Background
Krüppel-like factor 4 (KLF4) [
1,
2] belongs to the Krüppel-like factor family of zinc-finger transcription factors that are involved in numerous important cellular processes such as growth, development, differentiation, proliferation, inflammation, apoptosis, and somatic cell reprogramming. KLF4 has been shown in a context-dependent manner to be an oncogene or tumor suppressor [
3], as respectively demonstrated by the high levels of KLF4 in primary breast ductal carcinoma and oral squamous cell carcinoma [
4,
5] and decreased levels of KLF4 in a variety of other human cancers including esophageal, gastric, bladder, pancreatic, colorectal, lung and urinary bladder cancers [
6‐
14].
We and others have reported that one of the functions of KLF4 is to maintain the proper progression and integrity of the cell cycle [
15]. KLF4 inhibits cell proliferation by functioning as a cell cycle checkpoint protein to activate transcription of the cyclin-dependent kinase inhibitor, p21 [
1,
16]. Additionally, KLF4 is an important mediator of p53-dependent growth arrest in the G
1/S and G
2/M transitions of the cell cycle following DNA damage [
17]. More recently, we reported that KLF4 is important for the maintenance of genetic stability. This was demonstrated by the appearance of genetic instability in mouse embryonic fibroblasts (MEFs) null for the
Klf4 gene in the forms of increased DNA double strand breaks (DSBs), chromosomal aberrations and centrosome amplification [
18]. Since genetic instability plays a crucial role in the development and progression of human cancer [
19], we sought to determine whether re-expression of Klf4 in
Klf4
−/−
MEFsMay correct the observed genetic instability in these cells.
Discussion
Previously, we demonstrated that deletion of Klf4 from MEFs cells leads to increased genetic instability.
Klf4
−/−
MEFs display significantly higher levels of DNA damage as indicated by the increased presence of γ-H2AX foci compared with
Klf4
+/+
MEFs with and without γ-irradiation [
18,
23]. Additionally, the loss of Klf4 leads to defective cell-cycle checkpoint functions, aberrant centrosome duplication and increased aneuploidy. In view of these findings, we set to determine if reintroduction of Klf4 into
Klf4
−/−
MEFs will correct the observed genetic instable phenotype.
Cancer cells generally contain the full complement of biomolecules that are necessary for survival, proliferation, differentiation, and cell death [
25]. However, it is the failure to regulate these functions that results in an altered phenotype in cancer. Defects in checkpoint control increase genetic instability and contribute to uncontrolled proliferation. We have previously shown that relative to wild-type cells, MEFs deficient in Klf4 had a higher rate of BrdU incorporation that, was seemingly offset by a higher level of apoptosis [
18]. KLF4 is required for cell cycle arrest in G
1, G
2 or both in many cell types by modulating expression of cell cycle regulatory genes [
16,
17,
26]. Moreover, transcriptional profiling of KLF4 in cell lines suggests that KLF4 functions as a negative regulator of cell cycle progression [
27,
28]. As shown in Figure
1A, following Klf4 re-introduction in
Klf4
−/−
MEFs, the growth rate was significantly reduced. Also, consistent with previous reports that KLF4 exerts a cell cycle checkpoint effect by activating the expression of p21 [
16,
29], the level of p21 was upregulated when compared to control
Klf4
−/−
MEFs (Figure
1C). However, given the modest p21 upregulation in Klf4-transfected
Klf4
−/−
MEFs when compared to control
Klf4
+/+
MEFs (Figure
1C), it is possible that such a robust inhibition of cell proliferation observed in
Klf4
−/−
MEFs following Klf4 over expression might not be attributed to a single factor alone. In response to the high basal DNA damage and genetic instability observed in
Klf4
−/−
MEFs, such a robust suppression of proliferation following Klf4 overexpression could be the result of a cumulative effect of the upregulation of additional cell-cycle progression inhibitors that have been shown to be upregulated by Klf4, such as 14-3-3-sigma [
27] and other Cip/Kip family members p57 [
27] and p27 [
30], this in addition to the suppression of promoters of the cell cycle progression such as cyclin E (Figure
1C and [
22]), cyclin B1 [
26] and cyclin D1 [
31], Such notion requires further investigation.
