Regulation of haematopoietic stem cell fate through conditional gene expression could improve understanding of healthy haematopoietic and leukaemia initiating cell (LIC) biology. We established conditionally immortalised myeloid progenitor cell lines co-expressing constitutive Hoxa9.EGFP and inducible Meis1.dTomato (H9M-ciMP) to study growth behaviour, immunophenotype and morphology under different cytokine/microenvironmental conditions ex vivo upon doxycycline (DOX) induction or removal. The vector design and drug-dependent selection approach identified new retroviral insertion (RVI) sites that potentially collaborate with Meis1/Hoxa9 and define H9M-ciMP fate. For most cell lines, myelomonocytic conditions supported reversible H9M-ciMP differentiation into neutrophils and macrophages with DOX-dependent modulation of Hoxa9/Meis1 and CD11b/Gr-1 expression. Here, up-regulation of Meis1/Hoxa9 promoted reconstitution of exponential expansion of immature H9M-ciMPs after DOX reapplication. Stem cell maintaining conditions supported selective H9M-ciMP exponential growth. H9M-ciMPs that had Ninj2 RVI and were cultured under myelomonocytic or stem cell maintaining conditions revealed the development of DOX-dependent acute myeloid leukaemia in a murine transplantation model. Transcriptional dysregulation of Ninj2 and distal genes surrounding RVI (Rad52, Kdm5a) was detected. All studied H9M-ciMPs demonstrated adaptation to T-lymphoid microenvironmental conditions while maintaining immature myelomonocytic features. Thus, the established system is relevant to leukaemia and stem cell biology.
Genetic modification of the haematopoietic stem cells (HSC) via tetracycline-regulated gene transfer allows inducible and/or reversible expression of growth-controlling factors. The controllability of gene expression is essential since over-expressed transcription factors (TF) can trigger side effects resulting in cell exhaustion or malignant transformation, irreversible growth arrest or cell death due to apoptosis. Improved lentiviral doxycycline (DOX) controlled systems expressing single or multiple TFs could be useful to study both the benign and malignant expansion of genetically modified HSCs and open new routes in reprogramming, stem cell, and leukaemia biology1,2. However, tetracycline-regulated lentiviral vector efficiencies are often limited when in vivo transplantation models are used3.
Thus, a better understanding of intrinsic and extrinsic components influencing growth behaviour, survival, differentiation and possible malignant transformation of retrovirally modified HSCs in surrogate assays, as well as the influence of the surrounding microenvironment, could be critical. Elucidating the specific molecular and cellular properties that mediate formation and survival of leukaemia initiating cells (LIC) under optimal and sub-optimal conditions is an essential step toward creating efficient approaches for improved therapeutic leukaemia treatment4,5.
Constitutive co-expression of TFs such as Hoxa9 and Meis1 (H9M) is a conventional approach to transform haematopoietic cells ex vivo6. Hoxa9 is critical for the development and self-renewal of healthy HSCs, but its ectopic co-expression with Meis1 in haematopoietic stem and progenitor cells leads to rapid acute myeloid leukaemia (AML) onset in mice7,8. The number and fate impact of potential Hoxa9 and Meis1 collaborating genes is not completely understood.
Here, we developed tetracycline-regulated multimodal retroviral vectors (MRVs) based on a gammaretroviral vector (GV) backbone9, with the tetracycline-regulated promoter (TRP) T1110 inserted into the U3 self-inactivating (SIN) deletion of the 3′ long terminal repeat (LTR). After provirus integration into the host genome, constitutive Hoxa9 expression should be supplemented by inducible Meis1 expression in the presence of DOX. MRV design using GV backbone allows drug-controlled co-expression of selected TFs in combination with a potential propensity to activate neighbouring cellular sequences in target cells after MRV integration. It was shown before that SIN GV might transform cells ex vivo by insertional mutagenesis (IM) when strong internal retroviral enhancers/promoters are used11.
We established a robust tetracycline-regulated ex vivo model based on conditionally immortalised (ci) myeloid progenitor cell lines co-expressing Hoxa9 and Meis1 (H9M-ciMP) in the presence of DOX. The MRV design and DOX-dependent selection approach obtained retroviral insertion (RVI) sites that potentially collaborate with Meis1/Hoxa9 to define H9M-ciMP formation and fate. Among them, RVI into the first intron of the adhesion molecule Ninj2 (nerve injury-induced protein 2)12 resulted in multiple gene dysregulations within the locus. The LIC capacities of H9M-ciMPs that had Ninj2 RVI and were cultured under myelomonocytic2 or stem cell maintaining13 conditions were evaluated in a murine serial transplantation model, which revealed the rapid development of DOX-dependent AML.
We analysed H9M-ciMP growth behaviour, immunophenotype and morphology under different microenvironmental conditions ex vivo: myelomonocytic2, stem cell maintaining13 and T-lymphoid based on co-culture with OP9 stromal cells expressing the Notch ligand Delta-like 1 (OP9-DL1)14,15. We demonstrated that exponential growth and myeloid differentiation arrest are H9M-ciMP hallmarks in the presence of DOX under tested microenvironmental conditions ex vivo. After DOX removal and further reapplication, myelomonocytic conditions supported the efficient restoration of immature H9M-ciMP exponential growth.
The established tetracycline-regulated H9M-ciMP system can be efficiently employed to reveal new events that collaborate with Hoxa9 and Meis1 and define intrinsic and extrinsic signalling pathways that regulate immortalised cell line fate ex vivo and in vivo.
Generation of H9M-ciMP cell lines co-expressing Hoxa9 and Meis1 in the presence of DOX
To establish H9M-ciMP cell lines as a robust system to study conditional HSC immortalisation and differentiation, we developed tetracycline-regulated MRVs based on a GV vector backbone9, containing constitutive and inducible gene expression cassettes. To track the constitutive Hoxa9 and inducible Meis1 expression, we used Enhanced Green Fluorescent Protein (EGFP) and red fluorescent protein dTomato, respectively. The Hoxa9.EGFP constitutive cassette was cloned under the control of the murine phosphoglycerate kinase (mPGK) promoter1. The TRP T1110 was inserted into the U3 SIN deletion of the 3′ LTR of the same vector. Thus, constitutive Hoxa9.EGFP expression should be supplemented by inducible Meis1.dTomato expression in the presence of DOX (Fig. 1a). The MRV was equipped with a 304 bp linker cloned in front of the T11 TRP to provide an additional sequence for ligation-mediated PCR (LM-PCR) primer design to investigate RVIs. Additionally, an MRV vector without a linker (MRV*) was used.
