C-X-C motif chemokine 16, modulated by microRNA-545, aggravates myocardial damage and affects the inflammatory responses in myocardial infarction

Background Myocardial infarction (MI), a common type of coronary heart disease, is the major cause of morbidity and mortality around the world. Chemokine-mediated inflammatory cell infiltration and local inflammatory damage response are recent research hotspots. Hence, we attempted to examine the role of C-X-C motif chemokine 16 (CXCL16) as a potential candidate in MI. Methods Human cardiomyocytes were treated with hypoxia/reoxygenation (H/R) to establish an in vitro cell model. GEO database provided the clinical data of MI patients and GSEA verified the relationship of chemokine and MI. CCK-8 and flow cytometry analyses were used to measure cell viability and apoptosis. Bioinformatics analysis and luciferase reporter assay were conducted to determine the correlation between CXCL16 and miR-545. qRT-PCR and western blot assays were performed to investigate the expression level of the indicated genes. The activity of lactate dehydrogenase (LDH) and the levels of TNF-α, IL-6, IL-1β, and IL-10 were explored using ELISA assay. Results CXCL16 was increased in MI. CXCL16 knockdown can reverse the inhibitory effect of H/R treatment on cell viability, while overexpression of CXCL16 showed the opposite trend. MiR-545 directly targeted CXCL16 and negatively regulated CXCL16 levels. MiR-545 promoted cell proliferation and inhibited apoptosis in the MI cell model, which attenuated the CXCL16-induced injury on cardiomyocytes. Conclusion These findings demonstrated that CXCL16 aggravated MI damage through being directly targeted by miR-545 and mediating inflammatory responses, thereby providing potential therapeutic targets for MI therapy. Supplementary Information The online version contains supplementary material available at 10.1186/s40246-021-00314-7.

greatly improve the condition of MI patients and attenuate mortality.
Chemokine-mediated inflammatory cell infiltration and local inflammatory damage responses emerge as hotspots in recent years. Therefore, we performed Gene Set Enrichment Analysis (GSEA) to explore whether the progression of MI is linked with the chemokine signaling pathway. Chemokines are a string of small chemotactic cytokines with molecular weights of 8-12 kDa, which play a central role in the migration of leukocyte and other cellular motilities [5]. Interestingly, the migration of leukocyte into the vessel wall induced by chemokine is considered to be an early event in atherosclerosis development, as well as the major cause of MI [6]. Song et al. indicated that the increasing mesenchymal stem cell platelet in peripheral blood of MI patients is associated with the CXCR4/SDF-1 axis [7]. The potential effect of CXCL9 in MI has been investigated by Lin et al., which suggested that upregulation of CXCL9 in MI might exert an important role in post-MI cardiac fibrosis via activating cardiac fibroblasts [8]. Chronopharmacological targeting CCL2/CCR2 axis can ameliorate atherosclerosis [9]. Among the currently known chemokines, CXCL16 is somewhat peculiar with a glycosylated mucin-like stalk, and sensitive to a disintegrin and metalloprotease [10]. CXCL16 is expressed in both transmembrane and soluble forms [11]. CXCL16 can chemo attract immune cells to the inflammatory sites and act as the scavenger receptor for oxidized lipoproteins, which manifest its potential crucial role in MI [12]. Notably, in a soluble form, CXCL16 has been identified as an independent factor of cardiovascular death and morbidity in acute coronary syndromes [13]. However, the biological functions of soluble CXCL16 in MI and the underlying mechanism have not been fully illustrated.
MiRNAs are a class of endogenous and non-coding small single-stranded RNAs and could bind with the 3′ untranslated regions of target genes to regulate the translation process. Emerging evidences have shown that miRNAs are implicated in multiple biological processes and also act as important biomarkers in cardiovascular diseases, including MI. For example, miR-208a elevates the expression of myocardial endoglin and promotes myocardial fibrosis in acute MI [14]. miR-98 inhibits the MI-induced apoptosis through downregulating caspase-3 [15]. miR-135b prevents cardiomyocytes from infarction via restraining the NLRP3/caspase-1 signaling pathway [16]. The role of miR-545 in human disease has attracted continuous attention. miR-545 increases the replication of enterovirus 71 by targeting phosphatase and tumor necrosis factor receptor-associated factor 6 [17]. miR-545 is reduced in glioma cells, which may correlate with the upregulation of circPRKCI. Targeting circPRKCI/ miR-545 cascade might efficiently suppress human glioma cells [18]. Additionally, miR-545 could promote cell proliferation via targeting RIG-I or MT1M in hepatocellular carcinoma [19,20]. However, the effect of miR-545 on the progression of MI remains unknown.
In this present report, the effect of CXCL16 on the H/ R-treated human neonatal cardiomyocytes was evaluated by using loss/gain-of-function assays. The regulatory role of miR-545 on CXCL16 expression, as well as their interactions, was investigated to further reveal the potential mechanisms. In addition, the levels of inflammatory cytokines were detected to identify whether CXCL16 is implicated in the inflammatory responses post-MI.

