SLAMF6/Ly108 promotes the development of hepatocellular carcinoma via facilitating macrophage M2 polarization.

Tumor-associated macrophages (TAMs) are capable of worsening hepatocellular carcinoma (HCC) prognosis by accelerating tumor growth and progression. Signaling lymphocyte activation molecule family member 6 (SLAMF6; Ly108 in mice) is an immune regulator that is involved in numerous diseases. However, whether SLAMF6 might affect macrophage function in HCC has not yet been reported. Therefore, the present study aimed to determine the relationship between SLAMF6 expression on macrophages and HCC progression. In the present study, the expression of SLAMF6 in human blood samples and mice was analyzed by flow cytometry. Furthermore, macrophage-related polarization markers were detected via reverse transcription quantitative PCR. Clonogenic formation and Transwell assay were performed to determine the proliferation, migration and invasion of HCC cells. In addition, a murine HCC model was established to detect the function of SLAMF6 in vivo. The results demonstrated that SLAMF6 expression was increased in CD14+ cells obtained from patients with HCC. It was also determined that this increase was associated with a positive hepatitis B virus DNA status and high levels of α-fetoprotein. Polarized TAMs from THP-1 cells, murine peritoneal macrophages and murine bone marrow-derived macrophages all exhibited higher levels of SLAMF6 compared with M1 cells. Furthermore, an increased expression of Ly108 was detected in macrophages obtained from mice tumor tissues, indicating that the tumor microenvironment may promote Ly108 expression and macrophage M2 polarization. Ly108 small interfering RNA was applied to macrophages, which resulted in the suppression of M2 polarization. Ly108-silenced macrophages attenuated HCC cell migration and invasion and prevented tumor growth by inhibiting the nuclear factor-κB pathway. Altogether, the results from the present study suggested that SLAMF6/Ly108 was upregulated in TAMs, which may in turn accelerate the development of HCC. Copyright: © Meng et al.

Introduction

Liver cancer was the seventh most common type of cancer and the second leading cause of cancer-associated mortality worldwide in 2020 (1). Among patients with liver cancer, hepatocellular carcinoma (HCC) accounts for >90% of cases. Patients with HCC typically demonstrate a poor prognosis, which can be attributed to a diagnosis at an advanced stage (2). Previous studies have reported that immunotherapy can serve an important role in the treatment of HCC (3,4). Based on these previous studies, it is necessary to evaluate the functional molecules associated with HCC in order to determine a potential therapeutic target in the HCC immune microenvironment.

Tumor-associated macrophages (TAMs) are a type of primary tumor-infiltrating immune cells (5) that have been demonstrated to promote tumor growth, metastasis and invasion (6,7). TAMs can be divided into two main types as follows: The classically activated M1 phenotype and the alternatively activated M2 phenotype (8). M1 macrophages are polarized by the activation of interferon gamma (IFN-γ), promoting the T-helper (Th)1 immune response and antitumor activity (9,10). M2 macrophages are polarized by interleukin (IL)-4/IL-13 and are associated with the anti-inflammatory Th2 immune response, which demonstrates a pro-tumor activity (11). Previous studies have revealed that most TAMs are of the M2 phenotype, which promote tumor growth and progression and therefore worsen the prognosis of patients with HCC (12,13). To further validate the results of these studies, it is necessary to explore and block the key stages of macrophage M2 polarization in order to inhibit HCC progression.

