INTRODUCTION

Top Abstract Introduction Materials & Methods Results Discussion References

Acute promyelocytic leukemia (APL) is defined as the accumulation of malignant myeloid cells blocked at the intermediate promyelocytic stage of myeloid differentiation. APL has now been associated with four chromosomal translocations, all resulting in the fusion of the retinoic acid receptor alpha (RAR) gene, located on chromosome 17, with genes encoding a number of nuclear proteins, including PML-t(15;17) (13, 17, 25), promyelocytic leukemia zinc finger (PLZF)-t(11;17)(q23;21) (9, 10, 36), nucleophosmin-t(5;17) (52), and nuclear matrix-associated antigen (NuMA)-t(11;17)(q13;q21) (67). Over 95% of patients with APL harbor chromosomal translocation t(15;17) (19, 65), and malignant promyelocytes from these patients express the PML-RAR fusion protein. These individuals can be successfully treated with all-trans retinoic acid (ATRA), resulting in the differentiation of immature promyelocytes into mature granulocyte forms and elimination of the malignant clone (11). Similarly, promyelocytes from a patient with t(5;17) and NPM-RAR expression can undergo terminal granulocytic differentiation in vitro (51). A patient with a NuMA-RAR fusion and t(11;17)(q13;q21) also clinically responded to ATRA therapy. In striking contrast, t(11;17)(q23;q21)-associated APL is not responsive to ATRA therapy (20, 36), and no patients with this disease have achieved lasting clinical remission with conventional chemotherapy. In all four forms of APL, an aberrant RAR is generated, perhaps leading to the promyelocytic phenotype due to a block in RA-mediated signaling. The singular failure of APL associated with fusion of PLZF and RAR to respond to ATRA may be due to disruption of PLZF function in hematopoiesis.

The PLZF protein, which is highly conserved among humans, mice, and chickens (12), is a transcription factor containing nine Krüppel-like C₂H₂ zinc fingers. PLZF binds DNA in a sequence-specific manner and represses transcription through its cognate binding site (35, 59). The amino terminus of PLZF contains a poxvirus and zinc finger (POZ) domain, which is the most highly conserved domain in the protein (6). POZ domains are also found in the mammalian zinc finger proteins Bcl-6 and ZF5, as well as in a number of Drosophila transcription factors and viral proteins (2, 46, 70). The POZ domain of PLZF mediates its abilities to homodimerize (14) and repress gene transcription (35), the latter likely by interaction with nuclear corepressors that affect deacetylation of histones (18, 21-23, 40).

PLZF, as expected for a transcriptional regulator, is localized to the nucleus, where, as seen in early hematopoietic progenitors and the more mature HL60 and MDS cell lines, it has a distinct speckled pattern of expression (30, 37, 53). PLZF colocalizes with the PML protein in large nuclear bodies of unknown function (8, 15, 29, 66). In t(15;17)-associated APL, these large nuclear-body structures are disrupted and both PML and PLZF are found in a diffuse microspeckled pattern throughout the cell due to the action of PML-RAR. Treatment of these leukemic cells with ATRA leads to the restoration of the wild-type staining pattern. PML was defined as a repressor of cell growth (1, 28, 44), and it was hypothesized that the nuclear body plays a role in cell growth control. This suggested that PLZF might also play a role in the control of cell proliferation. In the hematopoietic compartment, relatively high levels of PLZF are expressed in CD34⁺ cells of the bone marrow (10, 53) and in immature erythroid, lymphoid, and myeloid cell lines. When cells are induced to differentiate, PLZF levels generally decline, leading to the notion that down-regulation of PLZF may be required for the normal program of cell division accompanied by terminal cell differentiation.

To explore the role of the PLZF gene in myeloid development, we engineered the expression of PLZF in 32Dcl3G/GM (32DG/GM), a murine interleukin-3 (IL-3)-dependent myeloid cell line that differentiates into granulocytes after exposure to granulocyte colony-stimulating factor (G-CSF) and into macrophages and granulocytes after exposure to granulocyte-macrophage colony-stimulating factor (GM-CSF) (31). The 32Dcl3 cell line is an established model of hematopoietic development which has been used to study the effect of oncogenes (3, 41, 54), tumor suppressor genes (60), and growth factors (58). Our studies demonstrated that PLZF has pleiotropic effects when expressed in 32DG/GM cells: it inhibits transit through the cell cycle, blocking cells in G₀/G₁; it inhibits differentiation; and it yields cells with a more immature immunophenotypic profile. PLZF expression was also associated with the secretion of an autocrine growth-inhibitory factor. These data suggest that PLZF may help control the quiescent state of hematopoietic progenitor cells. Disruption of this function in t(11;17) APL may contribute to the ATRA-resistant phenotype of this disease.

