Forkhead Box F2 Regulation of Platelet-derived Growth Factor and Myocardin/Serum Response Factor Signaling Is Essential for Intestinal Development*

Background: Transcriptional regulation of smooth muscle cells is an understudied component of intestinal development and physiology. Results: Foxf2 deletion from smooth muscle causes intestinal malformations and colon remodeling. Conclusion: Foxf2 regulation of PDGF and myocardin/SRF signaling is essential for intestinal development and homeostasis. Significance: Better understanding of transcriptional mechanisms regulating postnatal intestine development and homeostasis may provide therapeutic approaches for congenital and acquired gastrointestinal diseases. Alterations in the forkhead box F2 gene expression have been reported in numerous pathologies, and Foxf2−/− mice are perinatal lethal with multiple malformations; however, molecular mechanisms pertaining to Foxf2 signaling are severely lacking. In this study, Foxf2 requirements in murine smooth muscle cells were examined using a conditional knock-out approach. We generated novel Foxf2-floxed mice, which we bred to smMHC-Cre-eGFP mice to generate a mouse line with Foxf2 deleted specifically from smooth muscle. These mice exhibited growth retardation due to reduced intestinal length as well as inflammation and remodeling of the small intestine. Colons of Tg(smMHC-Cre-eGFP+/−);Foxf2−/− mice had expansion of the myenteric nerve plexus and increased proliferation of smooth muscle cells leading to thickening of the longitudinal smooth muscle layer. Foxf2 deficiency in colonic smooth muscle was associated with increased expression of Foxf1, PDGFa, PDGFb, PDGF receptor α, and myocardin. FOXF2 bound to promoter regions of these genes indicating direct transcriptional regulation. Foxf2 repressed Foxf1 promoter activity in co-transfection experiments. We also show that knockdown of Foxf2 in colonic smooth muscle cells in vitro and in transgenic mice increased myocardin/serum response factor signaling and increased expression of contractile proteins. Foxf2 attenuated myocardin/serum response factor signaling in smooth muscle cells through direct binding to the N-terminal region of myocardin. Our results indicate that Foxf2 signaling in smooth muscle cells is essential for intestinal development and serum response factor signaling.

. However, knowledge pertaining to the regulation of postnatal visceral smooth muscle development remains scarce.
The forkhead box (Fox) family of transcription factors has been shown to mediate a wide variety of cellular activities, including embryonic and postnatal cell growth, tissue repair after injury, cell migration, and tumor formation (13). The Foxf subgroup contains two members, Foxf1 and Foxf2 (1,14). Lessons from knock-out mice indicate that both Foxf members are critical for embryonic development as Foxf1 Ϫ/Ϫ mice die in utero (15,16), and Foxf2 Ϫ/Ϫ as well as compound heterozygotic (Foxf1 ϩ/Ϫ /Foxf2 ϩ/Ϫ ) mice die shortly after birth (17). Several Fox proteins, including Foxo4, Foxq1, and Foxf1, have been shown to be critical for smooth muscle cell development via regulation of the myocardin/serum response factor (SRF) axis (18 -20). Using in situ hybridization, embryonic Foxf2 expression has been found in the mesenchyme of the oral cavity, limb buds, genitalia, CNS, eyes, lung, prostate, ear, and placenta as well as the lamina propria region and smooth muscle of the developing GI tract (21,22). During embryonic development, Hedgehog signaling from the epithelium induces Foxf2 expression (17); however, postnatal Foxf2 expression and signaling remain poorly characterized. Studies have shown alterations in Foxf2 expression in prostate cancer (23) and that Foxf2 decreases the size and frequency of colonic polyps in colon adenoma (24). Foxf2 has been further shown to mediate cardiac metabolism (25), and a W174R amino acid substitution has been shown to cause anterior segment mesenchymal dysgenesis in the eye (Foxf2 W174R ) (26). However, molecular mechanisms for Foxf2 signaling in smooth muscle cells have not been previously elucidated due to lack of mouse models allowing conditional inactivation of Foxf2.
