stromal cells are employed in various different clinical settings in order to modulate immune response. However, relatively little is known about the mechanisms responsible for their immunomodulatory effects, which could be influenced by both the cell source and culture conditions. Design and Methods We tested the ability of a 5% platelet lysate-supplemented medium to support isolation and ex vivo expansion of mesenchymal stromal cells from full-term umbilical-cord blood. We also investigated the biological/functional properties of umbilical cord blood mesenchymal stromal cells, in comparison with platelet lysate-expanded bone marrow mesenchymal stromal cells. Results The success rate of isolation of mesenchymal stromal cells from umbilical cord blood was in the order of 20%. These cells exhibited typical morphology, immunophenotype and differentiation capacity. Although they have a low clonogenic efficiency, umbilical cord blood mesenchymal stromal cells may possess high proliferative potential. The genetic stability of these cells from umbilical cord blood was demonstrated by a normal molecular karyotype; in addition, these cells do not express hTERT and telomerase activity, do express p16(ink4a) protein and do not show anchorage-independent cell growth. Concerning alloantigen-specific immune responses, umbilical cord blood mesenchymal stromal cells were able to: (i) suppress T- and NK-lymphocyte proliferation, (ii) decrease: cytotoxic activity and (iii) only slightly increase interleukin-10, while decreasing interferon-gamma secretion, in mixed lymphocyte culture supernatants. While an indoleamine 2,3-dioxygenase-specific inhibitor did not reverse mesenchymal stromal cell-induced suppressive effects, a prostaglandin E-2-specific inhibitor hampered the suppressive effect of both umbilical cord blood- and bone marrow-mesenchymal stromal cells on alloantigen-induced cytotoxic activity. Mesenchymal stromal cells from both sources expressed HLA-G. Conclusions Umbilical cord blood- and bone marrow-mesenchymal stromal cells may differ in terms of clonogenic efficiency, proliferative capacity and immunomodulatory properties; these differences may be relevant for clinical applications.
引用
收藏
页码:1649 / 1660
页数:12
相关论文
共 56 条
[1]  
Anker PSI, 2003, HAEMATOLOGICA, V88, P845
[2]   Cotransplantation of ex vivo-expanded mesenchymal stem cells accelerates lymphocyte recovery and may reduce the risk of graft failure in haploidentical hematopoietic stem-cell transplantation [J].
Ball, Lynne M. ;
Bernardo, Maria Ester ;
Roelofs, Helene ;
Lankester, Arjan ;
Cometa, Angela ;
Egeler, R. Maarten ;
Locatelli, Franco ;
Fibbe, Willem E. .
BLOOD, 2007, 110 (07) :2764-2767
[3]   Morpho-Functional Characterization of Human Mesenchymal Stem Cells from Umbilical Cord Blood for Potential Uses in Regenerative Medicine [J].
Barachini, Serena ;
Trombi, Luisa ;
Danti, Serena ;
D'Alessandro, Delfo ;
Battolla, Barbara ;
Legitimo, Annalisa ;
Nesti, Claudia ;
Mucci, Ilaria ;
Acunto, Mario D' ;
Cascone, Maria G. ;
Lazzeri, Luigi ;
Mattii, Letizia ;
Consolini, Rita ;
Petrini, Mario .
STEM CELLS AND DEVELOPMENT, 2009, 18 (02) :293-305
[4]   Mesenchymal stem cells: clinical applications and biological characterization [J].
Barry, FP ;
Murphy, JM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2004, 36 (04) :568-584
[5]   Optimization of in vitro expansion of human multipotent mesenchymal stromal cells for cell-therapy approaches: Further insights in the search for a fetal calf serum substitute [J].
Bernardo, M. E. ;
Avanzini, M. A. ;
Perotti, C. ;
Cometa, A. M. ;
Moretta, A. ;
Lenta, E. ;
Del Fante, C. ;
Novara, F. ;
De Silvestri, A. ;
Amendola, G. ;
Zuffardi, O. ;
Maccario, R. ;
Locatelli, F. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 211 (01) :121-130
[6]   Human bone marrow-derived mesenchymal stem cells do not undergo transformation after long-term In vitro culture and do not exhibit telomere maintenance mechanisms [J].
Bernardo, Maria Ester ;
Zaffaroni, Nadia ;
Novara, Francesca ;
Cometa, Angela Maria ;
Avanzini, Maria Antonietta ;
Moretta, Antonia ;
Montagna, Daniela ;
Maccario, Rita ;
Villa, Raffaella ;
Daidone, Maria Grazia ;
Zuffardi, Orsetta ;
Locatelli, Franco .
CANCER RESEARCH, 2007, 67 (19) :9142-9149
[7]  
BERNARDO ME, 2007, BONE MARROW TRANSPL, V39, pS1
[8]   Marrow stromal stem cells [J].
Bianco, P ;
Robey, PG .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (12) :1663-1668
[9]   Critical parameters for the isolation of mesenchymal stem cells from umbilical cord blood [J].
Bieback, K ;
Kern, S ;
Klüter, H ;
Eichler, H .
STEM CELLS, 2004, 22 (04) :625-634
[10]  
Brando B, 2000, CYTOMETRY, V42, P327, DOI 10.1002/1097-0320(20001215)42:6<327::AID-CYTO1000>3.0.CO