The signaling lymphocyte activation molecule (SLAM) family comprises the following nine members: CD150 (SLAMF1), CD48 (SLAMF2), CD229 (SLAMF3), CD244 (SLAMF4), CD84 (SLAMF5), CD352 (SLAMF6), CD319 (SLAMF7), CD353 (SLAMF8) and CD84-H1 (SLAMF9) (14). These are surface molecules that are expressed on hematopoietic cells. They are also a type of immune molecule that can regulate innate and adaptive immunity by activating associated immune cells (14,15). Among these nine molecules, SLAMF6 (Ly108 in mice) is highly expressed in activated T and B cells. Its expression can also be increased in dendritic cells and macrophages via inflammatory signals (16), functioning as both a positive and negative regulator of the immune response (17). SLAMF6 can inhibit the secretion of T-dependent and T-independent antibodies (18). It has also been reported that SLAMF6 can activate natural killer cells to induce cytotoxicity and influence IFN-γ production (19,20). SLAMF3 is involved in the inhibition of HCC progression and cell proliferation (21,22). In addition to SLAMF6, there are several SLAMF family members that are expressed on the macrophage surface, including SLAMF3, SLAMF4, SLAMF5 and SLAMF7 (23). SLAMFs have been demonstrated to negatively influence the function of macrophages by reducing IL-6 production and increasing IL-13 secretion (24).

As a membrane protein that is expressed on immune cells, SLAMF6 has been proven to serve a role in numerous diseases (25–28). For example, although the expression of SLAMF6 on peripheral T cells is not markedly different in patients with systemic lupus erythematosus, it has been determined that the co-stimulatory function of SLAMF6 is lacking (25). In addition, SLAMF6 can promote Th17 differentiation (26). SLAMF6 can also stimulate the interaction between colonic innate immune cells and Gram-negative bacteria, thus reducing mucosal protection and enhancing inflammation, resulting in lethal colitis in mice (27). The administration of anti-SLAMF6 antibodies combined with ibrutinib, which is a Bruton tyrosine kinase inhibitor that serves as an anticancer targeted drug, can effectively eliminate tumor cells in the spleen, bone marrow, liver and peritoneal cavity (28). SLAMF6 can affect the function of Th2 by binding to downstream proteins and transcription factors, such as nuclear factor-κB (NF-κB) (29), which serves a role in macrophage polarization (30).

The present study investigated the expression of SLAMF6 in the peripheral CD14+ monocytes of patients with HCC to determine whether this expression was associated with the clinicopathological characteristics of these patients. Furthermore, SLAMF6 expression on different phenotype macrophages was detected in order to explore the relationship between this and HCC progression. This may provide a novel therapeutic target for HCC treatment.

Materials and methods

Blood sampling and mononuclear cell isolation

Blood samples were obtained from 34 patients with HCC and 33 healthy individuals at the Shandong Cancer Hospital and Institute (Jinan, China). Patients with HCC did not receive any form of antitumor therapy and were pathologically diagnosed with HCC prior to sampling. None of the healthy donors were positive for hepatitis B virus (HBV), hepatitis C virus or human immunodeficiency virus, consumed excessive alcohol or received any chemotherapy prior to sampling. Human peripheral mononuclear cell isolation was performed by centrifuging (800 × g; 15 min; 25°C) blood samples with an EZ-Sep™ lymphocyte separation tube (Dakewe Biotech Co., Ltd.). The mono-macrophages were marked with corresponding markers immediately after the isolation. The present study was approved by the Medical Ethics Committee of Shandong Cancer Hospital and Institute and informed consent was obtained from each participant. The clinicopathological characteristics of the healthy donors and patients with HCC are summarized in Table I.

Table I.

Clinicopathological characteristics of patients with hepatocellular carcinoma and healthy donors.

Variable	HCC patients (n=34)	Healthy donors (n=33)
Sex
Male, n (%)	26 (76.47)	25 (75.76)
Female, n (%)	8 (23.53)	8 (24.24)
Age, mean years (range)	60 (41–80)	44 (21–62)
HBV-DNA, n (+, %)	12 (35.29)	0
AFP, n (>100, %)	14 (41.18)	0
Single tumor, n (%)	13 (38.24)	0
Lymphatic metastasis, n (%)	10 (29.41)	0
Distant metastasis, n (%)	7 (20.59)	0
TNM stage I–II, n (%)	13 (38.24)	0

AFP, α-fetoprotein; HBV, hepatitis B virus; TNM, Tumor-Node-Metastasis.

