miR-24-3p Controls Growth and Development of Chicken Muscle Fat Cells by Blocking ANXA6

All animal experiments in this study were approved by the Institutional Animal Care and Use Committee of Sichuan Agricultural University (approval no. DKY2020202025). A total of 200 female Daheng broilers were raised at the Sichuan Daheng Poultry Breeding Co., Ltd. (Chengdu, China) to obtain breast muscle at age of 60 day, 90 day, 120 day, 150 day, 180 day, 240 day, and 300 day. Eleven tissue samples, including heart, liver, kidney, breast muscle, leg muscle, subcutaneous fat, abdominal fat, brain, gizzard, glandular stomach, and small intestine, were collected from three 90-day-old female Daheng broilers. These samples were stored immediately in liquid nitrogen for further analysis. Besides, sufficient 14-day-old chicks were prepared for primary intramuscular preadipocytes isolation. All experimental birds were euthanized by cervical dislocation.

Primary intramuscular preadipocytes were isolated from breast muscle tissues of 14-day-old chicks. Briefly, after removing the fascia and connective tissues, breast muscles were cut to pieces by ophthalmic scissors. Collagenase type I and type II (Biofroxx, Heidelberg, Germany) were used to digest tissue homogenate for 1.5 h, which were then passed through cell strainers (Biologix, Jinan, China) with pore sizes of 70 μm and 45 μm. The cell precipitate was gained via centrifugation at 1000 r/min for 10 min. Subsequently, these cells were maintained in DMEM/F12 medium (Gibco, Grand Island, NY, USA) supplemented with 10% fetal bovine serum (Hyclone, Logan, UT, USA) and 1% penicillin/streptomycin (Invitrogen, Carlsbad, CA, USA) in an incubator with 37 °C, 5% CO₂, and a humidified atmosphere. Because the adherent time of muscle satellite cells exceeded 3 h, after differential adherence for 2 h, the supernatant was removed and replaced with fresh complete medium to obtain relatively pure preadipocytes. Once the preadipocytes grew confluent, a differentiation medium containing 10 μg/mL insulin, 250 μM oleic acid, 0.5 mM 3-isobutyl-1-methylxanthine, and 1 μM dexamethasone was replaced to induce differentiation for 2 day. Then, a maintenance medium containing 10 μg/mL insulin and 250 μM oleic acid was replaced to maintain differentiation for 2 day. Finally, the complete medium was replaced every 2 day until the cells were differentiated into mature adipocytes. The differentiation time lasts for 10 day. All trials performed on cells contained at least three biological replicates.

Briefly, the RNA oligonucleotides or plasmids were diluted in Lipofectamine 3000 (Invitrogen, Carlsbad, CA, USA) and Opti-MEM medium (Gibco, Grand Island, NY, USA) according to the manufacturer’s instructions. Then, these mixed liquids were added to cell culture plates of different specifications in corresponding proportions. After incubation for 6–8 h, fresh complete medium was replaced in the cell culture plates. RNA oligonucleotides for miR-24-3p, including mimics of the negative control (NC), miR-24-3p mimics, inhibitor NC, and miR-24-3p inhibitor, as well as three small interfering RNAs (siRNAs) for ANXA6, were designed and synthesized by GenePharma (Shanghai, China) (Supplementary Table S1). Overexpression vector pcDNA3.1+ANXA6 was constructed by two restriction enzymes, BamHI and XhoI.

Total RNA was extracted from cells and tissues using Trizol reagent (TaKaRa, Dalian, China), and its concentration and purity were determined by NanoDrop 2000C spectrophotometer (Thermo, San Jose, CA, USA). Subsequently, cDNA was synthesized through reverse transcription of mRNA by PrimeScript RT Reagent Kit (TaKaRa, Dalian, China). CFX Connect Real-Time System was used to conduct quantitative real-time PCR (qPCR). Relative expression was calculated by the 2^−ΔΔCt method, with GAPDH and U6 being reference gene. All the primers used in qPCR assay were devised from Prime Premier 6 (Premier Biosoft, Palo Alto, CA, USA) and presented in Supplementary Table S2.