Data analysis
Gene Expression Omnibus (GEO) database was accessed to download the corresponding data sets for CXCL16 (GSE60993) and miR-545 (GSE24548) expression in MI, respectively. The data set GSE60993 was collected from peripheral blood containing 17 patients and 7 control samples, while miRNA expression profiling of GSE24548 was analyzed in platelets from 4 patients with first acute MI and in 3 controls. The differentially expressed genes (DEGs) or miRNAs (DEmiRs) between patients and controls were analyzed by GEO online analysis tool GEO2R. The criteria were |log fold change (FC)| ≥ 1 and P < 0.05. Gene set enrichment analysis (GSEA) was utilized to verify the correlation between chemokine and MI.
Transfected cells were collected for further experiments after 24 h transfection.

Cell counting kit 8 analysis
After 24 h post-transfection, cells (1000 cells/100 μL suspension) were inoculated into a 96-well plate and cultured under conditions of 37°C with 5% CO 2 . After H/R treatment, 10 μL of CCK-8 solution was added into each well and cultivated with these cells for 1.5 h at 37°C and 5% CO 2 . The optical density (OD) value was measured at 450 nm under the microplate reader (Infinite M200, TECAN).

Annexin V-FITC/propidium iodide (AV/PI) staining
Cells were collected at 24 h after transfection. Next, transfected cells were exposed to the H/R condition. Afterwards, cells were suspended to the final density of 1-5 × 10 6 /mL using pre-cold PBS and 1× binding buffer. Following staining with Annexin V-FITC and PI in the dark, cell apoptosis capability was examined by flow cytometry and analyzed using Flowjo software.

QRT-PCR
TRIzol solution (Invitrogen) was utilized to extract total RNA from cells. PrimeScript RT Reagent Kit (Takara, Japan) and SYBR Premix Ex Taq II (TaKaRa) were employed to synthesize cDNA through reverse transcriptions and performed real-time PCR on 7900HT realtime PCR system to measure the expression of CXCL16.
The cDNA of miR-545 was reversed transcribed with the aid of MiScript Reverse Transcription kit (Qiagen). Real-time PCR was performed using MiScript SYBR-Green PCR kit (Qiagen) to assess the expression level of miR-545.
The relative expression of CXCL16 and miR-545 were normalized to GAPDH or U6. Each experiment was conducted in three times and all reactions were repeated in triplicate. The 2 −ΔΔCt method was used to calculate the relative expression levels and primers used in this investigation are as follows:

Western blot analysis
After 48 h transfection, total proteins of cells were isolated with radio immunoprecipitation (RIPA) buffer containing phenylmethyl sulfonylfluoride (PMSF, protease inhibitor) and quantified by BCA method. Subsequently, isolated proteins were denatured at 95°C for 5 min and separated in 12% SDS-PAGE. Next, the separated proteins were transferred onto the PVDF membranes. The 5% non-fat milk was utilized to block PVDF membranes for 1 h at room temperature and indicated primary antibodies were then used to incubate PVDF membranes overnight at 4°C against CXCL16, PCNA, and GAPDH. Following washed by TBST three times, PVDF membranes were reacted using corresponding secondary antibody at room temperature for 1 h. The protein bands were observed by enhanced chemiluminescence (ECL) and quantified with QUANTITY ONE software.

Enzyme-linked immunosorbent (ELISA) experiment
Following specific transfections and H/R stimulation, cell culture supernatant was harvested for ELISA assay. The lactate dehydrogenase (LDH; Nanjing Jiancheng Bioengineering, Nanjing, China) and ELISA (Roche, Germany) were used to explore the activity of LDH and levels of TNF-α, IL-6, IL-1β, and IL-10 as the protocols of manufacturers.

Statistical analysis
GraphPad Prism 5.0 and SPSS 22.0 software were applied for all statistical analysis. Differences of two groups were determined by Student's t test, and comparisons in multiple groups were analyzed using one-way ANOVA followed by Tukey's post hoc test. All data were exhibited as mean ± standard deviation (SD). P < 0.05 was considered as significantly significant.

