Retinoic acid induces HL-60 cell differentiation via the upregulation of miR-663
© Jian et al; licensee BioMed Central Ltd. 2011
Received: 8 April 2011
Accepted: 25 April 2011
Published: 25 April 2011
Differentiation of the acute myeloid leukemia (AML) cell line HL-60 can be induced by all trans-retinoic acid (ATRA); however, the mechanism regulating this process has not been fully characterized.
Using bioinformatics and in vitro experiments, we identified the microRNA gene expression profile of HL-60 cells during ATRA induced granulocytic differentiation.
Six microRNAs were upregulated by ATRA treatment, miR-663, miR-494, miR-145, miR-22, miR-363* and miR-223; and three microRNAs were downregulated, miR-10a, miR-181 and miR-612. Additionally, miR-663 expression was regulated by ATRA. We used a lentivirus (LV) backbone incorporating the spleen focus forming virus (SFFV-F) promoter to drive miR-663 expression, as the CMV (Cytomegalovirus) promoter is ineffective in some lymphocyte cells. Transfection of LV-miR-663 induced significant HL-60 cell differentiation in vitro.
Our results show miR-663 may play an important role in ATRA induced HL-60 cell differentiation. Lentivirus delivery of miR-663 could potentially be used directly as an anticancer treatment in hematological malignancies
Differentiation of the acute myeloid leukemia (AML) cell line HL-60 can be induced by all trans-retinoic acid (ATRA); however, the mechanism regulating this process is not yet fully understood . Erkel et al. reported that growth arrest and induction of differentiation of HL-60 cells in response to Sch 52900 is due to induction of the cell cycle inhibitor p21WAF, and inhibition of the extracellular signal-regulated kinase (ERK) signaling pathway, leading to activation of the transcription factor AP-1 . Microarray analysis has shown ATRA can induce upregulation of genes involved in differentiation, the oxidase activation pathway and adhesion molecules. In HL-60 cells, ATRA treatment induces differential expression of a variety of genes from several pathways, including the differentiation pathway [3–5]. So far, few studies have focused on expression of microRNAs during HL-60 differentiation, and the expression profiles of human miRNAs during cell differentiation remain largely unknown.
This study analyzed the microRNA expression profile in HL-60 cells treated with ATRA. to investigate whether ATRA can induce growth arrest via upregulation of miR-663 expression, which has been linked to modulation of the cell cycle and mitotic growth arrest . Our results showed both ATRA and miR-663 can significantly inhibit HL-60 cell proliferation and induce differentiation.
MicroRNAs regulate the expression of genes involved in the control of development, proliferation, apoptosis, and stress responses [7–9]. Analysis of microRNA expression and function during hematopoiesis has unraveled the existence of several complex regulatory loops by which microRNAs fine-tune hematopoietic differentiation and proliferation. The expression profiles of miR-142 [10, 11], miR-181 [12–14] and miR-223 [14–16] have been described in B cells, T cells, monocytes, granulocytes and erythroid cells in murine hematopoiesis. Ectopic expression of these miRNAs dramatically alters the proportion of differentiated murine hematopoietic cell lineages in vitro and in vivo [17–21]. This suggests miRNAs can play an important lineage-specific role in mammalian cell differentiation. In humans, miR-107 and miR-223 are upregulated during ATRA induced granulocytic differentiation. Both miR-107 and miR-223 are postulated to downregulate their target gene NFI-A, and mediate a regulatory loop during cell differentiation . This data suggests miRNAs can function as oncogenes or tumor suppressors, and play important roles in the genesis of leukemia. Using a bioinformatic approach followed by in vitro experiments, we identified the microRNA gene expression profile of the AML cell line HL-60 during ATRA induced granulocytic differentiation. We further demonstrated that miR-663 expression level is regulated by ATRA.
