- Open Access
MEIS1, PREP1, and PBX4 Are Differentially Expressed in Acute Lymphoblastic Leukemia: Association of MEIS1 Expression with Higher Proliferation and Chemotherapy Resistance
- Judith A Rosales-Aviña†1,
- Jorge Torres-Flores†1,
- Adriana Aguilar-Lemarroy1,
- Carmen Gurrola-Díaz2,
- Georgina Hernández-Flores1,
- Pablo C Ortiz-Lazareno1,
- José M Lerma-Díaz1,
- Ruth de Celis1,
- Óscar González-Ramella3,
- Esperanza Barrera-Chaires4,
- Alejandro Bravo-Cuellar1 and
- Luis F Jave-Suárez1Email author
© Rosales-Aviña et al; licensee BioMed Central Ltd. 2011
Received: 14 September 2011
Accepted: 20 December 2011
Published: 20 December 2011
The Three-amino acid-loop-extension (TALE) superfamily of homeodomain-containing transcription factors have been implicated in normal hematopoiesis and in leukemogenesis and are important survival, differentiation, and apoptosis pathway modulators. In this work, we determined the expression levels of TALE genes in leukemic-derived cell lines, in blood samples of patients with Acute lymphoblastic leukemia (ALL), and in the blood samples of healthy donors.
Here we show increased expression of MEIS1, MEIS2, and PREP1 genes in leukemia-derived cell lines compared with blood normal cells. High levels of MEIS1 and PREP1, and low levels of PBX4 expression were also founded in samples of patients with ALL. Importantly, silencing of MEIS1 decreases the proliferation of leukemia-derived cells but increases their survival after etoposide treatment. Etoposide-induced apoptosis induces down-regulation of MEIS1 expression or PREP1 up-regulation in chemotherapy-resistant cells.
Our results indicate that up-regulation of MEIS1 is important for sustaining proliferation of leukemic cells and that down-regulation of MEIS1 or up-regulation of PREP1 and PBX genes could be implicated in the modulation of the cellular response to chemotherapeutic-induced apoptosis.
Three-amino-acid loop extension (TALE) genes belong to the homeobox group and are distinguished by the presence of three extra amino acids in the loop binding the first to the second alpha helix of the homeodomain . TALE proteins include subfamilies MEINOX and PBC. MEINOX is composed of the members MEIS1, MEIS2, the recently described MEIS3, PREP1, and PREP2 in humans [1, 2]. The PBC subfamily contains PBX1, PBX2, PBX3, and PBX4 proteins [3, 4]. Expression of TALE genes has been related with normal development, differentiation, survival, apoptosis, and with the hematopoietic process [5–10]. Indeed, some TALE genes are targets for viral insertion or for chromosome translocations during leukemogenesis. In this regard, MEIS1 has been characterized as a common proviral integration site in BXH-2 mice ; in these mice, leukemic tumors that contain a viral integration site at the MEIS1 locus frequently possess an additional co-integration site in some HOX genes , which suggests the required cooperative effect of MEIS and HOX during leukemogenesis. Over-expression of MEIS1 in CD34+ hematopoietic cells has been related with suppression of differentiation, promotion of proliferation, and self-renewal. Interestingly, high levels of MEIS1 in myeloid progenitors have been shown to regulate the cellular response to some cytokines, favoring self-renewal or differentiation. Moreover, in the murine myeloid cell line 32Dcl3, it has been observed that MEIS1 can block granulocytic differentiation in response to G-CSF . MEIS1 has been also found over-expressed in human leukemic cells .
