Progenitor expansion in apc mutants is mediated by Jak/Stat signaling
© Lin et al; licensee BioMed Central Ltd. 2011
Received: 2 September 2011
Accepted: 2 December 2011
Published: 2 December 2011
Mutations in APC, a negative regulator of the Wnt/ß-catenin pathway, can cause cancer as well as profound developmental defects. In both cases, affected cells adopt a proliferative progenitor state and fail to differentiate. While the upregulation of some target genes of Wnt/ß-catenin signaling has been shown to mediate these phenotypes in individual tissues, it is unclear whether a common mechanism underlies the defects in APC mutants.
Here we show that stat3, a known oncogene and a target of ß-catenin in multiple tissues, is upregulated in apc mutant zebrafish embryos. We further demonstrate that Jak/Stat signaling is necessary for the increased level of proliferation and neural progenitor gene expression observed in apc mutants.
Together, our data suggest that the regulation of Jak/Stat signaling may represent a conserved mechanism explaining the expansion of undifferentiated cells downstream of APC mutations.
Apc loss causes progenitor expansion in development and disease
The Wnt/ß-catenin signaling pathway acts to maintain the undifferentiated progenitor state in multiple epithelial tissues, and overactivation of this pathway is a major contributor to cancer. The tumor suppressor APC normally functions to inhibit Wnt/ß-catenin signaling, and APC mutations are oncogenic in tissues such as the colorectal epithelium . During normal embryonic development, Wnt and APC activities are balanced to allow both progenitor cell expansion and differentiation of postmitotic derivatives. Zebrafish embryos homozygous for apc mutations exhibit mispatterning and failure of differentiation in multiple tissues including the central nervous system (CNS) [2, 3]. Furthermore, in the CNS of other vertebrates, loss of APC function specifically leads to arrest in the neural progenitor state . Despite a clear picture of the cellular phenotypes following loss of APC, the molecular pathways underlying CNS progenitor cell expansion are largely unknown. These pathways may represent good candidates for mediators of oncogenesis in other epithelial cells.
Transcriptional targets of Wnt signaling mediate APC mutant phenotypes
The main downstream output of Wnt/ß-catenin signaling is the transcriptional regulation of target genes, mediated by Lef/Tcf family members. Typically, these targets are repressed by Lef/Tcf factors in the absence of Wnt signaling, and following Wnt activation ß-catenin translocates to the nucleus where it binds to Lef/Tcf proteins and acts as a co-activator. The identification of Wnt/ß-catenin transcriptional targets has thus been a major focus of investigation in past studies of the pathway's role in development and disease. Some identified target genes have been shown to be common targets in both normal embryos and the oncogenic state. For example, mitf is a direct target of Lef1 during melanocyte specification, and also plays an important role in melanoma progression downstream of Wnt pathway hyperactivation [5, 6]. Similarly, Wnt targets such as ascl2 and lgr5 may function in both intestinal epithelium homeostasis as well as colon cancer [7, 8].
Stat3 functions synergistically with Wnt signaling in cancer
Like Wnt signaling, the Jak/Stat pathway has been shown to mediate proliferation and tumor growth in cancer. In particular, constitutive Stat3 activity is associated with malignancy in colon cancer , the primary carcinoma caused by APC mutations. A previous study showed that Wnt signaling can stimulate Stat3 activity during early zebrafish development , but the mechanism underlying this activation was not characterized. One potential mechanism of regulation has been suggested by a study in esophageal carcinoma, where Stat3 was shown to be a transcriptional target of ß-catenin via Tcf4 . Intriguingly, Stat3 has also been suggested to be a target of Wnt signaling in ES cells , suggesting that this pathway may represent a developmentally important mechanism. However, the regulatory relationship between Wnt signaling and Stat3 activation has not been explored in vivo in untransformed tissue.
Here we demonstrate that stat3 is a direct transcriptional target of Wnt/ß-catenin signaling in developing zebrafish embryos. We show that increased stat3 expression in apc mutants correlates with increased proliferation and failure of neuronal differentiation in the developing hypothalamus. Conditional inhibition of Jak/Stat signaling rescues proliferation defects as well as ectopic expression of progenitor markers, but not the general activation of Wnt targets or the complete process of neurogenesis. Together, these data indicate a specific function for Jak/Stat activation in mediating neural progenitor expansion downstream of APC mutations, and suggest a conserved role for this pathway in development and disease.
