Introduction

Diagnosis of fatal hypothermia is carried out based on a combination of several common findings, such as the difference in colour between blood from the right and left ventricles, Wischnewski’s spot, haemorrhage of iliopsoas muscle and so on, which are often observed in corpses exposed to cold1,2,3,4. However, these findings are also observed in other pathologies such as carbon monoxide poisoning, hydrocyanic acid poisoning, and stress5,6,7. In addition, it is possible that the above findings may be recognised when cold exposure and another cause of death compete, further complicating diagnosis. Accordingly, a specific diagnostic marker is necessary for accurate diagnosis of fatal hypothermia.

Various studies using biochemical, pathological, morphological, and molecular biological approaches in the adrenal gland8, pituitary gland9,10,11, kidney12, and serum13,14 have been performed to identify diagnostic markers of fatal hypothermia. We previously reported supporting markers for diagnostic of fatal hypothermia utilising mRNA of hypothalamus15 and iliopsoas muscle16. Importantly, as corpses are often found after a postmortem interval, examinations often do not represent the state at the time of death. Thus, when studying forensic samples, it is important to consider the effects of postmortem interval. mRNA is structurally unstable, and mRNA isolated from forensic samples is often degraded as a result of the postmortem interval. However, it has been reported that even highly degraded RNA can yield molecular information in postmortem tissues17, but with limitations. Although mRNA is relatively stable in a cold environment, a molecular marker that can withstand the postmortem interval is required. Recently, microRNA (miRNA) has been proposed as a molecule that can withstand the postmortem interval18,19,20. Therefore, we focused on body temperature-dependent miRNA expression in the iliopsoas muscle, which plays an important role in maintaining mammalian body temperature in a cold environment21,22. In this study, we used the hypothermic rat model we previously reported16, and performed body temperature-dependent miRNA expression analysis of the iliopsoas muscle using microarray.

The aim of this study was to elucidate the molecular mechanism in iliopsoas muscle during the course of fatal hypothermia, and identify useful molecular markers for the diagnosis of fatal hypothermia.

Results

Seventeen miRNAs were upregulated by severe hypothermia

We performed a moderated t test (cut-off < 0.05) and Storey with bootstrapping for microarray data using GeneSpring. Microarray analysis showed that in the severe hypothermia group, expression levels of 17 miRNAs were more than doubled compared with control, mild, and moderate hypothermia groups (Fig. 1A, Table 1); whereas, levels of eight miRNAs in the severe hypothermia group were decreased to less than half compared with the other groups (Supplementary Table 1). Here, we focused on upregulated miRNAs. We predicted the mRNAs targeted by the 17 upregulated miRNAs using GeneSpring. Consequently, more than 100 mRNAs were extracted as target gene candidates (partial results are shown in Table 2). We focused on four miRNAs (rno-miR-126a-5p, rno-miR-145-5p, rno-miR-190a-5p, and rno-miR-374-5p) because the 100 target mRNAs were shown to be primarily controlled by these four miRNAs.

Figure 1
figure 1

(A) Microarray analysis. A total of 17 miRNAs exhibited double the level of expression in severe hypothermia compared with the other groups. (B, C) Relative expression of rno-miR-126a-5p and -miR-145-5p in iliopsoas muscle. Both miRNAs were upregulated by a decrease in body temperature, but not significantly changed. (D, E) Relative expression of rno-miR-190a-5p and rno-miR-374-5p in iliopsoas muscle. Both miRNAs were significantly upregulated only by severe hypothermia. (F) In situ hybridisation showing localization of rno-miR-374-5p in iliopsoas muscle cells. Scale bar = 100 µm and 50 µm. Graphs show mean ± SD (n = 4–6). The statistical significance of differences between means was assessed by one-way ANOVA, followed by Tukey’s multiple comparison test. *P < 0.05, **P < 0.01, ***P < 0.001.

Table 1 Microarray fold-change analysis.
Table 2 Predicted target genes of the four examined miRNAs.

Severe hypothermia altered expression of rno-miR-190a-5p and rno-miR-374-5p

qRT-PCR using the SYBR Green I assay revealed that the expression of rno-miR-126a-5p and rno-miR-145-5p in iliopsoas muscle increased with decreasing body temperature, but did not change significantly (Fig. 1B,C). In contrast, expression of rno-miR-190a-5p and rno-miR-374-5p was significantly increased only by severe hypothermia compared with control, mild, and moderate hypothermia animals (Fig. 1D,E).

