Chemokine-Like Receptor 1 mRNA Weakly Correlates with Non-Alcoholic Steatohepatitis Score in Male but Not Female Individuals

Abstract

The chemokine-like receptor 1 (CMKLR1) ligands resolvin E1 and chemerin are known to modulate inflammatory response. The progression of non-alcoholic fatty liver disease (NAFLD) to non-alcoholic steatohepatitis (NASH) is associated with inflammation. Here it was analyzed whether hepatic CMKLR1 expression is related to histological features of NASH. Therefore, CMKLR1 mRNA was quantified in liver tissue of 33 patients without NAFLD, 47 patients with borderline NASH and 38 patients with NASH. Hepatic CMKLR1 mRNA was not associated with gender and body mass index (BMI) in the controls and the whole study group. CMKLR1 expression was similar in controls and in patients with borderline NASH and NASH. In male patients weak positive correlations with inflammation, fibrosis and NASH score were identified. In females CMKLR1 was not associated with features of NAFLD. Liver CMKLR1 mRNA tended to be higher in type 2 diabetes patients of both genders and in hypercholesterolemic women. In summary, this study shows that hepatic CMKLR1 mRNA is weakly associated with features of NASH in male patients only.

1. Introduction

Non-alcoholic fatty liver disease (NAFLD) is a widespread cause of chronic liver injury and its progressive form non-alcoholic steatohepatitis (NASH) is characterized by hepatic inflammation and fibrosis [1,2]. NAFLD is related to the metabolic syndrome, and importantly, these patients have a high prevalence of developing hypertension, type 2 diabetes and dyslipidemia [3]. Chemokine-like receptor 1 (CMKLR1) is expressed by immune cells including subsets of dendritic cells, macrophages and natural killer cells [4,5]. The adipokine chemerin attracts CMKLR1-expressing cells to sites of inflammation [4,5]. Hepatic chemerin levels are changed in NAFLD, suggesting a function of this chemoattractant factor herein [6,7,8]. Importantly, higher chemerin expression has been described in human NASH while levels are unchanged in patients with borderline NASH and even reduced in human fatty liver [6,7,8]. Serum chemerin is increased in obesity and positive associations with serum lipids, blood glucose and blood pressure suggest a function of this chemokine in metabolic diseases [9]. Data on serum chemerin in NAFLD are not concordant and higher as well as normal levels have been described [10].

CMKLR1 also binds the potent anti-inflammatory mediator resolvin E1 which is generated from ω-3 eicosapentaenoic acid [11].

CMKLR1 deficiency in mice is not related to changes in body weight, inflammation, glucose tolerance and dyslipidemia. Importantly, comparable results have been obtained in animals fed a standard chow and mice given a high-fat diet [12]. In a second study, a high-fat, high-cholesterol diet did not differentially affect body weight and insulin resistance in CMKLR1-null mice and the respective control animals. Of note, hepatic inflammation and expression of fibrotic genes is unchanged in the liver of CMKLR1-deficient mice [13]. Nevertheless, reduced body weight and body fat irrespective of low- or high-fat diet has also been reported in CMKLR1 knock-out mice. Despite decreased hepatic and adipose tissue inflammation, these animals have impaired glucose disposal in muscle and fat [14].

CMKLR1 is highly abundant in the liver and is expressed by primary human hepatocytes, hepatic stellate cells, Kupffer cells and bile duct cells [15]. In patients with chronic hepatitis C, liver CMKLR1 mRNA is, however, not related to the inflammatory activity grade. CMKLR1 mRNA levels are comparable in males and females and expression is significantly reduced in women with advanced liver fibrosis [16].

In human NASH liver, CMKLR1 mRNA is even induced and IL-6 is suggested to contribute to CMKLR1 upregulation [7]. Associations of hepatic CMKLR1 expression with hepatocyte ballooning, lobular inflammation and fibrosis have not been identified in human NAFLD [7]. The limitation of this study is that only three patients with NASH were enrolled [7]. To our knowledge, gender-specific expression of CMKLR1 in human NAFLD has not been analyzed so far.

Here, hepatic CMKLR1 was quantified in a relatively large cohort of patients with histologically proven NAFLD. Analysis was performed for both genders separately to identify possible sex-related differences.