Murine haematopoietic progenitor cells (HPC) from Rosa26rtTA-nls-Neo2 (Rosa26rtTA) mice16,17,18 were transduced with MRV or MRV* (in three biological replicates) under myelomonocytic cytokine conditions (36S: IL3, IL6, SCF) without DOX. One day after transduction, cultures were split and half of the cells were treated with 1 µg/mL DOX (DOX+)1,2 (Fig. 1b). The other half was cultured further without DOX (DOX-) as a negative control (Fig. 1b). This experimental design ensures similar transduction levels for different DOX conditions for cells that are derived from the same biological replicate and enables identification of the insertional mutagenesis targets that potentially collaborate with Hoxa9 and Meis1 under DOX supplementation. Thus, double-positive HOXA9.EGFP+/MEIS1.dTomato+ (DOX+) or single-positive HOXA9.EGFP+/MEIS1.dTomato− (DOX-) cells were sorted, and limiting dilution assays were accomplished, which resulted in a higher number of potential cell lines for DOX+ conditions (Fig. 1b,c). Under DOX- conditions, cells did not proliferate sufficiently.
Cell lines generated in the presence of DOX were cultured under myelomonocytic 36S (DOX+) conditions and the cell lines that showed constant double-positive HOXA9.EGFP+/MEIS1.dTomato+ expression over time and stable proliferation were pre-selected (Fig. 1d,e; Supplementary Table S1). Of note, at this pre-selection step, the normally applied DOX concentration (1 µg/mL), which is sensitive to cell density, may not have provided a stably high level of double-positive HOXA9.EGFP+/MEIS1.dTomato+ expression in all cultures due to varying H9M-ciMP cell number and proliferation rate (Fig. 1d,e).
Average vector copy numbers (VCN) for all 36S pre-selected H9M-ciMPs were determined as one (1.1 ± 0.1, mean ± SD, n = 21) except for cell line #12 (Fig. 1f). The insertional analysis of 22 pre-selected H9M-ciMP cell lines demonstrated the relevant pattern and number of specific RVIs (Supplementary Fig. S1; Supplementary Table S1, S2). As it was previously shown that multiple distal genes surrounding a single insertion event could be dysregulated19,20,21,22, we annotated genes located within ~ ± 250 Kb from the RVI (Supplementary Table S2). Some H9M-ciMP cell lines obtained from the same biological replicates demonstrated identical RVIs (e.g. #1 and #5) into the first intron of Ninj212 (Supplementary Fig. S1; Supplementary Table S1, S2). Other H9M-ciMP of different origin exhibited RVIs into the same gene locus at a different position, e.g. Cmah (cytidine monophospho-N-acetylneuraminic acid hydroxylase)23,24 (Supplementary Table S2). Remarkably, the Cmah locus also revealed identical RVIs in related H9M-ciMPs #24, 25, 28 and 29, which originated from the same biological replicate (Supplementary Table S1, S2). Interestingly, neighbouring genes surrounding the RVIs in all H9M-ciMPs were found to be involved in oncogenesis, immune response, developmental and/or differentiation processes, or were evolutionary essential metabolic genes (Supplementary Table S2).
To study H9M-ciMPs under myelomonocytic DOX+/DOX- conditions, we focused on 8 H9M-ciMP cell lines originating from pre-selected MRV and MRV* derived cell lines. These cell lines had RVIs in the vicinity of the Ninj2 gene promoting neurite outgrowth12, Vps45 (vacuolar protein sorting 45)/Otud7b (OTU domain containing 7B)25,26, Plet1 (placenta expressed transcript 1)27, Thada (thyroid adenoma associated)28, Cmah23,24, and Chsy1 (chondroitin sulfate synthase 1)29 (Supplementary Table S1, S2).
After cryopreservation, these eight H9M-ciMP cell lines demonstrated a high percentage of EGFP+dTomato+ double-positive cells (94.7% ± 4.1%, mean ± SD, n = 8) (Fig. 1g) and were selected for further characterisation using DOX ON/OFF/re-ON conditions.
Myelomonocytic conditions supported the reversibility of DOX-dependent H9M-ciMP differentiation
We investigated the H9M-ciMP growth behaviour and differentiation status upon ON/OFF/re-ON switching under myelomonocytic conditions (Fig. 2, Supplementary Fig. S2). DOX+ conditions (ON) resulted in very rapid exponential growth, with increased viable cell numbers of up to 6767.8 ± 1848.9 fold (mean ± SD, n = 8) within 21 days (D) (Fig. 2a–c). At D0/ON, co-expression of HOXA9.EGFP and MEIS1.dTomato (94.7% ± 4.1%, mean ± SD, n = 8) was accompanied by high Meis1 and Hoxa9 transcriptional co-expression (Fig. 2d–f; Supplementary Fig. S2a,b).
After DOX withdrawal (OFF) at D7, the percentage of HOXA9.EGFP+/MEIS1.dTomato+ double-positive cells decreased to 1.5% ± 1.0% (mean ± SD, n = 8) with no significant change of VCNs (Fig. 2d; Supplementary Fig. S2b,c). However, the percentage of constitutively expressed HOXA9.EGFP+ cells also decreased (28.6% ± 32.6%, mean ± SD, n = 8), although to a different degree in distinct H9M-ciMPs (Fig. 2d; Supplementary Fig. S2d). In line with this, not only Meis1 but also Hoxa9 transcriptional expression decreased when compared to mock non-transduced non-cultured Lin− cells (Fig. 2f). It was previously described for similar vector systems that DOX induction leads to increased gene expression by both tetracycline-regulated T11 and constitutive mPGK promoters located in the same vector, and DOX removal results in downregulation of expression under both promoters1.
This could be explained by the presence of “read-through” transcript driven by the T11 promoter, spanning the Hoxa9 region and supplementing constitutive mPGK Hoxa9 transcriptional expression under DOX application (Supplementary Fig. S3a). Thus, here we measured the relative transcriptional expression of Hoxa9 is cumulative and determined as “Hoxa9-total” (Fig. 2f; Supplementary Fig. S3a). After drug-removal (D7/OFF), “read-through” transcription expression is efficiently down-regulated (Supplementary Fig. S3), and only constitutive Hoxa9 transcript is abundant, explaining the drop in Hoxa9 transcriptional expression (Fig. 2f).
To track H9M-ciMP differentiation, we used CD11b and Gr-1 marker expression levels to directly correlate differentiation and maturation of cells of the myelomonocytic lineage30,31 and morphology analysis32.