Mouse HCC model establishment and macrophage isolation

C57BL/6 mice were purchased from Beijing Weitonglihua Laboratory Animal Co., Ltd. and maintained in a controlled room (specific pathogen free; 12-h light/dark cycle; free access to food and water, temperature, 20–26°C; relative humidity, 40–70%). All experiments involving mice were approved by the Animal Care Committee of Shandong Cancer Hospital and Institute and performed according to the Animal Management Rules of the Chinese Ministry of Health. To establish a murine model of HCC, 100 µl PBS solution containing 1×106 H22 cells (cat. no. CL-0341; American Type Culture Collection) was subcutaneously injected into eight C57BL/6 male mice (8–10 weeks old; average weight, 22.32±0.19 g). After 14 days, the mice were euthanized via intraperitoneal injection of 100 mg/kg sodium pentobarbital followed by cervical dislocation (average weight, 24.17±0.62 g). The subsequent experiments were conducted immediately after the tissues were collected. The infiltrating lymphocytes from each type of tissue were isolated by centrifugation (800 × g; 20 min; 25°C) over 40% Percoll solution (GE Healthcare) (31), after which the expression level of SLAMF6 was evaluated by flow cytometry.

Flow cytometry

Flow cytometry was performed to detect the expression of SLAMF6 and various surface markers in macrophages. Human peripheral blood mononuclear cells (CD14+) were stained with anti-human SLAMF6-PE [cat. no. 317208; 3 µl stock solution/test (1×106 cells); BioLegend, Inc.] and anti-human CD14-FITC [cat. no. 301804; 5 µl stock solution/test (1×106 cells); BioLegend, Inc.] antibodies for 30 min at 4°C. Furthermore, murine macrophages (CD11b+) were stained with anti-mouse SLAMF6-PE [cat. no. 2124557; 3 µl stock solution/test (1×106 cells); eBioscience; Thermo Fisher Scientific, Inc.] and anti-mouse CD11b-PE-cy7 [cat. no. E07514-1633; 2 µl stock solution/test (1×106 cells); eBioscience; Thermo Fisher Scientific, Inc.] antibodies for 30 min. A total of ~10,000 cells were analyzed using BD FACSAria II (BD Biosciences) equipment and cells were gated according to their forward and side scatter properties.

Cell culture

Murine HCC cell lines, including H22 [cultured in RMPI-1640 containing 10% FBS and 1% penicillin/streptomycin mixture (cat. no. 15140-122; Gibco; Thermo Fisher Scientific, Inc.)] and Hepa1–6 (cat. no. CL-0105; cultured DMEM containing 10% FBS and 1% penicillin/streptomycin mixture), were obtained from the American Type Culture Collection. Murine peripheral macrophages (PMs) and bone marrow-derived macrophages (BMDMs) were cultured in DMEM containing 10% FBS and 1% penicillin/streptomycin mixture and placed at 37°C in a humidified incubator containing 5% CO2. The human monocyte cell line THP-1 (cat. no. BNCC100407; BeNa Culture Collection; Beijing Beina Chunglian Institute of Biotechnology) was cultured in RMPI-1640 supplemented with 10% FBS and 1% penicillin/streptomycin mixture. DMEM (cat. no. C11995500CP) was obtained from Gibco; Thermo Fisher Scientific, Inc., RMPI-1640 (cat. no. SH30809.01) was purchased from HyClone; Cytiva and FBS (cat. no. WXBD5226V) was obtained from Sigma-Aldrich; Merck KGaA.