	MATERIALS AND METHODS

Top Abstract Introduction Materials & Methods Results Discussion References

Generation of PLZF-expressing cell pools. The murine IL-3-dependent 32DG/GM cell line, which was previously described (31), was grown in Iscove's modified Dulbecco medium (Gibco BRL) supplemented with 10% heat-inactivated fetal bovine serum (FBS; HyClone), 50 U of penicillin per ml, 50 µg of streptomycin per ml, 2 mM glutamine (Gibco BRL), and 10 ng of recombinant murine IL-3 (Genzyme, Cambridge, Mass.) per ml. The 2 retroviral packaging cell line was maintained in Dulbecco's modified Eagle medium supplemented with 10% FBS, penicillin-streptomycin, and glutamine. Stable retroviral packaging lines were generated by using a retroviral vector, pBabepuro-PLZF, which was constructed by insertion of a 2.1-kb EcoRI fragment containing the PLZF cDNA (9) into pBabepuro (43). To create the packaging cell lines, 2 cells were electroporated at 300 V and 250 µF with 10 µg of pBabepuro or pBabepuro-PLZF which had been linearized by digestion with NotI. The transfected cells were selected with 1.5 µg of puromycin per ml for 2 weeks, and individual clones were isolated. The supernatant from packaging clones was screened for its ability to confer puromycin resistance to 3T3 cells. The resulting positive clones were expanded, and lysates of these cells were screened by immunoblotting with an anti-PLZF antibody. To generate stable pools of 32DG/GM cells expressing PLZF, 5 × 10⁶ cells were cocultivated with 2 packaging cells overnight, removed, and allowed to grow without selection for 48 h. Stable pools were then selected in medium containing 1.5 µg of puromycin per ml for 2 to 3 weeks. PLZF-expressing 32Dcl3 cell pools 7 and 8 were generated by coculture with 2 packaging cell line PLZF12, and pools 9 and 10 were generated from the 2 line PLZF14. Pools 2 and 3 were created by infection of 32Dcl3 cells with a pool of PLZF-harboring retroviruses derived 48 h after transient transfection, utilizing calcium phosphate, of the BOSC packaging cell line with the pBABEpuro-PLZF vector (49).

Growth and morphological assessment. Cells were plated at a density of 5 × 10⁴/ml, and live, trypan blue-excluding cells were counted by using a Thomas' hemocytometer every other day. 32DG/GM vector cells were plated at a density of 10⁵/ml with or without 50% conditioned medium (CM). CM was generated by plating control or PLZF-expressing cells at a density of 10⁴/ml and removing the medium after 3 days. The effect of IL-3 withdrawal on growth and survival was studied by washing cells twice with 5 ml of phosphate-buffered saline (PBS) and then incubating them in complete medium without IL-3. For morphological characterization, cells were collected, washed, and spun at 400 rpm in a cytocentrifuge (Shandon, Sewickly, Pa.) onto poly(L-lysine)-coated glass slides in PBS with 1% bovine serum albumin, after which they were treated with modified Giemsa stain (Sigma Diagnostics, St. Louis, Mo.). All slides were coded to eliminate bias and counted at least twice.