In the presence of DOX, the percentages of CD11b+Gr-1+ cells were stable and did not reveal significant differences between the initial (D0/ON) and end (D21/ON) time points of exponential growth (Fig. 2e). At D0/ON, the percentage CD11bhighGr-1high cells was only 0.4% ± 0.3% (mean ± SD, n = 8) (Fig. 2d; Supplementary Fig. S2e). In the presence of DOX, H9M-ciMPs showed blockade of myelomonocytic differentiation characterised by the high percentage of immature myelomonocytic cells (90.7% ± 3.8%, mean ± SD, n = 8, D7/ON) (Fig. 2g,h).
After DOX withdrawal and Meis1/Hoxa9 transcriptional downregulation (D7/OFF), morphology analysis revealed myeloid differentiation into mostly neutrophils associated with the increased population of CD11bhighGr-1high cells (37.5% ± 20.1%, mean ± SD, n = 8) (Fig. 2g,h; Supplementary Fig. S2e).
After seven days of DOX reapplication (re-ON) (D14 from the initial day of the experiment, see D14 re-ON at Fig. 2a), only five (#1, 5, 11, 12, 40) from eight H9M-ciMPs survived DOX removal, as tracked by viable cell number (Fig. 2c). In these “reversible” cell lines, the transcriptional Hoxa9 and Meis1 co-expression level was re-established as well as the percentage of HOXA9.EGFP+/MEIS1.dTomato+ double-positive cells (97.4% ± 1.4%, mean ± SD, n = 5) (Fig. 2a,d,f; Supplementary Fig. S2b). The myeloid progenitor morphology returned and percentage of CD11bhighGr-1high cells decreased to only 1.4% ± 0.9% (mean ± SD, n = 5) (Fig. 2d,g,h; Supplementary Fig. S2e).
Interestingly, “reversible” H9M-ciMP cell lines demonstrated significantly higher percentages of HOXA9.EGFP+ cells at D7/OFF when compared to “nonreversible” cell lines (#24, 25, 29) (Supplementary Fig. S2d). Accordingly, at D7/OFF, “reversible” cell lines demonstrated significantly higher percentages of immature myelomonocytic cells, while the majority of “nonreversible” cells differentiated towards the band and/or segmented neutrophils or macrophages (Fig. 2h). Even at D11/OFF, “reversible” H9M-ciMP revealed a mixture of immature and differentiated myelomonocytic cells (Supplementary Fig. S4), thus explaining the lack of exponential or linear expansion of H9M-ciMPs under DOX- conditions (Fig. 2i). Prolonged survival of HOXA9.EGFP+ immature myelomonocytic cells under suboptimal DOX- conditions in “reversible” cell lines could be essential for the rapid reconstitution of an exponentially growing pool of immature myeloid cells after DOX reapplication (Fig. 2j).
Thus, myelomonocytic conditions supported the efficient and rapid reconstitution of exponentially proliferating immature myeloid cells after DOX removal and reapplication, but not for all investigated H9M-ciMP cell lines. Such survival heterogeneity could be determined by intrinsic properties of “nonreversible” H9M-ciMPs (#24, 25, 29) obtained from the same biological replicate, characterised by identical RVIs into the evolutionary remarkable Cmah gene23,24 and showing rapid terminal differentiation after DOX removal (Supplementary Table S1, S2, Fig. 2h). Murine models indicate the impact of Cmah on the innate immune response suggesting that loss of CMAH during human evolution primed the monocyte-macrophage lineage toward inflammatory and phagocytic state33. It was also shown that inactivation of murine Cmah was associated with enhanced atherosclerosis or impaired hearing23,24.
Distinct H9M-ciMPs demonstrated exponential growth under stem cell maintaining cytokine conditions in the presence of DOX
It was previously shown that HSCs and LICs survival and proliferation ex vivo could be defined by similar cytokine conditions. For instance, the stem cell maintaining cytokine combination significantly promoted both HSC and LIC proliferation13,34,35. To address this, we investigated H9M-ciMP fate and growth behaviour in the presence of DOX under stem cell maintaining13,34 conditions (STIF: SCF, TPO, IGF2, FGF1). Only 6 of 22 investigated H9M-ciMP cell lines demonstrated sufficient proliferation (Fig. 3a; Supplementary Table S1). Selective survival could be explained by the requirement of additional insertional events34, e.g. identical RVI into the 1st intron of adhesion molecule Ninj2 in H9M-ciMP #1 and #5, suggesting that these cell lines may have arisen from a common ancestor (Supplementary Fig. S1a; Supplementary Table S2). Ninj2 was previously reported to contribute to neurite outgrowth and enhance growth, survival and proliferation of glioma and colorectal cancer cells12,36,37. Another candidate that survived, cell line #40, was characterised by RVI into the vicinity of the Chsy1 gene, which is involved in neutrophil and macrophage survival and differentiation29.
Cell lines #1, #5 and #40 are “reversible” H9M-ciMPs as shown in ON/OFF/re-ON experiments under 36S conditions (Fig. 2c,f,j). They demonstrated exponential growth in the second independent experiment under STIF conditions, however, the proliferation rate was relatively low (Fig. 3b). Thus, the first point available for analysis was D10 after initiation of the experiment. Percentages of EGFP+dTomato+ and CD11b+Gr-1+ cells at D10 (98.7% ± 1.5%, mean ± SD, n = 3; 69.9% ± 9.5%, n = 3 respectively) did not reveal significant differences from D17 (Fig. 3c,d). The real-time quantitative PCR (RT-qPCR) confirmed the relative transcriptional upregulation of Hoxa9 and Meis1 in H9M-ciMPs under STIF cytokine conditions and DOX (1 μg/mL) supplementation when compared to mock non-transduced controls (Fig. 3e).
Interestingly, at D10/ON under STIF conditions, H9M-ciMPs demonstrated only 76.0% ± 8.9% (mean ± SD, n = 3) of immature myelomonocytic cells and up to 22.0% ± 8.7% of more differentiated myelocytes and metamyelocytes32 (Fig. 3f). This may indicate that an adaptative phase could take place, influencing the exponential growth rate (Fig. 3b). More long term experiments are required to fully characterise the H9M-ciMP immunophenotype and cell morphology under STIF conditions.
Murine serial transplantation of H9M-ciMPs bearing RVI into the Ninj2 locus cultured under myelomonocytic or STIF cytokine conditions resulted in DOX-dependent AML development
To investigate if the H9M-ciMPs cultured under myelomonocytic or stem cell maintaining conditions are transplantable in vivo, we performed serial murine transplantation. To select cell lines, we considered the following: H9M-ciMP “reversibility” after DOX reapplication under myelomonocytic conditions, and increased survival under STIF conditions.
We chose cell lines #1 and #5, as they fulfil these criteria and have identical insertional patterns (Supplementary Fig. S1a, Supplementary Table S1, S2). Cell lines #1 and #5 were pooled together after culturing under 36S or STIF conditions (Material and Methods) and used as donor cells (Fig. 4a, Supplementary Table S1). DOX was administered to all primary (1°) and secondary (2°) recipients before and throughout the experiment.
