aml cell lines set2  (DSMZ)

Journal: Frontiers in immunology

Article Title: Platelet-derived microparticles provoke chronic lymphocytic leukemia malignancy through metabolic reprogramming.

doi: 10.3389/fimmu.2023.1207631

Figure Lengend Snippet: FIGURE 2 Impact of mitochondria acquisition on CLL viability. CLL cell lines were evaluated for cell viability at varying co-culture ratios (1:10 and 1:100) and incubation time (24 and 48 hours) with either (A) PMPs or (B) purified mitochondria isolated from the Set2 megakaryocytic cell line. Viability was established using a cell-based colorimetric assay (Cell Titer-Blue, Promega) combined a multi-well plate spectral analysis from a Synergy H1 Hybrid Multi-Mode Microplate Reader (Ex/Em: 560/590 nm). Each value is the mean ± SEM of six separate experiments. The asterisk (*) indicates significantly different (*p < 0.05, ***p < 0.001). (C) Light microscopy (40X) of CLLs co-incubations with PMPs or Set2-derived mitochondria was also performed for morphological examination.

Article Snippet: Human leukemic cell lines CII (#ACC 773), MEC-1 (ACC 497), and the megakaryocytic Set2 cell line (#ACC 608) were purchased from the Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Culture (DSMZ Braunschweig, Germany).

Techniques: Co-Culture Assay, Incubation, Isolation, Colorimetric Assay, Light Microscopy, Derivative Assay

Journal: Frontiers in immunology

Article Title: Platelet-derived microparticles provoke chronic lymphocytic leukemia malignancy through metabolic reprogramming.

doi: 10.3389/fimmu.2023.1207631

Figure Lengend Snippet: FIGURE 3 Impact of PMPs on CLL metabolic functions. CLL cell lines (CII and MEC-1) were evaluated for metabolic functions at varying co-culture ratios (1:10 and 1:100) and incubation periods (24 and 48 hours) with either PMPs or purified mitochondria isolated from the Set2 megakaryocytic cell line. (A) Oxygen consumption rate (OCR) was determined using an Oroboros-O2k for: ROUTINE respiration as the basal state; the non-phosphorylating resting state (LEAK respiration); and the electron transport system (ETS) capacity. (B) Total ATP and glycolytic ATP levels were evaluated using a firefly luciferase-based assay. Relative ATP concentrations related to specific pathways (oxidative phosphorylation/OXPHOS versus glycolysis) were determined by cell treatments to inhibit mitochondrial complexes I and III using Rotenone (ROT) and Antimycin A (AmA), respectively. (C, D) Cells were treated with AmA, ROT, and phorbol 12-myristate 13-acetate (PMA) as ROS inducers. Thereafter, samples were mixed with (C) CellROX green reagent and SYTOX Red Dead Cell Stain prior analysis by flow cytometry at Ex/Em: 508/525 nm (CellROX green) and 640/658 nm (SYTOX Red Dead Cell Stain) to determine intracellular total ROS content; or with (D) MitoSOX™reagent prior analysis by flow cytometry at Ex/Em: 510/580 nm to determine mitochondrial superoxide content. N-acetylcysteine (NAC) and Tert-butyl hydroperoxide (TBHP) were used as negative and positive controls, respectively. Results are expressed as the mean ± SEM of six biological experiments. One-way ANOVA followed by Tukey’s multiple comparisons test show significant differences in the values presenting different superscript letters (p < 0.05).

Article Snippet: Human leukemic cell lines CII (#ACC 773), MEC-1 (ACC 497), and the megakaryocytic Set2 cell line (#ACC 608) were purchased from the Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Culture (DSMZ Braunschweig, Germany).

Techniques: Co-Culture Assay, Incubation, Isolation, Luciferase, Phospho-proteomics, Staining, Cytometry

Journal: Haematologica

Article Title: Ruxolitinib in combination with prednisone and nilotinib exhibit synergistic effects in human cells lines and primary cells from myeloproliferative neoplasms

doi: 10.3324/haematol.2018.201038

Figure Lengend Snippet: Screening for signaling proteins affected by 32 nM ruxolitinib (R), 1.6 μM nilotinib (N), 0.8 μM prednisone (P), and their combinations, using a phospho-protein array. C: Control. The SET2 cell line was incubated with R, N, P or their combination for 48 hours and phosphoprotein analysis was performed.

Article Snippet: The SET2 cell line (DSMZ, Braunschweig, Germany), which harbors the JAK2 -V617F mutation, was cultured in RPMI 1640 with 20% FBS.

Techniques: Protein Array, Control, Incubation

Journal: Cancer research

Article Title: BONE MARROW STROMA SECRETED CYTOKINES PROTECT JAK2 V617F -MUTATED CELLS FROM THE EFFECTS OF A JAK2 INHIBITOR

doi: 10.1158/0008-5472.CAN-10-4002

Figure Lengend Snippet: Human SET2 cells were co-cultured directly (cell on cell) or indirectly (separated by 0.4 μm micropore membranes) with HS5, NK.tert, or TM-R1 stromal cells with or without 1μm atiprimod for 48 hours. Induction of apoptosis was assessed by flow cytometry to compare the direct or indirect effect of stromal monolayers.

Article Snippet: Human SET2 leukemia cell line with JAK2 V617F mutation was purchased from DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen Braunschweig, Germany), and maintained in RPMI1640 medium supplemented with 20% FCS.

Techniques: Cell Culture, Flow Cytometry