Immunoblotting. Whole-cell extracts from the stable cell pools were prepared by boiling an equal number of trypan blue-excluding cells in 1× sample buffer (6.25 mM Tris [pH 6.8], 2% sodium dodecyl sulfate, 10% glycerol, 5% 2-mercaptoethanol). The cellular proteins were separated through sodium dodecyl sulfate-7.5% or -10% polyacrylamide gels and transferred to Immobilon polyvinylidene difluoride membranes (Millipore, Bedford, Mass.) in a buffer (192 mM glycine, 25 mM Tris base) overnight at 25 V. The filters were blocked in 5% nonfat milk powder dissolved in TBST (10 mM Tris [pH 8.0], 150 mM NaCl, 0.05% Tween 20) for 1 h and then washed three times for 5 min each with 0.5% nonfat dry milk in TBST. The filters were incubated for 1 h with a 1:1,000 dilution of anti-PLZF polyclonal rabbit antiserum or affinity-purified anti-PLZF antibodies at a concentration of 0.5 µg/ml. The filters were washed three times for 5 min each with TBST and then incubated with a 1:7,500 dilution of goat anti-rabbit immunoglobulin G (IgG) or goat anti-mouse IgG coupled to horseradish peroxidase (Boehringer Mannheim, Indianapolis, Ind.) for 1 h; this was followed by five washes with TBST. Immunoreactive proteins were visualized by chemiluminescence and autoradiography (ECL; Amersham, Buckinghamshire, United Kingdom).

Immunostaining and flow cytometry. Immunostaining was performed on 10³ to 10⁶ cells per sample, depending on the cell pool and cell availability. Cell surface staining was performed first, followed by the intranuclear antigen staining and, finally, by DNA staining when necessary. 32DG/GM cells were first blocked in PBS containing 2% FBS and 2% mouse serum for 30 min at room temperature; this was followed by addition of the primary antibody against the cell surface antigen and incubation for an additional 30 min. The cells were then washed three times with PBS-2% FBS. Secondary antibody was added only if cell surface staining was performed. When intranuclear staining was performed, cells were permeabilized by incubation in PBS-0.2% Tween for 15 min at 37°C followed by incubation with the antibody against the intranuclear antigen for 30 min. Next, the cells were washed three times in PBS, incubated with the appropriate fluorochrome-conjugated secondary antibody for 30 min, and washed three more times with PBS. All antibodies were diluted in the blocking solution, and all incubations were carried out in 100-µl volumes at room temperature. For DNA staining, cells were incubated with 10 mg of propidium iodide (PI) per ml in PBS and 2.5 µg of DNase-free RNase (Boehringer Mannheim) per ml for at least 30 min. Samples were kept at 4°C for up to 1 day and then subjected to flow cytometry and analyzed with CellFit or ModFit software (Nippon Becton Dickinson).

Antibodies. Polyclonal rabbit anti-mouse IL-3R antibody (Santa Cruz Biotechnology) was used at a concentration of 0.3 µg/ml; polyclonal nonspecific rabbit IgG was purchased from R&D Systems; rat anti-GR-1-phycoerythrin (PE), PE-conjugated rat anti-Sca-1, and PE-conjugated rat IgG2b (PharMingen, San Diego, Calif.) were each used at a concentration of 0.2 µg/sample. Monoclonal mouse anti-PLZF antibody 2A9 was raised in the Hybridoma Core Facility of the Mount Sinai School of Medicine and used at a concentration of 1 µg/ml.

Flow cytometric analysis of apoptosis. Apoptosis was assessed by a modified terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay (Apotag; Oncor, Gaithersburg, Md.). Cells were fixed in 1% paraformaldehyde followed by 70% ethanol. Free 3' hydroxyl ends of DNA were extended with digoxigenin-conjugated nucleotides by using terminal transferase and labeled with fluorescein-conjugated antidigoxigenin antibody. Fluorescence emissions were recorded by using a FACscan flow cytometer and analyzed with LYSIS software (Nippon Becton Dickinson). Another approach for the assessment of apoptosis was based on the ability of annexin V to recognize phosphoserine-containing lipids on the surfaces of the dying cells (ApoAlert; Clontech, Palo Alto, Calif.). Live cells were stained with PI and fluorescein isothiocyanate (FITC)-conjugated annexin V, washed, and analyzed. PI-positive (necrotic) cells were excluded from analysis, and PI-negative cells were analyzed for FITC staining.