We have previously shown that
Klf4
−/−
have a higher level of apoptosis than
Klf4
+/+
MEFs [
18,
23]. Here we demonstrated that overexpression of Klf4 has no apparent effect on basal level of apoptosis in
Klf4
+/+
but trended to reduce apoptosis in
Klf4
−/−
MEFs (Figure
1B). These results suggest that under basal conditions, overexpression of Klf4 in cells with endogenous Klf4has no additional advantage on reduction of apoptosis and that overexpression of Klf4 in absence of endogenous Klf4 might be advantageous to cell survival by reducing the apoptotic level.
Abnormal duplication of centrosomes is a major reason for chromosome instability in cancer because it leads to multipolar spindles which direct unequal segregation of chromosomes during mitosis, thus increasing the frequency of mitotic defects [
32,
33]. We have previously shown that Klf4 plays a role in regulating centrosome duplication in MEFs as evidenced by the presence of centrosome amplification (defined as ≥3 centrosomes per cell) in
Klf4
−/−
MEFs when compared to
Klf4
+/+
MEFs [
18]. Centrosome amplification occurs when its duplication becomes dysregulated. It is known that the p53-p21-cyclin E axis of pathway plays a major role in regulating centrosome duplication. p53 is a tumor suppressor that induces the expression of p21 [
34,
35], which inhibits the activity of Cdk2/cyclin E [
36]. Previous work has shown that disruption of this pathway (loss of p53 or p21, or overexpression of cyclin E) can induce centrosome amplification [
37]. Recently, we demonstrated that genetic instability in the absence of Klf4 is likely due to elevated cyclin E and p53 levels, which are normally suppressed by Klf4 [
18]. The current study demonstrates that Klf4 may play a role in correcting abnormal centrosome amplification in
Klf4
−/−
MEFs. A potential mechanism by which this is achieved is indicated by the results in which Klf4 overexpression in
Klf4−/−MEFs lowered the levels of p53 and cyclin E and increased that of p21, cumulating in a restoration of the normal centrosome duplication process.
The DNA damage response (DDR) is essential for the maintenance of genetic stability and an unstable genome leads to the accumulation of mutations and cancer development [
38,
39]. Inefficient DNA double-strand break (DSB) repair can result in chromosomal translocation, deletion and chromosome fusion or loss [
40]. DDR signaling involves a large number of proteins that act as sensors, mediators, transducers and effector proteins [
41,
42]. Recruitment of the DDR protein γ-H2AX, BRCA1, and 53BP1 to DNA DSBs is a key event in the DDR [
43‐
45]. Defective recruitment of repair factors at DNA DSBs, such as delay in foci assembly and disassembly, is associated with defective DDR.
Klf4
−/−
MEFs contain a high level of phosphorylated histone 2AX (
y-H2AX), a marker for double-strand DNA breaks, and exhibit chromosome aberrations including dicentric chromosomes, double minute chromosomes, and chromatid breaks [
18]. The current study shows that a significantly higher fraction of
Klf4−/−MEFs contained γ-H2AX foci as compared to
Klf4+/+MEFs over 24 h in response to γ-irradiation (Figure
3B). In
Klf4
−/−
MEFs we observed no appreciable DNA repair response, showing a persistently elevated percentage of cells with 53BP1 foci 24 h post-irradiation compared to a robust DNA repair response in
Klf4+/+MEFs post irradiation (Figure
3C). These results suggest that Klf4 may be involved in the DNA repair response. This role is further substantiated by the ability of Klf4 to correct DNA damage present in
Klf4−/−MEFs after its reintroduction as demonstrated by lower number of foci of both γ-H2AX and 53BP1 with and without irradiation (Figure
4B and C). Taken together these results suggest that KLF4 plays a role in repairing DNA damage but the exact mechanism by which KLF4 accomplishes this requires further exploration.