2. Results

2.1. Hepatic Chemokine-Like Receptor 1 (CMKLR1) mRNA in the Human Liver

Recently, Döcke et al. analyzed CMKLR1 mRNA in 34 controls, 10 patients with a NASH score of 3–4 (undefined or borderline NASH) and three patients with a score equal or above 5 [7]. Because in that cohort the number of patients with definite NASH was quite small, we decided to determine CMKLR1 mRNA in a larger study group. CMKLR1 mRNA was measured in a cohort of 118 patients including 33 controls with normal liver, 47 patients with a NASH score ranging from 1.0 to 4.5 (borderline NASH) and 38 patients with a NASH score equal or above 5 (

Table 1. Characteristics of the cohort enrolled in the present study. Data are given as median values and range of the values. Uppercase numbers are shown where data were not available for all of the patients. Significant differences between controls and patients with borderline non-alcoholic steatohepatitis (NASH) are identified by *, between controls and patients with NASH with ^# and between patients with borderline NASH and NASH with ^&.

	Control	Borderline NASH	NASH	p-Values
Males/Females	16/17	22/25	24/14
Age	58 (20–82)	60 (24–84)	66 (33–82)	0.015 #
Body mass index (BMI) kg/m2	24.7 (18.3–30.5)	28.0 (22.0–46.0)	28.4 (21.0–57.7)	<0.001 *,#
Type 2 Diabetes	0	4	11	0.01 #
Hypertension	7	21	17
Hypercholesterolemia	0	4	10
Alanine aminotransferase U/L	21 (8–50) 32	35 (17–623) 36	32 (10–984) 35	<0.001 *,#
Aspartate aminotransferase U/L	23 (8–42) 27	31 (11–688) 35	30 (9–389) 34	0.014 * 0.012 #
Alkaline phosphatase U/L	102 (46–203) 29	97 (37–444) 36	91 (45–826) 35
Bilirubin mg/dL	0.6 (0.19–1.95) 30	0.56 (0.19–1.99) 37	0.53 (0.20–0.53) 36
Steatosis	0 (0–0)	2 (1–2)	2.5 (1–3)	<0.001 *,#,&
Inflammation	0 (0–0)	0 (0–2)	2 (0–3)	0.005 * <0.001 #,&
Fibrosis	0 (0–0)	0 (0–2)	2 (0–4)	0.047 * <0.001 #,&
NASH Score	0 (0–0)	2 (1–4.5)	6 (5–9)	<0.001 *,#,&

).

Indications for surgery (hepatocellular carcinoma, adenoma, hepatic metastases of extrahepatic tumours, focal nodular hyperplasia of the liver and cholangiocarcinoma) were not associated with altered CMKLR1 mRNA levels in the liver tissues used herein (Figure 1A).

In the patients with normal liver and in the whole study group, CMKLR1 mRNA did not correlate with age (r = −0.249, p = 0.162 in the control group and r = 0.050, p = 0.596 in the whole cohort) or Body mass index (BMI) (r = −0.189, p = 0.292 in the control group and r = 0.057, p = 0.546 in the whole cohort; data not shown). CMKLR1 mRNA was similarly expressed in the liver of normal-weight (BMI ≤ 25 kg/m²), overweight (BMI > 25 and < 30 kg/m²) and obese patients (BMI ≥ 30 kg/m²) (Figure 1B). CMKLR1 mRNA was not related to gender (Figure 1C).

2.2. Hepatic CMKLR1 mRNA in Human Non-Alcoholic Fatty Liver Disease (NAFLD)

In patients with definite NASH (NASH score ≥ 5), CMKLR1 mRNA was not significantly increased compared to controls and compared to patients with borderline NASH (NASH score < 5) (Figure 2A). When the first two groups with similar median values of CMKLR1 mRNA were combined, levels were significantly lower compared to NASH patients (Figure 2B). Receiver operating characteristic (ROC) curve analysis (Figure 2C) revealed an area under the curve (AUC) of 0.648 excluding analysis of CMKLR1 mRNA as a tool for NASH diagnosis. Alanine aminotransferase (r = 0.025, p = 0.802), aspartate aminotransferase (r = −0.79, p = 0.447), alkaline phosphatase (r = 0.139, p = 0.167) and bilirubin (r = −0.104, p = 0.295) in serum were not associated with hepatic CMKLR1 mRNA (data not shown). CMKLR1 did not correlate with steatosis grade (r = 0.146, p = 0.114) but positively correlated with inflammation (r = 0.248, p = 0.007), fibrosis (r = 0.425, p < 0.001) and NASH score (r = 0.272, p = 0.003) (Figure 2D–F and data not shown).