To determine which cells expressed rno-miR-190a-5p and rno-miR-374-5p in iliopsoas muscle, we performed in situ hybridisation (ISH). ISH results showed that rno-miR-374-5p was predominantly expressed in iliopsoas muscle cells (Fig. 1F), but rno-miR-190a-5p was not expressed (data not shown). Accordingly, we focused on rno-miR-374-5p.

Expression of target mRNAs was altered with decreasing body temperature

Abca8a, Ccnl1, Slc25a33, and Zfp423, which belong to “mitochondrial part”, “cell differentiation”, and “regulation of transcription” GO analysis terms (Table 2), are target gene candidates of rno-miR-374-5p. Expression of these genes was significantly altered with decreasing body temperature (Fig. 2A–D). In particular, expression of Ccnl1 and Slc25a33 was significantly increased only by severe hypothermia compared with control, mild, and moderate hypothermia animals.

Figure 2
figure 2

(AD) Relative expression of Abca8, Ccnl1, Slc25a33, and Zfp423 in each hypothermia group. These genes were induced by a decrease in body temperature. Expression levels were normalised to glyceraldehyde-3-phosphate dehydrogenase (Gapdh). Graphs show mean ± SD (n = 4–6). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001.

Expression of rno-miR-374-5p was significantly increased only by severe hypothermia, suggesting that these genes might not be controlled by rno-miR-374-5p under hypothermic conditions. In our study, rno-miR-30c-1-3p was downregulated in the severe hypothermia group compared with the control group (Supplementary Table 1). TargetScan predicted Slc25a33 as a target gene of rno-miR-30c-1-3p (https://www.targetscan.org/cgi-bin/targetscan/vert_72/view_gene.cgi?rs=ENST00000302692.6&taxid=10116&showcnc=0&shownc=0&shownc_nc=&showncf1=&showncf2=&subset=1). This result indicates that Slc25a33 might be primarily regulated by rno-miR-30c-1-3p under hypothermic conditions. Accordingly, it is possible that in hypothermic conditions, factors such as other miRNAs promote the expression of these genes, and this mechanism is even more effective during severe hypothermic conditions. This issue will be a focus of future research.

Expression of Mex3B exhibited an inverse correlation with rno-miR-374-5p expression

Expression of Mex3B was significantly decreased by moderate and severe hypothermia compared with control and mild hypothermia animals (Fig. 3A). In addition, the level of Mex3B protein after moderate and severe hypothermia was significantly decreased compared with the other groups (Fig. 3B). Expression of rno-miR-374-5p was gradually increased with decreasing body temperature, suggesting that this gene might be controlled by rno-miR-374-5p under hypothermic conditions.

Figure 3
figure 3

(A) Relative expression of Mex3B in each hypothermia group. These genes were induced by moderate and severe hypothermia. Expression levels were normalised to glyceraldehyde-3-phosphate dehydrogenase (Gapdh). (B) Relative level of MEX3B in each hypothermia group. Graphs show mean ± SD (n = 4–5). *P < 0.05. (C) Alignment of rno-miR-374-5p seed sequences and corresponding seed sequences of Mex3B mRNA. rno-miR-374-5p is predicted to bind with high affinity to the 3′-UTR of Mex3B. A luciferase reporter vector encoding the 3′-UTR was co-transfected with rno-miR-374-5p mimic or mutant into 3T3 cells. A decrease in luciferase activity indicated binding of the miRNA mimic to the 3′-UTR of the target sequence. Graphs show mean ± SD (n = 6–7). The statistical significance of differences between means was assessed by Mann–Whitney U test. *P < 0.05, **P < 0.01. (D) Relative expression of Mex3B and MEX3B in iliopsoas muscle cells transfected with rno-miR-374-5p mimic, mutation #2, rno-miR-374-5p inhibitor, or inhibitor control. Graphs show mean ± SD (n = 3). The statistical significance of differences between means was assessed by unpaired t test. *P < 0.05, **P < 0.01.