Irrespective of cytokine conditions, all 1° recipients at week eight following transplantation developed AMLs characterised by remarkably increased spleen weights (36S: 365.5 ± 134.6 mg; STIF: 300.5 ± 81.9; median ± SD, n = 4) and peripheral white blood cell (WBC) numbers (36S: 122.1 ± 111.3 × 103/µL, n = 4; STIF: 310.0 ± 125.8 × 103/µL, n = 3; median ± SD) (Fig. 4b,c).
2° recipients transplanted with bone marrow (BM) from selected 1° 36S (#222) or STIF (#225) animals (Supplementary Table S1) in the presence of DOX developed very rapid (within two weeks) AMLs characterised by normal spleen weight, but high numbers of peripheral WBCs (36S: 108.3 ± 23.4 × 103/µL, STIF: 34.6 ± 9.7 × 103/µL; median ± SD, n = 4) (Fig. 4b,c).
Transcriptional expression demonstrated significantly higher levels of Meis1 and Hoxa9 in BM cells of DOX-treated 1° STIF animals when compared to 1° 36S mice (Fig. 4d). In line with this observation, average VCNs in total BM were close to one, but significantly higher in BM of 1° and 2° STIF mice in comparison with 36S animals: (1° STIF 1.2 ± 0.1 versus 1° 36S 0.8 ± 0.1; 2° STIF 1.1 ± 0.03 versus 2° 36S 1.0 ± 0.03; mean ± SD, n = 4) (Fig. 4e). However, no statistically significant differences in the percentages of EGFP+dTomato+ cells were observed in BM from 36S and STIF 1°and 2° mice (Fig. 4f; Supplementary Fig. S5).
EGFP+dTomato+ and EGFP−dTomato+ cells infiltrating BM of 1° and 2° 36S and STIF mice were highly positive for the myeloid marker CD11b (1° 36S: 99.5% ± 0.5%, mean ± SD, n = 4; 1° STIF: 98.2% ± 0.9%, n = 4) (Fig. 5a,b; Supplementary Fig. S5b). Percentages of cells positive for the myeloid marker Gr-1 were lower: 88.1% ± 11.5% (mean ± SD, n = 4, 1° 36S) to 76.2% ± 7.3% (n = 4, 1° STIF) and thus consistent with previously described murine Hoxa9/Meis1 induced AML7 (Fig. 5a,b; Supplementary Fig. S5b).
EGFP+dTomato+ and EGFP−dTomato+ cells of the spleen, lymph nodes and thymus of 1° 36S and STIF recipients revealed comparable co-expression of CD11b and Gr-1 markers and were mostly negative for B220 and CD25 (Supplementary Fig. S6, S7).
EGFP+dTomato+ and EGFP−dTomato+ cells in all haematopoietic organs highly expressed the adhesion molecule CD44 (e.g. BM 1° 36S: 99.9% ± 0.1%, mean ± SD, n = 4; BM 1° STIF: 99.9% ± 0.1%, n = 4), which was reported to be required for homing and engraftment of murine LICs and related with poor prognosis38,39 (Fig. 5a,c; Supplementary Fig. S5b). CD44 was co-expressed with c-KIT, another marker associated with LIC biology40, in both 1° and 2° BM cells: 1° 36S: 17.6% ± 5.8%, mean ± SD, n = 4; 1° STIF: 13.3% ± 6.7%, n = 4 (Fig. 5a,c; Supplementary Fig. S5b).
Morphologically, the BM of 1° and 2° 36S and STIF recipients demonstrated dense infiltration with cells showing myelomonocytic and monoblastic differentiation (Fig. 5d), resembling AML M4/M5, which is commonly associated with MLL translocations and overexpression of HOXA9 and MEIS1 in patients41,42.
LM-PCR analysis of bone marrow of 1° and 2° 36S and STIF recipients confirmed a single integration into the 1st intron of adhesion molecule Ninj2 (Supplementary Table S2). The location of this integration was identical to that initially described for H9M-ciMPs #1 and #5 in vitro (Fig. 5e; Supplementary Fig. S1a, S8, S9; Supplementary Table S2), indicating successful engraftment of H9M-ciMP #1 and #5 cultured under 36S or STIF conditions, which resulted in AML.
It was described that genes located distantly from common proviral insertional sites are as frequently deregulated as proximal genes, with multiple genes affected per integration19,20,21,22. Transcriptional expression analysis of several genes located in the Ninj2 locus within ~ ± 250 Kb from the RVI demonstrated down-regulation of Ninj2, Rad52 (RAD52 homolog, DNA repair protein)43 and epigenetic regulator Kdm5a (lysine (K)-specific demethylase 5A)44 when compared to non-transplanted DOX-treated murine cells (Fig. 5f,g). Wnk1 (WNK lysine deficient protein kinase 1)45 transcription remained mostly unchanged, suggesting that the degree of downregulation correlated not only with the distance from RVI, but also with forward provirus orientation in regards to gene transcription direction (Fig. 5f,g; Supplementary Table S2).
According to the BloodSpot database46, NINJ2 is also downregulated in human AMLs. BloodSpot is a database that provides gene expression in AML in comparison with corresponding healthy cells and is an aggregated and integrated dataset grouping the results of multiple studies that focus on AML46. To conclude, serial transplantations demonstrated that H9M-ciMPs bearing RVI into the Ninj2 locus possess LIC ability under DOX supplementation and could be defined as ciLICs.
H9M-ciMPs demonstrated exponential growth of immature myelomonocytic cells under T-lymphoid cytokine conditions in the presence of DOX
A novel tumour suppressor role for Notch signalling in AML was reported recently, suggesting that Notch pathway activation could represent a therapeutic strategy in AML treatment. Thus, co-culture with OP9-DL4 stromal cells resulted in cell cycle arrest, differentiation and apoptosis of AML-initiating cells47.
Here, H9M-ciMP were cultured under DOX+ T-lymphoid (T-Ly: SCF, FLT3L, IL7) conditions48 using OP9-DL1 stromal cells14,15 following 36S (36S.T-Ly, n = 8) or STIF conditions (STIF.T-Ly, n = 3) (Fig. 6a). Surprisingly, under both 36S.T-Ly and STIF.T-Ly conditions, H9M-ciMPs revealed stable exponential growth (Fig. 6b). Survival under T-lymphoid conditions was confirmed by a high percentage of viable H9M-ciMPs, with 91.5% ± 2.6% (mean ± SD, n = 8) viability for 36S.T-Ly and 88.4% ± 5.1% (n = 3) viability for STIF.T-Ly conditions (D14) (Fig. 6c).
