Protective role of microRNA-9-5p in oxygen glucose deprivation/reperfusion-induced injury in liver sinusoidal endothelial cell

doi:10.21203/rs.3.rs-19922/v1

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Protective role of microRNA-9-5p in oxygen glucose deprivation/reperfusion-induced injury in liver sinusoidal endothelial cell

https://doi.org/10.21203/rs.3.rs-19922/v1

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Background: Maintenance of the function and survival of liver sinusoidal endothelial cells (LSECs) play a crucial role in hepatic ischemia/reperfusion (I/R) injury, a major cause of liver impairment during surgical treatment. Emerging evidence indicate a critical role of microRNAs in I/R injury. This study aims to investigate whether miR-9-5p exert a protective effect on LSECs in vitro .

Methods: We transfected LSECs with miR-9-5p mimic or mimic NC. LSECs were treated with oxygen and glucose deprivation (OGD, 5% CO2 and 95% N2), followed by glucose-free DMEM medium for 6 h, and high-glucose (HG, 30 mmol/L glucose) DMEM medium for 12 h. The biological role of miR-9-5p in I/R-induced LSEC injury was determined.

Results: In the in vitro model of OGD/HG injury in LSECs, the expression levels of miR-9-5p were significantly downregulated and those of CXC chemokine receptor-4 (CXCR4) upregulated. LSEC I/R injury led to deteriorated cell death, enhanced oxidative stress and excessive inflammatory response. Mechanistically, we showed that miR-9-5p overexpression significantly upregulated both mRNA and protein levels of CXCR4, followed by rescue of LSECs, ameliorated inflammatory response, and deactivation of pro-apoptotic signaling pathways.

Conclusion: miR-9-5p promotes LSEC survival and inhibits apoptosis and inflammatory response in LSECs following OGD/HG injury via downregulation of CXCR4.

Gastroenterology & Hepatology

MicroRNA-9-5p

CXC chemokine receptor-4

sinusoidal endothelial cell

ischemia-reperfusion injury

OGD/HG injury

Hepatic ischemia/reperfusion (I/R) injury, a major complication of liver surgeries, liver transplantation, and hemorrhagic shock, is attributable to deteriorated post-operational hepatic dysfunction, elongated hospital stay, as well as aggravated morbidity and mortality[1–3]. A crucial event during this process is the death of liver sinusoidal endothelial cells (LSECs), which takes place only a few minutes following reperfusion, several hours prior to detectable hepatocyte death[1, 4]. Apoptosis and inflammatory responses are pivotal underlying mechanisms of I/R-induced endothelial damage[5–7]. LSECs, which line the primary barrier between the hepatocytes and the bloodstream, play complex roles and are prone to viability[8]. Therefore, understanding the biological function of LSECs is essential to elucidate liver pathology during I/R injury.

One potential mechanism of LSEC survival is the alterations of epigenetic regulators, particularly microRNAs (miRNAs)[9]. MiRNAs usually regulate target functional proteins via binding to complementary seed sequences in 3′ untranslated regions (3′-UTRs) of mRNA, leading to their degradation or inhibition of translation[10–12]. MiR-9-5p have been extensively studied in malignant diseases, such as oral squamous cell carcinoma, nasopharyngeal carcinoma, papillary thyroid cancer, and prostate cancer, etc.[13–17] Depending on the specific cell type and pathological conditions, miR-9-5p may exert either pro-apoptotic or anti-apoptotic functions. We previously have shown that miR-9-5p protected human umbilical vascular endothelial cells (HUVEC) against apoptosis and excessive inflammatory response via downregulation of CXC chemokine receptor-4 (CXCR4)[18]. Nevertheless, the precise biological role of miR-9-5p in LSECs remain unknown.