rno-miR-374-5p directly regulated Mex3B translation in vitro

To verify that the mRNA we identified were bona fide targets of rno-miR-374-5p, we employed a luciferase reporter assay, qRT-PCR, and western blotting. rno-miR-374-5p is predicted to bind with high affinity to Mex3B. In luciferase reporter assays, a decrease in luciferase activity indicates binding of the miRNA mimic to the 3′-UTR of the target sequence. Luciferase reporter assay, qRT-PCR, and western blotting results showed that the rno-miR-374-5p mimic could effectively inhibit Mex3B expression (Fig. 3C,D); thus, we concluded that rno-miR-374-5p directly regulates Mex3B expression in vitro.

rno-miR-374-5p and Mex3B were involved in regulation of GTPase activity

As Mex3B is involved in the induction of apoptosis by cellular stress and belongs to the GO term “positive regulation of GTPase activity” (Table 2), we focused on Ras, a GTPase that functions as a molecular switch for signalling pathways regulating cell survival, growth, and so on. We examined the expression of Kras, Pik3ca, Akt1, Bad, and Bcl2l1, which are involved in apoptosis according to the KEGG pathway. qRT-PCR using the SYBR Green I assay revealed that Kras expression in iliopsoas muscle increased with decreasing body temperature (Fig. 4A). Expression of Pik3ca was slightly increased with decreasing body temperature, but did not significantly change (Fig. 4B). Expression of Akt1 was not significantly changed (Fig. 4C), but AKT1 expression significantly increased with decreasing body temperature (Fig. 4D). Expression of Bad significantly decreased with decreasing body temperature (Fig. 4E). In contrast, Bcl2l1 expression significantly increased with decreasing body temperature (Fig. 4F).

Figure 4
figure 4

(AF) Relative expression of Kras, Pik3ca, Akt1, AKT1, Bad, and Bcl2l1 in each hypothermia group. Expression levels were normalised to glyceraldehyde-3-phosphate dehydrogenase (Gapdh) or β-actin. Graphs show mean ± SD (n = 3–6) (G) Relative expression of Mex3B and Kras between Mex3B siRNA and Mex3B siRNA mutant. Graphs show mean ± SD (n = 4). H. Relative expression of rno-miR-374-5p, Mex3B, and Kras between rno-miR-374-5p inhibitor and Mex3B siRNA and control. Graphs show mean ± SD (n = 3). The statistical significance of differences between means was assessed by unpaired t test. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001.

To examine whether Mex3B regulated Kras expression, we synthesised siRNA for Mex3B and transfected iliopsoas muscle cells. As a result, Mex3B siRNA induced decreased Mex3B expression, followed by inactivation of Kras expression (Fig. 4G). This result contradicted observed Kras expression in the animal model. When we co-transfected iliopsoas muscle cells with the rno-miR-374-5p inhibitor and Mex3B siRNA, or transfected only rno-miR-374-5p inhibitor, Kras expression showed the same expression pattern as Mex3B (Figs. 3D, 4H and Supplementary Fig. 1A). However, when we transfected iliopsoas muscle cells with the rno-miR-374-5p mimic, Mex3B expression decreased and was followed by an increase in Kras expression (Fig. 3D and Supplementary Fig. 1B), consistent with the observed expression pattern in the animal model. Accordingly, these results suggest that Kras expression might be regulated not only by Mex3B, but also indirectly by activated rno-miR-374-5p in iliopsoas muscle cells.

rno-miR-374-5p was involved in regulation of apoptosis in iliopsoas muscle cells

Western blotting results revealed that overexpression of rno-miR-374-5p induced decreased activation of cleaved CASP3 and CASP6 in iliopsoas muscle cells compared with cells overexpressing rno-miR-374-5p mutant #2 (Fig. 5A,B). In addition, expression of CASP8 was slightly suppressed by overexpression of rno-miR-374-5p (Fig. 5C). These results indicate that activation of rno-miR-374-5p might enhance the viability of iliopsoas muscle cells.

Figure 5
figure 5

(AC) Relative expression level of CASP3, CASP6, and CASP8 in iliopsoas muscle cells transfected with rno-miR-374-5p mimic, mutation #2, rno-miR-374-5p inhibitor, or inhibitor control. Graphs show mean ± SD (n = 3). The statistical significance of differences between means was assessed by unpaired t test. *P < 0.05.