For 36S.T-Ly conditions, a slight initial decrease in the % of EGFP+dTomato+ cells (91.7% ± 7.8%, mean ± SD, n = 8) was observed at D0 (corresponds to 4 days of T-Ly pre-conditioning) (Fig. 6a,d,e). At D17, percentages of EGFP+dTomato+ cells increased to 98.1% ± 1.2% (mean ± SD, n = 8) indicating only initial adaptation to the new microenvironment (Fig. 6a,d,e). Interestingly, no significant adaptation drop in the % of EGFP+dTomato+ cells was detected for STIF.T-Ly treated H9M-ciMPs: 95.3% ± 6.7% for D0 and and 97.6% ± 0.7% for D17 (n = 3) (Fig. 6e).
For both 36S.T-Ly and STIF.T-Ly conditions, efficient Hoxa9 and Meis1 transcriptional upregulation was detected already at D0 (Fig. 6f).
In line with this, cytospin analysis of H9M-ciMPs cultured under both 36S.T-Ly and STIF.T-Ly conditions at D0 and D17 revealed blockade of myelomonocytic differentiation, but with a transient increase in the percentage of more differentiated myelocytes and metamyelocytes for 36S.T-Ly at D0 in comparison with D17 (Fig. 6g,h).
Although a statistically significant difference in the percentage of CD11b+Gr-1+ cells was observed between D0 and D17 for 36S.T-Ly (Fig. 6i), the expression pattern of CD44/CD25 markers did not change over this time (Fig. 6d; Supplementary Fig. S10a). Thus, both 36S.T-Ly and STIF.T-Ly cultured H9M-ciMPs were ~ 100% CD44+CD25– on D0 (99.4% ± 0.5%, mean ± SD, n = 8; 99.4% ± 0.5%, n = 3, respectively) (Fig. 6d). On D17, H9M-ciMPs CD44/CD25 expression pattern was similar (36S.T-Ly: 98.8% ± 1.4%, mean ± SD, n = 8; STIF.T-Ly: 99.3% ± 0.2%, n = 3), demonstrating efficient support of myeloid cells under T-lymphoid microenvironment conditions as reported recently48 (Supplementary Fig. S10a).
Importantly, mock non-transduced Lin− cells already showed T-lymphoid differentiation at D17, with percentages of cells in the double-negative (DN) stages corresponding to previously described in vitro assays48: DN1, 3.1%; DN2, 13.2%; DN3, 73.5%; and DN4, 10.2% (Supplementary Fig. S10b).
Investigation of the transcriptional expression of Notch signalling genes in H9M-ciMPs kept under 36S.T-Ly or STIF.T-Ly conditions in the presence of DOX showed transcriptional upregulation of Notch receptor Notch3 and Notch ligand Jag1 (Supplementary Fig. S11a). Mock non-transduced non-cultured Lin− cells were selected as reference material. Notch target Hes1, which plays a role in stemness, metastasis and multidrug resistance49,50, was also upregulated (Supplementary Fig. S11a). Interestingly, for H9M-ciMPs cultured under 36S and STIF conditions (Figs. 2a; 3b), Notch3 and Hes1 were either down-regulated or unchanged (Supplementary Fig. S11b).
Although the role of Notch3 is poorly understood51,52, recent studies using a zebrafish model suggested that Notch3 is required to activate Notch signalling, and this activation is necessary for further HSC specification52. Thus, Notch3 up-regulation in H9M-ciMPs under T-Ly conditions might be considered as a part of adaptative H9M-ciMP properties.
Interestingly, after DOX removal, H9M-ciMPs cultured under 36S.T-Ly or STIF.T-Ly did not show any significant increase in viable cell number after DOX withdrawal (P > 0.05), indicating myeloid differentiation and depletion after DOX removal (Supplementary Fig. S12). Of note, a similar observation was obtained for STIF conditions after DOX removal (Supplementary Fig. S12).
To conclude, H9M-ciMPs revealed efficient adaptation to T-Lymphoid conditions. For H9M-ciMPs pre-cultured in STIF (STIF.T-Ly), exponential growth under T-Ly conditions was more remarkable.
Tetracycline-regulated models for genetic modifications of HSCs help explore the role of collaborating and single genes in complex signalling networks that control the fate decision process in normal and malignant haematopoiesis. Improved understanding of immortalised cell growth behaviour, mechanisms that trigger differentiation and microenvironmental influences on these processes could help develop optimised strategies for HSC ex vivo manipulation and leukaemia treatment.
Here, we present an inducible model based on tetracycline-regulated co-expression of Hoxa9 and Meis1 in murine HPCs potentially collaborating with genes targeted via insertional mutagenesis and showing myelomonocytic arrest under different cytokine/microenvironmental conditions.
The vector design and drug-dependent selection approach allowed us to isolate H9M-ciMP cell lines with DOX-dependent exponential growth under myelomonocytic2, stem cell maintaining13 and T-lymphoid conditions14,15,48. Limiting dilution assays to select H9M-ciMPs in the presence or absence of DOX demonstrated that MRV integration without simultaneous Hoxa9/Meis1 co-expression did not lead to the efficient selection of long-term proliferating cell lines.
The insertional analysis identified a number of potential genes involved in cancerogenesis, immune response, differentiation and metabolism, which may potentially cooperate with Hoxa9/Meis1 in cell line establishment (Supplementary Table S2). Hypothesising that insertional dysregulation of these genes could contribute to H9M-ciMP survival/differentiation under suboptimal intrinsic and extrinsic conditions, we initially focused on eight H9M-ciMP cell lines that had RVIs in the loci of Ninj212 (#1, 5), Vps45/Otud7b25,26 (#11), Plet127/Thada28 (#12), Cmah24 (#24, 25, 29) and Chsy129 (#40) (Supplementary Table S1, S2).
Investigation of transgene modulation (i.e. ON/OFF/re-ON experiments) under myelomonocytic conditions revealed selective H9M-ciMP survival and reversibility. Thus, five H9M-ciMP cell lines with RVIs into loci of Ninj212 (#1, 5), Vps45/Otud7b25,26 (#11), Plet127 (#12) or Chsy129 (#40) showed rapid restoration of exponential growth after DOX reapplication, which was related to slower differentiation after DOX removal and probably longer LIC preservation.