In this study, we generated a novel Foxf2-floxed (Foxf2 fl ) mouse line to investigate the importance of Foxf2 in smooth muscle cells. By breeding these mice with smooth muscle myosin heavy chain-Cre mice (smMHC-Cre-eGFP) (27), we were able to efficiently delete Foxf2 from mature smooth muscle in the gut. Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice were viable and fertile. Juvenile mice showed no difference in size or morphology; however, adult Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice were significantly smaller in stature and had a significant decrease in the length of the GI tract (both large and small intestine). Adult mice had focal inflammatory regions in the small intestine and a significant increase in thickness of the smooth muscle and enteric neuron layers in the colon. We used colon smooth muscle from Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice and cultured Foxf2 Ϫ/Ϫ smooth muscle cells to demonstrate that Foxf2 regulates the PDGF pathway and physically interacts with myocardin to inhibit SRF signaling in visceral smooth muscle cells.

Generation of Foxf2-floxed Mice and Deletion of Foxf2 from Smooth Muscle Myocytes-A LoxP site was inserted into the
Foxf2 promoter via the Foxf2-targeting vector and the PGK-gb2 LoxP/FRT-flanked neomycin (neo) cassette was placed into the first intron (Fig. 1D). Electroporation of mouse ES cells (C57Bl/ 6 ϫ 129/SVEV) with the Foxf2 fl -targeting vector, following neo (G418) selection, was performed at the inGenious Targeting Laboratory (Stony Brook, NY). PCR analysis with multiple primer sets identified ES cells with the appropriate Foxf2 fl -targeted locus. Foxf2 fl ES cells were subsequently used to generate chimeric mice by injection into mouse blastocysts. Mice containing the Foxf2 fl -targeted allele were determined by PCR amplification with primers flanking the LoxP sequence located in the Foxf2 promoter (P1 and P2) ( Table 1) and primers located in the 3Ј region of the Foxf2 fl allele (P3 and P4). Chimeric mice were bred with C57Bl/6 mice in the animal facility at Cincinnati Children's Research Foundation to produce Foxf2 fl/ϩ mice. The neo cassette was deleted by breeding Foxf2 fl/ϩ mice with ACT-FLP1 mice (The Jackson Laboratory) (Fig. 1D). The loss of neo in Foxf2 fl/ϩ mice was confirmed by PCR using P5 and P6 primers ( Table 1) and sequencing of the Foxf2 locus using mouse tail DNA. Foxf2 fl/ϩ mice were backcrossed to generate viable Foxf2 fl/fl mice that were bred into the C57Bl/6 background for 10 generations. Deletion of the Foxf2 fl alleles from visceral smooth muscle was accomplished through breeding with smooth muscle myosin heavy chain-Cre-eGFP (smMHC-Cre-eGFP) transgenic mice (C57Bl/6) (27). Animal studies were approved by the Animal Care and Use Committee of Cincinnati Children's Research Foundation.
Tissue Collection-Intestinal tracts were collected from Foxf2 fl/fl and Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice and placed in ice-cold, calcium-free, sterile PBS. Colons and small intestines were separated at this time. Luminal contents were manually forced out by gentle manipulation with forceps. Tissues destined for immunohistochemistry were placed in 4% paraformaldehyde at this time. Tissues for whole organ RNA were placed in RNA-STAT-60. To enrich the smooth muscle layer of the colon, colons were split along their length and laid flat with the smooth muscle side down. A scalpel was then used to scrape away the epithelium and other layers leaving behind a smooth muscle enriched segment that was then placed in RNA-STAT-60 for RNA isolation or used for enzymatic digestion to prepare a single cell suspension as described previously (18).
