Upregulation of miR-376c-3p alleviates oxygen–glucose deprivation-induced cell injury by targeting ING5
The expression level of miR-376c-3p is significantly lower in infants with neonatal hypoxic-ischemic encephalopathy (HIE) than in healthy infants. However, the biological function of this microRNA remains largely elusive.
We used PC-12 and SH-SY5Y cells to establish an oxygen–glucose deprivation (OGD) cell injury model to mimic HIE in vitro. The miR-376c-3p expression levels were measured using quantitative reverse transcription PCR. The CCK-8 assay and flow cytometry were utilized to evaluate OGD-induced cell injury. The association between miR-376c-3p and inhibitor of growth 5 (ING5) was validated using the luciferase reporter assay. Western blotting was conducted to determine the protein expression of CDK4, cyclin D1, Bcl-2 and Bax.
MiR-376c-3p was significantly downregulated in the OGD-induced cell injury model. Its overexpression elevated cell viability and impaired cell cycle G0/G1 phase arrest and apoptosis in PC-12 and SH-SY5Y cells after OGD. Downregulation of miR-376c-3p gave the opposite results. We further demonstrated that ING5 was a negatively regulated target gene of miR-376c-3p. Importantly, ING5 knockdown had a similar effect to miR-376c-3p-mediated protective effects against cell injury induced by OGD. Its overexpression abolished these protective effects.
Our data suggest that miR-376c-3p downregulated ING5 to exert protective effects against OGD-induced cell injury in PC-12 and SH-SY5Y cells. This might represent a novel therapeutic approach for neonatal HIE treatment.
KeywordsmiR-376c-3p Oxygen–glucose deprivation ING5 Cell cycle Apoptosis
Cell Counting Kit-8
Dulbecco’s modified Eagle medium
fetal bovine serum
Neonatal hypoxic-ischemic encephalopathy
horse radish peroxidase
inhibitor of growth family member 5
sodium dodecyl sulfate-polyacrylamide gel electrophoresis
Neonatal hypoxic-ischemic encephalopathy (HIE), which is also known as neonatal stroke, is caused by a disruption of cerebral blood vessels and leads to hypoxic or ischemic injury . It is considered a major cause of disability in children after the neonatal period, with 0.1–0.2% incidence in term or near-term infants [2, 3]. Up to 40% of HIE patients usually suffer from devastating disability, including cerebral palsy, mental retardation, epilepsy and learning impairment [4, 5, 6]. Therapeutic hypothermia is the only recognized treatment for HIE, but it needs to be applied within 6 h of birth in a tertiary care center, which limits its application [7, 8]. Thus, it is important to better understand the molecular mechanisms of HIE.
MicroRNAs (miRNAs or miRs) are small endogenous non-coding RNAs that regulate a wide variety of biological processes, including differentiation, proliferation and apoptosis, by targeting mRNAs [9, 10, 11]. In recent years, researchers have found that miRs are closely associated with the pathogenesis of hypoxic-ischemic diseases. For example, miR-29b promotes neurocyte apoptosis by targeting MCL-1 during cerebral ischemia/reperfusion (I/R) . MiR-451 has been reported to target CELF2, protecting against apoptosis and oxidative stress induced by oxygen and glucose deprivation/reoxygenation (OGD/R) . Most recently, O′ Sullivan et al. found that the expression levels of three miRs (miR-374a-5p, miR-376c-3p and miR-181b-5p) are significantly lower in infants diagnosed with HIE than in healthy control infants . This was determined by performing miRNA profile pattern analysis in umbilical cord whole blood.
Notably, miR-376c-3p has been shown to regulate cell growth, proliferation and migration in different cancer types [15, 16]. We thus speculated that miR-376c-3p might play an important role in neuronal cell survival under ischemic conditions.