We herein hypothesized that miR-9-5p may play a critical role in attenuation of oxygen and glucose deprivation/high glucose (OGD/HG)-induced LSEC impairment in vitro. In this study, we established an in vitro model by incubating LSECs with oxygen and glucose deprivation followed by high-glucose medium to mimic reperfusion. This enables us to observe the intracellular effects of OGD/HG injury in LSCEs. We then tested whether overexpression of miR-9-5p sufficiently ameliorate activated apoptosis, inflammatory response and cell death in OGD/HG-treated LSECs.

In vitro model of ischemia/reperfusion and cell transfection

Briefly, LSECs (Ningbo mingzhou biotechnology co. LTD, MZ-M0395) were incubated in an Eppendorf Galaxy 170R incubator under hypoxia conditions (5% CO2 and 95% N2 at 5L/min) for 30 minutes till oxygen concentration reached 1%. The hypoxia mixture gas was continuously injected to maintain O2 concentration less than 1% in the incubator. Then, cells were treated with glucose-free Dulbecco’s modified Eagle’s (DMEM) medium for 6 h, followed by high glucose (HG, 30 mmol/L glucose) DMEM medium containing 10% fetal bovine serum (FBS) at 5% CO2 for 12 h. The sequences of miR-9-5p mimic and miR-9-5p mimic NC were provided by the Shanghai GenePharma Co., Ltd. (Shanghai, China). LSECs were inoculated into a 6-well plate 24 h prior to transfection. Upon reaching approximately 50% of cell confluence, the cells were incubated with 200 µL of transfection reagent and plasmids, as instructed by the manual from Lipofectamine 2000 transfection kit (11668-027; Invitrogen Inc., Carlsbad, CA, USA). The medium was changed after 6 h and collected after 48 h, according to the manufacturer’s instructions. This study is exempted from approval from the ethics’ board.

RNA isolation and quantitation

Total RNA of transfected cells was isolated using the Trizol reagent according to the manufacturer’s protocol. 2 ug of RNA were reverse-transcribed into cDNA. The primers of miR-9-5p and CXCR4 were designed and synthesized by Beijing Augct biotechnology Co., Ltd. (Beijing, China), with U6 acting as the internal reference for miR-9-5p, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) for CXCR4. The relative transcriptase mRNA levels of the target gene were calculated by conducting the relative quantitative method: ΔCT = Ct target gene - Ct internal reference.

Western blot analysis

Proteins were extracted from cultured LSECs and homogenized in lysis buffer. following centrifugation at 12000 r/min for 10 min, the supernatant was collected and the concentration of protein was determined using a protein quantitative kit, adjusting protein concentration to the same level. Proteins were treated with the sample buffer and prepared on 15% separation gel. After 2 h of protein electrophoresis, proteins were transferred to the polyvinylidene fluoride (PVDF) membranes. The membranes were blocked with 5% of skim milk powder for 2 h at room temperature on a horizontal shaking table. Then, the membranes were incubated with primary antibodies: CXCR4 (1:100, ab124824), Bcl-2-associated X protein (Bax) (1:1000, ab32503), B-cell lymphoma 2 (Bcl-2) (1:2000, ab182858), cleaved caspase 3 (1:500, ab32042), cleaved caspase 9 (1:1000, ab2324), and β-actin (1:2000, ab8227) overnight at 4 °C. All antibodies were purchased from Abcam Inc., Cambridge, MA, USA). PVDF membranes were then washed using a phosphate buffer saline Tween-20 (PBST) [phosphate buffer saline (PBS) containing 0.1% Tween-20] for 4 times, 15 min each wash, followed by incubation with a secondary antibody horseradish peroxidase (HRP) labeled goat anti-rabbit IgG antibody (1:3000) for 1 h at room temperature. Membranes were treated with enhanced chemiluminescence (ECL) agent before photographed and analyzed using Jetta image analysis system. The relative protein expression was defined as the ratio of the gray value of target protein band to the internal reference β-actin or GAPDH.

Detection of Malondialdehyde (MDA) content

The MDA content was detected via the thiobarbituric acid method in accordance with the instructions provided by the MDA kit. Cells were inoculated in a 24 well plate (4 wells set up each experimental group) with the density rate of approximately 1 × 10⁵ cells per well, followed by grouping and processing using methods mentioned above. 100 µL supernatant of each group was collected from the cultured cells. The optical density (OD) at 532 nm wavelength was measured by a 752-type ultraviolet grating spectrophotometer. The MDA content of each group was calculated.