Other TALE proteins that have been also related with normal hematopoiesis and leukemogenesis comprise members of the PBX group. PBX proteins were first identified as HOX cofactors involved in developmental gene regulation [15, 16]. PBX1 plays a role in the development of blood cell populations because hematopoietic stem cells from PBX1-/- embryos have reduced colony-forming activity and are unable to establish multilineage hematopoiesis in competitive reconstitution experiments . PBX-PREP1 complexes are required for the production of normal CD4 and CD8 T-lymphocytes. Furthermore, PBX-MEIS complexes have been implicated in megakaryocyte differentiation, and PBX-PREP complexes have been also connected with the regulation of Interleukin (IL)-10 production in macrophages during the phagocytosis of apoptotic cells . PREP proteins are also important during development; for instance, deletion of PREP1 in mice and zebrafish induces embryonic lethality [18, 19]. Mice hypomorphic for PREP1 exhibit defects in T-cell development, with a decreased number of single-positive thymocytes, increased apoptosis of double-positive thymocytes, and abnormalities in the expression of αβ and γδ T-cell receptors . Additionally, reduction in PREP1 expression directly affects the expression of MEIS and PBX and consequently, normal embryonic hematopoiesis .
In summary, TALE genes codify for important transcription factors involved in hematopoiesis and leukemogenesis and are important survival, differentiation, and apoptosis pathway modulators in hematopoietic cells. In this study, we analyzed the expression of TALE genes in leukemia-derived cell lines, in samples of patients with Acute lymphoblastic leukemia (ALL), and in samples of clinically healthy donors. We observed consistent up-regulation of MEIS1 and PREP1 and down-regulation of PBX4 in leukemic cell lines and in the samples of patients with ALL. Interestingly, RNA-mediated down-modulation of MEIS1 lowers leukemic cell proliferation. Additionally, chemotherapeutic treatment of lymphoblastic cell lines induces an increment in PREP1, PBX2, and PBX4 messenger RNA (mRNA) levels that could be related with a more resistant phenotype.
Higher Expression Levels of MEIS1, MEIS2, and PREP1 Genes in Leukemia-derived Cell Lines Compared with Normal Cells
Primer pairs used for PCR reactions
F: CCC CAG CAC AGG TGA CGA TGA T
R: TGC CCA TTC CAC TCA TAG GTC C
F: CCA TCG ACC TCG TCA TTG AT
R: CCT CCT TTC TTC TGG CGT TTT T
F: GGT TTT GGC CTG ATT CTA TTG C
R: GTG GGG AGG GAG TGG TG
F: GCC ACC AAT ATA ATG CGT TCT T
R: GTG TTC CAA GCC CAG GTC
F: CTA ACT CGC CCT CAA CTC C
R: GTG TCC AGA TTG GCT GAA ATA G
F: GGC GGC TCT TTC AAT CTC TCA
R: GTC TCG TTA GGG AGG GGA TGA C
F: CAA GGG TCC CAA GTC GG
R: TGG CCT AAT TGG ATA AAG TGC T
F: ATG GGG AAG TTT CAA GAA GAG G
R: ATC TCG AGT CGC AGC AGA C
F: CAC TGC CAC CCA GAA GAC TGT G
R: TGT AGG CCA TGA GGT CCA CCA C
F: GCA TTG ACA ACA GGG TTC GTA G
R: ATT TAA ACA GAA AAC GTG CAC A
F: TCC GCA AAG ACC TGT ACG
R: AAG AAA GGG TGT AAC GCA ACT A
Up-regulation of MEIS1 and PREP1 and Down-regulation of PBX4 in ALL Samples vs. Those of Healthy Individuals
Overview of controls and patients
MEIS1 Silencing Decreases the Proliferation Rate of Leukemic-derived Cell Lines
Expression of MEIS1 and PREP1 Is Modulated in Response to Apoptosis Induction by Etoposide
Given that K562 cells show a chemotherapeutic-resistant phenotype and that response of these cells to etoposide exposure is the down-modulation of MEIS1, and because we observed that Jurkat cells increased MEIS1 expression and were the most sensitive cells, we postulate that MEIS1 down-regulation could be a mechanism for resistance to etoposide-induced apoptosis. In this regard, Jurkat clones with MEIS1-silenced should be more resistant than Jurkat infected with the empty virus (pLVX) or with parental Jurkat cells. We tested this hypothesis exposing the cells to etoposide and measuring the percentage of surviving cells (Figure 6C). From this approach, we observed that Jurkat clones in which MEIS1 was silenced demonstrated a higher percentage of cell survival compared with pLVX infected cells or parental cells. MEIS1 silencing in K562 cells did not further increased the percentage of surviving cells.