Genes surrounding the corresponding RVI loci (window ~ ± 250 Kb) in “reversible” cell lines were shown to be involved in haematological disorders or solid tumour proliferation. For instance, enhanced NINJ2 expression was reported to be associated with enhanced growth, survival and proliferation of human glioma and colorectal cancer cells36,37. The epigenetic regulator Kdm5a44, a member of the gene group, often mutated in myelodysplastic syndrome (MDS) (Supplementary Table S2), was found to be one of the genes within ~ ± 250 Kb from the RVI in the Ninj2 locus. Mutations in Vps45 are associated with congenital neutrophil defect syndrome and impaired neutrophil function25. Chsy1 may have a role in the generation and maintenance of neutrophils and macrophages, involved in neurodegenerative processes and proliferation promotion in colorectal cancers29,53.
Importantly, three H9M-ciMP cell lines with identical RVI into the Cmah locus (#24, 25, 29) rapidly differentiated towards neutrophils/macrophages and were incapable of reversibility after DOX removal.
The “reversible” H9M-ciMP cell lines #1 and 5, which had identical RVI into the Ninj2 locus, demonstrated exponential proliferation under stem cell maintaining13 conditions and were selected for serial murine transplantation. The LIC potential of these cell lines was verified by the rapid development of DOX-dependent AMLs and verification of the RVI in the Ninj2 intron 1 in bone marrow cells. The immunophenotype and morphology of immature myelomonocytes co-expressing Meis1 and Hoxa9 and infiltrating haematopoietic organs did not significantly depend on cytokine conditions used before transplantation (myelomonocytic or stem cell maintaining).
Interestingly, while myelomonocytic conditions are commonly used in murine transplantation models and leading to AML7, stem cell maintaining conditions were described to contribute to lymphoid leukaemia development34. The latter was described even for shorter exposure of retrovirally transduced HPCs to STIF conditions than in the present experiment34.
We characterised the transcriptional expression of the following genes within of ~ ± 250 Kb from RVI in the affected Ninj2 locus: Ninj2, Kdm5a, Rad52 and Wnk1. RVI into the 1st intron of Ninj2 resulted in its transcriptional down-regulation when compared to non-transplanted DOX-treated murine cells. Significantly, NINJ2 is also downregulated in human AMLs according to the integrated BloodSpot database46. Interestingly, the dysregulation level of other investigated genes was not directly related to gene location regarding of RVI. Thus, more distal Kdm5a and Rad52 (~ 240 Kb upstream and ~ 213 Kb downstream of RVI, respectively) were down-regulated, while Wnk1 (~ 77 Kb upstream) expression remained similar when compared to non-transplanted DOX-treated murine cells. However, the orientation of the retroviral vector sequence may be important as the provirus was in the forward orientation for all down-regulated transcriptional units (Supplementary Table S2).
Of note, in contrast to selective survival of H9M-ciMPs under STIF conditions, all investigated H9M-ciMP cell lines survived in T-lymphoid conditions after a short adaptation period. Thus, cell lines co-expressing Hoxa9 and Meis1 and possessing different RVIs demonstrated the exponential growth of immature myelomonocytic cells. Therefore, we suggest that co-expression of Hoxa9 and Meis1 is necessary for microenvironmental adaptation properties ex vivo and maintaining myelomonocytic memory.
Myelomonocytic conditions initially used to generate H9M-ciMPs defined the myelomonocytic immature signature kept under both stem cell maintaining and T-lymphoid conditions in the presence of DOX. Our results are in accordance with previous findings that demonstrated myeloid differentiation to be critical for LIC formation and AML development54. Together with the possible RVI influence, this suggests a unique role of myelomonocytic conditions for H9M-ciMP survival (Fig. 7).
A limitation of the current study is that AML in vivo data were obtained for only two conditionally immortalised H9M-ciMP cell lines characterised by identical RVI in the Ninj2 locus, indicating that they may have originated from a common ancestor. Thus, additional in vivo experiments are needed to test LIC capacities of other H9M-ciMPs that have other RVIs. Obtained fate differences depending on RVI present in a given H9M-ciMP cell line and the direct implication of IM targeted genes could be of particular interest in future experiments. This system may also be useful to study if H9M-ciMPs can maintain LIC ability in vivo after culturing under T-lymphoid conditions. In summary, the ciLIC system co-expressing Hoxa9 and Meis1 provides a promising tool to study LIC properties.
The TRP T1110 was inserted into the 3′ LTR of the self-inactivating gammaretroviral vector9 (Fig. 1a). No linker (MRV*) or a 304 bp linker (MRV) was cloned in front of the T11 TRP. Such linker provides an additional sequence for LM-PCR primer design to investigate insertion sites. Both vector versions were used in two independent experiments for H9M-ciMP generation. The coding DNA for murine Hoxa91 was located under the control of mPGK promoter in the constitutive module of the vector. Correspondently, coding DNA for murine Meis11 was cloned into the inducible module of the vector resulting in construct RSF91.Meis1.idTomato.mPGK.Hoxa9.P2a.EGFP.pre.T11 (Fig. 1a). To track the Hoxa9 expression, EGFP was linked by 2A self-cleavage sites1. To track the Meis1, we introduced the red fluorescent protein dTomato via an internal ribosomal entry sequence (IRES) derived from encephalomyocarditis virus downstream of the reading frame. Vectors and cloning details are available on request.
Vector production and titration was performed as described before2,55. In short, 293T cells were transfected with 10 µg of retroviral vector, 3 µg of pcDNA3.MLVsyn g/p, 2 µg of pMD.G (VSVg) using the calcium phosphate method. Viral supernatant was concentrated by ultracentrifugation and titrated using the SC1-rtTA2 cell line as described before2.
H9M-ciMP generation and cultivation under the myelomonocytic and stem cell maintaining conditions
Lin− cells were magnetically sorted from BM using lineage-specific antibodies (Lineage Cell Depletion Kit, Miltenyi Biotech, Bergisch Gladbach, Germany). To generate H9M-ciMPs, Lin− cells were prestimulated for 24 h and transduced overnight with multiplicities of infection 10 in the absence of doxycycline in serum-free StemSpan medium (Stem Cell Technologies, Vancouver, Canada) supplemented with 1% penicillin/streptomycin (Pan Biotech), 2 mM l-glutamine (Biochrom, Berlin, Germany), as described before using myelomonocytic conditions 36S: 6 ng/mL of murine interleukin 3 (mIL3); 10 ng/mL of human interleukin 6 (hIL6); 20 ng/mL of murine stem cell factor (mSCF) (all cytokines from Peprotech, Hamburg, Germany)1,2,7. Doxycycline Hyclate (DOX) (Sigma-Aldrich, St. Louis, MO) was added (1.0 µg/mL) 1 day after transduction to half of the transduced cells. Another half was kept in the DOX absence as the negative control. On days 13–23 post-transduction, HOXA9.EGFP+/MEIS1.dTomato+ cells and HOXA9.EGFP+/MEIS1.dTomato− kept under DOX + and DOX- conditions respectively were sorted on a FACSAria Fusion instrument by the Hannover Medical School (MHH) Cell Sorting Unit. Limiting dilution assay was performed by seeding 1 (MRV*) or 10 (MRV) cells per well in 96 well plates. Limiting dilution assay of sorted HOXA9.EGFP+/MEIS1.dTomato− cells (kept before sorter under DOX- conditions) was performed under DOX- (MRV*) and DOX+ (MRV) conditions, and did not result in the selection of stably proliferating cell lines. Only H9M-ciMPs kept under DOX+ conditions before sorting and under limiting dilution assay (MRV* and MRV) were cryopreserved on day 60–85 post-transduction. H9M-ciMPs were generated in two independent experiments performed in three biological replicates for DOX+ conditions and two biological replicates for DOX- conditions.