Chromatin Immunoprecipitation (ChIP) Assays-Stably transfected mouse rhabdomyosarcoma cells with a dual His/FLAGtagged Foxf2 construct were generated and used for ChIP analysis. The pMIEG3 retroviral vector was used for dual-tagged protein expression in mammalian cells and has been described previously (43). To generate a double-tagged construct, Foxf2 ORF was PCR-amplified using high fidelity Pfx polymerase with N-terminal FLAG and C-terminal His 6 affinity epitopes according to manufacturer's protocol (Invitrogen). Nuclear extracts from transfected mouse rhabdomyosarcoma cells were cross-linked by addition of formaldehyde, sonicated, and used for immunoprecipitation with anti-His 6 -tagged rabbit polyclonal antibodies (Abcam) as described previously (44 -48). DNA fragments were ϳ500 bp as verified by agarose gel. Reverse cross-linked ChIP DNA samples were subjected to PCR, using oligonucleotides specific to promoter regions of mouse PDGFa, PDGFb, PDGFR␣, Foxf1, and myocardin genes ( Table 3). Potential FOXF2-binding sites were identified using the MacVector program and the previously published FOXF2 consensus binding sequence TA(G)TTTA(G)T (44). DNA sites with the highest homology to the published FOXF2 consensus binding sequence were investigated via ChIP. DNA binding was normalized to control ChIP DNA samples, which were immunoprecipitated using control rabbit IgG.
Luciferase and Mammalian Two-hybrid Assays-Foxf2 was amplified by RT-PCR from mRNA isolated from mouse intestine. The encoded protein of 446 amino acids is identical to that encoded by NM_010225.2. A Foxf1 mammalian expression construct was amplified by PCR from an HFH8 clone obtained from Robert Costa (44). This resulted in expression of a FOXF1 protein of 353 amino acids identical to that encoded by NM_010426.1. Fox expression plasmids were transfected together with SRF expression plasmid, telokin promoter luciferase reporter gene (Ϫ256 to ϩ147), and telokin-Renilla luciferase internal control into 10T1/2 cells, and luciferase assays were performed as described previously (46). The Foxf1 lucif-  Table lists inventoried TaqMan probes used for qRT-PCR analysis of gene expression.

Gene name
Assay no. acta2

TABLE 3 ChIP primers
Primer sets in table were used in ChIP analysis of Foxf2 binding to gene promoter regions (listed in parentheses). MARCH 20, 2015 • VOLUME 290 • NUMBER 12

JOURNAL OF BIOLOGICAL CHEMISTRY 7565
erase reporter (Ϫ5.3 kb Foxf1 ϩ 3Ј response element) and Foxf2 luciferase reporter (six repeats of Foxf2-binding sequence) genes were transfected into U2OS cells, and luciferase assays were performed as described previously (46,49). Mammalian two-hybrid assays utilizing SRF fused to the GAL4 DNA bind-ing domain and myocardin fused to the GAL4 activation domain were performed as described previously (50). GST Pulldown Assays-GST-SRF and GST-myocardin bacterial expression plasmids were described previously (50 -53).

Foxf2 Is Essential for Intestinal Development
ing amino acids 1-628) and GST-CT MRTFA (encoding amino acids 618 -929) were generated by PCR amplification of MRTFA fragments from the MRTFA mammalian expression vector (52). All expression constructs were confirmed by DNA sequencing. Full-length and fragments of Foxf2 were PCR-amplified and cloned into pET vectors for expression in bacteria.
GST pulldown assays were performed as described previously (53).