	RESULTS

Top Abstract Introduction Materials & Methods Results Discussion References

Generation of pools of 32DG/GM cells expressing PLZF. To address the biological role of PLZF in myeloid cell differentiation, we engineered the expression of PLZF in 32DG/GM cells. To avoid possible artifacts due to clonal selection, pools of PLZF-expressing cells were created by using three different sources of retrovirus. 32DG/GM cells were infected with a PLZF-expressing, replication-deficient retrovirus by coculture with two different 2-PLZF packaging lines and by incubation with supernatant containing a pool of retroviruses derived after transient transfection of the BOSC packaging line with the PLZF vector. PLZF expression in the stable pools was demonstrated by immunoblotting (Fig. 1A). PLZF was detected as an 85- to 90-kDa protein in PLZF-infected pools but was not detected in control pools transduced with a pBabepuro vector lacking a cDNA insert. The six PLZF-expressing 32DG/GM cell pools analyzed all expressed similar levels of PLZF that were much higher than the amount of PLZF endogenously expressed in 32DG/GM cells, in which PLZF mRNA is detectable by reverse transcription-PCR (53) but the protein is not detected by immunoblot analysis (Fig. 1A).

View larger version (28K): [in this window] [in a new window]   FIG. 1.   Analysis of retrovirus-infected 32DG/GM cell pools and transfected NB4 cells for exogenous expression of PLZF. (A) In vitro-translated PLZF (TNT) and whole-cell lysates prepared from equal numbers of trypan blue-excluding cells from each of the pools infected with the pBabepuro or pBabepuro-PLZF retrovirus were separated by electrophoresis through a denaturing 10% polyacrylamide gel, transferred to a polyvinylidene difluoride membrane, and blotted with monoclonal mouse anti-PLZF antibody 2A9. (B) Immunoblot of extracts from a vector-infected pool, a growth-suppressed PLZF 7 pool, and two pools which had reverted from the growth-suppressed phenotype, PLZF 8R and PLZF 10R. The positions of molecular mass markers are shown to the left of the gels.

PLZF expression in 32DG/GM cells is associated with growth suppression and G₁ arrest. PLZF-expressing pools of 32DG/GM cells proliferated poorly in culture (Fig. 2A). Wild-type and vector-infected cells had very similar growth curves and reached plateaus of growth at about day 5 at densities exceeding 10⁶/ml, while PLZF pools, despite being infected with viral vectors derived from three different packaging cell lines, all showed the same phenotype of severe growth suppression and never reached a density of greater than 10⁵ cells/ml. The PLZF2 pool could be maintained in culture for a limited time period. The doubling time for wild-type and vector-control cell lines was less than 24 h. In contrast, it took PLZF pools on average more than 3 days to double their populations. Growth suppression by PLZF was not limited to the murine 32DG/GM cells, since human NB4 APL cells overexpressing PLZF were significantly growth retarded, as were lymphoid BaF/3 cells overexpressing PLZF (data not shown).

View larger version (13K): [in this window] [in a new window]   FIG. 2.   Effect of PLZF overexpression on cell proliferation. (A) Duplicate cultures derived from recently thawed PLZF-expressing or control 32DG/GM cells were plated at a density of 5 × 104/ml in complete medium. Live-cell numbers were determined at 2-day intervals, and the averages were plotted. (B) Growth curves of revertant 32DG/GM cell lines which lost PLZF expression and of control vector pools. The control and PLZF pools were maintained in continuous culture in parallel for at least 6 weeks prior to performance of the experiment at a time when the PLZF pools reverted to fast cell growth. WT, wild type.

View larger version (24K): [in this window] [in a new window]   FIG. 3.   Effect of PLZF expression on cell cycle profile of 32DG/GM cells. (A) The cell cycle distributions of control and PLZF-expressing pools of 32DG/GM cells. Cells were plated at an initial density of 5 × 104/ml, grown for 2 days, and analyzed by PI staining and FACS analysis. Hypodiploid cells were excluded from this analysis. (B) Representative DNA content histograms of PLZF pool 10 and a vector-infected control pool. Curves modeling the G0/G1, S, and G2 compartments are shown.

View larger version (33K): [in this window] [in a new window]   FIG. 4.   Pools expressing PLZF are delayed in the G1 phase of the cell cycle. Vector control and PLZF-expressing 32DG/GM pool 7 cells were plated at an initial density of 5 × 104/ml and grown in the presence or absence of 1.5 µg of nocadazole/ml for 48 h. Cells were stained with PI and analyzed by FACS to determine their DNA content and cell cycle phase at the start of the experiment and after 48 h of growth in the presence of nocadazole. Curves modeling the G0/G1, S, and G2 compartments, derived by using the ModFit program, are shown. Cell number is plottted on the y axes, and DNA content is plotted on the x axes.