TALE genes are a particular group of homeobox genes that are important in the regulation of proliferation, apoptosis, and normal cell differentiation. Anomalous expression of these genes has been involved in the development of hematological malignancies . In this work, we first analyzed variations in the expression of TALE genes in leukemia-derived cell lines compared with normal control cells. In that we observed dissimilar MEIS1, MEIS2, and PREP1 expression levels, we wished to confirm whether these changes were also observed in samples of patients with leukemia. Interestingly, we found variations in MEIS1, PREP1, and PBX4 expression. It has been reported that over-expression of MEIS1 blocks myeloid cell differentiation; thus, high levels of MEIS1 are required to maintain hematopoietic cells in an undifferentiated state . We observed high levels of MEIS1 mRNA in leukemia-derived cell lines and also in the blood samples of patients with ALL; our results are in agreement with observations that lower levels of MEIS1 are unfavorable for cell life, because MEIS1 down-regulation has been related with decreased proliferation and poor survival of neuroblastoma and leukemia cell lines [24, 25]. Moreover, Kawagoe et al. reported that down-regulation of MEIS1 is required to induce differentiation of hematopoietic cells . Our findings support the notion that this gene plays an oncogenic role and that its expression is required to sustain proliferation and block differentiation in leukemia cells [24, 27]. Controversially, it has been reported that high levels of this protein can also trigger apoptosis; we observed that high MEIS1-expressing K562 cells were more resistant to apoptosis induction than Jurkat cells, which exhibited lower levels of MEIS1; however, it is also well known that MEIS1 requires the presence of protein partners to achieve its different functions [16, 28, 29]; one explanation for the contradictory effects reported for MEIS1 could be that, regardless of higher MEIS1 expression, cells can regulate the action of this protein by modulating the expression of MEIS1 cofactors, such as HOX. The availability of the later can transform MEIS1 action from proliferative into pro-apoptotic .
In the cell lines studied, we observed that an apoptotic stimulus induces MEIS1 up- and down-regulation (Jurkat and K562, respectively). A strategy of tumor cells for survival could be down-regulation of MEIS1. In this respect, through lowering its proliferation rate, tumor cells avoid DNA damage, which can induce apoptosis.
Regarding MEIS2 expression, this gene has been found in immature neuronal precursor cells, lens proliferative cells, ovarian cancer, and other tumor cell types, which underlies its possible role in sustaining proliferation . We observed strong expression in leukemia-derived cell lines compared with control cells, which is in agreement with the findings of Smith et al. ; however, when we analyzed its expression in patients, we found no variation in the expression of this gene (Figure 3).
To a greater extent, we observed that all studied cell lines express PREP1, but not PREP2. PREP1 has been described to be ubiquitously expressed in adult tissues  and PREP2 is depicted as possessing more restricted expression, being negative in peripheral blood leukocytes . After apoptosis induction by etoposide, CEM cells greatly increase PREP1 gene expression, PREP1 has been directly involved in the regulation of apoptosis: it has been described that BCL XL , an intrinsic apoptotic-pathway regulator, is a direct target of PREP1 . PREP proteins interact with PBX members to achieve their functions . Interaction of PREP with PBX1 and PBX2 increases the stability of PBX proteins and additionally increases the affinity of PREP for DNA binding [34, 35]; the expression of BCLXL and p53 has been reported to be regulated by PREP1 in cooperation with PBX1b [22, 36]. In etoposide-treated CEM cells, it was observed that expression of PBX2 and PBX4 increases (Additional file 1); PBX2 has been reported as a negative apoptosis modulator through negative regulation of BCL2 . Up-regulation of PREP1 together with down-regulation of PBX genes could account for the etoposide-resistant phenotype of CEM cells; this resistance could be mediated by BCLXL and p53. High levels of p53 have been associated with apoptosis but, in the presence of BCLXL-mediated survival signals, p53 can induce senescence instead of apoptosis .