Genetic instability, which includes both numerical and structural chromosomal abnormalities, is a hallmark of cancer. We recently reported that
Klf4
−/−
MEFs exhibit aneuploidy [
18]. The current study demonstrated a role of Klf4 in preserving genetic integrity by correcting aneuploidy in
Klf4
−/−
MEFs. Re-expression of Klf4 in
Klf4
−/−
cells resulted in a decrease in the number of cells exhibiting aneuploidy when compared to control
Klf4
−/−
MEFs (Figure
5). The role of KLF4 in maintaining genetic stability is further substantiated by the ability of Klf4 to suppress micronuclei formation in
Klf4−/− cells (Figure
6) as micronuclei is considered a biomarker of chromosomal damage, genome instability, and eventually of cancer risk [
46]. The mechanism by which Klf4 maintain ploidy and chromosome integrity is currently being investigated.
Methods
Cells and cell culture
The wild type (
Klf4+/+) and null (
Klf4−/−) for
Klf4 mouse embryonic fibroblasts (MEFs) were generated as previously described [
23]. Studies involving experimental animals have been reviewed and approved by the Stony Brook University Institutional Review Board (Protocol #245765). Cells were Maintained in Dulbecco’s Modified eagle’s Medium (DMEM) supplemented with 10% FBS, 1% penicillin/streptomycin at 37°C in atmosphere containing 5% CO
2. To overexpress Klf4-GFP and GFP-control in MEFs, cells were transiently transfected with 3 μg plasmid DNA (per well in a 6-well plate) or 0.6 μg plasmid DNA (per well in a 4-well glass slide) using Lipofectamine 2000 reagent (Life Technologies) according to Manufacturer’s instructions. For cell proliferation assay, cells were seeded onto 6-well plates at a density of 10
5 cells per well in triplicate. Cells were harvested by trypsinization every 24 h for 3 days and counted using Z1 Coulter Particle Counter (Beckman Coulter). For DNA-damage analysis cells were treated or not with γ-irradiation using
137Cs -irradiator at 0.75 Gy/min for a total of 2 Gy. Media were refreshed and treated cells were allowed to recover for 1, 4 or 24 h before fixation for immunostaining.
Plasmids
Expression vector pEGFP-N1 was purchased from Clontech. For generation of Klf4-GFP fusionMKLF4 ORF was excised from pGBKT7-Klf4 vector [
48] using
Nco I and
Eco RI restriction enzymes. ExcisedMKlf4 ORF was then inserted in frame in pRSET B vector, and the stop codon of theMKlf4 was removed by PCR site directed mutagenesis. TheMKlf4minus stop codon was then excised using
Kpn I restriction enzyme and inserted in pEGFP-N1.
Cytogenetic analysis
Cytogenetic analysis by Metaphase spreading of MEFs was performed as described previously [
49]. Colcemid (0.5 μg/ml, Life Technologies) was added to MEFs 4 h before harvesting. After treatment, floating rounded-up Mitotic and adherent cells (obtained from the Medium and a PBS wash or after trypsinization, respectively) were pooled and pelleted by centrifugation at 10,000 rpm for 5 min. Cells were swollen in hypotonic solution (0.075 M KCl) at 37°C for 15 min and fixed in fresh, Carnoy’s fixative (methanol: glacial acetic acid at 3:1) for 10 min at room temperature. Cells were spun down at 1000 rpm for 10 min, and washed three times in Carnoy’s fixative and then dropped onto glass slides and aged in a 60°C oven overnight. Cells were subjected to hoechst staining for nucleus visualization. Metaphase spreads images were acquired using a Nikon eclipse 90iMicroscope (Nikon Instruments Inc.) equipped with a DS-Qi1Mc and DS-Fi1, CCD cameras (Nikon Instruments Inc.). The numbers of chromosomes in Metaphase (n = 100 cells) from each genotype were counted and analyzed.