Detection of glutathione peroxydase (GSH-PX) activity

GSH-PX activity was evaluated using a GSH-PX kit based on the 5–5′-dithio-2-dinitrobenzoicacid (DTNB) method, according to the manufacturer’s instructions. Cells were inoculated into 24 well plates (4 wells in each experimental group 1 × 10⁵ cells per well). 100 µL supernatant of each group was collected and the absorbance value was measured at 412 nm wavelength. Three independent experiments were performed.

Cell counting Kit-8 (CCK-8) assay

When the cell confluency reached approximately 80%, the cells were treated with 0.25% trypsin to prepare the single cell suspension. After counting, the cells were inoculated in a 96-well plate (200 µL/well) with the density amounting to 3 × 10³ − 6 × 10³ cells/well, 6 replicates were established. Cells were cultured in an incubator, and the cell proliferation was exanimated at 0 h, 24 h, 48 h, and 72 h. Cells in each well were added with 10 µL CCK-8, followed by culturing for 2 h. The OD values were measured at 450 nm wavelength by the enzyme linked immunosorbent assay (ELISA) reader. Cell viability curve was drawn (time point as the abscissa, OD value as the ordinate). The proliferative ability of cells was determined

ELISA

A commercially available ELISA kit was employed to test for the expression levels of interleukin-1 (IL-1), IL-6 and tumor necrosis factor-α (TNF-α), following the protocol provided. We measured OD values at 450 nm wavelength using a Swiss TECAN multifunctional ELIS reader.

Statistical analysis

The statistical analysis was conducted using the SPSS 21.0 software (IBM Corp. Armonk, NY, USA). Data were tested conforming to normal distribution and homogeneity of variance. The measurement data were presented by the mean ± standard deviation. Comparisons made between two groups were performed using t-test, while comparisons among multiple groups were analyzed by the one-way analysis of variance (ANOVA). Pairwise comparisons in multiple groups were performed using Tukey post-test data. The repeated measure ANOVA was used for analysis of the data at different time points. All experiments were performed three times. P < 0.05 was considered statistically different

miR-9-5p is downregulated and CXCR4 upregulated in an ischemia/reperfusion injury model in vitro.

We generated an experimental model of ischemia/reperfusion injury in vitro by incubating liver sinusoidal endothelial cells (LSECs) in with oxygen and glucose deprivation (OGD, 5% CO2 and 95% N2), which imitates the low oxygen and glucose conditions during pathological conditions such as liver surgery. The LSECs were then treated with glucose-free DMEM medium for 6 h, followed by high-glucose (30 mmol/L glucose) DMEM medium for 12 h. RT-qPCR and Western Blot analysis were used to detect the expression levels of miR-9-5p and CXCR4 in LSECs, respectively. Intriguingly, ischemia/reperfusion suppressed the mRNA levels of miR-9-5p by 37.4%, but enhanced that of CXCR4 by 2.05-fold in vitro (Fig. 1A). This expression pattern was further confirmed by detection of CXCR4 protein expression levels post- ischemia/reperfusion injury in LSECs (Fig. 1B). Thus, these data indicate that miR-9-5p and CXCR4 may exert functional roles in ischemia/reperfusion injury in LSECs. Their precise biological impacts, however, remain to be explored.