The inhibitor of growth family member 5 (ING5) is composed of four molecular domains: a nuclear localization signal (NLS), a novel conserved region (NCR), a leucine zipper-like (LZL) domain, and a plant homeodomain (PHD) . A related study indicated that ING5 is a key factor in DNA replication, cell cycle regulation and apoptosis . ING5 overexpression could decrease cell proliferation and induce apoptosis in lung cancer  and esophageal squamous cell carcinoma . Interestingly, Zhu et al. reported that ING5 suppresses cell viability and promotes cell apoptosis in human pulmonary artery smooth muscle cells under hypoxic conditions . This highlights its potential for the treatment of hypoxic pulmonary hypertension. These results suggest that targeting ING5 might be beneficial for developing novel therapeutic strategies for HIE injury.
In this study, we constructed an OGD cellular model as the most commonly applied in vitro model of HIE [22, 23] to investigate the functional significance of miR-376c-3p in regulating neuron survival. Here, PC-12 [24, 25, 26, 27] and SH-SY5Y  cells were used to construct an OGD cell injury model to mimic HIE. We confirmed whether miR-376c-3p exerted protective effects on OGD-injured cells. Furthermore, we explored the molecular mechanisms underlying miR-376c-3p in OGD cell injury.
Materials and methods
PC-12 cells and SH-SY5Y cells were purchased from the American Type Culture Collection (ATCC) and cultured in Dulbecco’s modified Eagle medium (DMEM; HyClone) supplemented with 10% fetal bovine serum (FBS; Gibco). The culture was maintained at 37 °C in a humidified incubator containing 5% CO2.
OGD cell injury model
Cells were cultured in glucose-free culture medium and placed into a hypoxia incubator with 94% N2, 5% CO2, 1% O2 for 2 h at 37 °C. Growth medium containing glucose was used to replace the culture medium and cells were cultured at 37 °C under normal conditions in an atmosphere with 5% CO2.
MiR-376c-3p mimic (mimic), miR-NC, anti-miR-376c-3p, anti-miR-NC, small interfering RNA targeting ING5 (si-ING5) and si-NC were all synthesized by GenePharma. The open reading frame of ING5 without its 3′-UTR was inserted into pcDNA3.1 vector (Sangon Biotech) to produce pcDNA3.1/ING5 vector. Lipofectamine 2000 (Invitrogen) was used to perform cell transfection prior to OGD.
Quantitative reverse transcription PCR
Total RNA was isolated using Trizol Reagent and RNA was reverse transcribed using the TaqMan MicroRNA Reverse Transcription Kit or AMV reverse transcriptase random primers (Sigma-Aldrich) according to the manufacturer’s instructions. PCR was performed using TaqMan Universal Master Mix II (Sigma-Aldrich) for miR-376c-3p or SYBR Premix Ex Taq II kit (Takara) for ING5 with the following primer sequences: miR-376c-3p forward: 5′-AACATAGAGGAAATTCCACG-3′ and reverse: 5′-CAGTGCGTGTCGTGGAGT3′; U6 forward: 5′-CTCGCTTCGGCAGCACA-3′ and reverse: 5′-AACGCTTCACGAATTTGCGT-3′; ING5 forward: 5′-GGGAGATGATTGGCTGTG-3′ and reverse: 5′-CCTTTGGGTTTCGTGGTA-3′; GAPDH forward: 5′-AGAAGGCTGGGGCTCATTTG-3′ and reverse: 5′-CGATCCACACGGAGTACTTGC-3′.
The PCR amplification parameters were: 95 °C for 5 min, followed by 40 cycles of 95 °C for 15 s, 60 °C for 30 s and 72 °C for 30 s. The relative expression levels of miR-376c-3p and ING5 were calculated using the 2−ΔΔCt method  with the respective internal controls U6 and GAPDH.
Cell viability assay
Cells from different groups were seeded into 96-well plates (4 × 103 cells per well) and incubated with 10 μl CCK-8 solution (Dojindo Laboratories) for 1 h. Using a Bio-Rad Microplate Reader, we measured the optical density values at 450 nm and used them to calculate relative cell viability in experimental groups compared with the control group.