Total protein was extracted from cells transfected for 48 h using the Total Protein Extraction Kit (BestBio, Shanghai, China). The concentration of protein samples was detected and homogenized by BCA Protein Quantitative Kit (BestBio, Shanghai, China). Then, briefly, about 25 μg of the protein sample was separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The region containing the target protein was isolated and transferred to polyvinylidene fluoride membranes. After blocking with blocking buffer (Beyotime, Haimen, China) on a decolorization shaker for 1 h at room temperature, the membranes were incubated with primary antibodies overnight at 4 °C, including anti-β-Tubulin (ZenBio, Chengdu, China; 1:5000 dilution), anti-CDK2 (ZenBio, Chengdu, China; 1:1000 dilution), anti-PCNA (ZenBio, Chengdu, China; 1:1000 dilution), anti-PPARγ (ABclonal, Wuhan, China; 1:1000 dilution), and anti-FASN (ZenBio, Chengdu, China; 1:1000 dilution). Subsequently, western wash buffer (Beyotime, Haimen, China) was used to wash the membranes for three times. Secondary antibodies, horseradish peroxidase-conjugated IgG of anti-mouse (ZenBio, Chengdu, China; 1:5000 dilution) or anti-rabbit (ABclonal, Wuhan, China; 1:2000 dilution), were used to incubate the membranes for 1 h at 4 °C. Finally, the Ultra Hypersensitive ECL Chemiluminescence Kit (Beyotime, Haimen, China) was used to visualize the specific protein bands, whose quantitative analysis was performed by Image J 1.8 software.

Intramuscular preadipocytes were cultured in 96-well plates. After transfection, cell proliferation was monitored using the Cell Counting Kit-8 (Meilun, Dalian, China). Specifically, 10 µL of CCK-8 reagent was added to incubate the cells for 2 h. Optical density (OD) value in each well was detected by Microplate Reader (Thermo, San Jose, CA, USA) at 450 nm after transfection of 12 h, 24 h, 36 h, and 48 h.

EdU assay was performed on preadipocytes plated in 96-well plates by Cell-Light EdU Apollo567 In Vitro Kit (RiboBio, Guangzhou, China) according to the manufacturer’s protocol after transfection for 12 h. Briefly, 50 μM EdU reagent was added to each well and incubated for 2 h at 37 °C. Cell nuclei were stained by Hoechst 33342 reagent. Biological microscope (Olympus, Tokyo, Japan) was used to capture randomly selected fields, with the number of EdU positive cells and total cells being counted using Image-Pro Plus 6.0 software (Media Cybernetics, Rockville, MD, USA).

After transfection for 48 h, preadipocytes in 6-well plates were induced to mature adipocytes for 10 d. Subsequently, the adipocytes were washed with PBS once and fixed with 4% paraformaldehyde for 30 min. Fixed cells were washed with distilled water twice, soaked with 60% isopropanol for 5 min, and dyed with Oil Red O (Solarbio, Beijing, China) for 20 min. Then, they were washed with distilled water five times. IX53 biological microscope (Olympus, Tokyo, Japan) was used to capture images of stained cells. In order to quantify lipid droplets, 100% isopropanol was used to dissolve Oil Red O in each well. Finally, OD value was detected at 510 nm.

The upstream miRNAs of ANXA6 were predicted with miRDB 6.0 software. A complementary pattern diagram of the miR-24-3p and ANXA6 3′UTR region was created by RNAhybrid 2.1 software. Dual-luciferase reporter assay was performed in chicken embryo fibroblast line (DF-1 cells). Briefly, the DF-1 cells cultured in 48-well plates were co-transfected with reporter vector (ANXA6 3′UTR wild type or mutant type) and mimics NC or miR-24-3p mimics. Following transfection for 48 h, luciferase activity was detected using the Dual Luciferase Reporter Gene Assay Kit (Beyotime, Haimen, China) according to the manufacturer’s instructions.

All data are displayed as mean ± standard error (SEM). One-way ANOVA analysis or unpaired Student’s t-test was conducted by SPSS 26.0 software, with the Tukey–Kramer method being used for multiple comparisons. The significant levels were regarded as * p < 0.05, ** p < 0.01, and ^a–dp < 0.05.

The tissue expression profile of ANXA6 in broilers was investigated by qPCR assay, which presented that ANXA6 was enriched in gizzard, and also highly expressed in subcutaneous fat, abdominal fat, as well as liver (Figure 1A). We determined the mRNA levels of ANXA6 in chicken breast muscle from 60 d to 300 d after hatching. The results suggested that ANXA6 reached the highest expression in breast muscle of 90 d and 180 d broilers (Figure 1B). Subsequently, we detected the expression of ANXA6 during the differentiation process of chicken intramuscular preadipocytes into mature adipocytes, showing that ANXA6 expression hit peak levels on the second day after differentiation, and then decreased gradually (Figure 1C).