PLZF overexpression leads to apoptosis. Although PLZF repressed cell growth by inhibition of the cell cycle, we did studies to determine whether PLZF could also affect the process of programmed cell death. PI staining of PLZF-expressing cells generally showed a greatly expanded sub-G₀/G₁ shoulder, indicative of apoptosis (Fig. 3 and 5A). While less than 1% of the control pools contained hypodiploid cells, 7 to 20% of the PLZF-expressing pools contained such cells. To further demonstrate the occurrence of apoptosis, we used the TUNEL assay to detect free 3' hydroxyl ends of DNA (Fig. 5B). As a positive control for apoptosis, 32DG/GM cells were withdrawn from IL-3 for 48 h; 25% of the cells subsequently stained positive by the TUNEL assay (data not shown). When 32DG/GM cells were infected with an insertless retroviral vector grown in the presence of IL-3, 0 to 3% of the cells stained dimly positive in the TUNEL assay, likely a reflection of a low-level physiological turnover of cells. For PLZF pool 2, in contrast, up to 5% of the cells stained brightly positive for apoptosis in the TUNEL assay (Fig. 5B). Apoptosis was also demonstrated by the binding of annexin V to phosphoserines on the outer membrane of the dying cell (63). PLZF-expressing 32DG/GM pools on average had two- to threefold more annexin V-positive, apoptotic cells (Fig. 5C) than did the vector pools. The results of the three assays for apoptosis are concordant with each other and demonstrate increased cell death in the PLZF pools. The correlation between PLZF expression and apoptosis was further demonstrated by dual-channel FACS analysis of a PLZF pool, assaying simultaneously for PLZF expression and the presence of 3' hydroxyl ends by the TUNEL assay (Fig. 6). The experiment was internally controlled: the PLZF-positive or bright population was compared to the PLZF-negative or dim population. This experiment yielded two notable findings. First, virtually all of the TUNEL-positive apoptotic cells expressed high levels of PLZF. Second, less than half of the cell population expressed high levels of PLZF despite the marked growth suppression of the entire pool (Fig. 1).

View larger version (22K): [in this window] [in a new window]   FIG. 5.   PLZF expression increases spontaneous apoptosis in 32DG/GM cells grown in the presence of IL-3. (A) The percentage of cells with a sub-G1/G0 content of DNA was derived by integration of the DNA content histograms from cells plated at an initial concentration of 5 × 104/ml and grown for 2 days in complete medium containing IL-3. (B) Apoptotic cells were detected by modified TUNEL assay. The percentage of TUNEL-positive cells and the mean fluorescence of the cells from two trials are indicated. (C) Apoptotic cells were stained with FITC-conjugated annexin V. Necrotic cells, which are nonspecifically stained by annexin V, were eliminated from the analysis by gating out cells which stained with PI. The data represent the averages (+ standard deviation) of from two to four independent determinations.

View larger version (20K): [in this window] [in a new window]   FIG. 6.   Expression of PLZF in 32DG/GM cells is closely linked to induction of apoptosis. 32DG/GM PLZF pool 2 cells were plated at a density of 5 × 104/ml and allowed to grow in complete medium containing IL-3 for 2 days. The cells were fixed in 1% formaldehyde and simultaneously stained for expression of PLZF with monoclonal mouse anti-PLZF antibody 2A9 (1 µg/ml) and for apoptosis by the TUNEL assay. After being stained, the cells were analyzed by two-channel FACS, with PLZF expression displayed on the ordinate and TUNEL-positive, apoptotic cells displayed on the abscissa. In parallel, the cells were stained with an isotype control for the PLZF monoclonal antibody and incubated with a Texas red-conjugated secondary antibody and a fluorescein-conjugated antidigoxigenin antibody in the absence of terminal transferase (TdT) to set the upper limits for nonspecific fluorescence.