Statistical Analysis-Student's t test was used to determine statistical significance. p values Ͻ0.05 were considered significant. Values for all measurements were expressed as means Ϯ S.E.  immunostaining with anti-FOXF2 antibodies showed restriction of FOXF2 to mesenchymal layers of the developing GI tract at E14.5 and E17.5. Postnatally, Foxf2 was expressed in lamina propria (L) and circular muscle layer (C) but was absent from the longitudinal muscle layer (LM) and epithelium (E). C, qRT-PCR analysis of adult whole organ mRNA showed that Foxf2 is more highly expressed in the jejunum and ileum than the duodenum of the small intestine and more highly expressed in the colon than small intestine. Expression levels were normalized to ␤-actin (n ϭ 3). D, schematic shows Foxf2-floxed targeting construct. LoxP sites (solid triangles) were inserted to flank the first exon (E1) of the Foxf2 gene. Locations of primers (P) and sizes of PCR products are indicated. Primers used are listed in Table 1. Foxf2 fl/fl mice were bred with ACT-FLP1 mice to remove neo and later with smMHC-Cre-eGFP mice to delete Foxf2 from smooth muscle cells. E, visualization of immunofluorescence in frozen-fixed cross-sections of adult ileum and colon from smMHC-Cre-eGFP mice crossed with the Cre-dependent mT/mG reporter strain. Membrane-bound enhanced GFP is detected in the smooth muscle layers as well as the muscularis mucosa but not lamina propria. eGFP is expressed stronger in the muscularis mucosa of colon compared with ileum. The abbreviations used are as follows: CM, circular muscle; LM, longitudinal muscle; MP, myenteric nerve plexus; MM, muscularis mucosa; SMF, submucosal fibroblasts; EP, epithelium. F and G, PCR analysis of mouse tail DNA shows the presence of the neo cassette, Cre transgene, as well as wild type and Foxf2-floxed alleles. Scale bar, 10 m.

Generation of Mice with Foxf2 Deletion from Smooth Muscle
Cells-As Foxf2 expression has been poorly studied and the emergence of reliable commercial antibodies fairly recent, we performed immunohistochemistry on embryonic (E14.5 and E17.5), newborn, juvenile (P12), and adult (8 -12 weeks) wild type mice to investigate FOXF2 expression patterns in the GI tract during development. As early as E14.5 and at E17.5, FOXF2-positive nuclei were detected in the intestinal mesenchyme located adjacent to the epithelial layer (Fig. 1A). In the newborn, P12, and adult, FOXF2 was detected in the lamina propria and inner circular smooth muscle layer of the muscularis externa in both the small intestine and colon (Fig. 1B). FOXF2 was not detected in the outer longitudinal smooth muscle layer (Fig. 1B). FOXF2 was not expressed in vascular smooth muscle cells (data not shown). qRT-PCR analysis indicated that Foxf2 expression increases along the cranial to caudal axis in the adult gut, with little expression in the duodenum and highest expression in the colon (Fig. 1C).
To assess Foxf2 requirements in smooth muscle cells, we created a PGK-Neo-Foxf2 targeting construct and used it for electroporation of ES cells ( Fig. 1D and "Experimental Procedures"). A Foxf2-floxed (Foxf2 fl ) mouse line was generated and confirmed by PCR amplification of tail genomic DNA (Fig. 1, F  and G). The neo cassette was deleted by crossing the mice with ACT-FLP1 transgenic mice (Fig. 1D). Foxf2 fl/fl mice contain LoxP sites flanking exon one of the Foxf2 gene, which contains the DNA binding domain and one of two transcriptional activation domains of the FOXF2 protein. Foxf2 fl/fl mice were bred with smMHC-Cre-eGFP mice to delete Foxf2 from intestinal smooth muscle. Analysis of Cre-dependent reporter mice demonstrated that the smMHC-Cre-eGFP transgene directs robust Cre activity in the smooth muscle layers as well as muscularis mucosa but not lamina propria of small intestine and colon (Fig.  1E).
Foxf2 Binds to Promoter Regions of PDGFa, PDGFb, PDGF Receptor ␣, Myocardin, and Foxf1 Genes-Because expression of genes critical for the PDGF and Hedgehog signaling pathways was altered in the smooth muscle of Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ colons (Fig. 5A), we examined whether FOXF2 could directly bind to promoter regions of these genes. Potential FOXF2-binding sites (TGTTTAT, TATTTAT, or TATTTGT (44)) were identified in the promoter regions of PDGFa, PDGFb, PDGFR␣, and Foxf1 genes. Subsequently, a mouse myosarcoma cell line was created that stably expressed a His-and FLAG-tagged Foxf2 construct. ChIP with anti-His antibodies demonstrated that His-FOXF2 bound to the promoter regions of the PDGFa, PDGFb, and PDGFR␣ genes (Fig.   6A). His-FOXF2 protein also bound to promoter regions of myocardin, a critical co-activator of SRF signaling, and Foxf1 transcription factor, a downstream target of Hedgehog signaling (Fig. 6B). In co-transfection experiments, FOXF2 repressed Foxf1 promoter activity in a concentration-dependent manner as shown by luciferase assay (Fig. 6C). Thus, Foxf1 is a direct transcriptional target of Foxf2.