After sorting/cryopreservation, H9M-ciMPs were kept in Iscove's Modified Dulbecco's medium (Biochrom) supplemented with 15% fetal bovine serum Brazil One (FBS; Pan Biotech, Aidenbach, Germany), 1% penicillin/streptomycin, 2 mM l-glutamine, using myelomonocytic (36S) or stem cell maintaining cytokine conditions, STIF: 50 ng/mL of mSCF, 20 ng/mL of murine thrombopoietin (mTPO), 20 ng/mL of murine insulin-like growth factor 2 (mIGF2), 10 ng/mL of human fibroblast growth factor 1 (hFGF1) (all cytokines from Peprotech) with 10 µg/mL of heparin (Sigma-Aldrich)13,56.
T-lymphoid conditions using OP9-DL1 co-culture assay
OP9-DL114,48 cells were cultured in alpha minimum essential medium (α-MEM) freshly reconstituted from a powder (Gibco, Paisley, Scotland, United Kingdom) supplemented with 20% FBS Brazil One (Pan Biotech, Aidenbach, Germany), 1% penicillin/streptomycin, and 2.2 g/L sodium bicarbonate (Pan Biotech). H9M-ciMPs were transferred to OP9-DL1 feeder layer in complete α-MEM supplemented with 20 ng/mL of mSCF (Peprotech), 5 ng/mL of human FMS-like tyrosine kinase 3 ligand (hFLT3L; Peprotech), and 2 ng/mL of human interleukin 7 (hIL7; Cytheris S.A., Issy Les Moulineaux, France) and cultured as described before48.
Cells were stained with the following anti-mouse antibodies: CD11b APC-Cy7 (M1/70), Gr-1 PE-Cy7 (RB6-8C5 ), CD44 BV711 (IM7), CD25 APC (PC61) (all from Biolegend, San Diego, CA); c-KIT APC (2B8) and B220 PerCP-Cy5.5 (RA3.6B2) (both from eBioscience, San Diego, CA). Sample acquisition was performed using CytoFLEX S (Beckman Coulter Life Sciences, Brea, CA) or FACSCalibur (Becton Dickinson, Heidelberg, Germany) flow cytometers. DAPI (4′,6-diamidine-2′-phenylindole dihydrochloride; Sigma-Aldrich) or PI (propidium iodide; Sigma) were used to label dead cells. The data were analysed with FlowJo 10 software (Tree Star, Ashland, OR).
Mice and transplantation conditions
C57BL/6J mice were purchased from the Hannover Medical School (MHH) central animal facility (Hannover, Germany) and Charles River (Sulzfeld, Germany). Rosa26rtTA-nls-Neo2 (Rosa26rtTA) mice expressing the reverse tetracycline-inducible transactivator (rtTA2) under the control of the ubiquitously active Rosa26 locus, were purchased from the central MHH animal facility (Hannover, Germany)16,17,18. Both C57BL/6J and Rosa26rtTA mice were housed in micro-isolators under pathogen-free conditions in MHH animal facility. Rosa26rtTA mice (female, age 16 (MRV) or 28 (MRV*) weeks) served as the source of Lin− cells for immortalisation setup ex vivo (see H9M-ciMP generation). For the in vivo 1° transplantation assay, H9M-ciMPs #1 and #5 cultured in 36S (Fig. 1b,d) or STIF (Fig. 3a) cytokine conditions were pooled accordingly (Supplementary Table S1). 0.8 × 106 (36S, ~ month 4) or 0.7 × 106 (STIF, day 23) viable H9M-ciMPs were transplanted intravenously per 1° recipient C57BL/6J (female, age 10 weeks) after conditioning by myeloablative irradiation (9 Gy) (Supplementary Table S1). 3 × 105 freshly isolated total bone marrow cells were co-transplanted per 1° recipient for radioprotection. For in vivo 2° transplantation assay, 1.8 × 106 cells of the selected 1° recipient were transplanted intravenously per 2° recipient (age 13 weeks) after 9 Gy irradiation (Supplementary Table S1). For doxycycline administration, 1° and 2° recipients received standard dry food supplemented with doxycycline hyclate (Sigma-Aldrich) at a final concentration 625 mg/kg (Ssniff, Soest, Germany), starting one week before transplantation and throughout the experiment56. All transplanted mice received 100 µg/ml of ciprofloxacin (Fresenius Kabi, Bad Homburg, Germany) within the drinking water for the first two weeks. The animal experiment protocol (TS11/0607) was approved by MHH’s central animal facility (Hannover, Germany) and Lower Saxony State Office for Consumer Protection and Food Safety [LAVES] (Lower Saxony, Germany), which includes an ethical review. All experiments were performed in accordance with their guidelines and regulations. As soon as symptoms of myeloproliferative disease or acute leukaemia were detected, the animals were immediately euthanised and analysed in detail. The animal experiments were carried out in compliance with the following ARRIVE guidelines (https://arriveguidelines.org/arrive-guidelines) Essential 10: study design, sample size, inclusion and exclusion criteria, randomisation, blinding, outcome measures, statistical methods, experimental animals, experimental procedures, and results.
Analysis of leukaemias
Peripheral blood cells were taken by retro-orbital bleeding and measured using an automatic analyser (ABC Counter, Scil, Vierheim, Germany). Mice were euthanised when symptomatic and macroscopically examined for pathological abnormalities. Enlarged organs were weighed. Bone marrow, spleen, lymph nodes and thymus cell suspensions were prepared for cytospins and flow cytometry analysis as described before1,56.
qPCR to determine the VCNs was performed on an Applied Biosystems StepOnePlus System (Foster City, CA) in triplicates using the Quantitect SYBR Green Kit (Qiagen, Hilden, Germany) as described before1. Briefly, a plasmid standard containing the sequences of woodchuck hepatitis virus post-transcriptional regulatory element (wPRE) and fetal liver kinase 1 (Flk1) gene as internal reference control was used for quantification with the described primer sets1.