OGD/HG induces LSEC injury

Next, we sought to evaluated the effects of OGD/HG insults on LSECs. Cell viability was determine using a non-radioactive cell counting kit-8 (CCK-8) assay. Accordingly, OGD/HG injury significantly reduced LSEC survival by 67.3% (Fig. 2A). Given that oxidative stress, inflammatory response and apoptosis are essential pathological processes that underlie liver ischemia/reperfusion injury, we investigated these mechanisms in our LSEC model in vitro. The oxidative degradation of lipids, detected by the OD value of MDA, results in free radicals taking electrons from the lipids, leading to cell damage. Thus, it is essential to assess oxidative stress. The Glutathione Peroxidase (GSH-Px) plays a crucial role in the protection of liver tissues from oxidative damage, their activities were also examined and quantified. We observed a significant elevation of OD value of MDA (3.62-fold, Fig. 2B) and an ~ 27.5% decrease in GSH-PX content (Fig. 2C). Indeed, these data demonstrate that OGD/HG injury in LSECs led to enhanced oxidative stress. Then, we examined the impact of this injury on inflammatory response in LSECs. Using ELISA analyses, we detected expression levels of crucial pro-inflammatory factor, namely TNF-α, IL-1 and IL-6. As expected, their expression levels were all significantly increased (Fig. 2D). Collectively, OGD/HG insults in LSECs aggravated cell oxidative stress and inflammatory response, leading to worsened cell survival rate.

Overexpression of miR-9-5p largely mitigated OGD/HG LSEC injury

To investigate the functional role of miR-9-5p on OGD/HG -induced LSEC injury, we further tested these effects in the setting of miR-9-5p overexpression. LSECs were transfected with empty mimic NC or miR-9-5p mimic (Fig. 3A). RT-qPCR confirmed the efficacy of transfection, as indicated by a 2.3-fold increase in miR-9-5p mRNA expression levels. Importantly, miR-9-5p overexpression significantly reduced the mRNA expression levels of CXCR4 to 53.9% of that of mimic NC controls (Fig. 3A), suggesting that CXCR4 is a target of miR-9-5p during LSEC injury. The data was consolidated by Western blot analysis, as the protein expression level of CXCR4 decreased by 51.8% following miR-9-5p overexpression (Fig. 3B). Next, we determined whether changes in the expression pattern of miR-9-5p and CXCR4 impact on OGD/HG-induced LSEC injury. Indeed, our data showed that a 2.24-fold increase in miR-9-5p expression significantly improved the OD value of CCK-8 assay by 23.4% and 44.9% at 24 hours and 48 hours post-injury, respectively (Fig. 3C). In accordance with these findings, miR-9-5p overexpression also led to significant downregulation of pro-apoptotic proteins Bax, cleaved-caspase 3 and cleaved-caspase 9, as well as upregulation of anti-apoptotic protein Bcl2 (Fig. 3D). Furthermore, LSECs transfected with mimic miR-9-5p were also more resistance to inflammatory response, as determined by decrease expression levels of TNF-α, IL-1 and IL-6. In conclusion, our data indicate that miR-9-5p targets CXCR4 and exerts a protective role in OGD/HG -induced LSEC damage in vitro (Fig. 4).

Although tremendous effort has been made in the past decades to decipher the underlying mechanisms of I/R injury, therapies that successfully translated into clinical practice remain scarce[1, 2]. The present study depicts a previously unidentified role of miR-9-5p in the LSEC pathological processes using an in vitro I/R model. We showed that miR-9-5p is downregulated and CXCR4 upregulated in an OGD/HG model in hepatic sinusoidal endothelial cells, suggesting their potential role in I/R injury. Upon OGD/HG insults, LSECs underwent enhanced oxidative stress, apoptosis and inflammatory response, as well as aggravated cell death. Importantly, we revealed that CXCR4 is a downstream target of miR-9-5p. Indeed, overexpression of miR-9-5p diminished both mRNA and protein expression levels of CXCR4, thus preserving LSEC survival and suppressed the activation of Bax/Bcl2 pro-apoptotic signaling pathway and synthesis of pro-inflammatory factors including TNF-α, IL-1 and IL-6 (Fig. 4). Therefore, miR-9-5p/CXCR4 may represent a promising therapeutic target for LSEC protection during liver I/R injury.