Foxf2 Directly Interacts with Myocardin and Influences Myocardin/SRF Signaling-Gene expression studies in Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice suggest that Foxf2 may regulate multiple signaling pathways during gut morphogenesis. Next, we focused our studies on the myocardin/SRF signaling pathway. SRF and myocardin are known to be essential for smooth muscle development and function (18). Having shown that FOXF2 was able to bind to the myocardin promoter, we investigated the effects of the FOXF proteins on myocardin/SRF signaling in vitro. Co-transfection experiments with an SRF-dependent luciferase reporter (telokin promoter) showed that both FOXF proteins, FOXF1 and FOXF2, can increase SRF-dependent stimulation of the telokin reporter gene in the absence of myocardin, although FOXF2 to a lesser extent (Fig. 7A). A mammalian two-hybrid assay, examining the binding of SRF to myocardin also showed that FOXF1 promotes the interaction of SRF with myocardin, whereas FOXF2 does not (Fig. 7B). Utilizing a glutathione pulldown assay, we showed that FOXF2 protein has a direct physical interaction with myocardin protein (Fig. 7C). FOXF2 was found to bind strongly to the N terminus of myocardin (Myo NT (1-585)). FOXF2 weakly bound to SRF, the C terminus of myocardin (Myo CT(585-935)) and the N terminus of the myocardin family member, MRTFA (Fig.  7C). Further analysis of myocardin deletion mutants determined that FOXF2 binds to a region within the first 350 amino acids of myocardin (Fig. 7D), which contains two RPEL motifs (58). Interestingly, this is distinct from FOXF1 which binds to the myocardin SAP domain (18).
To investigate functional consequences of FOXF2 binding to myocardin on expression of SRF target genes, adenoviral Cremediated deletion of Foxf2-floxed alleles was performed in a primary culture of colon smooth muscle cells purified from Foxf2 fl/fl mice. Foxf2 mRNA was nearly completely ablated indicating efficient Foxf2 deletion from primary smooth muscle cells (Fig. 7E). Foxf2 deletion significantly increased Foxf1 mRNA (Fig. 7E), a finding consistent with increased Foxf1 expression in Foxf2-deficient colons (Fig. 5A). Foxf2 knockdown increased expression of the SRF target gene smooth muscle 22␣ (sm22␣), ␣SMA, ␥SMA, smMHC, and myocardin in vitro (Fig. 7E). Furthermore, increased mRNA levels of SRF target genes were observed in colon tissue obtained from adult Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice (Fig. 7F). Thus, Foxf2 deficiency in colonic smooth muscle cells causes increased expression of genes regulated by the SRF signaling pathway. Altogether, our results indicate that FOXF2 directly binds to myocardin and inhibits myocardin/SRF signaling in smooth muscle cells.