Immunofluorescence analysis
For all the immunostaining experiments, cells grown on glass coverslips were washed briefly with PBS and fixed with 3.7% formaldehyde for 30 min at room temperature followed by three times wash with PBS. For centrosome count, at 24 h post-transfection, untransfected and transfected cells were fixed and washed as mentioned above. Cells were then incubated with blocking solution (3% bovine serum albumin (BSA), 0.2% Triton X-100 in PBS) for 1 h at room temperature, probed with rabbit anti-γ-tubulin polyclonal antibody (10732; Santa Cruz) overnight at 4°C and detected with Alexa Fluor 568-conjugated goat anti-rabbit IgG antibody (A11011, Life Technologies) for 1 h at 37°C. Cells were then washed once and counterstained with hoechst for 5 min at room temperature in the dark. Finally cells were washed two times and Mounted in Prolong Antifade kit (Life Technologies), and visualized with Nikon microscope. Antibody dilutions and washes after incubations were performed in blocking solution. For γH2AX and 53BP1 foci staining, cells were transfected as mentioned above, and left untreated or γ-irradiated (2 Gy) at 24 h post-transfection, and incubated for 1, 4, or 24 h. Cells were fixed and immunostaining was carried out as Mentioned above. Cells were probed with Mouse anti-γH2AXMonoclonal antibody (05–636; Millipore) or rabbit anti-53BP1 polyclonal antibody (ab21083, Abcam) overnight at 4°C, and detected with Alexa Fluor 568-conjugated goat anti-mouse IgG antibody or Alexa Fluor 568-conjugated goat anti-rabbit IgG antibody, respectively, for 1 h at 37°C. For cleaved caspase 3 staining, cells were transfected as Mentioned above. At 24 h post-transfection, cells were fixed and immunostaining was carried out as Mentioned above. Cells were probed with rabbit anti-cleaved caspase 3 polyclonal antibody (9664S, Cell signaling) overnight at 4°C and detected with Alexa Fluor 568-conjugated goat anti-rabbit IgG antibody for 1 h at 37°C.
Micronucleus assay
Cells were seeded onto coverslips and transfected as mentioned above. Five hours post transfection cells were treated with 4 μg/ml cytochalasin B (C6762, Sigma) in fresh media and incubated overnight. At 24 h post-cytochalasin B addition, cells were stained with hoechst for 5 min at room temperature in the dark. Finally cells were washed two times mounted in Prolong Antifade kit (Life Technologies) and visualized with Nikon microscope.
Immunoblotting
Cells were lysed in lyses buffer containing 100 mm Tris–HCl (pH6.8), 2% sodium dodecyl sulfate (SDS) and 20% glycerol, and vortexed for 3–4 min for homogenization. Insoluble material was removed by centrifugation at 12,000 rpm for 5 min, and the supernatant was collected for protein quantification. Following quantification, β-mercaptoethanol and bromophenol blue were added to a final concentration of 5% (v/v) and 0.1% (w/v), respectively, and samples were heated at 95-100°C for 10 min. Samples were cooled to room temperature and then used for SDS-PAGE gel electrophoresis. Following protein transfer, the membranes were immunoblotted with the following primary antibodies: rabbit anti-KLF4 (PM07,MBL), goat anti-p53 (6243, Santa Cruz), Mouse anti-p21 (556431, BD Biosciences), Mouse anti-cyclin E (05–363, Millipore), and rabbit anti-γH2AX (05–636, Millipore), and mouse anti-β-actin (A1978, Sigma-Aldrich). The blots were then incubated with appropriate horseradish peroxidase-conjugated secondary antibodies for 1 h at room temperature. The antibody-antigen complex was visualized by ECL chemiluminescence (Millipore).
Statistical analysis
Statistical analysis for significance between treatments was performed by t-test.
Competing interests
None of the authors had any competing financial interests in relation to the work describe.
Authors’ contributions
EE carried out the all the experimental studies, participated in the design of the study and drafted the manuscript. EH participated in cell transfections and in Western blots. AG carried out microscope imaging and the statistical analysis. BY participated in the irradiation experiments. VY conceived of the study, and participated in its design and coordination and drafted the manuscript. All authors read and approved the final manuscript.