Flow cytometry analysis
Cells were collected and fixed at 4 °C with cold ethanol overnight. After two washes in phosphate-buffered saline (PBS), the cells were re-suspended in 200 μl binding buffer, followed by staining with 400 μl PI (BestBio) for 30 min in the dark. Next, the cell cycle distribution was analyzed via flow cytometry with FlowJo software (BD Bioscience).
To assess cell apoptosis, cells were collected, re-suspended and stained with Annexin V-FITC and PI (BestBio) for 20 min in the dark at room temperature. The numbers of early (Annexin V+/PI-), late (Annexin V+/PI+) and total apoptotic cells were determined using a flow cytometer equipped with CellQuest Pro software (BD Bioscience).
Luciferase reporter assay
TargetScan Bioinformatics software (www.targetscan.org/vert_72) was searched to seek the putative target genes associated with the effects of miR-376c-3p on cell growth. For the luciferase reporter assay, the wild-type (WT) or mutant (MUT) 3′-untranslated region (3′-UTR) of ING5 was cloned into the pmirGLO dual luciferase reporter vectors (Promega) by RIBOBIO. These were transfected into HEK293T cells with mimic or miR-NC using Lipofectamine 2000 (Invitrogen). Cells were harvested after 48 h transfection and relative luciferase activities were determined using the Dual-Luciferase Reporter Assay System (Promega).
Western blot analysis
RIPA lysis buffer and enhanced BCA Protein Assay kit (Beyotime) were respectively used to extract total protein and determine protein concentration. Approximately 30 μg of protein samples were separated using sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) with 12% sodium dodecyl gel. The separated protein was transferred onto PVDF membranes where it underwent blocking with 5% nonfat milk for 2 h. Subsequently, the membranes were incubated with anti-ING5 and anti-GAPDH (Abcam) overnight at 4 °C, followed by incubation with horse radish peroxidase-labeled secondary antibody for 2 h at room temperature. The protein bands were visualized with GAPDH as an internal control using enhanced chemiluminescence (Pierce).
Quantitative data were expressed as means ± SD from at least three experiments. GraphPad Prism 6.0 Software was used to perform statistical analysis. Differences were evaluated using Student’s t-test (2 groups) and one-way ANOVA followed by a Bonferroni post-hoc test (multiple groups). Values of p less than 0.05 were considered to be statistically significant.
The levels of miR-376c-3p decrease in the OGD-induced cell injury model
Then, we evaluated the OGD cell injury model. The CCK-8 assay showed that the cell viability of PC-12 and SH-SY5Y cells decreased significantly after OGD (Fig. 1b, p < 0.01). Moreover, the percentages of PC-12 cells and SH-SY5Y cells in G0/G1 phase increased significantly (p < 0.01), while the percentages of those in G2/M phase and S phase decreased after OGD (p < 0.01), indicating that OGD induced cell cycle G0/G1 phase arrest (Fig. 1c).
Furthermore, the percentage of apoptotic cells was remarkably elevated in the OGD group compared with the control group in both PC-12 and SH-SY5Y cells (Fig. 1d). These results reveal that downregulation of miR-376c-3p might play an important role in the OGD-induced cell injury model.
MiR-376c-3p significantly attenuates OGD-induced injury
We further confirmed the protective role of miR-376c-3p against OGD-induced injury with loss-of-function assays. Anti-miR-376c-3p transfection significantly suppressed the expression of miR-376c-3p in PC-12 cells (Fig. 2e). As expected, downregulation of miR-376c-3p promoted OGD-induced impaired cell viability (Fig. 2f), cell cycle G0/G1 phase arrest (Fig. 2g) and apoptosis (Fig. 2h) in PC-12 cells. These results suggest that miR-376c-3p exerts protective effects against OGD-induced injury.