DISCUSSION
To circumvent perinatal lethality in Foxf2 Ϫ/Ϫ mice, we generated a novel mouse model in which Foxf2 is selectively deleted  MARCH 20, 2015 • VOLUME 290 • NUMBER 12 from smooth muscle cells beginning at mid-gestation and throughout the life of the mouse. Loss of Foxf2 from smooth muscle decreased the length of the intestinal tract, truncating both the small intestine and colon. Foxf2 deletion resulted in increased thickness of longitudinal smooth muscle and expansion of the myenteric nerve plexus. PDGF receptor ␣-positive nerves have been previously observed in the GI tract (54), and staining of control and Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ colons showed PDGF receptor ␣ clearly localized to the myenteric plexus with increased staining in Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice. Tg(smMHC-Cre-eGFP ϩ/Ϫ ); Foxf2 Ϫ/Ϫ colons also had elevated expression of PDGFa and FIGURE 7. FOXF2 regulates myocardin/SRF signaling in smooth muscle cells. A, FOXF1 and, to a lesser extent, FOXF2 stimulate a SRF-dependent telokin reporter in the absence of myocardin. SRF, Foxf1, and Foxf2 expression plasmids were co-transfected with the SRF-dependent telokin reporter gene into 10TI1/2 cells. **, p Ͻ 0.01. B, mammalian two-hybrid assay examining the binding between SRF and myocardin in the presence or absence of FOXF1 or FOXF2. In these assays, SRF was fused to the GAL4 DNA binding domain and myocardin to the GAL4 activation domain. Interaction between the SRF binding domain and myocardin activation domain results in activation of a GAL4-dependent reporter gene (SRF/Myoϩvector compared with SRF/pACTϩvector: pACTϪ empty GAL4 activation domain vector). FOXF1 promotes myocardin binding to SRF, although FOXF2 has no effect on myocardin-SRF binding. C, GST pulldown assays in which bacterially expressed FOXF2 was incubated with SRF, myocardin, or MRTFA-GST fusion proteins. Following extensive washing, glutathionebound fusion proteins were analyzed by Western blot (upper panel). Input GST-fusion proteins visualized by Ponceau staining are shown in the lower panel. FOXF2 protein physically binds to SRF, the N-terminal half of myocardin (Myo NT 1-585), more weakly to the C-terminal half of myocardin (Myo CT 585-935), and weakly with the N-terminal half of MRTFA but not the C-terminal half of MRTFA. D, upper panel, schematic representation of myocardin structural domains. Middle panel, GST pulldown assays using various fragments of myocardin fused to GST. The GST fusion protein-bound FOXF2 is shown in the middle panel and GST fusion protein inputs in the lower panel. FOXF2 specifically bound to the first 220 amino acids of the myocardin protein, which contains RPEL motifs. Weak binding was also observed for amino acids 221-350 of myocardin. E, adenoviral Cre-mediated deletion of Foxf2 fl alleles from primary colon smooth muscle cells increased mRNA levels of Foxf1 as well as expression of myocardin/SRF target genes SM22␣, ␣SMA, ␥SMA, smMHC, and myocardin. mRNA expression levels were quantitated by qRT-PCR and normalized to ␤-actin (n ϭ 6). *, p Ͻ 0.05 versus control. F, mRNA levels of myocardin/SRF target genes SM22␣, ␣SMA, ␥SMA, and smMHC were increased in adult Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mouse colons (n ϭ 4).

Foxf2 Is Essential for Intestinal Development
PDGFb. Increased PDGF signaling can contribute to expansion of the myenteric plexus in Foxf2-deficient colons as PDGF signaling has been previously shown to induce neural mitosis and hyperplasia (55,59,60). Interestingly, Foxf2 Ϫ/Ϫ mice have been reported to lack ganglia in the colon (17), which is in stark contrast to the increased myenteric plexus observed in our Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice. The reason for this discrepancy could be due to the contribution of Foxf2-regulated signals from the lamina propria, which is not targeted by smMHC-Cre-eGFP and thus not Foxf2-deficient in our mouse model. Foxf2 may regulate the expression of genes essential for neural crest cell migration, proliferation, or survival. Alternatively, the difference may be due to the timing in which Foxf2 is deleted, as smMHC-Cre-eGFP is not detected prior to E12.5 (27), which is after the initiation of neural crest infiltration of the colon (61).