In conclusion, our study shows that MEIS1 and PREP1 mRNA levels are significantly up-regulated in patients with ALL in comparison with healthy controls and inversely, that PBX4 is down-regulated in patients with ALL. Importantly, utilizing silencing assays, we confirmed that down-modulation of MEIS1 produces a lower leukemic-cell proliferation rate, an effect that was most notorious in the K562 myeloblastic cell line. Etoposide- induced apoptosis leads to changes in the expression of PREP1 and MEIS1; up-regulation of PREP1 and down-regulation of MEIS1 were independently related with resistance to apoptosis. Taken together, these results support the important role that TALE genes play in leukemic cell proliferation and survival, in addition to their probable involvement during leukemia development. Therefore, it could be important to evaluate MEIS1 and PREP1 expression in patients with leukemia prior to and after chemotherapeutic treatment and to correlate these findings with the clinical response.
Cells and cell culture
We used five commercially available human leukemia-derived cell lines: MOLT-4; Jurkat and CEM cells derived from lymphoid leukemia; HL-60 derived from promyelocytic leukemia, and K562 from erythroleukemia. Cells were grown in RPMI-1640 medium supplemented with 10% Fetal bovine serum (FBS), penicillin (100 U/mL,) and streptomycin (100 μg/mL); all products mentioned previously were obtained from GIBCO™ (Invitrogen Corp., Carlsbad, CA, USA). Cultures were maintained at 37°C in a humidified atmosphere with 5% CO2.
Patients and sample collection
Peripheral blood samples were collected from 14 patients with Acute lymphoblastic leukemia (ALL) according to World Health Organization (WHO) classification criteria at the Centro Médico Nacional de Occidente of the Mexican Social Security Institute (CIBO-IMSS) and the Hospital Civil de Guadalajara Fray Antonio Alcalde. Additionally, blood samples from 19 healthy donors were also collected from the IMSS Blood Bank. Letters of informed consent and protocols were approved by the CLIS-1305 Ethical Board of CIBO-IMSS.
Drugs and in vitro cell treatments
Etoposide was obtained from Lemery Laboratorios, México. The drug was stored at 4°C for <4 days and adjusted to the desirable concentration with DMEM culture medium immediately prior to utilization. The concentration employed was 170 μM etoposide.
RNA extraction and cDNA synthesis
Total RNA was isolated by using the PureLink™ Micro-to-Midi Total RNA Purification System (Invitrogen Corp.) from 5 × 106 cultured cells as described by the manufacturer. Peripheral blood samples from patients with leukemia and from healthy donors were collected with EDTA as anticoagulant and mixed immediately after collection with 45 mL of RNA/DNA Stabilization Reagent for Blood/Bone Marrow (Roche Applied Science, Germany) and stored at ‒80°C for preservation. The stabilized samples were utilized for mRNA isolation via a two-step procedure by means of magnetic separation employing the mRNA Isolation kit for blood/bone marrow (Roche Applied Science). mRNA was finally eluted from the magnetic pearls in 20 μL of water and stored at ‒80°C until use.
cDNA synthesis was performed from 5 μg of total RNA or 12 uL mRNA employing the Transcriptor First Strand cDNA Synthesis kit primed with oligo(dT) (cat. no. 04897030001, Roche Applied Science). The protocol was conducted as recommended by the manufacturer. cDNA were stored at ‒20°C and aliquots were utilized as templates for PCR and RT-PCR reactions.
PCR and RT-PCR
PCR reactions were carried out utilizing the set of primers presented in Table 1; the primers were designed using Oligo v6.0 software from sequences obtained from the NCBI-website GenBank Nucleotide database. PCR was performed using Taq DNA Polymerase (cat. no. 11146173001, Roche Applied Science) and Deoxynucleoside triphosphates (cat. no. 1969064, Roche Applied Science) in a PX2 Thermal Cycler (Thermo Electron Corp.). All reactions were conducted in 20 μL at the specified Tm (see Table 1). PCR products were resolved in 2% agarose gels containing 0.1 μg/mL ethidium bromide (Sigma Aldrich, Germany), visualized under Ultraviolet (UV) light, and documented with a DigiDoc-It System, (UVP, UK). RT-PCR analysis was achieved by employing the LightCycler-FastStart DNA MasterPLUS SYBR Green I kit (cat. no. 03515885001, Roche Applied Science) in the LightCycler 1.5 System (Roche Diagnostics GmbH, Mannheim, Germany). Data were normalized to the expression of the reference genes RPL32 (L32 Ribosomal Protein) and ACTB (β-actin).