Lentiviral technology represents a powerful method to genetically modify leukemia cells. We chose to use a viral expression backbone driven by the spleen focus forming virus (SFFV-F) promoter, as the CMV (Cytomegalovirus) promoter has been shown to be ineffective in some lymphocyte cells. We focused on miR-663 as a candidate molecule which is important for HL-60 cell differentiation. The virus expressing the miR-663 precursor was compared to a control mock virus containing GFP. Lentivirus transfection showed LV-miR-663 significantly induces HL-60 cell differentiation in vitro. miR-663 may play important role in the differentiation of HL-60 cells treated with ATRA and miR-663 lentivirus could potentially be used directly as an anticancer treatment in he
2.1 Cell line and reagents
HL-60 cells were obtained from our own laboratory. ATRA, RPMI 1640, MTT, DMSO, TPA and NBT were obtained from Sigma Co. DMEM was obtained from Invitrogen. PCR primers were synthesized by Shanghai Sangon Biotechnology Co. Ltd. PE-conjugated CD11b (ITGAM integrin alpha M) antibody was purchased from Pharmingen Co.
2.2 Cell culture and induction
HL-60 cells were cultured in RPMI 1640 standard medium with 2 mmol/L L-glutamine supplemented with 10% heat-inactivated fetal calf serum, 100 U/ml penicillin and 100 μg/ml streptomycin at 37°C in 5% CO2. Exponentially growing cells (approximately 1 × 107) were incubated with 0.1 μmol/L ATRA, 0.1% alcohol or untreated RPMI 1640 for 1 to 3 days.
2.3 MTT proliferation assay
Cell proliferation was determined using the MTT (methyl thiazolyl tetrazolium) assay. HL-60 cells (5 × 105/well in 96-well plates) were incubated with 0.1 μmol/L ATRA , 0.1% alcohol or untreated RPMI 1640 for 24 to 72 h, then 10 μl 5 mg/m1 MTT was added to each well for 4 h. The reaction was stopped by addition of 150 μl DMSO and absorbance (A) at 490 nm was determined on a plate reader (Bio-Rad). Each group was analyzed in triplicate samples. Cell inhibition rate = 100% × (control group A values -experimental group A values)/control group A values.
2.4 NBT and CD11b differentiation assays
Differentiation of HL-60 cells was assessed using the NBT (nitroblue tetrazolium) reduction test and flow cytometry detection of the cellular surface differential antigen CD11b. Briefly, 100 μl 1 × 106/m1 HL-60 cells in 96-well plates were incubated with 0.1 μ mol/L ATRA  for 1 to 3 days. RPMI 1640 was used as a blank control and 0.1% alcohol was used as the solvent control. 100 μl 1 mg/ml NBT and 200 μl 1 mg/ml TPA were added to each well and incubated at 37°C in 5% CO2 for 1 h, after which the cells were centrifuged for 5 min and then subjected to Wright's staining. When NBT is phagosomed by cells, the intracellular dye converts to insoluble blue formazan crystals . The number of positive cells containing blue formazan crystals was determined from two hundred cells using microscopy with an oil immersion objective. For detection of the cell differentiation antigen CD11b [25, 26], 1 × 106 cells were washed twice with PBS, incubated with PE-conjugated CD11b antibody or PE-conjugated IgG1isotype control antibody at 4°C for 30 min and analyzed by flow cytometry using a FACScan flow cytometer and Cell Quest software (Becton Dickinson, Mountain View, CA). The expression rate of CD11b positive cells was determined from 1 × 104 cells for each group.
2.5 MicroRNA expression profiling
MicroRNAs were extracted using the mirVana miRNA isolation kit (AM1560, Applied Biosystems, USA). Samples which were successfully isolated were analyzed using an Agilent miRNA Chip version 10.0 at the Microarray Core Facility, Baylor College of Medicine, USA. In total, 637 images were acquired, calculated, normalized and filtering of signal intensity for each spot and batch-effect adjustment was performed. A total of 235 microRNA probes met the filtering criteria for subsequent analysis using significance analysis of microarrays (SAM, Version 3.0, 2007, http://www-stat.stanford.edu/~tibs/SAM/).