In addition to expression in enteric neurons, PDGF receptor ␣, and PDGF ligands are expressed in colon smooth muscle (1,57). PDGF has been shown to be a potent mitogenic agent in smooth muscle cells (62), and a cell autonomous role for PDGF signaling in smooth muscle proliferation has been previously demonstrated (63). Although we did not observe any smooth muscle cell proliferation in the colon of adult Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice, we did observe increased proliferation during early postnatal development. Unlike vascular smooth muscle, smooth muscle of the GI tract continues to proliferate for the first few days after birth. By 12 days after birth, proliferation of colon smooth muscle cells in control mice appears to have ceased. In contrast, in Tg(smMHC-Cre-eGFP ϩ/Ϫ );Foxf2 Ϫ/Ϫ mice there was still detectable proliferation in the circular muscle layer of the colon and marked proliferation in the longitudinal muscle layer. The increased expression of PDGF ligands and receptor in Foxf2-deficient colons could thus be stimulating proliferation of the neonatal colonic smooth muscle and/or delaying cell cycle exit. It has been previously shown that PDGF ligands originate from the circular muscle layer and myenteric plexus of the gut, and PDGF receptor ␣ is more highly expressed in the longitudinal muscle than the circular smooth muscle layer (57). This expression pattern could explain why the circular muscle layer is less affected by Foxf2 deletion, because it lacks the receptor to respond to PDGF ligands. Increased expression of PDGF proteins, however, does not appear to prevent colonic smooth muscle cells from ultimately exiting the cell cycle and differentiating. Cell cycle exit coupled with the direct increase in myocardin expression seen following loss of Foxf2 likely contributes to increased expression of contractile proteins in the adult colon.
The experiments performed in this study provide novel insight into the in vivo signaling of Foxf2 as well as regulatory pathways for postnatal visceral smooth muscle development, particularly in the intestines. It was previously shown that FOXF1 and FOXF2 bind to the same consensus cis-acting regulatory element sequence (28). This together with analysis of global knock-out and compound Foxf1/f2 heterozygous mice suggests that Foxf1 and Foxf2 may be partially redundant (17). In contrast, our studies have clearly shown that Foxf1 and Foxf2 have quite distinct roles in GI smooth muscle cells. We have previously shown that loss of Foxf1 from smooth muscle cells results in decreased contractile protein expression (18); however, in this study we found that loss of Foxf2 increases expression of these genes. Binding experiments show that FOXF1 and FOXF2 bind to different regions of myocardin (this study and Ref. 18), and the effects of this binding are quite distinct. FOXF2 is a weak activator of SRF-regulated genes as compared with FOXF1, and binding of FOXF1 to myocardin promotes its interaction with SRF, whereas the binding of FOXF2 to myocardin does not. Our data indicate that Foxf2 may act as a functional decoy for Foxf1, having only minimal co-stimulatory activity, at least as pertains to myocardin/SRF signaling. In addition, FOXF2 inhibits Foxf1 promoter activity, which can further exacerbate diminished myocardin/SRF signaling.
In addition to regulating the activity of myocardin/SRF complexes through protein-protein interactions, FOXF2 also directly affects the expression of myocardin through binding to a forkhead site in the myocardin promoter. ChIP analysis showed that FOXF2 can bind to the promoter region of myocardin, implicating Foxf2 in transcriptional regulation of the myocardin gene. Our data indicate that Foxf2 influences GI tract development via regulation of PDGF, SRF and Hedgehog pathways, all of which have been shown to be critical for GI tract development and physiology. Foxf2 may directly or indirectly regulate expression of genes critical for all three pathways and through this regulation mediate postnatal intestinal development and maintenance.
In summary, we generated a novel mouse line containing Foxf2-floxed alleles and used it to create smooth muscle-specific Foxf2 knock-out mice. Utilizing this model, we demonstrated a distinct phenotype for smooth muscle Foxf2 deletion compared with Foxf2 Ϫ/Ϫ mice. We also showed that FOXF2 bound to the promoter region of the myocardin gene as well as several members of the PDGF and Hedgehog signaling pathways. FOXF2 directly binds to and inhibits Foxf1 promoter activity and regulates SRF signaling through a protein-protein interaction with myocardin. By its capacity to regulate PDGF, Hedgehog and SRF signaling, Foxf2 is a critical regulator of GI tract development and maintenance.