Discussion

In forensic practice, various biochemical, pathological, and molecular biological examinations are performed using blood and tissues collected from the corpse to assess the cause of death8,9,10,11,12,13,14,15,16. However, because corpses are often found with a postmortem interval, examinations often do not represent the state at the time of death. Accordingly, an index for diagnosis of cause of death that can withstand the postmortem interval is required. We have reported specific molecular markers using mRNA that support the diagnosis of fatal hypothermia, one of the pathologies for which the diagnosis of cause of death is difficult15,16. In a cold environment, mRNA is relatively stable, but a molecular marker that can withstand the postmortem interval is required. Recently, microRNA (miRNA) has been proposed as a molecule that can withstand the postmortem interval18. The iliopsoas muscle performs shivering- or non-shivering-thermogenesis to maintain body temperature when the body temperature declines extremely23, and haemorrhage of the iliopsoas muscle is observed in fatal hypothermia3. In our previous study, the iliopsoas muscle might have been activated because haemorrhage was observed in this muscle of rats with extreme hypothermia16. Therefore, we focused on miRNA expression in the iliopsoas muscle.

In this study, expression of rno-miR-190a-5p and rno-miR-374-5p in iliopsoas muscle was increased with decreasing body temperature. Previous reports suggest that the expression of both miRNAs fluctuates dynamically in response to hypoxia24,25. Hypothermic conditions induce tissue asphyxiation because blood is cooled by the inhalation of low-temperature air, and oxygen and hemoglobin do not dissociate in a cold environment. Therefore, both miRNAs may be activated by tissue asphyxiation induced by severe hypothermia and, therefore, be potential markers of hypoxia in a cold environment.

The expression of target gene candidates (Abca8a, Ccnl1, Slc25a33 and Zfp423) of rno-miR-374-5p increased with decreasing body temperature and showed similar expression to rno-miR-374-5p. These results indicate that these genes may not be regulated by rno-miR-374-5p. Abca8 is a sinusoidal efflux transporter for cholesterol and taurocholate in mouse and human liver26, but is function in hypothermia is still unknown. Zfp423 is involved in skeletal muscle regeneration and proliferation after injury27. Increased expression of Zfp423 may contribute the promotion of iliopsoas muscle repair. Expression of Ccnl1 and Slc25a33 was only increased by severe hypothermia. Inhibited expression of Ccnl1, a cell cycle regulatory gene, by forced expression of a specific miRNA suppressed cell proliferation and invasion, arrested cell cycle progression, and promoted cell apoptosis28. Hence, Ccnl1 may contribute to cell survival during cellular stress such as cold stimulation. Slc25a33 is reportedly involved in mitochondrial oxidative phosphorylation for ATP synthesis29. Accordingly, it is suggested that Slc25a33 expression might be induced by the promotion of thermogenesis accompanying a decrease in body temperature. Moreover, Ccnl1 and Slc25a33 represent novel findings that will potentially complement the diagnosis of fatal hypothermia because the expression of both genes was induced only by severe hypothermia.

Our study showed that significantly decreased Mex3B expression in moderate and severe hypothermia was directly regulated by rno-miR-374-5p. Mex3B is reportedly involved in the induction of apoptosis following cell stresses such as heat, cold shock, reactive oxygen species, and radiation30. Accordingly, overexpression of miR-374b-5p inhibited apoptosis and contributed to the elevation of cell survival31. Our results indicate that Mex3B directly or indirectly regulated Kras expression, which was accompanied by subsequent activation of downstream molecules such as Bcl2l1 in the Ras signalling pathway. Kras is a GTPase that functions as a molecular switch for signalling pathways regulating cell proliferation, survival, growth, and differentiation32. Bcl-2 family proteins regulate apoptosis through protein–protein interactions. Previous reports suggest that overexpression of Bcl‐2 inhibits apoptosis and plays an important role in the development of inflammation-related disorders33,34. Accordingly, these results suggest activation of a novel rno-miR-374-5p/Mex3B/Kras pathway to elevate cell viability in extreme hypothermia.

In conclusion, our results indicate that rno-miR-190a-5p and rno-miR-374-5p may be activated by tissue asphyxiation induced by severe hypothermia and, thus, serve as potential markers of hypoxia in a cold environment. In addition, Ccnl1 and Slc25a33 may be upregulated by cellular stresses such as cold shock and the promotion of thermogenesis accompanying decreases in body temperature. Thus, these miRNAs and mRNAs are potential novel supporting markers for the diagnosis of fatal hypothermia. In addition, a novel rno-miR-374-5p/Mex3B/Kras pathway may be involved in the pathological process of fatal hypothermia. However, further investigation of these genes is necessary before they can be applied to forensic practice.