To explore the effects of ANXA6 on chicken intramuscular preadipocytes, the cells were transfected with overexpression vector (pcDNA3.1+ANXA6) or siRNAs (siRNA-ANXA6-1, siRNA-ANXA6-2, and siRNA-ANXA6-3). The expression of ANXA6 was raised in the overexpression group more than 100 times compared with the control group (Figure 2A). Contrarily, both siRNA-ANXA6-1 and siRNA-ANXA6-3 significantly attenuated the mRNA levels of ANXA6, with siRNA-ANXA6-3 possessing the highest interference efficiency of 44.7% (Figure 2B). The mRNA levels of cell-proliferation-related genes (MKI67 and CDK2) were reduced or increased after overexpression or interference of ANXA6 (Figure 2C,D), so did the protein levels of CDK2 and PCNA (Figure 2E,F,L). Nevertheless, the change of PCNA protein expression was not significant after ANXA6 interference. CCK-8 assay suggested that cell proliferation was inhibited following ANXA6 overexpression (Figure 2G) but promoted following ANXA6 knockdown (Figure 2H). EdU assay indicated that EdU positive cell ratio was decreased or increased after ANXA6 overexpression or interference (Figure 2I–K). Together, these results revealed that ANXA6 inhibits the proliferation of chicken intramuscular preadipocytes.

The expression of adipogenic genes (CEBPA, ADIPOQ, FASN, and ACACA) was measured in chicken intramuscular preadipocytes following transfection. The results demonstrated that the mRNA levels of CEBPA and FASN were ascended after ANXA6 overexpression (Figure 3A), while ANXA6 knockdown reduced the mRNA levels of CEBPA, ADIPOQ, FASN, and ACACA (Figure 3B). The protein levels of FASN also showed a similar trend (Figure 3C–E). However, PPARγ protein expression remained stable whether overexpression or interference of ANXA6. After preadipocytes were induced to differentiation for 10 d, we stained them with Oil red O, which showed that the formation of lipid droplets increased following ANXA6 overexpression but decreased following ANXA6 knockdown (Figure 3F,G). The determination of OD values at 510 nm further confirmed the above results (Figure 3H). All these results proved that ANXA6 promotes the differentiation of chicken intramuscular preadipocytes.

Through applying miRDB software for bioinformatic analysis, we discovered that miR-24-3p is an upstream regulatory miRNA of ANXA6. The seed region of miR-24-3p is evolutionarily conserved and complementary to the 3′UTR of ANXA6 (Figure 4A,B). The mRNA levels of ANXA6 were decreased following transfection of miR-24-3p mimics but raised following transfection of both miR-24-3p mimics and ANXA6 overexpression vector (Figure 4C) or miR-24-3p inhibitor (Figure 4D). Dual-luciferase reporter assay indicated that miR-24-3p mimics significantly restrained the luciferase activity of ANXA6 wild-type plasmid compared with mimics NC (Figure 4E), presenting that miR-24-3p can directly bind to the 3′UTR of ANXA6.

To explore the effects of miR-24-3p on chicken intramuscular preadipocytes, the cells were transfected with miR-24-3p mimics or inhibitor. The expression of miR-24-3p was raised more than 140 times in the mimics group compared with the NC group (Figure 5A) and the interference efficiency achieved 95.7% (Figure 5B). The mRNA levels of MKI67 and CDK2 were increased following transfection of miR-24-3p mimics but decreased following transfection of both miR-24-3p mimics and ANXA6 overexpression vector (Figure 5C) or miR-24-3p inhibitor (Figure 5D). The same phenomenon was observed in the protein levels of CDK2 and PCNA, although the change of CDK2 protein expression was not significant in the mimics group compared with co-transfection group and the change of PCNA protein expression was not significant in the inhibitor group compared with the NC group (Figure 5E–G). The CCK-8 assay showed that cell proliferation was promoted after transfection of miR-24-3p mimics (Figure 5H) but inhibited after transfection of both miR-24-3p mimics and ANXA6 overexpression vector (Figure 5I) or miR-24-3p inhibitor (Figure 5J). EdU assay suggested that EdU positive cell ratio was raised following transfection of miR-24-3p mimics but reduced following transfection of both miR-24-3p mimics and ANXA6 overexpression vector or miR-24-3p inhibitor (Figure 5K–M). Thus, we speculated that miR-24-3p promotes the proliferation of chicken intramuscular preadipocytes through targeting ANXA6.

The qPCR results demonstrated that the expression of CEBPA, ADIPOQ, FASN, and ACACA were inhibited following transfection of the miR-24-3p mimics but promoted following transfection of both the miR-24-3p mimics and ANXA6 overexpression vector (Figure 6A) or the miR-24-3p inhibitor (Figure 6B). The protein levels of FASN showed the same trend as the above results (Figure 6C–E). Nevertheless, the protein levels of PPARγ were not significantly influenced whether transfection of the miR-24-3p mimics, both the miR-24-3p mimics and the ANXA6 overexpression vector, or the miR-24-3p inhibitor. Oil red O staining presented that the formation of lipid droplets decreased after transfection of the miR-24-3p mimics but decreased after transfection of both the miR-24-3p mimics and the ANXA6 overexpression vector (Figure 6F) or the miR-24-3p inhibitor (Figure 6G), which was in accordance with the results of the OD value determination at 510 nm (Figure 6H).