Macrophage polarization

Mouse peritonitis was induced by intraperitoneal injection of 1 ml sterile 6% starch solution in six 8–10 week old male C57BL/6 mice. After 72 h, mice were euthanized via intraperitoneal injection of 100 mg/kg sodium pentobarbital followed by cervical dislocation. The peritoneal cells were harvested by irrigating the abdominal cavity and the PMs were enriched by quick adhesion. Model establishment, harvesting of cells and quick adhesion were described previously (32). PMs were polarized into M1 phenotypes using 100 ng/ml lipopolysaccharide (LPS) for 24 h at 37°C, while M2 macrophages were polarized using 20 ng/ml IL-4 for 24 h at 37°C. PBS was used as a control. Furthermore, six 4–6 week old male C57BL/6 mice were euthanized via intraperitoneal injection of 100 mg/kg sodium pentobarbital followed by cervical dislocation. The BMDMs were collected by flushing the femurs and tibias (32). BMDMs were polarized into the M1 phenotype using 20 ng/ml granulocyte macrophage colony-stimulating factor (cat. no. AF-315-03-20; PeproTech, Inc.) treatment for 5 days at 37°C, while the M2 phenotype was obtained using 100 ng/ml macrophage colony-stimulating factor (cat. no. AF-315-02-10; PeproTech, Inc.) treatment for 5 days at 37°C. Samples were then stimulated using 100 ng/ml LPS for 24 h to induce M1 or 20 ng/ml IL-4 for 24 h to induce M2.

HCC conditioned medium (HCM)

After culturing H22 cells for 24 h, serum-free DMEM was collected for use as HCM. Newly isolated PMs (2×105 per well) seeded into 12-well-plates were exposed to 200 µl HCM, producing a final volume of 1,000 µl with complete medium (DMEM containing 10% FBS). The control group was treated with 200 µl FBS-free DMEM added to 800 µl complete medium. The final percentage of HCM was 20%.

SLAMF6 interference

SLAMF6 expression was inhibited in murine PMs via transfection with SLAMF6 small interfering RNA (siRNA). Three siRNAs were tested and all sequences were working. The sequences of the siRNAs are presented in Table II. SLAMF6 siRNA (120 pmol) or non-targeting negative control siRNA (120 pmol) (Biosune Biotechnology Co., Ltd.) were transfected into the PMs in each of the 12 wells using lipofectamine RNAiMAX (cat. no. 13778-150; Invitrogen; Thermo Fisher Scientific, Inc.) for 24 h at 37°C. After 24 h, the PMs, which had been transfected with siRNAs, were treated with Bay11-7082 (10 µM; cat. no. HY-13453; MedChemExpress), an inhibitor of NF-κB, for 2 h before IL-4 (20 ng/ml) was added for 24 h. SLAMF6-silenced PMs, negative control PMs and their culture supernatants were collected (immediately or after storage at −80°C in an ultra-low temperature freezer within 1 month) to examine the effect of SLAMF6 on cell proliferation and invasion, since macrophages exert their function on tumor cells via secretion of cytokines.

Table II.

Sequence of Ly108 small interfering RNAs used for transfection and of primers used for RT-qPCR.

Primer	Sequence
Small interfering RNA
Control, sense	UUCUCCGAACGUGUCACGUTT
Ly108-366, sense	GCUAAUGAAUGGCGUUCUATTUAGAACGCCAUUCAUUAGCTT
Ly108-567, sense	CCUGCAAAUCAGCAACCUUTTAAGGUUGCUGAUUUGCAGGTT
Ly108-1190, sense	CCAUGACAAUUUACUCCAUTTAUGGAGUAAAUUGUCAUGGTT
RT-qPCR
Homo-β-actin, forward	CATGTACGTTGCTATCCAGGC
Homo-β-actin, reverse	CTCCTTAATGTCACGCACGAT
Homo-SLAMF6, forward	GGCCCAGGGAATGTAGTTTCA
Homo-SLAMF6, reverse	ACTGACTCCCCCAGAATCCC
Homo-TNF-α, forward	GAGGCCAAGCCCTGGTATG
Homo-TNF-α, reverse	CGGGCCGATTGATCTCAGC
Mouse-β-actin, forward	CGGGCCGATTGATCTCAGC
Mouse-β-actin, reverse	TACAGCCCGGGGAGCATCGT
Mouse-ly108, forward	CCTTCAGGGTAATGGGTTGGTT
Mouse-ly108, reverse	CCTTCAGGGTAATGGGTTGGTT
Mouse-arg-1, forward	TGTCCCTAATGACAGCTCCTT
Mouse-arg-1, reverse	GCATCCACCCAAATGACACAT
Mouse-TNF-α, forward	GCCACCACGCTCTTCTGTCT
Mouse-TNF-α, reverse	TGAGGGTCTGGGCCATAGAAC
Mouse-iNOS, forward	GCCACCAACAATGGCAACAT
Mouse-iNOS, reverse	TCGATGCACAACTGGGTGAA
Mouse-IL-1β, forward	ACCTTCCAGGATGAGGACATGA
Mouse-IL-1β, reverse	AACGTCACACACCAGCAGGTTA