Type 2 diabetes, hypertension and dyslipidemia are commonly diagnosed in NASH patients [3]. Systemic chemerin positively correlates with low-density lipoprotein cholesterol, insulin resistance and systolic as well as diastolic blood pressure [9]. Whether hepatic CMKLR1 is associated with metabolic diseases such as hypercholesterolemia or type 2 diabetes has not been evaluated to our knowledge so far.

CMKLR1 mRNA was similar in the 14 patients with and those without hypercholesterolemia (data not shown). In the 45 hypertensive patients, hepatic CMKLR1 mRNA was not changed (data not shown). CMKLR1 mRNA was elevated in the 15 patients with type 2 diabetes (Figure 2G). Type 2 diabetes is a risk factor for NAFLD [2] and the NASH score was significantly higher (p = 0.001) in this group.

In the NASH group 11 patients had diabetes, and here, CMKLR1 mRNA was comparable to that of non-diabetic NASH patients (p = 0.201, Figure 2H). Similarly, CMKLR1 mRNA was unchanged in the 10 patients with NASH and hypercholesterolemia (p = 0.935) and the 17 hypertensive NASH patients (p = 0.367) compared to NASH patients not suffering from these co-morbidities (data not shown).

2.3. Hepatic CMKLR1 mRNA in Females

Recently, gender-specific associations of hepatic CMKLR1 expression with liver histology have been identified in chronic hepatitis [16]. Therefore, CMKLR1 mRNA was analyzed in both genders separately. In the female patients 22 had a normal weight, 15 were overweight and 19 were obese. CMKLR1 mRNA expression was, however, not associated with BMI (r = 0.031, p = 0.823; Figure 3A). Of the 56 female patients, 17 had normal liver, 25 borderline NASH and 14 NASH. CMKLR1 mRNA was similarly expressed in the three groups (Figure 3B). There was no difference in the hepatic levels of CMKLR1 mRNA compared to the combined values of the controls and those with borderline NASH (p = 0.609). CMKLR1 mRNA did not correlate with steatosis grade (r = 0.075, p = 0.582), inflammation (r = 0.054, p = 0.693), fibrosis (r = 0.248, 0.068) and NASH score (r = 0.137, p = 0.314) (Figure 3C and data not shown). Alanine aminotransferase (r = −0.040, p = 0.787), aspartate aminotransferase (r = −0.234, p = 0.113), alkaline phosphatase (r = 0.170, p = 0.249), and bilirubin (r = −0.066, p = 0.647) in serum were not associated with hepatic CMKLR1 mRNA (data not shown).

CMKLR1 levels tended to be increased in the six females with hypercholesterinemia (Figure 3D). There was a modest trend to a higher expression in the liver of the five females with type 2 diabetes (p = 0.103, Figure 3E). CMKLR1 expression was not related to hypertension diagnosed in 16 females (data not shown).

2.4. Hepatic CMKLR1 mRNA in Males

In the male cohort 17 patients had a normal weight, 28 were overweight and 17 were obese. CMKLR1 mRNA was not associated with BMI (r = 0.068, p = 0.607; Figure 4A). Of the 62 male patients, 16 had normal liver, 22 borderline NASH and 24 NASH. CMKLR1 mRNA was similar in the liver of male NASH patients compared to those with borderline NASH and controls. When the last two cohorts were combined, CMKLR1 mRNA was lower compared to that of NASH patients (Figure 4C). ROC analysis (Figure 4D) revealed an AUC of 0.723. The optimal cut-off point was 1.7 with a sensitivity of 88% and a specificity of 48% to detect NASH. CMKLR1 mRNA positively correlated with inflammation score (r = 0.404, p = 0.001), fibrosis score (r = 0.555, p < 0.001; Figure 4E) and NASH score (r = 0.392, p = 0.002).

Alanine aminotransferase (r = 0.028, p = 0.839), aspartate aminotransferase (r = 0.055, p = 0.705), alkaline phosphatase (r = 0.225, p = 0.108) and bilirubin (r = −0.132, p = 0.346) in serum were not associated with hepatic CMKLR1 mRNA (data not shown).

In males, CMKLR1 expression tended to be higher in the 10 patients with type 2 diabetes (p = 0.058, Figure 4F). Expression was not related to hypertension (29 patients) and hypercholesterinemia (8 patients) (Figure 4G and data not shown).

