HUVECs were obtained from the American Type Culture Collection (ATCC; Manassas, VA, USA) and cultured in Endothelial Cell Growth Medium-2 (EGM-2; Lonza, Portsmouth, NH, USA) at 37°C in a humidified atmosphere of 5% CO₂ as previously described (18). The HUVECs were transfected with oligonucleotides in 6-well plates using Lipofectamine 2000 reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. Briefly, 100 pmol of miR-7 mimics, miR-7 inhibitors (miR-ASO) or small interfering RNAs (siRNAs) against KLF4 (GenePharma, Shanghai, China) were formulated with 500 µl serum-free RPMI-1640 medium (Invitrogen). The transfection complex was directly added to the cells and replaced with fresh complete medium 6 h later. Analyses of the effects of miRNAs or siRNAs on recipient cells were performed 48 h after transfection as previously described (11,19).

The 3′-untranslated region (3′-UTR) of KLF4 was amplified from human genomic DNA and cloned into the pGL3-control vector (Promega, Madison, WI, USA) (19). Mutation of the miR-7 binding core sequence on the 3′-UTR region of the KLF4 gene was achieved using overlap extension PCR methods using primers as previously reported (19). HUVECs were seeded in 24-well plates and then transfected with 500 ng of wild-type or mutant reporter plasmid, 25 ng of Renilla luciferase expression vector, along with miR-7 mimics (10 nM) or the negative control (10 nM) using Lipofectamine 2000 reagent. After 48 h, the cell extract was used to determine firefly and Renilla luciferase activities with the Dual-Luciferase Reporter Assay system (Promega).

Total RNA was isolated from the cells using TRIzol reagent (Invitrogen) according to the manufacturer's instructions. RNAs were reverse transcribed into cDNA using miScript Reverse Transcription kit (Qiagen, Valencia, CA, USA). All PCR conditions were optimized to produce a single product in the exponential range. Quantitative real-time PCR was performed using SYBR-Green Master Mix and analyzed using an ABI Step One Real-Time PCR system (Applied Biosystems, Foster City, CA, USA). GAPDH was used as an internal loading control. Quantitative RT-PCR for KLF4, VEGF and GAPDH was performed using the following primers: KLF4 forward, 5′-CCCACATGAAGCGACTTCCC-3′ and reverse 5′-CAGGTCCAGGAGATCGTTGAA-3′; VEGF forward, 5′-AGGGCAGAATCATCACGAAGT-3′ and reverse 5′-AGGGTCTCGATTGGATGGCA-3′); GAPDH forward, 5′-TCACCAGGGCTGCTTTTAAC-3′ and reverse, 5′-GACAAGCTTCCCGTTCTCAG-3′.

After placing the PCR tubes into the thermal cycler, the process entailed an initial denaturation step at 95°C for 10 min followed by a second step at 95°C for 15 sec and 60°C for 30 sec for 40 cycles with a melting curve analysis. The level of target mRNA was normalized to the level of GAPDH and was compared with the control. For the detection of miR-7, miRNA from cultured cells was extracted by mirVana miRNA Isolation kit (Ambion, Carlsbad, CA, USA) according to the manufacturer's instructions. TaqMan MicroRNA Reverse Transcription kit was used to produce cDNA for TaqMan MicroRNA assay (Applied Biosystems). Human miR-7 expression was quantified in real-time with FAM dye-labeled MGB-probes and normalized to snU6 (Applied Biosystems). Data were analyzed using the ΔΔC_T method.

HUVECs were seeded in a 6-well plate (8×10⁴ cells/well) and transfected with 50 nM miRNA mimics with Lipofectamine 2000 reagent in serum-free medium. After 4 h, the medium was replaced with complete EGM-2 medium. A 96-well plate was coated with 50 µl Matrigel™ (BD Biosciences, San Jose, CA, USA) and incubated for 30 min at 37°C. After incubation for 48 h, the transfected HUVECs were counted, prepared in a cell suspension in EGM-2 medium and seeded on top of the Matrigel™ (7,500 cells/well). After incubation for 17 h, the wells were imaged with a Nikon TE2000 microscope at a magnification of ×10. Tubule formation was quantified by counting the number of branch points in at least three independent wells under similar conditions using NIH ImageJ software.