Arg-1, arginase-1; IL-1β, interleukin 1β; iNOS, inducible nitric oxide synthase; RT-qPCR, reverse transcription quantitative PCR; SLAMF6, signaling lymphocytes activation molecule family member 6; TNF-α, tumor necrosis factor-α.

Analysis of tumor cell migration, invasion and proliferation, and in vivo assessment

The culture supernatant of SLAMF6-silenced PMs and control PMs was used to culture Hepa1–6 cells. Transwell assay cell migratory and invasive abilities were determined using 24-well transwell chambers with an 8-µm pore polycarbonate membrane insert (Corning, Inc.; cat. no. 3422). For invasion assay only, the membrane was pre-coated with 50 µl Matrigel (cat. no. 356234; BD Biosciences) for half an hour. Then, ~2.5×104 Hepa1–6 cells suspended in 200 µl serum-free DMEM were loaded onto the upper chamber, while 600 µl medium collected from corresponding macrophages, as aforementioned in the SLAMF6 interference section, was added to the lower chamber. After 16 h (migration) or 24 h (invasion), the cells on the lower chamber were stained with 0.1% crystal violet for 10 min at room temperature. The number of invaded cells were counted under a light microscope (magnification, ×200).

To prepare murine hepatoma homografts, 2×105 H22 cells in 100 µl PBS were subcutaneously injected into the groins of 14 C57BL/6 male mice (8–10 week old; average weight, 22.72±0.17 g), which were anesthetized by intraperitoneal injection with 50 mg/kg sodium pentobarbital. At 8 days after H22 cell injection, SLAMF6-silenced PMs and control PMs were injected into the tumor site, after which time the size of tumors was measured. Tumor volume was calculated using the following formula: 1/2ab2 (a, long diameter; b, short diameter). The procedure was repeated every other day. On the 18th day, all mice were euthanized via intraperitoneal injection of 100 mg/kg sodium pentobarbital followed by cervical dislocation (average weight, 25.03±0.71 g), after which tumors were collected and their size and weight were determined. The maximum tumor volume was as follows: 1/2×17.0×16.5×16.5=2,314.125 mm3.

RNA isolation and reverse transcription quantitative (RT-q)PCR

According to the manufacturer's protocol, RNA was extracted from THP-1 cells and PMs using the Fastagen RNA isolation kit (cat. no. 220011; Fastagen Biotech). Subsequently, RNA was reverse transcribed into cDNA using the Takara reverse transcription kit (cat. no. RR037A; Takara Biotechnology Co., Ltd.). The PCR thermocycling conditions (Bio-Rad Laboratories, Inc.) were as follows: 95°C for 30 sec, followed by 40 cycles of 95°C for 5 sec. The relative expression levels were normalized to endogenous control and were expressed as 2−ΔΔCq (33). The primers used for PCR are listed in Table II.