To exclude that the higher number of type 2 diabetic patients accounts for associations of CMKLR1 mRNA with NASH in male patients; correlation analysis was performed using data of the 52 males without this co-morbidity. CMKLR1 mRNA still correlated with inflammation (r = 0.378, p = 0.006), fibrosis (r = 0.547, p < 0.001) and NASH score (r = 0.312, p = 0.024).

3. Discussion

We present evidence that hepatic CMKLR1 mRNA expression is associated with NASH in male patients. Here, positive correlations of CMKLR1 mRNA with inflammation score, fibrosis score and consequently NASH score have been identified. The correlation coefficients are rather low but associations are highly significant. In females, hepatic CMKLR1 expression is not related to features of NASH. Although the current study could not identify increased CMKLR1 expression in human NASH, a recent study reported elevated CMKLR1 in those patients. Gender-related analysis has not been performed in this cohort [7].

CMKLR1 mRNA is comparable in both genders in the cohort analyzed herein. Levels of mRNA are also similar in female and male patients with chronic hepatitis C [16]. In hepatitis C patients, CMKLR1 mRNA is not related to inflammation and a negative association with fibrosis has been identified in females only [16]. CMKLR1 mRNA regulation in chronic liver disease is therefore influenced by gender and etiology of hepatic injury. The prevalence of NASH is higher in males, and this may be due to the fact that sex hormones affect NASH severity [17,18]. Modest upregulation of CMKLR1 in male NASH patients obviously contributes an additional factor responsible for gender-related differences in NASH pathology.

Obesity is a risk factor for NAFLD [1]. The mature-onset obesity phenotype has been observed in male but not female CMKLR1-deficient mice [12]. Our results do not show any relation between hepatic CMKLR1 mRNA and BMI, arguing against an association of liver CMKLR1 levels and body weight.

Interestingly, hepatic CMKLR1 tends to be increased in type 2 diabetes patients in both genders and upregulation is significant in the whole cohort. This suggests that elevated CMKLR1 mRNA in the liver of these patients is not necessarily related to NASH which has a higher prevalence in type 2 diabetes [2]. There is, however, no difference in CMKLR1 mRNA in male NASH patients with and without type 2 diabetes. Hypercholesterinemia in females is also linked to an increase in hepatic CMKLR1. Blockage of cholesterol synthesis in adipocytes does not affect CMKLR1 protein levels, while chemerin is strongly reduced [19]. In hepatocytes, elevation of cellular cholesterol does not change CMKLR1 protein [15]. Therefore, CMKLR1 levels seem not to be related to cellular cholesterol concentrations. Dyslipidemia may nevertheless affect hepatic CMKLR1 activity in females independent of NAFLD. A limitation of the current study is the relatively low number of patients with type 2 diabetes and hypercholesterolemia. There are no patients suffering from these co-morbidities in the control group and only few patients in the borderline NASH group. Therefore, the association of CMKLR1 with type 2 diabetes and/or hypercholesterolemia has to be evaluated in different cohorts using patients who ideally do not suffer from NASH. The main intention of the present study was, however, to identify NAFLD-related changes of this hepatic chemokine receptor. CMKLR1 mRNA was still associated with inflammation, fibrosis and NASH score when those suffering from type 2 diabetes were excluded.

The association of CMKLR1 with NASH score in male NASH patients may suggest a higher activity of CMKLR1-related signaling pathways.

Chemerin is abundantly expressed in the liver, and in patients with chronic hepatitis C mRNA levels are similar in males and females [8,16]. In human NASH, hepatic chemerin expression is induced [7] while Deng et al. described lower levels in human fatty liver [6]. Gender-related regulation of liver chemerin has not been evaluated so far. Serum chemerin is found increased in females in some but not all studies [20]. The CMKLR1 receptor is only activated by proteolytic cleaved chemerin [9] and we are unaware of data on gender-related activation of this adipokine. Additional investigations are needed to evaluate whether chemerin signaling is indeed enhanced upon higher expression of hepatic CMKLR1. Further, the physiological and pathophysiological roles of CMKLR1/chemerin signaling in the liver have to still be clarified.

Resolvin E1 is an additional ligand of CMKLR1 [11]. In ob/ob mice, this lipid ameliorates insulin sensitivity and hepatic steatosis [21]. In a murine model of liver fibrosis induced by Schistosoma japonicum infection, resolvin E1 treatment reduces the growth of granulomas and thereby delays hepatic fibrogenesis [22]. However, resolvin E1 fails to improve liver injury in mice fed an atherogenic diet to induce NASH [23]. Resolvins are derived from ω-3 polyunsaturated fatty acids [24] and ethyl-eicosapentanoic acid could not ameliorate NASH in a clinical trial [25]. Therefore, the potential beneficial effects of resolvins in NASH have to be proven in future studies.