PLZF overexpression inhibits myeloid differentiation. 32DG/GM cells undergo myeloid differentiation in response to G-CSF and GM-CSF. The morphology of defined cell pools is demonstrated in Fig. 7A. When grown in medium containing IL-3, cells from all pools, including those expressing PLZF, demonstrated the immature morphology characteristic of myeloblasts, with round nuclei and a high nucleus/cytoplasm ratio. Wild-type and vector-infected pools, after exposure to G-CSF and GM-CSF, showed morphological evidence of maturation. The nuclei of the vector cells became lobulated, or bean shaped, and smaller in proportion to the cytoplasm, and in GM-CSF-treated cells the characteristic ring-nucleated murine neutrophils appeared (Fig. 7A, top row, extreme right panel). In contrast, PLZF-overexpressing pools showed fewer signs of differentiation, with their cell morphology being relatively unchanged after exposure to differentiating factors (Fig. 7A). Further examination of cells from each pool indicated that the block to differentiation was not complete. About 20% of the 32DG/GM cells spontaneously showed some evidence of differentiation when grown in the presence of IL-3, reflecting the partially differentiated phenotype of this subline of 32Dcl3 cells. The number of cells showing morphological differentiation at baseline was slightly depressed in the PLZF-expressing pools (Fig. 7A). Upon stimulation with G-CSF or GM-CSF, PLZF-expressing pools generally showed a minor increase in differentiated forms, such that generally 30 to 40% of the population of cells exhibited cytological differentiation. In contrast, G-CSF and GM-CSF induced morphological evidence of differentiation in about 90% of the control cells (Fig. 7B).

View larger version (64K): [in this window] [in a new window]   View larger version (14K): [in this window] [in a new window]   FIG. 7.   PLZF overexpression inhibits the ability of 32DG/GM cells to differentiate in response to G-CSF or GM-CSF. (A) 32DG/GM cells were grown in the presence of IL-3, G-CSF, or GM-CSF for 2 weeks and visualized by staining with modified Wright-Giemsa stains. Representative fields are shown. (B) The morphology of the cells grown in medium containing IL-3 or in the presence of G-CSF and GM-CSF was judged based on the nucleus/cytoplasm ratio and nuclear shape. At least 300 cells were counted on each slide, and the percentages of differentiated cells were plotted. Data from two independent experiments (Exp 1 and 2) are presented.

View larger version (23K): [in this window] [in a new window]   FIG. 8.   Expression of myeloid cell surface differentiation markers in control and PLZF-expressing pools. Cells were maintained in medium containing IL-3, G-CSF, or GM-CSF for 2 weeks, harvested, stained with anti-Sca-1 or anti-Gr-1 antibody, and analyzed by FACS. The percentages (± the standard deviations for three to five trials) of cells positive for the expression of the indicated cell surface markers are plotted. Due to poor growth, pool 9 was assayed only once.

PLZF-expressing cells secrete a growth-suppressive factor. Growth suppression by PLZF was profound in 32DG/GM cells (Fig. 1), although FACS analysis (Fig. 6) indicated that high levels of PLZF were found in less than 50% of the cells in a pool. Therefore, we hypothesized that PLZF pools of 32DG/GM cells could secrete an inhibitory factor into the growth medium. To detect such a factor, control 32DG/GM cells stably infected with the parental pBabepuro vector were cultured in medium conditioned by PLZF-expressing cells. As a result, the growth of these cells was inhibited, reaching a 50% lower peak density and exhibiting an increase in estimated doubling time from 24 to 48 h (Fig. 9). Contamination with PLZF-expressing cells was eliminated by filtering the CM. Furthermore, the medium from PLZF-expressing 32DG/GM cells did not contain packaged retroviruses because the CM failed to confer puromycin resistance to NIH 3T3 cells (data not shown). When CM was taken from denser cultures (~10⁵ to 10⁶ cells/ml) of 32DG/GM-PLZF cells, the effect of CM on the growth of control cells was more pronounced. The growth-suppressive effect was strongest when cells were cultivated with 50% CM, with cells reaching a threefold-lower cell density; it diminished with 20% CM and, in one case, was lost with 10% CM (Fig. 9). CM derived from the pBabepuro-infected pool did not suppress the growth of a fresh culture of 32DG/GM cells despite the fact that the vector-infected cells grew noticeably faster than the PLZF-expressing pools, leading to increased acidity of the CM and, presumably, depletion of some nutrients.

View larger version (25K): [in this window] [in a new window]   FIG. 9.   PLZF-expressing pools secrete a growth-inhibitory factor. 32DG/GM cells infected with the pBabepuro retroviral vector lacking an insert were plated in triplicate at a density of 105/ml in the presence or absence of medium conditioned by growth in the presence of PLZF-expressing 32DG/GM cell pools. Live cells were counted by hemocytometer and plotted (± standard deviations). The upper panel represents the effect on cell growth produced by 50% CM derived from an initial culture of 104 PLZF-expressing cells/ml. The lower panel displays the effect of different dilutions of CM derived from higher-density cultures (approximately 2 × 105 cells/ml) of PLZF-expressing cells on the growth of 32DG/GM vector cells.