Western blotting

PMs were transfected with negative control or Ly108 siRNA and lysed with RIPA lysis buffer (cat. no. P0013B; Beyotime Institute of Biotechnology) at 4°C. Proteins (5 µg/lane), the concentration of which was determined by the BCA protein determination method (cat. no. A53225; Thermo Fisher Scientific, Inc.), were separated by 10% SDS-PAGE and transferred onto PVDF membranes. After blocking membranes with 5% bovine serum albumin (cat. no. A8010; Beijing Solarbio Science & Technology Co., Ltd.) for 2 h at room temperature, membranes were incubated with primary antibodies against phosphorylated (p)-NF-κB p65 (Cell Signaling Technology, Inc.; cat. no. 3033; 1:1,000); NF-κB (Cell Signaling Technology, Inc.; cat. no. 8242; 1:1,000) and β-actin (Cell Signaling Technology, Inc.; cat. no. 3700; 1:1,000) at 4°C overnight. The secondary antibodies (anti-mouse IgG, HRP-linked, cat. no. 7076S, 1:2,000, Cell Signaling Technology, Inc.; anti-rabbit IgG (H+L) antibody conjugated to biotin, cat. no. 14708S, 1:2,000, Cell Signaling Technology, Inc.) were incubated with the membranes at 25°C for 1 h. A western blot Imaging System (Tanon Science and Technology Co., Ltd.) was used to detect protein bands and obtain images using the Alldoc-ECL 2019 software (Tanon Science and Technology Co., Ltd.). The data were analyzed via densitometry and normalized to expression of the internal control (β-actin).

Statistical analysis

All data were analyzed using GraphPad Prism 8 software (GraphPad Software Inc.). A Student's t-test was used to determine differences between two groups. One-way ANOVA followed the Tukey's post hoc test was used to determine the differences between more than two groups. Data are presented as the mean ± standard error of the mean. P<0.05 was considered to indicate a statistically significant difference.

Results

Enhanced SLAMF6 expression in TAMs is related to the severity of HCC

SLAMF6 expression level was detected in the peripheral CD14+ monocytes of patients with HCC and healthy donors. As presented in Fig. 1A, the percentage of peripheral CD14+ monocytes expressing SLAMF6 in patients with HCC was significantly higher compared with healthy donors. The relationship between SLAMF6 expression level and the severity of HCC was subsequently analyzed. As presented in Fig. 1B, the expression level of SLAMF6 was assessed in six groups of patients categorized according to the following criteria: i) The HBV status (negative or positive); ii) the α-fetoprotein (AFP) level (> or <100 ng/ml); iii) the number of tumors (single or multiple); iv) the lymphatic metastasis occurrence (yes or no); v) the distant metastasis occurrence (yes or no); and vi) the different stages of tumors. Among these groups, only two presented with differences in SLAMF6 expression. The expression level of SLAMF6 in CD14+ monocytes from patients with HCC who were HBV-positive was significantly higher than in HBV-negative individuals. Furthermore, an increased expression of SLAMF6 was demonstrated in patients with HCC whose serum AFP level was >100 ng/ml compared with those exhibiting AFP level <100 ng/ml, which indicated a relationship between SLAMF6 expression and HCC poor prognosis (34). Since the age distribution of the patients and the healthy donors was too different for SLAMF6 expression, we made the comparison between the low and high age groups and found no difference between the two age groups (Fig. S1).

Figure 1.

SLAMF6 expression level is increased in monocytes and tumor-associated macrophages. Peripheral CD14+ monocytes were isolated from 34 patients with HCC and 33 healthy donors. (A) Flow cytometry analysis was used to measure the percentage of SLAMF6+CD14+ cells among monocytes. The monocytes were assessed using CD14+ in human peripheral blood mononuclear cells. (B) Association between SLAMF6 expression level and the clinicopathological characteristics of patients with HCC. (C) Using flow cytometry, Ly108 expression level was evaluated in the infiltrating macrophages (assessed using CD11b+) isolated from the tumor and liver tissues of mice, which were subcutaneously injected with 1×106 H22 cells for 2 weeks. *P<0.05 and **P<0.01. SLAMF6, signaling lymphocyte activation molecule family member 6; HCC, hepatocellular carcinoma.