The cell growth-conditioned medium from the above experiments was collected and analyzed for VEGF levels with immunosorbent assay (ELISA) kits (ACEL, Kanagawa, Japan) according to the manufacturer's instructions. The data are presented as mean ± SEM.

ChIP was performed as previously described (20). Briefly, HUVECs were grown and then washed twice with phosphate-buffered saline (PBS) and cross-linked using 1% formaldehyde for 10 min. Following lysis of the cells and sonication, DNA-protein complexes in the lysates were subjected to immunoprecipitation using anti-KLF4 (HPA002926; Sigma, St. Louis, MO, USA) or control normal IgG. After precipitation of the immunocomplex with protein G-agarose, isolated DNA was used as a template in PCR with specific primers spanning the target region of the VEGF promoter. Primers used for amplification of the human VEGF promoter were as follows: VEGF-1 (−0.6 kb) forward, 5′-GCAGACGGCAGTCACTAGG-3′ and reverse, 5′-CACTCTCGAAGACGCTGCT-3′; VEGF-2 (−3.1 kb) forward, 5′-GAACATTTGGGAAATCTCTTGC-3′ and reverse 5′-TGTGGCTCTGAAGGCAGTT-3′; VEGF-3 (−3.2 kb) forward, 5′-GCCTTGGCCCAATCACTAC-3′ and reverse, 5′-GTGGAGAAAAGTGCGAAAGG-3′.

The cDNA of human transcription factor KLF4 (GenBank: BC030811/029923) was amplified by PCR, cloned into the vector pMD-18T (Takara, Dalian, China) and confirmed by DNA sequencing (20,21). The KLF4 open reading frame (ORF) was then subcloned into the lentiviral vector pLenti-6.3 (Invitrogen). Viral packaging and infection were performed according to the standard protocols as recommended by the manufacturer (Invitrogen).

Total protein was extracted from the cells using lysis buffer containing 20 mM Tris-HCl (pH 7.4), 150 mM NaCl, 5 mM EDTA, 1% Triton X-100, 1% DTT and 1% protease inhibitor cocktail (Roche). Equal amounts of protein extracts (40 µg) were separated by 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto a polyvinylidene fluoride (PVDF) membrane. Membranes were blocked with 5% w/v non-fat dry milk dissolved in Tris-buffered saline plus Tween-20 (TBS-T; 0.1% Tween-20; pH 8.3) at room temperature for 1 h, then incubated with primary antibodies at 4°C overnight. The primary antibodies used were rabbit anti-KLF4 and anti-β-actin (Sigma). After washing with TBS-T, the membranes were incubated with horseradish peroxidase (HRP)-labeled secondary antibodies (Sigma) for 30-45 min at room temperature. Immunobands were visualized using enhanced chemiluminescence (ECL) kit (GE Healthcare, Waukesha, WI, USA) according to the manufacturer's instructions and exposed to X-ray film. β-actin was used as a loading control.

All statistical analyses were performed using the GraphPad Prism software, version 4 (GraphPad Software, San Diego CA, USA). Data are expressed as mean ± SEM. Comparison of the means was performed using two-sided Student's t-test and a P<0.05 value was considered to indicate a statistically significant result.

We assessed the role of miR-7 in the angiogenesis of HUVECs by first transfecting HUVECs with a miR-7 inhibitor (miR-7 ASO). As shown in Fig. 1A, transient transfection of miR-7 ASO significantly decreased the miR-7 expression compared with that of the control. The tube formation assay was performed to evaluate the effect of miR-7 on the angiogenic potential of HUVECs. Knockdown of miR-7 significantly induced the tube formation of HUVECs (Fig. 1B and C) suggesting that miR-7 inhibition resulted in enhanced angio-genesis in the HUVECs.

VEGF plays a key role in endothelial cell migration and proliferation, and angiogenesis. We consequently assessed the VEGF expression following miR-7 inhibition. qRT-PCR analyses showed that VEGF mRNA levels were significantly increased in the HUVECs treated with miR-7 ASO (Fig. 1D). ELISA analyses further demonstrated significantly upregulated VEGF protein levels in the cell culture medium from the HUVECs treated with miR-7 ASO (Fig. 1E). Previous studies indicated that KLF4 is overexpressed in ECs and plays an important role in angiogenesis (15,16). We further assessed the KLF4 expression following miR-7 inhibition in the HUVECs and found that the mRNA levels of KLF4 were significantly induced by miR-7 ASO (Fig. 1D). Similarly, the KLF4 protein level was markedly upregulated in the HUVECs treated with miR-7 ASO (Fig. 1F). These results demonstrated that downregulation of miR-7 promoted angiogenesis of HUVECs, accompanied by the upregulation of the expression of VEGF and KLF4.