Results and Discussion
stat3 is a direct target of the Wnt pathway via Lef1
We next tested whether the endogenous expression of stat3 in the zebrafish embryo depends on Wnt-mediated transcription. We used a transgenic inducible repressor of Lef/Tcf target genes (hs:ΔTcf) to globally inhibit pathway activity in vivo. 28 hpf embryos were heat shocked for one hour, allowed to recover until 36 hpf, and then processed for in situ hybridization. We observed a qualitative decrease in stat3 expression throughout embryos expressing ΔTcf, including in the hypothalamus (Figure 1D,E). Together, these results suggest that stat3 is a direct transcriptional target of the Wnt pathway.
stat3 expression and Stat3 phosphorylation are increased in apc mutants
Increased proliferation in apc mutants can be rescued by blocking Jak/Stat signaling
In other tissues, APC mutations and Stat3 hyperactivation can both lead to increased cell proliferation. To quantify the proliferative increase in apc mutant zebrafish, we performed short-pulse (1 hour) BrdU labeling in wild-type and mutant embryos. At 36 hpf, significantly more cells within the developing hypothalamus of apc mutant embryos incorporated BrdU than in wild-type siblings (Figure 2C,D). These data are consistent with an increased number of progenitor cells in the CNS of apc mutants compared to wild-type embryos.
We next tested whether inhibition of Jak/Stat activity could reverse the increased proliferation found in apc mutants. To block Jak/Stat signaling, we used the Jak2 inhibitor AG-490, which has been demonstrated to prevent Stat3 phosphorylation in many other experimental systems including zebrafish  and allowed us to bypass early developmental defects resulting from stat3 knockdown. When wild-type embryos were incubated in 40µm AG-490 from 24-36 hpf, we did not observe a significant change in the BrdU labeling index compared to untreated controls (Figure 2C,D). In contrast, AG-490 incubation completely reversed the increase in proliferation observed in apc mutant embryos, restoring the BrdU labeling index to wild-type levels (Figure 2C,D). Together, these data indicate that Jak/Stat signaling is required for increased proliferation in apc mutant brains. Our observations of increased stat3 mRNA expression in apc mutants suggest that Stat3 levels may be limiting in the developing brain, and that regulation by the Wnt pathway may control the ability of Jak/Stat signaling to drive cell proliferation.
Increased progenitor marker expression in apc mutants requires Jak/Stat activity
In the zebrafish retina, otx1 expression marks the putative stem cell zone of the ciliary margin, and is expanded in apc mutants . Otx1 and Otx2 are also expressed in the developing vertebrate hypothalamus and label neural progenitors in the zebrafish hypothalamus. We observed increased otx1 mRNA expression in the hypothalamus of apc mutants (not shown), and to provide a more quantitative measurement, we examined the number of cells labeled with an antibody that recognizes both Otx1 and Otx2. Within the hypothalamus, apc mutants showed a significant increase in Otx1/2-positive cells at 36 hpf (Figure 3B,C), and this increase was rescued to wild-type levels by AG-490 incubation (Figure 3B,C). These data suggest that cells may be arrested in an Otx-positive progenitor state following apc inactivation, and that Jak/Stat function mediates this arrest.
Inhibition of Jak/Stat activity is not sufficient to rescue neurogenesis in apc mutants
Here we have shown that stat3 is a direct transcriptional target of Wnt signaling in the developing embryo, and that Jak/Stat signaling mediates the expansion and maintenance of CNS progenitor characteristics downstream of Wnt hyperactivation in apc mutants. Together, our data suggest that transcriptional regulation of stat3 may represent a general mechanism linking Wnt pathway overactivation to the expansion of undifferentiated cells in the disease state.
At higher doses of AG-490, we were able to completely eliminate both proliferation and progenitor marker expression in wild-type embryos (not shown). Combined with the endogenous expression pattern of stat3, and the fact that ΔTcf can repress stat3 in wild-type embryos, this suggests that a Wnt/Stat3 pathway may also play an important role in normal CNS development.
