Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study
Magin S, Körfer N, Partenheimer H, Lange C, Zander A, Noll T (2009)
Stem Cell and Development 18(1): 173-186.
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Autor*in
Magin, S;
Körfer, N;
Partenheimer, H;
Lange, C;
Zander, A;
Noll, ThomasUniBi
Einrichtung
Abstract / Bemerkung
Although umbilical cord blood (UCB) has been widely accepted as an alternative source of hematopoietic stem cells (HSC) for transplantation, its use in adults is restricted because of low absolute HSC numbers. To overcome this obstacle, expansion of HSC in coculture with feeder cells is a promising possibility. In this study, we compared the potential of three human primary cell types, namely, mesenchymal stem cells (MSC), human umbilical cord vein endothelial cells (HUVEC), and Wharton's jelly cells (WJC), for use as feeder cells in a potentially clinically applicable coculture system. In first experiments, we evaluated procedures needed to obtain feeder cells, the possibility to separate them from cells derived from CD34(+) cells after coculture, their ability to activate allogeneic T cells, and their survival in CD34(+)-adapted medium. Finally, we compared their support for UCB-derived CD34(+) expansion. MSC and WJC were superior to HUVEC in terms of ease and reliability of isolation procedures needed. None of the potential feeder cells expressed CD34 or CD45, thus providing markers for cell sorting after coculture. Other markers (CD31, CD90, CD105, CD166) were expressed differently on feeder cell types. While MSC in higher concentrations did not activate allogeneic T cells, those were stimulated by lower concentrations of MSC as shown by CD25, CD69, and CD71 expression. In contrast, HUVEC and WJC were proven to activate T cells at all ratios tested. Feeder cells survived a 7-day culture in CD34(+)-adapted medium. In cocultures of UCB CD34(+) cells with primary feeder cells, mononuclear cell expansion was 30- to 60-fold, colony-forming cell expansion 20- to 40-fold, and cobblestone area-forming cell expansion 10- to 50-fold. We conclude that after a careful further evaluation especially of their immunological properties, all three primary cell types might possibly be suitable for use in a potentially clinically applicable system for expansion from UCB CD34(+) cells, with WJC being best choice and MSC still superior to HUVEC.
Erscheinungsjahr
2009
Zeitschriftentitel
Stem Cell and Development
Band
18
Ausgabe
1
Seite(n)
173-186
ISSN
1547-3287
eISSN
1557-8534
Page URI
https://pub.uni-bielefeld.de/record/2395472
Zitieren
Magin S, Körfer N, Partenheimer H, Lange C, Zander A, Noll T. Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study. Stem Cell and Development. 2009;18(1):173-186.
Magin, S., Körfer, N., Partenheimer, H., Lange, C., Zander, A., & Noll, T. (2009). Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study. Stem Cell and Development, 18(1), 173-186. https://doi.org/10.1089/scd.2007.0273
Magin, S, Körfer, N, Partenheimer, H, Lange, C, Zander, A, and Noll, Thomas. 2009. “Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study”. Stem Cell and Development 18 (1): 173-186.
Magin, S., Körfer, N., Partenheimer, H., Lange, C., Zander, A., and Noll, T. (2009). Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study. Stem Cell and Development 18, 173-186.
Magin, S., et al., 2009. Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study. Stem Cell and Development, 18(1), p 173-186.
S. Magin, et al., “Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study”, Stem Cell and Development, vol. 18, 2009, pp. 173-186.
Magin, S., Körfer, N., Partenheimer, H., Lange, C., Zander, A., Noll, T.: Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study. Stem Cell and Development. 18, 173-186 (2009).
Magin, S, Körfer, N, Partenheimer, H, Lange, C, Zander, A, and Noll, Thomas. “Primary cells as feeder cells for clinical co-culture expansion of human hematopoietic stem cells from umbilical cord blood – a comparative study”. Stem Cell and Development 18.1 (2009): 173-186.
Daten bereitgestellt von European Bioinformatics Institute (EBI)
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Human vascular endothelial cells stimulate a lower frequency of alloreactive CD8+ pre-CTL and induce less clonal expansion than matching B lymphoblastoid cells: development of a novel limiting dilution analysis method based on CFSE labeling of lymphocytes.
Dengler TJ, Johnson DR, Pober JS., J. Immunol. 166(6), 2001
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Dengler TJ, Johnson DR, Pober JS., J. Immunol. 166(6), 2001
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Concise review: human umbilical cord stroma with regard to the source of fetus-derived stem cells.
Can A, Karahuseyinoglu S., Stem Cells 25(11), 2007
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Can A, Karahuseyinoglu S., Stem Cells 25(11), 2007
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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.
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Van Overstraeten-Schlogel N, Beguin Y, Gothot A., Eur. J. Haematol. 76(6), 2006
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Van Overstraeten-Schlogel N, Beguin Y, Gothot A., Eur. J. Haematol. 76(6), 2006
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Human mesenchymal stem cells support megakaryocyte and pro-platelet formation from CD34(+) hematopoietic progenitor cells.