2.6 miRNA extraction and real-time quantitative PCR (qRT-PCR) assays
Extraction of miRNA was performed using the mirVana miRNA isolation kit and TaqMan miRNA assays were used to detect and quantify mature miR-663 as previously described . Briefly, total RNA was reverse transcribed using the Reverse Transcription Kit (Applied Biosystems Inc., CA), according to the manufacturer's instructions. The RT primers were: U6 5'-CGCTTCACGAATTTGCGTGTCAT-3' and mir-663 5'-GTCGTATCCAGTGCGTGTCGTGGAGTCGGCAATTGCACTGGATACGACGCGGTCC-3'. The PCR primers used to quantify U6 expression were:
F: 5'-GCTTCGGCAGCACATATACTAAAAT-3' and R: 5'-CGCTTCACGAATTTGCGTGTCAT-3' and for mir-663 were: F: 5'-GTGCGTGTCGTGGAGTCG-3' and R: 5'-TTTAGGCGGGGCG-3'. mir-663 expression was normalized to endogenous U6 expression using the SDS relative quantification software (Applied Biosystems Inc, USA).
2.7 MicroRNA lentiviral expression constructs and lentivirus production
The lentiviral vector expressing miR-663 has been previously described . Briefly, an approximately 250 bp fragment containing the human miR-663 precursor hairpin loops was amplified by PCR using using primers flanked by BamH I and Xho I sites at the 5' and 3' ends, and cloned into the pDrive cloning vector (Qiagen) under the control of the RNA Pol III mouse U6 promoter. Positive clones were confirmed by sequencing and subcloned into the pHR' SINcPPT SFFV-WPRE vector under the control of the SFFV promoter. The GFP virus, driven by the SFFV promoter, has also been previously described . The vector plasmids, gag-pol plasmid (pD8.91) and the VSVG envelope encoding plasmid (pMD2-G), were amplified in E.Coli and purified using the Endofree Maxiprep Kit (Qiagen). 13 μg transfer vector, 10 μg pD8.91 and 6 μg pMD2-G was mixed with 1.5 mL 0.25 M CaCl2 (Sigma) and added to 1.5 mL 2 × HEPES (Sigma) and mixed while bubbling for 20 min to allow a precipitate to form. This was then added to a 175 cm2 flask of approximately 60% confluent 293T cells containing 20 mL DMEM supplemented with 10% fetal calf serum, 100 U/mL penicillin, 100 μg/mL streptomycin and 2 mM glutamine and incubated for 48 h at 37°C in 5% CO2. The supernatant was centrifuged at 1,700 g for 10 min to pellet cell debris, and ultracentrifuged at 121,603 g for 2 h. The pellet containing concentrated virus was resuspended in DMEM without supplements and stored at -80°C.
2.8 Statistical analysis
All data are presented as mean ± SD. Statistical analysis was performed using SPSS (Chicago, IL). Student's two-tailed t-tests were used to compare groups and p ≤ 0.05 was considered significant.
Results and discussion
ATRA also induced HL-60 mature granulocyte cell differentiation (Figures 1C and 1D). Treatment with ATRA for 1 to 3 days significantly increased the number of HL-60 cells expressing CD11b. After 1, 2 and 3 days the expression rates of CD11b in ATRA treated cells were 41.2 ± 9.1%, 57.4 ± 11.4% and 67.2% ± 12.4% respectively, compared with the solvent control group (0.56 ± 0.21%, p < 0.01). The percentage of NBT positive cells in HL-60 cells treated with ATRA for 1, 2 or 3 days (Figure 1E) was 12.5%±9.1%, 27.4% ± 10.3% and 47.2% ± 10.4% respectively, compared with the solvent control group 4.31% ± 2.3%, p < 0.01, providing further evidence that ATRA promotes HL-60 cell differentiation.
Transfection of the miR-663 lentivirus, LV-miR-663, inhibited HL-60 proliferation in a time-dependent manner. MTT assays indicated inhibition rates were 34.2 ± 13.1%, 45.2 ± 24.5% and 53.2 ± 21.3% at 1, 2 and 3 days respectively, compared with the mock transfected group, p < 0.01, Figure 4B. LV-miR-663 also induced HL-60 differentiation and lead to a significant increase in the rate of CD11b expression, indicating mature granulocyte differentiation.