Major liver surgery, including hepatectomy and transplantation, is the most effective and often the only treatment for liver cancer and other end-stage liver diseases[19, 20]. Hepatic ischemia injury, initially due to reduced blood supply, is followed by reperfusion injury mediated by a variety of pathophysiological processes, a major complication referred to as liver ischemia/reperfusion injury. This may be attributable to, at least in part, the therapeutic target cell type. The present study focuses on the Liver sinusoidal endothelial cells (LSEC). LSECs line the vascular endothelium of the hepatic tissue, which control vascular tone and thereby blood flow and delivery of nutrients and oxygen to hepatocytes. Thus, LSECs exhibit crucial biological functions including elimination of macromolecules and small particles from the blood supply, as well as immunological functions and facilitation of liver regeneration[21].

To the best of our knowledge, study in the role of miR-9-5p in ischemia/reperfusion injury is rudimentary, apart from our previous findings that it is vital for HUVEC survival during I/R injury. More importantly, given the essential role of LSECs in the maintenance of liver functioning, insight into the biological role of miR-9-5p in LSCEs is worthwhile. The conventional mouse model of liver I/R injury involves clamping the portal vein, bile duct and hepatic artery with microvascular clips to interrupt the blood supply, followed by reperfusion[22, 23]. The method, however, makes it difficult to elucidate cell type-specific role of the factor studied. Hence, we used an in vitro model by incubating LSECs with oxygen and glucose deprivation to mimic the low oxygen and glucose conditions as is experienced during liver transplantation. The LSECs were then treated with glucose-free DMEM medium for 6 h, followed by high-glucose (30 mmol/L glucose) DMEM medium for 12 h. This enables us to observe the intracellular effects of I/R injury in LSCEs. We depict that miR-9-5p is fundamental for two pivotal pathological processes in LSECs, inflammatory response and apoptosis. However, further investigation is warranted to test the protective role of miR-9-5p in vivo.

Excessive inflammatory response is considered to be a key mechanism of liver IR injury. Previous studies indicate the involvement of various inflammatory cells and humoral factors in liver IR injury[5, 6]. Upon I/R injury, activated SECs, neutrophils, and hepatocytes express pro-inflammatory cytokines and chemokines, such as TNF-α and interleukin-1, contributing to their damage. Previously, we showed that overexpression of miR-9-5p inhibited the release of inflammatory factors in human umbilical vascular endothelial cells (HUVEC)[18]. In contrast, a miR-9-5p inhibitor largely counteracted the anti-inflammatory effects upon CXCR4 inhibition in HUVEC[18], suggesting that miR-9-5p exerts anti-inflammatory effects. Nevertheless, whether miR-9-5p directly modulate this critical process in key hepatic components during I/R injury is less understood. Thus, we established an in vitro I/R injury model to test this hypothesis using LSECs. Our data demonstrate that TNF-α, IL-1, and IL-6 were all significantly downregulated in response to miR-9-5p overexpression in LSECs. In addition, IL-1 and IL-6 are also important mediators of ROS production[24–27]. Indeed, the enhanced production of TNF-α, IL-1, and IL-6 following OGD/HG insults is accompanied by increased OD value of MDA and decreased activity of GSH-PX, suggesting aggravated oxidative stress. In accordance with these data, we have showed previously that HUVECs overexpressing miR-9-5p exhibited opposite effects, i.e. decreased OD value of MDA and increased GSH-PX activity[18]. In line with our findings, recent studies showed an anti-inflammatory role of miR-9-5p in deep vein thrombosis and multiple sclerosis by targeting NF-κB[28–30]. Thus, the present study extended our knowledge of the potential targets of miR-9-5p during inflammatory response.