To explore the mechanism associated with the downregulation of miR-7 in angiogenesis, we searched for potential miR-7 target genes using miRNA target prediction tools, including TargetScan, PicTar and miRanda (22). We found that KLF4 is a potential miR-7 target. Previous studies have shown that KLF4 is a central regulator of sprouting angiogenesis via the Notch signaling pathway (20), and promoted epithelial cell transformation via targeting KLF4. These data suggested that miR-7 may inhibit angiogenesis by targeting KLF4 in HUVECs. To test this hypothesis, we analyzed the expression of KLF4 in HUVECs transfected with control or miR-7 mimics. Western blot analysis showed that miR-7 mimics decreased expression of KLF4 (Fig. 2A). Furthermore, qRT-PCR analysis revealed that the levels of KLF4 mRNA were obviously decreased in the HUVECs transfected with the miR-7 mimics (Fig. 2B). These results suggest that miR-7 may negatively regulate KLF4 expression by disrupting the stability of KLF4 mRNA.

To confirm that KLF4 is a direct target of miR-7, we constructed luciferase reporters with the KLF4 3′-UTR containing a miR-7 binding site (Fig. 2C). The constructs were transiently transfected into HUVECs along with miR-7 or NC mimics and the relative luciferase activity was measured at 48 h. The relative luciferase activity of the construct with wild-type 3′-UTR was significantly repressed by 60% following miR-7 mimic transfection (Fig. 2D). However, site-directed mutagenesis of the miR-7 binding site within the 3′-UTR of KLF4 completely abolished this suppression (Fig. 2D), indicating that miR-7 directly binds to this site in HUVECs.

KLF4 is a transcription factor. The simultaneous promotion of the expression of KLF4 and VEGF in HUVECs after miR-7 inhibition suggests that KLF4 may promote VEGF transcription. Indeed, bioinformatic analysis identified the presence of multiple DNA-binding elements of the KLF4 transcription factor in the VEGF promoter (Fig. 3A). We then performed a ChIP and found that the KLF4 antibody specifically pulled down the VEGF promoter in the HUVECs (Fig. 3B). We next overexpressed KLF4 by infecting HUVECs with a lentivirus cloned with KLF4 (Lv-KLF4). Compared with the control lentivirus (Lv-Luc), infection of Lv-KLF4 significantly increased the mRNA (Fig. 3C) and protein level (Fig. 3D) of KLF4 in the HUVECs. As expected, ectopic overexpression of KLF4 significantly induced the VEGF mRNA levels in the HUVECs treated with miR-7 ASO (Fig. 3E), and the concentration of VEGF protein in the cell culture medium from HUVECs treated with miR-7 ASO (Fig. 3F). These results indicate that KLF4 playsed a direct role in the transcriptional regulation of VEGF.

Our observations showed that KLF4 is a functional target of miR-7 and transcriptional activator of VEGF, which promotes angiogenesis, suggesting that knockdown of KLF4 may attenuate angiogenesis induced by miR-7 inhibition. We tested this hypothesis by transfecting exogenous KLF4 short hairpin RNA into the miR-7-transfected HUVECs using a previously described transient transfection system (11). KLF4 silencing significantly abolished the induction of VEGF mRNA in the HUVECs treated with miR-7 ASO (Fig. 4A) and the concentration of VEGF protein in the cell culture medium from HUVECs treated with miR-7 ASO (Fig. 4B). Consistent with the key function of VEGF in angiogenesis, KLF4 knockdown significantly prevented the induction of angiogenesis by the miR-7 inhibitor in the HUVECs (Fig. 4C and D). Taken together, the results indicate that KLF4 knockdown abrogates miR-7-knockdown-induced angiogenesis, suggesting that KLF4 is a functional mediator of miR-7 in the regulation of angiogenesis in HUVECs.