Natural Killer Cell Differentiation from Hematopoietic Stem Cells: A Comparative Analysis of Heparin- and Stromal Cell-Supported Methods

被引:26
作者
Dezell, Steven A. [1 ]
Ahn, Yong-Oon [1 ]
Spanholtz, Jan [3 ]
Wang, Hongbo [1 ]
Weeres, Matthew [1 ]
Jackson, Scott
Cooley, Sarah [2 ]
Dolstra, Harry [3 ]
Miller, Jeffrey S. [2 ]
Verneris, Michael R. [1 ]
机构
[1] Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Div Blood & Marrow Transplantat, Minneapolis, MN USA
[3] Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Lab Med,Lab Hematol, NL-6525 ED Nijmegen, Netherlands
基金
美国国家卫生研究院;
关键词
NK differentiation; Hematopoesis; Heparin; Stoma; Cytotoxicity; IFN-gamma; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; CORD BLOOD TRANSPLANTATION; NK CELLS; LYMPHOCYTE RECOVERY; CD34-POSITIVE CELLS; LEUKEMIA; BINDING; KIR; RECONSTITUTION;
D O I
10.1016/j.bbmt.2011.11.023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Natural killer (NK) cells differentiated from hematopoietic stem cells (HSCs) may have significant clinical benefits over NK cells from adult donors, including the ability to choose alloreactive donors and potentially more robust in vivo expansion. Stromal-based methods have been used to study the differentiation of NK cells from HSCs. Stroma and cytokines support NK cell differentiation, but may face considerable regulatory hurdles. A recently reported clinical-grade, heparin-based method could serve as an alternative. How the stromal-based and heparin-based approaches compare in terms of NK cell generating efficiency or function is unknown. We show that compared with heparin-based cultures, stroma significantly increases the yield of HSC-derived NK cells by differentiating less-committed progenitors into the NK lineage. NK cells generated by both approaches were similar for most NK-activating and -inhibiting receptors. Although both approaches resulted in a phenotype consistent with CD56(bright) stage IV NK cells, heparin-based cultures favored the development of CID56(+)CD16(+) cells, whereas stroma produced more NK cell immunoglobulin-like receptor-expressing NK cells, both of which are markers of terminal maturation. At day 21, stromal-based cultures demonstrated significantly more IL-22 production, and both methods yielded similar amounts of IFN-gamma production and cytotoxicity by day 35. These findings suggest that heparin-based cultures are an effective replacement for stroma and may facilitate clinical trials testing HSC-derived NK cells. Biol Blood Marrow Transplant 18: 536-545 (2012) (C) 2012 American Society for Blood and Marrow Transplantation
引用
收藏
页码:536 / 545
页数:10
相关论文
共 50 条
[1]   Immunological reconstitution and correlation of circulating serum inflammatory mediators/cytokines with the incidence of acute graft-versus-host disease during the first 100 days following unrelated umbilical cord blood transplantation [J].
Abu-Ghosh, A ;
Goldman, S ;
Slone, V ;
van de Ven, C ;
Suen, Y ;
Murphy, L ;
Sender, L ;
Cairo, MS .
BONE MARROW TRANSPLANTATION, 1999, 24 (05) :535-544
[2]   Activated Notch Supports Development of Cytokine Producing NK Cells Which Are Hyporesponsive and Fail to Acquire NK Cell Effector Functions [J].
Bachanova, Veronika ;
McCullar, Valarie ;
Lenvik, Todd ;
Wangen, Rosanna ;
Peterson, Karen A. ;
Ankarlo, Dave E. M. ;
Panoskaltsis-Mortari, Angela ;
Wagner, John E. ;
Miller, Jeffrey S. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2009, 15 (02) :183-194
[3]   Early Lymphocyte Recovery and Outcomes after Umbilical Cord Blood Transplantation (UCBT) for Hematologic Malignancies [J].
Burke, Michael J. ;
Vogel, Rachel Isaksson ;
Janardan, Sanyukta K. ;
Brunstein, Claudio ;
Smith, Angela R. ;
Miller, Jeffrey S. ;
Weisdorf, Daniel ;
Wagner, John E. ;
Verneris, Michael R. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2011, 17 (06) :831-840
[4]   A human natural killer cell subset provides an innate source of IL-22 for mucosal immunity [J].
Cella, Marina ;
Fuchs, Anja ;
Vermi, William ;
Facchetti, Fabio ;
Otero, Karel ;
Lennerz, Jochen K. M. ;
Doherty, Jason M. ;
Mills, Jason C. ;
Colonna, Marco .
NATURE, 2009, 457 (7230) :722-725
[5]  
Cichocki F, 2010, METHODS MOL BIOL, V612, P15, DOI 10.1007/978-1-60761-362-6_2
[6]   The transcription factor c-Myc enhances KIR gene transcription through direct binding to an upstream distal promoter element [J].
Cichocki, Frank ;
Hanson, Rebecca J. ;
Lenvik, Todd ;
Pitt, Michelle ;
McCullar, Valarie ;
Li, Hongchuan ;
Anderson, Stephen K. ;
Miller, Jeffrey S. .
BLOOD, 2009, 113 (14) :3245-3253
[7]   INTERACTION OF INTERLEUKIN-7 (IL-7) WITH GLYCOSAMINOGLYCANS AND ITS BIOLOGICAL RELEVANCE [J].
CLARKE, D ;
KATOH, O ;
GIBBS, RV ;
GRIFFITHS, SD ;
GORDON, MY .
CYTOKINE, 1995, 7 (04) :325-330
[8]   Donor selection for natural killer cell receptor genes leads to superior survival after unrelated transplantation for acute myelogenous leukemia [J].
Cooley, Sarah ;
Weisdorf, Daniel J. ;
Guethlein, Lisbeth A. ;
Klein, John P. ;
Wang, Tao ;
Le, Chap T. ;
Marsh, Steven G. E. ;
Geraghty, Daniel ;
Spellman, Stephen ;
Haagenson, Michael D. ;
Ladner, Martha ;
Trachtenberg, Elizabeth ;
Parham, Peter ;
Miller, Jeffrey S. .
BLOOD, 2010, 116 (14) :2411-2419
[9]   Donors with group B KIR haplotypes improve relapse-free survival after unrelated hematopoietic cell transplantation for acute myelogenous leukemia [J].
Cooley, Sarah ;
Trachtenberg, Elizabeth ;
Bergemann, Tracy L. ;
Saeteurn, Koy ;
Klein, John ;
Le, Chap T. ;
Marsh, Steven G. E. ;
Guethlein, Lisbeth A. ;
Parham, Peter ;
Miller, Jeffrey S. ;
Weisdorf, Daniel J. .
BLOOD, 2009, 113 (03) :726-732
[10]   Human NKp44+IL-22+ cells and LTi-like cells constitute a stable RORC+ lineage distinct from conventional natural killer cells [J].
Crellin, Natasha K. ;
Trifari, Sara ;
Kaplan, Charles D. ;
Cupedo, Tom ;
Spits, Hergen .
JOURNAL OF EXPERIMENTAL MEDICINE, 2010, 207 (02) :281-290