Materials and methods

All methods were performed according to relevant guidelines and regulation.

The Animal Care Committee of Nagasaki University approved this research protocol (approval number 1606081312-2).

Animals

Pathogen-free 8-week-old male Wistar rats (300–350 g in body weight) were obtained from Charles River Laboratories (Yokohama, Japan). Prior to experiments, rats were housed for 1 week under a 12/l2-h light/dark cycle (light on at 07:00 and off at 19:00) at a constant temperature and humidity, and allowed free access to food and water.

Experimental groups and thermal treatments

Twenty-three 9-week-old male Wistar rats were divided into four groups of 5–6 rats (control, mild, moderate, and severe hypothermia) and anesthetised by intraperitoneal injection of 0.3 mg/kg medetomidine, 2 mg/kg midazolam, and 2.5 mg/kg butorphanol. After 30 min, rats were exposed to cold (ambient temperature of 4 °C); rectal temperature (Ret) was continuously measured. Control rats were euthanised by cervical dislocation at 30 min after anesthesia. Mild hypothermia rats were euthanised by cervical dislocation when Ret reached 30 °C. Similarly, moderate and severe hypothermia rats were euthanised when Ret reached 22 °C and 12 °C, respectively16.

RNA isolation and evaluation of total RNA integrity

After euthanasia, the iliopsoas muscle was immediately dissected, immersed in Ambion RNAlater (Thermo Fisher Scientific, Waltham, MA), and stored overnight at 4 °C. Total RNA, including microRNA (miRNA), was extracted using a miRNeasy Mini kit and miRNeasy Micro kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions. RNA samples were stored at − 80 °C until use.

Total RNA purity was assessed using a Nano-Drop2000 spectrophotometer (Thermo Fisher Scientific). RNA integrity was assessed by on-chip capillary electrophoresis using an RNA 6000 Nano kit and Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA). RNA integrity number was calculated as described elsewhere35.

Microarray analysis

Microarray analysis was performed on a total of 12 samples (n = 3 per group) using a Rat miRNA V21.0 microarray in accordance with the manufacturer’s instructions (Agilent Technologies). Bioinformatic analyses were performed using GeneSpring v13 (Agilent Technologies). The data discussed in this publication have been deposited in NCBI’s Gene Expression Omnibus and are accessible through GEO Series accession number GSE139446.

cDNA synthesis from miRNA and mRNA, and quantitative real-time PCR

Total RNA (10 ng) was utilised as a template for complementary DNA (cDNA) synthesis and quantitative real-time PCR (qRT-PCR), which were performed using a miRCURY LNA RT Kit and miRCURY LNA SYBR Green PCR Kit for miRNA expression analysis (Qiagen), respectively. Primers [hsa-(rno-)miR-126-5p, hsa-(rno-)miR-145-5p, hsa-(rno-)miR-190a-5p, hsa-(rno-)miR-374b-5p, and 5S rRNA] were purchased from Qiagen.

Total RNA (500 ng) was utilised as a template for cDNA synthesis using a PrimeScript RT Reagent Kit for mRNA expression analysis (Takara Bio, Kusatsu, Japan) in accordance with the manufacturer’s instructions. qRT-PCR was performed in a 10-µL reaction system using SYBR Premix Ex Taq (Takara Bio) and a Thermal Cycler Dice Real-Time System (Takara Bio). Contents of the amplification mix and thermal cycling conditions were set in accordance with the manufacturer’s instructions. Primers [ATP binding cassette subfamily A member 8 (Abca8a), cyclin L1 (Ccnl1), solute carrier family 25 member 33 (Slc25a33), zinc finger protein 423 (Zfp423), Mex-3 RNA binding family member B (Mex3B), Kras proto-oncogene GTPase (Kras), phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha (Pik3ca), Akt serine/threonine kinase 1 (Akt1), Bcl2-associated agonist of cell death (Bad), apoptosis regulator Bcl-X (Bcl2l1) and glyceraldehyde-3-phosphate dehydrogenase (Gapdh)] were purchased from Takara Bio.

Relative quantification of miRNA and mRNA transcripts was performed using the ∆∆Ct method36.