To normalize target gene expression, we employed two different reference genes. We calculated the Crossing point (CP) for target and reference genes in each sample and subsequently calculated the ΔCP value of each sample, i.e., the target gene CP minus the reference gene CP. This facilitated analysis by taking only the intrinsic values of each sample. CPs from ACTB, and RLP32 were employed for this analysis. It is extremely noteworthy that ΔCP is inversely proportional to the expression of the target gene.
Lentivirus production and infection
Oligonucleotides used to construct shRNAs were: forward 5'- GAT CCG CGG GAC TCA CCA TCC TTC AAG TGA ATT CAA GAG ATT CAC TTG AAG GAT GGT GAG TCC CGT TTT TTG-3' and reverse 5'-AAT TCA AAA AAC GGG ACT CAC CAT CCT TCA AGT GAA TCT CTT GAA TTC ACT TGA AGG ATG GTG AGT CCC GCG-3' directed to MEIS1 exon 9 (E9); forward 5'-GAT CCG CCG TGT GTT TAG AAG CCT AAT TCA AGA GAT TAG GCT TCT AAA CAC ACG GCT TTT TTA CGC GTG-3 and reverse 5'- AAT TCA CGC GTA AAA AAG CCG TGT GTT TAG AAG CCT AAT CTC TTG AAT TAG GCT TCT AAA CAC ACG GCG-3' directed to MEIS1 exon 13 (E13); this latter sequence has been previously used . Complementary primers were annealed and cloned into the vector pLVX-shRNA1 (Clontech Laboratories, USA) using the restriction sites BamHI and EcoRI (NEB-Biolabs, USA). To produce infectious viral particles, Lenti-X 293T cells were transient-transfected by Lentiphos HT/Lenti-X HT Packaging Systems with lentiviral vectors pLVX-Puro or pLVX-shRNA1-E9 or pLVX-shRNA1-E13 as described by the manufacturer (Clontech Laboratories, USA). After 48 h, supernatants were checked with Lenti-X GoStix (Clontech Laboratories, USA) to determine whether sufficient viral particles were produced before transducing target cells. Supernatants were filtered through a 0.22-μm PES filter to eliminate detached cells, were aliquoted, and subsequently stored at ‒80°C until use. Jurkat and K562 cells (2.5 × 105) were transduced with approximately 4.5 × 105 IFU/mL of supernatants. RNA extractions were obtained after at least 2 weeks of puromycin selection (1 μg/mL).
Cell survival determination
Cell survival was determined by cleavage of tetrazolium salt WST-1 to formazan by cellular mitochondrial dehydrogenase enzymes. After different treatment periods, cells were incubated with 10 μL/well of WST-1/ECS solution (BioVision Research, Mountain View, CA, USA) for 3 h. Absorbance (450 nm) of treated and untreated samples was determined on a microtiter plate reader (Synergy™ HT Multi-Mode Microplate Reader; Biotek, Winooski, VT, USA). Data are reported as percentage of cell survival taking untreated control cells as 100% of cell survival.
Cell death was measured by flow cytometry using propidium iodide (cat. no. P4864, Sigma-Aldrich) and Annexin-V-FlUOS (cat. no. 1828681, Roche Applied Science) as recommended by these manufacturers. Cells were seeded in 6-well plates at a density of 3 × 105 cells per well in 1 mL RPMI medium containing or not etoposide (170 μM). After 5, 15, and 25 h, each sample was analyzed in a FACS Aria cytometer (BD Biosciences).
We thank our technicians María de Jesús Delgado-Ávila and Leticia Ramos-Zavala for their efficient support. This work was supported by grants CB-2005-25121/51502-M (CONACyT-México), FIS/2005/1/I/022, and FIS/2006/1A/I/051 (IMSS) to LFJ-S.
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