Cheng L, Qasba P, Vanguri P, Thiede MA., J. Cell. Physiol. 184(1), 2000
PMID: 10825234
Cheng L, Qasba P, Vanguri P, Thiede MA., J. Cell. Physiol. 184(1), 2000
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Expansion of LTC-ICs and maintenance of p21 and BCL-2 expression in cord blood CD34(+)/CD38(-) early progenitors cultured over human MSCs as a feeder layer.
Kadereit S, Deeds LS, Haynesworth SE, Koc ON, Kozik MM, Szekely E, Daum-Woods K, Goetchius GW, Fu P, Welniak LA, Murphy WJ, Laughlin MJ., Stem Cells 20(6), 2002
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Kadereit S, Deeds LS, Haynesworth SE, Koc ON, Kozik MM, Szekely E, Daum-Woods K, Goetchius GW, Fu P, Welniak LA, Murphy WJ, Laughlin MJ., Stem Cells 20(6), 2002
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The lactate issue revisited: novel feeding protocols to examine inhibition of cell proliferation and glucose metabolism in hematopoietic cell cultures.
Patel SD, Papoutsakis ET, Winter JN, Miller WM., Biotechnol. Prog. 16(5), 2000
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Patel SD, Papoutsakis ET, Winter JN, Miller WM., Biotechnol. Prog. 16(5), 2000
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Glutamate modulation of human lymphocyte growth: in vitro studies.
Lombardi G, Miglio G, Dianzani C, Mesturini R, Varsaldi F, Chiocchetti A, Dianzani U, Fantozzi R., Biochem. Biophys. Res. Commun. 318(2), 2004
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Lombardi G, Miglio G, Dianzani C, Mesturini R, Varsaldi F, Chiocchetti A, Dianzani U, Fantozzi R., Biochem. Biophys. Res. Commun. 318(2), 2004
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A human stromal-based serum-free culture system supports the ex vivo expansion/maintenance of bone marrow and cord blood hematopoietic stem/progenitor cells.
da Silva CL, Goncalves R, Crapnell KB, Cabral JM, Zanjani ED, Almeida-Porada G, Almeida-Porada G., Exp. Hematol. 33(7), 2005
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da Silva CL, Goncalves R, Crapnell KB, Cabral JM, Zanjani ED, Almeida-Porada G, Almeida-Porada G., Exp. Hematol. 33(7), 2005
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A systematic strategy to optimize ex vivo expansion medium for human hematopoietic stem cells derived from umbilical cord blood mononuclear cells.
Yao CL, Chu IM, Hsieh TB, Hwang SM., Exp. Hematol. 32(8), 2004
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Yao CL, Chu IM, Hsieh TB, Hwang SM., Exp. Hematol. 32(8), 2004
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A clinical-scale expansion of mobilized CD 34+ hematopoietic stem and progenitor cells by use of a new serum-free medium.
Ivanovic Z, Duchez P, Dazey B, Hermitte F, Lamrissi-Garcia I, Mazurier F, Praloran V, Reiffers J, Vezon G, Boiron JM., Transfusion 46(1), 2006
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Ivanovic Z, Duchez P, Dazey B, Hermitte F, Lamrissi-Garcia I, Mazurier F, Praloran V, Reiffers J, Vezon G, Boiron JM., Transfusion 46(1), 2006
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Cytokine-dependent proliferation of human CD34+ progenitor cells in the absence of serum is suppressed by their progeny's production of serine proteinases.
Goselink HM, Hiemstra PS, van Noort P, Barge RM, Willemze R, Falkenburg JH., Stem Cells 24(2), 2005
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Goselink HM, Hiemstra PS, van Noort P, Barge RM, Willemze R, Falkenburg JH., Stem Cells 24(2), 2005
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Maternal plasma or human serum albumin in wash buffer enhances enrichment and ex vivo expansion of human umbilical cord blood CD34+ cells.
Kwok YK, Tang MH, Law HK, Ngai CS, Lau YL, Lau ET., Br. J. Haematol. 137(5), 2007
PMID: 17488490
Kwok YK, Tang MH, Law HK, Ngai CS, Lau YL, Lau ET., Br. J. Haematol. 137(5), 2007
PMID: 17488490
Human marrow mesenchymal stem cell culture: serum-free medium allows better expansion than classical alpha-MEM medium.
Meuleman N, Tondreau T, Delforge A, Dejeneffe M, Massy M, Libertalis M, Bron D, Lagneaux L., Eur. J. Haematol. 76(4), 2006
PMID: 16519702
Meuleman N, Tondreau T, Delforge A, Dejeneffe M, Massy M, Libertalis M, Bron D, Lagneaux L., Eur. J. Haematol. 76(4), 2006
PMID: 16519702
Korhonen, Eur J Haematol 78(), 2007
Human platelet lysate can replace fetal bovine serum for clinical-scale expansion of functional mesenchymal stromal cells.
Schallmoser K, Bartmann C, Rohde E, Reinisch A, Kashofer K, Stadelmeyer E, Drexler C, Lanzer G, Linkesch W, Strunk D., Transfusion 47(8), 2007
PMID: 17655588
Schallmoser K, Bartmann C, Rohde E, Reinisch A, Kashofer K, Stadelmeyer E, Drexler C, Lanzer G, Linkesch W, Strunk D., Transfusion 47(8), 2007
PMID: 17655588
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