Total protein extraction and western immunoblot analysis

Iliopsoas muscles were homogenised using a TissueLyzer II (Qiagen). T-PER Reagent (Thermo Fisher Scientific), consisting of proteinase and dephosphorylation inhibitors, was then added. Debris was removed from the supernatant using an Ultrafree-MC 0.45-mm filter (Merck Millipore, Darmstadt, Germany). Filtered protein samples were quantified using a Direct Detect Spectrometer (Merck Millipore), separated on 4–12% NuPAGE Novex Bis–Tris gels (Thermo Fisher Scientific), transferred to polyvinylidene difluoride membranes, and blotted according to standard protocols (antibody details are listed in Table 3). Protein bands were visualised using ImmunoStar LD (Wako, Osaka, Japan), and band intensity was calculated using Multi Gauge version 3.X (Fujifilm, Tokyo, Japan). This method was performed according to our previous study37.

Table 3 List of antibodies.

Synthesis of DNA, miRNA mimic, inhibitor, siRNA, and mutant

Putative target genes of rno-miR-374-5p were predicted using GeneSpring (Agilent Technologies). DNA synthesis of Mex3B was performed by Hokkaido System Science (Sapporo, Japan). Luciferase reporter plasmids were constructed to confirm the regulation of target genes by rno-miR-374-5p. As a negative control, a rno-miR-374-5p mimic (chemically synthesised double-stranded mature rno-miR-374-5p) and mutant were chemically synthesised by GeneDesign (Ibaraki, Osaka, Japan). Similarly, inhibitor and siRNAs for rno-miR-374-5p, Mex3B and a mutant negative control were chemically synthesised by GeneDesign.

Cell culture and reagents

3T3 cells were cultured for the luciferase reporter assay in Dulbecco’s Modified Eagle’s Medium (DMEM, Wako) with high glucose, l-glutamine, 10% foetal bovine serum (FBS), and 1% penicillin–streptomycin. Cells were harvested, seeded onto a 96-well plate at a density of about 2.2 × 104 cells per well in DMEM (Wako) with 10% FBS, but without 1% penicillin–streptomycin, and cultured for 24 h. Subsequently, cells were washed with Opti-MEM (Thermo Fisher Scientific) and 100 µL of Opti-MEM was added to each well for incubation at 37 °C prior to transfection.

Transfection and luciferase reporter assay

The 3′-untranslated regions (UTRs) of rno-miR-374-5p targets were predicted using microT-CDS in DIANA TOOLS (https://diana.imis.athena-innovation.gr/DianaTools/index.php?r=microT_CDS/index). Vectors were constructed with pmirGLO Dual-Luciferase miRNA Target Expression Vector (Promega, Madison, WI) in accordance with the manufacturer’s instructions. Primers consisting of the 3′-UTRs of predicted rno-miR-374-5p target sequences and appropriate restriction sites were synthesised, annealed, and cloned downstream of the firefly luciferase reporter (luc2) gene in pmirGLO. Sequences were as follows (upper- and lowercase letters indicate the 3′-UTR and restriction sites for PmeI and XbaI, respectively): Mex3B sense 5′-aaacAACCTCATGGTCAAATACTAATATTATATt-3′, and Mex3B antisense 5′-ctagaATATAATATTAGTATTTGACCATGAGGTTgttt-3′. Sequences of the rno-miR-374-5p mimic and mutant of the seed sequence (as a negative control) were as follows: rno-miR-374-5p mimic 5′-AUAUAAUACAACCUGCUAAGUG-3′, rno-miR-374-5p mutation #1 5′-AUACAAUACAACCUGCUAAGUG-3′, and rno-miR-374-5p mutation #2 5′-AUGUAACACAACCUGCUAAGUG-3′.

3T3 cells (2.2 × 104 cells/100 µL) were co-transfected with the rno-miR-374-5p mimic or mutant, and a reporter plasmid containing the 3′-UTR of Mex3B. The rno-miR-374-5p mimic and mutant were added at a final concentration of 45 nM along with Lipofectamine3000 (Thermo Fisher Scientific). Luciferase activity was assessed 48 h after transfection using a Dual-Glo Luciferase Assay System (Promega) according to the manufacturer’s instructions.

