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| Status |
Public on Apr 23, 2015 |
| Title |
Gene expression of human blood Natural Killer (NK) cells directly after isolation and after manual or automated ex vivo expansion |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by array
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| Summary |
Ex vivo activation and expansion of natural killer (NK) cells is a strategy to produce sufficient numbers of these effector cells for adoptive immunotherapy. Therefore we aimed at the development of an automated, clinical scale NK cell expansion process and compared NK cells after manual and automated expansion.We found only a small subset of 124 genes that significantly varied between both sample groups. These genes were associated with movement of leukocytes were identified including a group of genes for NK cell movement (CMKLR1, CX3CR1, S1PR5, GNLY and CXCR1) which were slightly higher expressed after automated compared to manual expansion. Nevertheless, the expansion profiles of NK cells after automated or manual expansion were rather similar in comparison to the remarkable difference between primary and expanded NK cells in general represented by the vast majority of regulated genes between the analyzed sample groups. Pathway analysis revealed that most of regulated genes upon expansion were associated with cell cycle regulation, DNA replication, DNA recombination and DNA repair, regulation of apoptosis and cell survival as well as cytokine signaling. Furthermore, the expression of many NK cell relevant markers was changed upon expansion with the strongest effects on up regulation of TRAIL and FASL, inhibitory TIGIT and chemokine receptors CCR2, CCR5 and CXCR6. In addition, granzyme M was down regulated but other important effector molecules like TNFa, perforin and granzymes A, B and K were up regulated. In summary we could show that manual and automatically expanded NK cells show a similar expansion profile while the differ significantly from primary NK cells. Up regulation of many NK cell relevant markers indicate for an enhanced NK cell functionaility after ex vivo activation and expansion.
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| Overall design |
24 samples were analyzed in total. 6 biological replicates represented by cells from different donors. 4 different samples per donor: freshly isolated NK cells (d0) and NK cells expanded for 14 days under 3 different conditions: in co-culture with EBV-LCL feeder cells and 500 U/mL IL2 either cultivated manually in T75 flasks (T) or automatically using the CliniMACS Prodigy system (P); NK cells cultured with 500 U/ml IL2 without feeder cells (I)
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| Contributor(s) |
Granzin M, Kollet J, Knauel M, Rüberg S, Huppert V |
| Citation(s) |
25881519 |
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| Submission date |
Oct 23, 2014 |
| Last update date |
Jan 09, 2018 |
| Contact name |
Jutta Kollet |
| E-mail(s) |
jutta.kollet@miltenyibiotec.de
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| Organization name |
Miltenyibiotec GmbH
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| Department |
Bioinformatics
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| Street address |
Friedrich-Ebert-Str. 68
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| City |
Bergisch Gladbach |
| ZIP/Postal code |
51429 |
| Country |
Germany |
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| Platforms (1) |
| GPL17077 |
Agilent-039494 SurePrint G3 Human GE v2 8x60K Microarray 039381 (Probe Name version) |
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| Samples (24)
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| Relations |
| BioProject |
PRJNA264719 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE62654_RAW.tar |
296.0 Mb |
(http)(custom) |
TAR (of TXT) |
| Processed data included within Sample table |
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