The non-availability of protein from the respective liver tissues may be considered as a limitation of our study. Recently, our group has shown that CMKLR1 protein is reduced in human steatotic liver [15]. However, the liver tissue of only 14 patients was analyzed and gender-related regulation was not determined.

In summary, the present study demonstrates a weak association of hepatic CMKLR1 expression with features of NASH in male patients.

4. Materials and Methods

4.1. Study Group

Liver tissues of controls and patients with NAFLD were received and details of the patients are summarized in Table 1. These samples have been introduced in a recent study [26]. Details of the histological scoring which was done as described [27] are summarized in

Table 2. Scoring of steatosis, inflammation and fibrosis.

Scores	Description
Steatosis 0	<5% steatosis
Steatosis 1	5%–33% steatosis
Steatosis 2	>33%–66% steatosis
Steatosis 3	>66%
Inflammation 0	No foci/20 × field
Inflammation 1	<2 foci/20 × field
Inflammation 2	2–4 foci/20 × field
Inflammation 3	>4 foci/20 × field
Fibrosis 0	No fibrosis
Fibrosis 1	Zone 3 perisinusoidal/pericellular fibrosis; focally or extensively present
Fibrosis 2	Zone 3 perisinusoidal/pericellular fibrosis with focal or extensive periportal fibrosis
Fibrosis 3	Zone 3 perisinusoidal/pericellular fibrosis and portal fibrosis with focal or extensive bridging fibrosis
Fibrosis 4	Liver cirrhosis

. The scores were summed up and ranged from 0 to 9. Patients with a score of ≥5 were defined as NASH patients. Alcohol abuse, viral infections and drugs are known to cause liver injury, and therefore, these patients were excluded. Indications for surgery was hepatic metastases of extrahepatic tumours for 70 patients, focal nodular hyperplasia of the liver for nine patients, adenoma for six patients, cholangiocarcinoma for 15 patients, hepatocellular carcinoma for 12 patients and other diseases in 6 patients. Only healthy tissue was used for isolation of RNA. Hypertension, hypercholesterolemia and type 2 diabetes diagnosis had been documented. Serum lipids and glucose were not recorded. Experimental procedures accord to the guidelines of the charitable state controlled foundation Human Tissue and Cell Research and the study was authorized by the local ethical committee of the University of Regensburg (Identification code: 12-101-0048; date: 29 March 2012). The written informed consent was obtained from each patient.

4.2. Monitoring of Gene Expression by Real-Time RT-PCR

The LightCycler FastStart DNA Master SYBR Green I kit from Roche (Mannheim, Germany) was used for analyzing the expression of mRNA semi-quantitatively by real-time RT-PCR. Total cellular RNA was reverse transcribed using the Promega Reverse Transcription System (Promega, Madison, WI, USA). The cDNA was used for amplification in glass capillaries (LightCycler, Roche). Oligonucleotides were synthesized by Metabion (Planegg-Martinsried, Germany). Real-time RT-PCR was performed as described and sequencing of the amplified DNA fragments (Geneart, Regensburg, Germany) confirmed the specificities of the PCRs [19]. Serially diluted cDNA was used to create a standard curve for each gene analyzed. The second derivative maximum method was used for quantification with the LightCycler software. Primers to amplify human CMKLR1 were 5′-ACC TGC ATG GGA AAA TAT CCT-3′ and 5′-GAG GTT GAG TGT GTG GTA GGG-3′. The 18S rRNA was used for normalization and amplified with 5′-GAT TGA TAG CTC TTT CTC GAT TCC-3′ and 5′-CAT CTA AGG GCA TCA CAG ACC-3′.

4.3. Statistical Analysis

Data are displayed as box plots and median, lower and upper quartiles and range of the values are shown. The Mann-Whitney U Test (SPSS Statistics 21.0 program, IBM, Leibniz Rechenzentrum, München, Germany) was used for comparison of two data sets and Anova followed by a Dunnett post-hoc test was used for comparison of three data sets. ROC analysis and Spearman correlation were done using SPSS Statistics 21.0 program. Youden index was calculated to identify the best cut-off point. A value of p < 0.05 was regarded as significant. Distribution of gender and co-morbidities listed in Table 1 was analyzed with the Chi-square test.