ING5 is directly targeted by miR-376c-3p
The luciferase reporter assay was conducted to confirm direct target binding. Overexpression of miR-376c-3p significantly decreased the luciferase activity of a reporter vector containing the WT ING5 3′-UTR, but did not affect the luciferase activity of a reporter vector containing MUT ING5 3′-UTR in HEK293T cells (Fig. 3b, p < 0.01).
Subsequently, we analyzed the expression of ING5 in the OGD cell injury model using western blot analysis. The protein expression of ING5 was obviously elevated after OGD treatment in both PC-12 and SH-SY5Y cells (Fig. 3c). Furthermore, we demonstrated that overexpression of miR-376c-3p significantly decreased the mRNA (Fig. 3d) and protein (Fig. 3e) expression of ING5 in the OGD-induced PC-12 and SH-SY5Y cell injury model. By contrast, downregulation of miR-376c-3p elevated the mRNA (Fig. 3f) and protein (Fig. 3g) expression of ING5 in PC-12 cells. These results show that ING5 might be a direct target gene of miR-376c-3p.
Knockdown of ING5 and miR-376c-3p overexpression have similar protective effects against OGD-induced injury
Restoration of ING5 expression reverses the protective effect of miR-376c-3p against OGD-induced injury
MiR-376c-3p regulates cell cycle arrest and apoptosis-associated factors by targeting ING5 in the OGD-induced cell injury model
MiR-376c-3p levels are significantly lower in infants diagnosed with HIE than in healthy control infants . Consistently, we found that miR-376c-3p is significantly downregulated in response to OGD treatment. By performing gain-of-function and loss-of-function assays, we further found that miR-376c-3p significantly attenuates OGD-induced injury. The underlying mechanism for this might be reversal of cell cycle G0/G1 phase arrest and apoptosis, as confirmed by the upregulation of CDK4, cyclin D1 and Bcl-2 and downregulation of Bax after miR-376c-3p overexpression. Various studies have shown that miR-376c-3p is involved in regulating cell proliferation, cell cycle and apoptosis in neuroblastoma cells , gastric cancer  and hepatocellular carcinoma . From this evidence, we hypothesized that miR-376c-3p might play a neuroprotective role in OGD-induced cell injury.
ING5 is the last member of the ING candidate tumor suppressor family that has been implicated in multiple cellular functions, including cell cycle regulation, apoptosis and chromatin remodeling . Wu et al.  found that ING5 overexpression inhibits tumor growth in SH-SY5Y cells by suppressing proliferation and inducing apoptosis. In addition, ING5 has been reported as a potential target for breast cancer  and gastric cancer  treatment.
Our data show that the protein expression of ING5 is obviously elevated in OGD-induced cell injury. ING5 consistently and significantly aggravated hypoxic human pulmonary artery smooth muscle cells . In fact, miRNA directly binds to the 3′-UTR of target mRNAs via complementary pairing sequences to induce their degradation .
We then explored whether ING5 is the downstream target gene of miR-376c-3p in OGD-induced cell injury. As expected, we found miR-376c-3p directly binds to the 3′-UTR of ING5. Moreover, ING5 knockdown imitated and ING5 overexpression reversed the protective effect of miR-376c-3p against OGD-induced injury. Furthermore, the regulatory effects of miR-376c-3p on CDK4, cyclin D1, Bcl-2 and Bax were abolished by ING5 overexpression. Similarly, ING5 is a target gene of miR-196a and suppresses head and neck cancer cell survival and proliferation . Based on these data, we speculate that miR-376c-3p may downregulate ING5 expression in OGD-induced injury by regulating cell cycle and apoptosis-associated factors.
Our experiments have confirmed our initial hypothesis that miR-376c-3p affects OGD-induced cell injury by targeting ING5. This study provides a theoretical basis for further investigation into the protection of neurons against OGD-induced injury. Of course, the impacts of other miRNAs on more target genes for HIE will be explored in future studies.