PLZF expression increases survival of 32DG/GM cells after IL-3 withdrawal. Since PLZF is expressed in quiescent and apoptosis-resistant CD34⁺ progenitor cells (53), we studied the effect of PLZF overexpression on cell death induced by withdrawal of IL-3. Within 24 h after IL-3 withdrawal, wild-type and vector-infected cells underwent apoptosis, as determined by TUNEL assay and the appearance of cells with a hypodiploid DNA content (data not shown). Since PLZF cells have a higher incidence of apoptosis when cultured in the presence of IL-3, we expected to see a much faster induction of the death program in PLZF-expressing pools after IL-3 withdrawal. Surprisingly, PLZF-expressing 32DG/GM cells survived longer in the absence of the growth factor than did the control cells (Fig. 10A). Whereas all control cells were dead within 1 week of IL-3 withdrawal, more than 10% of the cells derived from PLZF-expressing pools of 32DG/GM survived 2 weeks without the growth factor (Fig. 10A) and exhibited the typical appearance of undifferentiated 32DG/GM cells (Fig. 10B). FACS analysis indicated that these surviving cells were blocked in the G₁ phase of the cell cycle (data not shown).

View larger version (38K): [in this window] [in a new window]   FIG. 10.   PLZF prolongs survival of 32DG/GM cells after IL-3 withdrawal. (A) Cells were washed free from IL-3 and plated in culture medium lacking IL-3; live cells were counted at the indicated time points. (B) Morphology of cells maintained for 2 weeks without IL-3. Cells were centrifuged onto slides, air dried, and visualized with a modified Wright-Giemsa stain.

	DISCUSSION

Top Abstract Introduction Materials & Methods Results Discussion References

APL associated with t(11;17)(q23;q21) is unique in its resistance to differentiation therapy with ATRA and to conventional chemotherapy (20, 36). Since the RAR gene is disrupted in a similar manner in all translocations associated with APL (19, 52, 62, 67, 68), we surmised that the properties of the PLZF gene disrupted in t(11;17) might explain the unique properties of the disease. PLZF encodes a DNA-binding transcriptional regulator (35, 59) which is expressed in the early hematopoietic precursor lineage (53). When such cells were placed into culture and allowed to differentiate, PLZF levels transiently increased and then declined (32). Engineered stable overexpression of PLZF in 32DG/GM cells yielded a striking suppression of cell growth, accumulation of cells in the G₀/G₁ phase of the cell cycle, and inhibition of differentiation in response to G-CSF and GM-CSF. Expression of PLZF was also associated with a more immature immunophenotype characterized by up-regulation of Sca-1, down-regulation of Gr-1, and a twofold decline in surface expression of the IL-3 receptor (data not shown). Hence, PLZF-expressing myeloid cells share many characteristics with hematopoietic progenitor/stem cells, including cell quiescence, expression of early hematopoietic markers, and reduced expression of growth factor receptors (47, 61). Together these data indicate that PLZF expression may be important for the maintenance or survival of hematopoietic stem cells.

Growth suppression and cell cycle delay induced by PLZF. Growth suppression associated with expression of PLZF was linked to inhibition of the cell cycle. When acutely expressed in 32Dcl3 cells by retroviral infection, PLZF can cause arrest in S phase, and when expressed in NIH 3T3 cells, it can lengthen the G₁/S transition (73). After selection of stable pools of 32Dcl3 cells expressing PLZF, the resulting population of cells showed an increased fraction in G₀/G₁. When treated with nocadazole, the PLZF cells failed to significantly accumulate in G₂, slowly passing through the G₁ and S phases of the cell cycle. The ability of PLZF to inhibit transit through the G₁ and S phases may be due to the ability of PLZF to repress transcription of the cyclin A2 gene (73). However, other cyclin or cyclin-dependent complexes involved in the G₁/S transition may be affected in 32Dcl3 cells, either by the direct action of PLZF or indirectly through secretion of growth-inhibitory substances.