RT-qPCR was performed as described before1. RT-qPCR analysis was performed on an Applied Biosystems StepOnePlus System in triplicates using the Quantitect SYBR Green Kit (Qiagen). Relative quantification of a target gene transcript in comparison with a reference β-actin transcript1 was performed using the method described by Pfaffl57. The program https://qpcr.probefinder.com/organism.jsp was used to design primers. RT-qPCR efficiencies were determined for all sets of designed primers57. Sequences of primers used: Hoxa9 forward (Fw), 5′- TCCCTGACTGACTATGCTTGTG-3′; Hoxa9 reverse (Rv), 5′-GTTGGCAGCCGGGTTATT-3′; Meis1 Fw, 5′-GACGCTTTAAAGAGAGATAAAGATGC-3′; Meis1 Rv, 5′- CATTTCTCAAAAATCAGTGCTAAGA-3′; Ninj2 Fw, 5′-CAGGACCTCCAGCAATCCTA-3′; Ninj2 Rv, 5′-TCAGGGACAAAGGCTGAAGT-3′; Wnk1 Fw 5′-GCAGCATCTTCCAGTGAAGG-3′; Wnk1 Rv, 5′-GCTACTGTCTGGGAAACTGGA-3′; Rad52 Fw, 5′-CCCCTTTTTCAGACATCACC-3′; Rad52 Rv, 5′-CCATCCACTGAAGCCAAAGTA-3′; Kdm5a Fw, 5′-GGAAGGACTGGAGGAGTCAA-3′; Kdm5a Rv, 5′-TCCTTTTGCTCTCGTTCTTTG-3′.
Identification of integration sites
Integration site analysis was performed by LM-PCR as reported before11,58. Genomic DNA was digested with CviQI restriction enzyme for MRV and with HaeIII for MRV* pre-selected H9M-ciMPs (New England BioLabs, Frankfurt/ Main, Germany). To amplify integration sites of MRV vectors, 5′ LM-PCR was performed using the following primers Rv1 5′-[bio] ACGTTCTCTATCACTGATAGGGAGTAAACTGG-3′; Rv2, 5′-CAGGCACAAGTGTTAAAGCAG-3′; Rv3, 5′-TCGAATTCACGTGTCGACGA-3′. To amplify integration sites of MRV* vectors, 3′ LM-PCR was performed using a primer that annealed in the wPRE sequence (SINPRE, 5′-[bio]GCACTGATAATTCCGTGGTGTTGTC-3′). For exponential PCR, the following primers were designed: SIN LTR2_1, 5′-GTTTGGCAAGCTAGCGAGACT-3′ and/or SIN LTR2_2, 5′-CCCTATCAGTGATAGAGAACGT-3′; SIN LTR3, 5′-CCCAATAAAGCCTCTTGCTGT-3′. PCR products were extracted after gel electrophoresis using QIA quick Gel Extraction Kit (Qiagen), sequenced and analysed using BLAST/BLAT searches at www.ensembl.org/Mus_musculus/Tools/Blast42 (Ensembl release 100 April 2020)59. LM-PCR for H9M-ciMP #38 did not reveal any specific bands. The images of full-length gels presented in Supplementary Figure S1, S9. The photos were taken using BIO-RAD Molecular Imager Gel Doc XR + System with Image Lab Software (Bio-Rad Laboratories, Inc. Hercules, California, USA).
2 × 104 − 2 × 105 cells were centrifuged in 150 µl PBS for 10 min at 800 rpm on microscope slides using a Thermo Shandon Cytospin 4 centrifuge (Thermo Fisher Scientific, Waltham, MA, USA). Cytospins were stained after Pappenheim (Giemsa/May-Grünwald): 5 min in May-Grünwald followed by 20 min in Giemsa staining solutions (Sigma-Aldrich, Steinheim, Germany). The cytospins were digitised at a 40 × magnification using the Hamamatsu NDP.scan software (version 3.2.17) with the Hamamatsu NanoZoomer S210 digital slide scanner equipped with a Nikon plan apochromat 20x (NA 0.75) objective lens and a colour CMOS sensor type 1/2.3 camera (pixel 4000 × 3000). Morphology was assessed using NDP.view 2.8.24 viewing software U12388-01 https://www.hamamatsu.com/eu/en/product/type/U12388-01/index.html by examination of digitised cytospins; a 90–200-cell differential count was performed. Any cell which did not fit a definition exactly was counted with the category, which it most closely resembled32. Representative pictures of digitised cytospins or light microscope pictures of cytospins (BX51 microscope, camera XC50, software Cell F version 3.4, all Olympus) are presented.
Ex vivo results were presented as the mean of individual parameters obtained from different H9M-ciMP cell lines. Animal experiment results were presented as the median for spleen weight and WBC count and as the mean for other results. Statistical analyses were performed using GraphPad Prism versions 4.00 or 5.00 for Windows (GraphPad software, San Diego, CA) or Matplotlib 3.1.1 https://matplotlib.org48,60. Comparisons were made using the non-parametric two-tailed Mann–Whitney test. P-values < 0.05 were considered statistically significant: *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.
The datasets generated and/or analysed during the current study are available from the corresponding authors on reasonable request.
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This study was supported by the German Research Foundation (DFG; REBIRTH Exc 62/1, 62/2; SFB738), German Academic Exchange Service (DAAD), and the European Union FP7 integrated project CELL-PID (HEALTH-2010-261387). This project received funding from the European Union's Horizon 2020 research and innovation program under grant agreement No. 755170 and 666908. We thank Girmay Asgedom for technical assistance with vector cloning. We thank Jörg Frühauf (Institute for Radiation Therapy and Special Oncology, Hannover Medical School) for support with the mouse irradiation procedure, staff of the animal facility of Hannover Medical School for mice handling and breeding. We thank Tobias Maetzig, Michael Rothe and Marc-Jens Kleppa, for useful advice. We acknowledge the assistance of the Cell Sorting Core Facility of the Hannover Medical School supported, in part, by Braukmann-Wittenberg-Herz-Stiftung and Deutsche Forschungsgemeinschaft. We thank Ivan Takmakov for help with graph plotting using Matplotlib.
Open Access funding enabled and organized by Projekt DEAL.
The authors declare no competing interests.
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Stahlhut, M., Ha, T.C., Takmakova, E. et al. Conditionally immortalised leukaemia initiating cells co-expressing Hoxa9/Meis1 demonstrate microenvironmental adaptation properties ex vivo while maintaining myelomonocytic memory. Sci Rep 11, 5294 (2021). https://doi.org/10.1038/s41598-021-84468-3
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