Zebrafish maintenance and embryo culture
Embryos were obtained from natural spawning of wild-type (AB*), Tg(hsp70l:tcf3-GFP) w26 , Df(LG01:lef1,msxb) x8 , and apc hu745 mutant zebrafish and were staged according to Kimmel et al., . lef1 deletion and apc mutant embryos were identified by morphology and hs:Δtcf embryos were identified by expression of a GFP fusion protein. All embryos were raised at 28.5°C and fixed in 4% PFA for analysis. 28 hpf hs:Δtcf embryos were heat shocked for 1 hour at 37°C, then allowed to recover at 28.5°C until 36 hpf. To block Jak/Stat signaling, embryos were treated with 40 uM AG-490 (Enzo) beginning at 24 hpf. For BrdU labeling, 35 hpf embryos were incubated in 10 mM BrdU in 15% DMSO for 30 minutes on ice, washed and allowed to recover for 1 hour at 28.5°C before fixation.
ChIP and qPCR
ChIP analysis was performed as described previously  with the following modifications. One hundred embryos at 36 hpf were dechorionated and fixed in 1% PFA in PBS for 15 minutes at room temperature, and then lysed in cell lysis buffer [10 mM Tris (pH 8.1), 10 mM NaCl, 0.5% NP- 40, and protease inhibitors] and nuclear lysis buffer [50 mM Tris-Cl (pH 8.1), 10 mM EDTA, 1% SDS and proteinase inhibitors] by pipetting. For each immunoprecipitation, 5 ug of anti-Lef1 antibody  was conjugated to 30 ul Dynabeads (Invitrogen) prior to applying nuclear extract. A detailed protocol is posted at: https://wiki.zfin.org/display/prot/ZFIN+Protocol+Wiki. Precipitated DNA fragments were purified and submitted for Illumina sequencing at the University of Utah HSC Core Facility and sequences were mapped to zebrafish genome (assembly zv7).
For qPCR analysis of ChIP fragments, total input chromatin and Lef1 immunoprecipitated chromatin from wild-type and Df(LG01:lef1,msxb) x8 mutant siblings was used. For qPCR analysis of stat3 mRNA levels, total RNA was isolated from 42 hpf wild-type and apc hu745 mutants using an RNAeasy extraction kit (Qiagen) followed by DNase treatment. cDNA was synthesized by SuperScript II reverse transcriptase (Invitrogen), and stat3 levels were normalized to beta actin cDNA. Quantitative real-time PCR was performed at the University of Utah HSC Core Facility.
Primers used for stat3 ChIP qPCR are: 5'-TGCGTATCACAACACGGTTT-3' 5'-ACATGTCTCTGACGCAGTCG-3' Primers used for stat3 cDNA qPCR are: 5'-CCGACTGGAAGAGGAGACAG-3' 5'-GCTGGACGGTGCTGAATAAT-3'
In situ hybridization
Whole mount in situ hybridization was performed as described previously . Probes for stat3  and otx1  were obtained from T. Piotrowski. Probes for ascl1b and axin2 were synthesized in our laboratory. Following staining, whole embryos were mounted in 80% glycerol and imaged on a dissecting microscope, or embedded in plastic, sectioned, and imaged on a compound microscope.
For BrdU and PCNA detection, fixed embryos were incubated for 1 hour in 2N HCl. Immunostaining was performed as described previously . Antibodies were obtained from the following sources: anti-BrdU (AbD Serotec, 1:500), anti-HuC/D (Molecular Probes, 1:500), anti-OTX1/2 (Chemicon, 1:500), anti-PCNA (Sigma, 1:1000), anti-pStat3 (Tyr708, MBL, 1:1000), and secondary antibodies conjugated to Alexa Fluor 647 (Invitrogen). Following immunohistochemistry, embryos were counterstained with TO-PRO-3 (Invitrogen), and whole brains were dissected for imaging. Embryos were mounted in Fluoromount-G (Southern Biotech), and confocal images were acquired using an Olympus FV1000 microscope.
Acknowledgements and Funding
Grant Sponsor: NIH (NINDS); R21NS055138
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