PLZF expression alters myeloid differentiation. Enforced expression of PLZF inhibited myeloid differentiation induced by G-CSF or GM-CSF. It was suggested that differentiation of myeloid cells usually occurs in two steps: a precommitment stage, in which inducers of differentiation alter the genetic program of the cell, and terminal differentiation, which is accompanied by G₁ arrest, generally occurring after a few rounds of cell division (71, 72). Since 60 to 80% of 32DG/GM-PLZF cells were already arrested in G₁ before the addition of G-CSF or GM-CSF differentiation factor, the failure of the PLZF-expressing pools to undergo differentiation cannot be explained by their inability to cease cell division. Instead, the problem may reside in the inability of the PLZF-expressing cells to undergo the rounds of division which accompany terminal differentiation. It is also possible that PLZF prevents expression of genes determining differentiation during the precommitment phase, maintaining the cells in an undifferentiated state. Sca-1 and Gr-1 themselves could be targeted by PLZF. This is supported by the fact that even when grown in the absence of differentiation factors, PLZF-expressing cells expressed considerably less Gr-1 and more Sca-1. PLZF expression led to either the induction of a more undifferentiated phenotype or preferential selection of 32DG/GM cells with this phenotype. This is consistent with the fact that PLZF is expressed in CD34⁺ cells and further supports the hypothesis that PLZF is necessary for the maintenance of dormant immature hematopoietic progenitors. PLZF-expressing 32DG/GM cells, in an aberrant manner, up-regulated Sca-1 after G-CSF or GM-CSF treatment. This altered phenotype also indicates that the growth suppression induced by PLZF is unlikely to be a nonspecific toxic effect but rather is due to a blockade of normal pathways of myeloid development. As a result, signals received by the cells through the actions of cytokines may be diverted to an aberrant differentiation program.

PLZF and altered cell death. Constitutive PLZF expression protected 10% of 32DG/GM cells from apoptotic death after 2 weeks of IL-3 withdrawal, with the surviving cells arrested in the G₀/G₁ phase of the cell cycle. This novel phenotype further indicates that PLZF has specific effects on cell growth and survival. The antiapoptotic effect of PLZF may reflect an important biological function, namely, to enhance the survival of quiescent stem cells. It is possible that decreased sensitivity to IL-3 withdrawal is the reflection of the decreased dependence on IL-3 to provide the proliferative signal, due to the diminished numbers of IL-3 receptors on the surfaces of the PLZF pool cells (73). It will be important to determine if other apoptotic stimuli, such as genotoxic damage and treatment with tumor necrosis factor, are also blunted in the PLZF-expressing pools. This would determine whether PLZF expression causes a more global change in the balance between cell life and death, possibly by altering the expression of bcl2 or related proteins. The effect of PLZF is very similar to that of bcl2, which, when overexpressed in 32Dcl3 cells, retards apoptosis after IL-3 deprivation (4, 64). Strikingly, bcl2 overexpression also inhibits differentiation of 32Dcl3 cells (39) even though it does not interfere with differentiation in other cell lines (45, 48, 69). By itself, protection from apoptosis is not sufficient to inhibit differentiation, since overexpression of bcl2 family member A1 protects 32Dcl3 from cell death but has no effect on differentiation (39).

The role of PLZF in t(11;17) APL. Our data have implications for understanding the pathogenesis of APL associated with t(11;17)(q23;q21). The blockade of the normal RA signal plays a critical role in the pathogenesis of APL, likely in selecting the promyelocyte phenotype. Both PML-RAR and PLZF-RAR inhibit the transcription of key myeloid differentiation target genes at low (10⁹ M) concentrations of ATRA. While PML-RAR can activate these genes after treatment with pharmacological doses of ATRA (10⁶ M), PLZF-RAR fails to activate such genes (55) due to the ability of the PLZF moiety of the fusion protein to interact with SMRT and N-Cor corepressor proteins even in the presence of ATRA (18, 21-23, 40). Thus, part of the resistant phenotype of t(11;17)-associated APL may be due to a reduced capacity of the PLZF-RAR chimeric protein to transduce ATRA-mediated differentiation signals. However, a transgenic model for t(11;17) APL yielded a myeloid leukemia that did respond to high-dose ATRA with an increase in differentiated granulocyte forms, suggesting that in the organism, PLZF-RAR, though leukemogenic, does not completely block differentiation (22).