CXCL16 expresses at higher levels in MI and human neonatal cardiomyocytes in response to H/R treatment
The appearance of chemokines is the main feature of inflammatory response after myocardial injury [5]. Thus, in order to investigate the relationship of chemokine and MI, GSEA was implemented based on the KEGG gene set of MSigDB database and revealed that chemokines were positively correlated with the MI process (P = 0.016, Fig. 1a) (Table S1). Then, we interacted the chemokine-related genes (n = 47) (Table S2) derived from GSEA with differentially expressed genes (DEGs; n = 147) (Table S3) in MI obtained from the GEO database, and two common genes CXCL16 and NCF1 were ultimately achieved (P = 0.016, Fig. 1b). We finally selected CXCL16 as the research project followed by a comprehensive analysis. GSE60993 data set showed that soluble CXCL16 was significantly increased in MI tissue specimens (n = 17) compared with human normal samples (n = 7) (P = 0.0019, Fig. 1c). Moreover, in the in vitro H/R cell model, the expression of CXCL16 was also increased relative to the control (**P < 0.01, Fig. 1d). These data indicated that CXCL16 might be associated with the progression of MI.
CXCL16 inhibits cell viability in human neonatal cardiomyocytes treated with H/R Subsequently, we regulated the expression of CXCL16 to determine its biological roles in cell viability after H/R Fig. 1 CXCL16 expression was elevated in MI and human neonatal cardiomyocytes in response to H/R treatment. a GSEA analysis was applied to detect the correction between chemokine-related genes and MI. b The Venn curve exhibited that there are two overlapped differentially expressed genes: CXCL16 and NCF1. Blue represents the DEGs obtained from the GEO database and yellow represents the upregulated chemokine genes in MI. c Relative expression of CXCL16 in MI tissues (n = 17) and normal specimens (n = 7) based on the GSE60993, P = 0.0019. d Relative expression of CXCL16 in human neonatal cardiomyocytes evoked by the H/R and control group, **P < 0.01 vs. control. n = 3 independent experiments. All data were exhibited as mean ± standard deviation (SD) treatment. QRT-PCR and western blot analyses exhibited that CXCL16 expression was remarkably decreased in cells due to the transfection of si-CXCL16#1 and si-CXCL16#2 (**P < 0.01, Fig. 2a, b). Meanwhile, both mRNA and protein expressions of CXCL16 were overexpressed after pcDNA3.1-CXCL16 transfection (**P < 0.01, Fig. 2c, d). After H/R treatment, cell viability was significantly inhibited (**P < 0.01, Fig. 2e, f). Downregulation of CXCL16 was observed to partially rescue the cell viability of cardiomyocytes that were repressed by H/R treatment ( ## P < 0.01, Fig. 2e), while overexpression of CXCL16 enhanced the inhibitory effect of H/R on cell viability ( ## P < 0.01, Fig. 2f). Collectively, CXCL16 can inhibit cell viability in H/R-induced cardiomyocytes.
MiR-545 directly targets CXCL16 and attenuates the expression level of CXCL16 in H/R-stimulated human neonatal cardiomyocytes Prediction website was employed to predict the upstream miRNAs of CXCL16 and a total of 37 miRNAs vector. e, f Cell viability was measured using CCK-8 analysis, n = 3 independent experiments. **P < 0.01 vs. control, ## P < 0.01 vs. H/R. All data were exhibited as mean ± standard deviation (SD) were obtained. Based on the GEO database, a total of 25 differentially expression miRNAs with lower expression levels was identified in MI. After intersection, miR-545 and miR-34a were achieved, and miR-545 was selected for the following research. As shown in Fig. 3a, miR-545 was markedly decreased in MI (P < 0.0001). In the in vitro cell model, the expression of miR-545 was decreased compared with the control group (**P < 0.01, Fig. 3b). The sequences of putative binding site between miR-545 and CXCL16 are exhibited in Fig. 3c. Compared with the negative control (NC), miR-545 mimic significantly reduced the luciferase activity of WT CXCL16 while miR-545 inhibitor elevated the luciferase activity of WT CXCL16. However, both miR-545 mimic and miR-545 inhibitor had no effects on the luciferase activity of MUT CXCL16 (**P < 0.01, Fig. 3c). Besides, miR-545 inhibitor significantly increased the expression level of CXCL16, whereas miR-545 mimic obviously inhibited CXCL16 expression (**P < 0.01, Fig. 3d-h). Furthermore, co-transfections of miR-545 inhibitor and si-CXCL16 or miR-545 mimic and CXCL16 could reverse the effects of si-CXCL16 or CXCL16 ( ## P < 0.01, Fig. 3d-h). In summary, miR-545 directly targets CXCL16 and inhibits the expression level of CXCL16 in MI.