In situ hybridisation

In situ hybridisation (ISH) was performed using a microRNA ISH buffer set and miRCURY LNA Detection 5′- and 3′-DIG-labelled probes (Qiagen) in accordance with the manufacturer’s instructions. In brief, 4% paraformaldehyde perfusion-fixed tissues were embedded in paraffin. Six-micrometer-thick sections were deparaffinised and incubated with Proteinase K solution (DAKO, Glostrup, Denmark) for 10 min at 37 °C. After washing in phosphate-buffered saline, sections were dehydrated. Hybridisation was performed using 40 nM miRNA probe in microRNA ISH buffer (Qiagen) at 50 °C for 3 h. Sections were rinsed in 5 × SSC buffer at 50 °C for 5 min, twice with 1 × SSC buffer at 50 °C for 5 min, twice with 0.2 × SSC buffer at 50 °C for 5 min, and with 0.2 × SSC buffer at room temperature for 5 min. Sections were treated with blocking solution (Nacalai Tesque, Kyoto, Japan) for 15 min at room temperature and then incubated with an anti-DIG antibody (1:800; Roche Diagnostics, Basel, Switzerland) in blocking solution (Nacalai Tesque) overnight at 4 °C. Sections were developed using NTB/BCIP (Roche Diagnostics) at 30 °C. Observations were made using a BZ-9000 (Keyence, Osaka, Japan). The obtained images were processed with analysis software (Keyence). This method was performed according to our previous study37.

Skeletal muscle cell culture and transfection

Rat iliopsoas muscle tissue was dissociated into a single-cell suspension using a skeletal muscle dissociation kit (Miltenyi Biotec, Bergisch Gladbach, Germany). For rno-miR-374-5p mimic or inhibitor or Mex3B siRNA assays, iliopsoas muscle cells were cultured in Skeletal Muscle Cell Growth Medium (SMCGM, Takara Bio). Cells were then harvested, seeded onto a six-well plate at a density of approximately 0.5–1.5 × 105 cells per well in SMCGM, and cultured for 24 h. Subsequently, cells were washed with Opti-MEM, supplemented with 3 mL of Opti-MEM in each well, and incubated at 37 °C prior to transfection.

Iliopsoas muscle cells were transfected with rno-miR-374-5p mimic, mutation #2, rno-miR-374-5p inhibitor, inhibitor control, Mex3B siRNA, or mutant siRNA. rno-miR-374-5p inhibitor, inhibitor control, Mex3B siRNA, and mutant siRNA sequences were as follows (upper- and lowercase letters indicate RNA and DNA, respectively): rno-miR-374-5p inhibitor sense 5′-GACGGCGCUAGGAUCAUCAACCACUUAGCAGGUUGUAUUAUAUCAAGUAUUCUGGU-3′, rno-miR-374-5p inhibitor antisense 5′-ACCAGAAUACAACCACUUAGCAGGUUGUAUUAUAUCAAGAUGAUCCUAGCGCCGUC-3′, rno-miR-374-5p inhibitor control sense 5′-GACGGCGCUAGGAUCAUCAACUAUCGCGAGUAUCGACGUCGAGGCCCAAGUAUUCUGGU-3′, rno-miR-374-5p inhibitor control antisense 5′-ACCAGAAUACAACUAUCGCGAGUAUCGACGUCGAGGCCCAAGAUGAUCCUAGCGCCGUC-3′, Mex3B siRNA sense 5′-ACAGCAGACACAUACAUAUtt-3′, Mex3B siRNA antisense 5′-AUAUGUAUGUGUCUGCUGUtt-3′, Mex3B siRNA mutation sense 5′-ACAUCAGACACACACAUAUtt-3′, and Mex3B siRNA mutation antisense 5′-AUAUGUGUGUGUCUGAUGUtt-3′.

rno-miR-374-5p mimic, mutation #2, rno-miR-374-5p inhibitor, or inhibitor control were added at a final concentration of 45 nM along with Lipofectamine RNAiMAX Transfection Reagent (Thermo Fisher Scientific). Mex3B siRNA and mutant siRNA were used at 25 pmol/well with Lipofectamine RNAiMAX Transfection Reagent. Expression of Mex3B, Kras, MEX3B, CASP3, CASP6, and CASP8 was assessed 48 h after transfection by qRT-PCR and western blotting, in accordance with the manufacturer’s instructions.

Data analysis

Data are shown as mean ± SD. Statistical significance of differences between means was assessed by Mann–Whitney U test, unpaired t test, and one-way ANOVA, followed by Tukey’s multiple comparisons test (GraphPad Software, San Diego, CA). A P-value < 0.05 was considered significant.