To determine the expression level of SLAMF6 in TAMs, a murine tumor model of HCC was established, after which the expression of Ly108 was determined in TAMs isolated from tumor and liver tissues. As presented in Fig. 1C, when compared with liver tissues, the TAMs isolated from tumor tissues expressed a higher level of Ly108. These results demonstrated that SLAMF6 expression was increased in TAMs, which may be associated with the poor prognosis of patients with HCC.

M2-like macrophages exhibit a higher SLAMF6 expression

As previously reported, TAMs are considered to be M2-like macrophages (35). The present study therefore compared the expression level of SLAMF6 in different types of macrophages. To achieve this, human THP-1, murine PMs and murine BMDMs were polarized into M1- and M2-like macrophages. As presented in Fig. 2A, different expression levels of TNF-α, a M1 marker, indicated that polarization was successful. In addition, the results from RT-qPCR demonstrated that the human M2-like phenotype exhibited higher SLAMF6 expression level compared with the M1-like phenotype. However, the results from flow cytometry analysis revealed that the human M1-like phenotype expressed a higher percentage of SLAMF6 compared with the M2-like phenotype.

Figure 2.

M2-like macrophages exhibit higher SLAMF6 expression level. (A) Flow cytometry analysis was used to determine the percentage of SLAMF6+ THP-1 cells, and the relative expression of SLAMF6 and TNF-α was evaluated via reverse transcription quantitative PCR. The percentage of Ly108+ cells, along with the mean fluorescence intensity of Ly108 expression was also determined in (B) PMs and (C) BMDMs. *P<0.05, **P<0.01 and ***P<0.001. NS, no significance; SLAMF6, signaling lymphocyte activation molecule family member 6; PM, peripheral macrophage; BMDM, bone marrow-derived macrophage; TNF-α, tumor necrosis factor α.

For murine PMs, the mean fluorescence intensity (MFI) of Ly108 expression in the M2-like phenotype was higher than that in the M1-like phenotype. However, the percentage expression of Ly108 did not significantly differ between the two groups according to flow cytometry analysis (Fig. 2B), which may be due to the fact that the PMs we collected were induced by the starch and already expressed ~90% Ly108. Regarding murine BMDMs, the percentage of expression and MFI of Ly108 in M2-like macrophages were higher than in M1-like macrophages (Fig. 2C). These results suggested that the M2-like phenotype exhibited higher SLAMF6 expression level compared with the M1-like phenotype.

Macrophage SLAMF6 expression and polarization is promoted in the tumor microenvironment

The aforementioned results indicated that the M2-like phenotype exhibited increased SLAMF6 expression level. Thus, the present study aimed to determine the reason behind this increase. The effect of HCC microenvironment on PMs was therefore assessed by using HCM. As presented in Fig. 3A, 200 µl HCM significantly promoted Ly108 expression in PMs and induced two positive peaks rather than one positive peak following the negative peak. This result may be due to the fact that HCM enhanced Ly108 expression in macrophages that already expressed a certain amount of Ly108, and HCM might trigger the Ly108 expression in macrophages that did express the molecule at a lower level. In addition, the expression levels of M2 marker arginase-1 (arg-1) and of the M1 markers TNF-α, IL-1β and inducible nitric oxide synthase (iNOS) were increased in the HCM group compared with the control group (Fig. 3B). It was therefore hypothesized that the tumor microenvironment may enhance SLAMF6 expression and that an unknown mechanism may promote M2 polarization in these conditions.

Figure 3.

Ly108 expression and macrophage polarization is promoted by the tumor microenvironment. (A) Flow cytometry was performed to analyze the expression of Ly108, after which the mean fluorescence intensity of Ly108 was measured in PMs cultured with or without hepatocellular carcinoma conditioned medium. (B) Reverse transcription quantitative PCR was subsequently performed to determine the relative expression of arg-1, TNF-α, IL-1β and iNOS in PMs. *P<0.05 and **P<0.01. PM, peritoneal macrophage; arg-1, arginase-1; IL-1β, interleukin 1β; iNOS, inducible nitric oxide synthase; TNF-α, tumor necrosis factor-α.