miR-545 elevates cell proliferation and eliminates apoptosis through targeting CXCL16
To further assess the underlying mechanism of miR-545/CXCL16 axis in MI, CCK-8 and flow cytometry experiments were conducted for the detection of cell viability and apoptosis, respectively. Results of the CCK-8 assay showed that the H/R-treated cardiomyocyte viability was promoted after miR-545 mimic and si-CXCL16 transfections compared with the H/R group (P < 0.01, Fig. 4a). The opposite tendency was exhibited after the transfection of miR-545 inhibitor and highregulated CXCL16 (P < 0.01, Fig. 4a). The addition of miR-545 mimic partially abolished the inhibitory impacts of CXCL16 on cell viability, and co-transfection of miR-545 inhibitor and si-CXCL16 attenuated the promoting effects of si-CXCL16 on cell viability in the H/R cell model (P < 0.01, Fig. 4a). As shown in Fig. 4b, in consistency with cell viability results, PCNA expression was significantly increased owing to the transfection of miR-545 mimic or si-CXCL-16 in H/R-induced cells, whereas CXCL16 overexpression or miR-545 inhibition dramatically abolished PCNA. Co-transfection of miR-545 mimic and pcDNA3.1-CXCL16 overturned the effect of miR-545 mimic or pcDNA3.1-CXCL16, and the co-transfection of miR-545 inhibitor and si-CXCL16 reversed the role of miR-545 inhibitor or si-CXCL16. Furthermore, cell apoptosis showed the opposite trends with the proliferative capability after various treatments (P < 0.01, Fig. 4c). To sum up, these above observations indicated that miR-545 can promote cell proliferation and inhibit apoptosis through negatively regulating CXCL16.

MiR-545/CXCL16 axis mediates the activity of LDH and the levels of inflammatory cytokines
Given the important role of inflammation in MI, we next detected the activity of LDH and inflammatory cytokines for further examination of the role of miR-545/CXCL16 axis. After H/R treatment, the activity of LDH and the levels of TNF-α, IL-6, and IL-1β were significantly increased (P < 0.01, Fig. 5a-d). Compared with the H/R group, they were inhibited in the H/R + mimic group and H/R + si-CXCL16 group, while they were promoted in the H/R + inhibitor group and H/R + CXCL16 group (P < 0.01, Fig. 5a-d). Moreover, the co-transfection of mimic and CXCL16 attenuated the promoting activity of LDH caused by H/R + mimic treatment, as well as inflammatory factors (TNF-α, IL-6, and IL-1β). Downregulation of LDH activity, TNF-α, IL-6, and IL-1β induced by H/R + si-CXCL16 were significantly elevated due to the addition of miR-545 inhibitor (P < 0.01, Fig. 5a-d). Likewise, the level of IL-10 was opposite with the above proinflammatory cytokines (P < 0.01, Fig. 5e). Therefore, we concluded that miR-545/CXCL16 axis might modulate the development of MI through regulating inflammation.