ATRA is the acid form of vitamin A, and can inhibit proliferation and induce differentiation in tumor cells. As a physiological inducer of differentiation, ATRA has been successfully applied in the treatment of hematological malignancies and has become a model of differentiation therapy (8). It has been demonstrated that PML-RARa is able to influence transcription of several miRNA genes [10, 13]. As the expression of these miRNAs is restored by ATRA, our results suggest the effects of successful clinical protocols to eradicate APL cells may be mediated, in part, by affecting microRNA expression. These findings also indicate that ATRA may also indirectly affect gene transcription through the ability of microRNAs to regulate of post-transcriptional mRNA processing.
In the present study, we characterized the expression profile of microRNAs during HL-60 ATRA-induced granulocytic differentiation, and identified a small number of microRNAs upregulated and downregulated in a time-dependent manner. Our findings are consistent with the previous observations of Croce CM, Norrild B and Barrera G [28–30]. We also observed that miR-663 is upregulated in response to ATRA treatment in HL-60 cells, which is the first report of the involvement of miR-663 in ATRA-induced differentiation. In HL-60 cells, Pizzimenti et al. reported miR-663 was upregulated by 4-Hydroxynonenal (HNE) treatment  and Kasashima et al. reported miR-663 was upregulated during 12-O-tetradecanoylphorbol-13-acetate (TPA) induced differentiation . Lutherburrow et al. reported expression of miR-663 is higher in M1 than M5 AML patients and hypothesized it may potentially be involved in blocking the differentiation of M1 blasts, and consequently monocytic differentiation .
MiR-663 seems to have dual functions, and the role it mediates varies in different experimental models. In human THP-1 monocytic cells and human blood monocytes, resveratrol upregulates miR-663 expression . MiR-663 is an oscillatory shear (OS) sensitive microRNA, and plays a key role in OS-induced inflammatory responses by mediating the expression of inflammatory genes in HUVECs . Downregulation of miR-663 in tumor cells may contribute to aberrant cell hyperplasia, leading to the development of gastric cancer .
Thousands of miR-663 target genes have been predicted by bioinformatic analysis and interestingly, most are transcription factors of AP-1 . In THP-1 cells, miR-663 decreases endogenous activator protein-1 (AP-1) activity and impairs lipopolysaccharide (LPS) induced upregulation of AP-1 by, in part, by directly targeting the Jun B and Jun D transcripts. Dose dependent downregulation of AP-1 activity and Jun B levels by resveratrol are miR-663 dependent. The specific targeting of genes encoding a subset of AP-1 factors by mir-633, such as Jun B and Jun D, may possibly explain some of the anti-leukemia function of ATRA. Bioinformatic tools have predicted TGF-β is also a target gene of miR-663, which is of interest as TBF-β is an important molecule with roles in many signaling pathways. These findings indicate miR-663 expression is upregulated during ATRA-induced differentiation, and lentivirus expressing miR-663 can significantly induce HL-60 differentiation. This study demonstrates miR-663 may play an important role in ATRA-induced differentiation in HL-60 cells; however, the function of miR-663 and the mechanism by which it affects HL-60 differentiation requires further study.
Our study is the first investigation of the effect of ATRA on microRNA expression, specifically the ability of ATRA treatment to upregulate miR-663 expression and lentiviral delivery of miR-663 can induce differentiation and inhibit proliferation in HL-60 cells.
Pan Jian, Ph.D. Immulogy. Graduated from State Key Laboratory of Molecular Oncology, Cancer Institute (Hospital), Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, PR China. Now is an associate professor of Department of Hematology and Oncology, Children's Hospital of Soochow University, Suzhou China, and an guest professor of Translational research center, Second Hospital, The Second Clinical School, Nanjing Medical University, Nanjing, China.
List of abbreviations used
acute myeloid leukemia
all trans-retinoic acid
extracellular signal-regulated kinase
methyl thiazolyl tetrazolium
spleen focus forming virus.
This work was supported by grants from the National Key Basic Research Program (NKBRP) (973 program) (No.2010CB933902) and the National Natural Science Foundation (30570818 and 30600279).
We thank Professor Zhihua Yang (Cancer Institute/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China) for her kind help.
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