Apoptosis of liver-resident cells, a crucial mechanism of liver injury, is common under pathological condition of stress and diseases[31, 32]. Given the small proportion of LSECs in the hepatic tissue, the importance of LSEC apoptosis, to some extent, may be underestimated. Intriguingly, miR-9-5p regulates apoptosis in various tissues and cell lines[13, 33, 34]. Its involvement in LSECs, however, remains unclear. Within minutes of I/R injury, LSEC undergo caspase dependent apoptotic cell death, followed by that of hepatocyte death few hours later[31, 32, 35–37]. The present and our previous study showed that miR-9-5p-mediated anti-apoptotic effects may be beneficial for survival of various endothelial cell lines including HUVEC and LSECs[18]. Bax is also expressed in LSECs[4]. When looking into the mechanism of apoptosis reduction associated with miR-9-5p, we observed that overexpression of miR-9-5p elevated protein expression levels of pro-apoptotic Bax, caspase-3 and caspase-9, while decreased expression levels of anti-apoptotic Bcl2, suggesting that miR-9-5p is a regulator of LSEC apoptosis following OGD/HG damage. Notably, an anti-apoptotic effect in LSECs may also prevent LSEC and hepatocyte injury[38]. Moreover, Tanoi et al. showed that inhibition of Bax in LSECs reduces apoptosis in both LSECs and hepatocytes[39]. In contrast to our finding, recent studies show that miR-9-5p may induce apoptosis in papillary thyroid cancer and oral squamous cell carcinoma[14, 15]. This may be attributable to cell type, pathological conditions, and more importantly, targeting factors.

MicroRNAs, approximately over 2000 in human genome, are a class of small non-coding RNAs that inhibit gene expression [10, 11]. They bind to complementary seed sequences in 3′ untranslated regions (3′-UTRs) of mRNA, resulting in degradation or inhibition of the translation of target functional proteins[12]. Although the cause of reduction of miR-9-5p in response to I/R injury remains unknown, we have shown that OGD/HG insults sufficiently reduced the expression levels of miR-9-5p in LSECs. Furthermore, the reduction of miR-9-5p correlated with enhanced expression of CXCR4 mRNA and protein levels. Notably, overexpression of miR-9-5p significantly diminished CXCR4 expression, suggesting that CXCR4 is a direct target of miR-9-5p. In line with our findings, Lu et al. and Ferrer-Marin et al. reported that miR-9 strongly reduced CXCR4 expression in nasopharyngeal carcinoma and human megakaryocytes [16, 17]. In addition, miR-9 directly bind to the 3′-UTRs of CXCR4[16]. The precise role of miR-9-5p may depend on specific cell context. Regarding endothelial cells, the present and our previous study show that miR-9-5p targets CXCR4 and therefore attenuates stress-induced apoptosis in HUVEC and LSEC. It is possible that miR-9-5p/CXCR4 axis may play a broader role in pathological conditions such as cardiovascular disease and neurological diseases, where endothelial cells are also vital for the initiation and progression of the disease[18, 40, 41].

Our data indicate a pro-survival role of miR-9-5p in LSEC. Upon OGD/HG injury in vitro, the expression levels of miR-9-5p is downregulated, resulting in enhanced CXCR4 expression. Consequently, LSECs underwent aggravated apoptosis, excessive inflammatory response, and impaired cell survival. Taken together, miR-9-5p may be a promising therapeutic target to rescue endothelial cells during liver I/R injury.

CXCR4, CXC chemokine receptor-4; LSECs, liver sinusoidal endothelial cells; I/R, ischemia-reperfusion injury; miR-9-5p, MicroRNA-9-5p; TNF-α, tumor necrosis factor α; IL-1, interleukin-1; IL-6, interleukin-6; ELISA, enzyme-linked immunosorbent assay; RT-qPCR, real-time quantitative polymerase chain reaction; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; Bax, Bcl-2-associated X protein; HG, high glucose.

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Competing interests:

The authors declare that they have no competing interests.

Funding:

No funding was received.

Authors’ contributions:

YD analyzed results, drafted the paper and was involved in experiment design, ZG designed and performed the majority of experiments, supervised and funded the study, and analyzed data; XW, YM and HZ contributed to data analysis and experiment design. All authors read and approved the final manuscript.

Acknowledgements:

Not applicable.

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Protective role of microRNA-9-5p in oxygen glucose deprivation/reperfusion-induced injury in liver sinusoidal endothelial cell

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