Discussion
The concept of cardiovascular disease is firstly proposed by Herberden in 1772 [21], while James Herrick did not define MI until 1912 according to the relationship between coronary thrombosis and coronary artery disease [22]. From then on, the research on the pathogenesis and mechanism of MI, that is, the possible correlation of leukocytes and inflammation, has gradually become a hotspot. Previous literatures suggested that complicated and multifaceted pathologies are implicated in the MI development. In our present study, GSEA analysis showed that chemokine signaling pathway was positively associated with MI. Chemokines are originally discovered as inducing factors for leukocyte migration to the site of inflammation [23]. In addition, chemokines and their receptors also can affect homeostasis, the formation of foam cell, leukocyte activation, and so on [24]. Assisted by the bioinformatics analyses, we obtained two common genes (CXCL16 and NCF1) that were both linked with chemokine signaling pathway and significantly increased in MI tissues. Ludwig et al. discovered that the vast majority of chemokines are soluble, while CXCL16 is a unique molecule, both in membrane-bound form and in soluble form [10]. Previous studies of CXCL16 in cardiovascular disease mainly focus on atherosclerosis. The soluble form of CXCL16 could promote inflammation and atherosclerosis via recruiting the inflammatory cells [25]. Furthermore, CXCL16 mRNA expression is upregulated in atherosclerotic plaques and mainly expresses in lipid-rich macrophages [26]. More importantly, CXCL16 plays an important role in the progression of heart failure through controlling the matrix remodeling [27]. CXCL16 has been reported to provide novel information in clinical cardiovascular risk assessment [28]. Xu et al. provided the first evidence that CXCL16 polymorphisms remarkably affect MI risk in China [29]. However, its specific significance has not been verified in MI. Thus, we finally selected CXCL16 as the topic project in this work. We analyzed the expression of CXCL16 and found that CXCL16 was significantly increased in MI tissues and the MI cell model. CCK-8 assay showed that CXCL16 inhibited cell viability of cardiomyocytes treated by H/R. These data suggested that CXCL16 might act as a vital regulator in MI development.
Considering the central role of miRNAs in heart diseases, we next used the TargetScan and other predicted tools to screen the upstream miRNAs of CXCL16 in MI. According to the bioinformatics analysis, miR-545 was selected as a putative upstream molecule of CXCL16. At present, accumulating evidences have demonstrated that miR-545 exerts an inhibitory effect in a variety of cancers, including gastric cancer [30], hepatocellular carcinoma [20], and cervical cancer [31]. Although several miRNAs have been found to be involved in the development of MI via regulating the inflammatory responses after MI, such as miR-370 [32], miR-155 [33], and miR-223 [34], there exist no reports of miR-545's function in MI. Thus, we accessed to GEO database and displayed that miR-545 was markedly decreased in MI tissue samples compared with normal cases, which was opposite with CXCL16 expression. Moreover, the expression of CXCL16 was attenuated by miR-545 in the H/R cell model. Loss/gain-of-functional in vitro experiments showed that miR-545 can partially eliminate the effect of CXCL16 on cell viability and apoptosis. PCNA, the most widely utilized proliferation labeling protein, is expressed in the nucleus and closely related with cell cycle [35]. The expression of PCNA detected by western blot confirmed that the regulation of CXCL16 in MI was associated with miR-545. Additionally, the primary receptor for CXCL16 is CXCR6. The CXCL16/CXCR6 axis could drive the cross-talk among cells within the brain and microglia, as well as infiltrating macrophages, and induce a neuroprotective or detrimental phenotype [36].
Mir et al. have determined the biological significance of the CXCL16/CXCR6 axis in lung cancer [37]. A controversial role of the CXCL16/CXCR6 axis was found in atherosclerosis [38,39], suggesting that there exists a complex molecular mechanism between CXCL16/ CXCR6. Maybe, this contradictory can be explained with miR-545 in MI. The innate immune system-induced inflammatory responses exert a crucial role in the cardiac pathological process after MI. The inflammatory responses can be triggered by MI; consequently, the release of cytokines TNF-α encourages the leukocyte infiltration and promotes the secretion of inflammatory cytokines, including IL-6 and IL-1β. These inflammatory cytokines next induce the inflammation cascade followed by myocardial dysfunction [40][41][42][43]. Levels of pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β) and anti-inflammatory cytokine IL-10 modulate homeostasis within the heart in response to damage. Thus, in order to detect the role of CXCL16/miR-545 on inflammatory responses post-MI, the levels of TNF-α, IL-6, IL-1β, and IL-10 were measured using ELISA assay. Compared with the H/R group, CXCL16 resulted in a reduction in the levels of TNF-α, IL-6, and IL-1β and in an obvious increase of IL-10. By contrast, miR-545 exerted the opposite role on the levels of inflammatory cytokines. The activity of LDH, the important marker for cellular damage [44], showed the same trend as the inflammatory cytokines, that is, CXCL16 may play a pro-inflammatory role in MI. This is consistent with a previous report, which suggests that upregulation of CXCL16 in neonatal rat cardiomyocytes can stimulate inflammation by increasing IL-1β [27]. However, Lepore et al. previously demonstrated that CXCL16 can function as a good target to modulate microglia phenotype in order to inhibit inflammation and glioma progression [36]. The opposite effects indicate that the role of CXCL16 in different diseases may be correlated with the cellular microenvironment, and its exact mechanism in MI is worthy of further investigation.
This investigation presents some limitations; for example, all results were collected from in vitro experiments, and thus, further in vivo experiments are required to validate the current observations. It is difficult to determine the clinical significance of miR-545 and CXCL16 in actual MI patient samples. To solve this problem, we are trying our best collecting the MI patient specimens. Actually, based on the bioinformatics analysis, we discovered two upstream molecules of CXCL16, miR-545 and miR-34a. The relationship between miR-34a and CXCL16 will be detected in another research in the future, as well as the mechanism of action of CXCL16 in the inflammatory pattern.