The study was supported by the Department of Pediatrics, Renmin Hospital of Wuhan University, Hubei Province, China.
HB conceived and designed the study. ZH and ZJ performed the experiments. ZMX analyzed the data. ZMX and YYJ wrote and edited the manuscript. All authors read and approved the final manuscript.
This study was supported by grant from the Applied Basic Research in Wuhan (no. 2017060201010211).
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
- 2.Rao R, Trivedi S, Vesoulis Z, Liao SM, Smyser CD, Mathur AM. Safety and short-term outcomes of therapeutic hypothermia in preterm neonates 34–35 weeks gestational age with hypoxic-ischemic encephalopathy. J Pediatr. 2017;183:37–42. https://doi.org/10.1016/j.jpeds.2016.11.019.CrossRefPubMedGoogle Scholar
- 3.Rong Z, Pan R, Chang L, Lee W. Combination treatment with ethyl pyruvate and IGF-I exerts neuroprotective effects against brain injury in a rat model of neonatal hypoxic-ischemic encephalopathy. Int J Mol Med. 2015;36:195–203. https://doi.org/10.3892/ijmm.2015.2219.CrossRefPubMedPubMedCentralGoogle Scholar
- 14.O’Sullivan MP, Looney AM, Moloney GM, Finder M, Hallberg B, Clarke G, Boylan GB, Murray DM. Validation of altered umbilical cord blood microRNA expression in neonatal hypoxic-ischemic encephalopathy. JAMA Neurol. 2019;76(3):333–41. https://doi.org/10.1001/jamaneurol.2018.4182.CrossRefPubMedGoogle Scholar
- 20.Zhang GJ, Zhao J, Jiang ML, Zhang LC. ING5 inhibits cell proliferation and invasion in esophageal squamous cell carcinoma through regulation of the Akt/NF-kappaB/MMP-9 signaling pathway. Biochem Biophys Res Commun. 2018;496:387–93. https://doi.org/10.1016/j.bbrc.2018.01.045.CrossRefPubMedGoogle Scholar
- 23.Garnier Y, Middelanis J, Jensen A, Berger R. Neuroprotective effects of magnesium on metabolic disturbances in fetal hippocampal slices after oxygen-glucose deprivation: mediation by nitric oxide system. J Soc Gynecol Investig. 2002;292:86–92.Google Scholar
- 26.Li J, Qu Y, Chen D, Zhang L, Zhao F, Luo L, Pan L, Hua J, Mu D. The neuroprotective role and mechanisms of TERT in neurons with oxygen-glucose deprivation. Neuroscience. 2013;252:346–58. https://doi.org/10.1016/j.neuroscience.2013.08.015.CrossRefPubMedGoogle Scholar
- 30.Tu L, Zhao E, Zhao W, Zhang Z, Tang D, Zhang Y, Wang C, Zhuang C, Cao H. hsa-miR-376c-3p regulates gastric tumor growth both in vitro and in vivo. BioMed Res Int. 2016;2016:1–7.Google Scholar
- 33.Gou WF, Shen DF, Yang XF, Zhao S, Liu YP, Sun HZ, Su RJ, Luo JS, Zheng HC. ING5 suppresses proliferation, apoptosis, migration and invasion, and induces autophagy and differentiation of gastric cancer cells: a good marker for carcinogenesis and subsequent progression. Oncotarget. 2015;6:19552–79. https://doi.org/10.18632/oncotarget.3735.CrossRefPubMedPubMedCentralGoogle Scholar
- 34.Qin X, Guo H, Wang X, Zhu X, Yan M, Wang X, Xu Q, Shi J, Lu E, Chen W, Zhang J. Exosomal miR-196a derived from cancer-associated fibroblasts confers cisplatin resistance in head and neck cancer through targeting CDKN1B and ING5. Genome Biol. 2019;20:12. https://doi.org/10.1186/s13059-018-1604-0.CrossRefPubMedPubMedCentralGoogle Scholar
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.