Ly108 silencing reverses M2 polarization and inhibits HCC progression

Previous studies have revealed that M2-like macrophages can promote HCC growth and invasion (6,8,12). Ly108 siRNA was therefore used to investigate the role of Ly108 in macrophage polarization and HCC progression. As presented in Fig. 4A, Ly108 expression was successfully decreased following siRNA transfection. The results also demonstrated that following Ly108 silencing, the expression of the M2 marker arg-1 was decreased, while the expression of certain M1 markers, including TNF-α, IL-1β and iNOS, was increased. The culture supernatant of macrophages treated with Ly108 or control siRNA was subsequently co-cultured with Hepa1–6 cells (Fig. 4B). Following co-culture, the proliferation, migration and invasion of Hepa1–6 cells was significantly decreased. These results suggested that Ly108 could inhibit the migratory and invasive abilities of Hepa1–6 cells.

Figure 4.

Ly108 promotes M2 polarization and hepatocellular carcinoma cell migration and invasion. (A) Reverse transcription quantitative PCR was performed to determine the relative expression of Ly108, arg-1, TNF-α, IL-1β and iNOS in PMs, which were transfected with SLAMF6 siRNA or negative control siRNA. (B) Clonogenic formation and Transwell assays were performed to evaluate the proliferation, migration and invasion of Hepa1–6 cells. *P<0.05, **P<0.01 and ***P<0.001. NC, negative control; si, small interfering; Arg-1, arginase-1; IL-1β, interleukin 1β; iNOS, inducible nitric oxide synthase; TNF-α, tumor necrosis factor-α.

Macrophage Ly108 promotes HCC growth in vivo

To improve our understanding of the effect of TAM Ly108 on HCC progression in vivo, a murine model of HCC was established. Ly108 siRNA or control siRNA was transfected into M2-like macrophages, which were subsequently injected into C57BL/6 mice. The results demonstrated that, compared with control M2-like macrophages, Ly108 siRNA-transfected M2-like macrophages inhibited the growth of H22 tumors in terms of growth rate, gross tumor volume and tumor weight (Fig. 5A).

Figure 5.

Ly108 promotes hepatocellular carcinoma growth by inhibiting the NF-κB signaling pathway. (A) A murine HCC model was prepared (n=6) and the resulting tumors were weighed at the time of sacrifice. Tumor images are presented in the left panel, while summary data are presented in the right panel. Tumor growth was measured via tumor size, as presented in the middle panel. (B) PMs were transfected with negative control siRNA or Ly108 siRNA, with or without Bay11-7082 prior to treatment with 20 ng/ml IL-4. Western blotting was performed to determine p65 and p-p65 expression. (C) Ly108 siRNA transfection and Bay11-7082 or control DMSO stimulation prior to IL-4 induction was performed on murine PMs. Reverse transcription quantitative PCR was performed to determine the relative expression of arg-1, TNF-α, IL-1β and iNOS. (D) The macrophage culture supernatants in Figure 5C were collected and co-cultured with Hepa1–6 cells for the transwell assays. Clonogenic formation assays were then performed. *P<0.05, **P<0.01 and ***P<0.001. HCC, hepatocellular carcinoma; NC, negative control; si, small interfering; Arg-1, arginase-1; IL-1β, interleukin 1β; iNOS, inducible nitric oxide synthase; TNF-α, tumor necrosis factor-α; NF-κB, nuclear factor-κB; IL-4, interleukin 4; Ctr, control; p, phosphorylated; PMs, peritoneal macrophages.

Ly108 promotes HCC growth via the NF-κB pathway

The present study aimed to determine the potential underlying mechanism of Ly108. As presented in Fig. 5B, the Ly108 siRNA-transfected group presented higher expression of p65 phosphorylation. Furthermore, treatment with Bay11-7082, an inhibitor of NF-κB, inhibited the phosphorylation of p65. In addition, when Ly108 siRNA-transfected macrophages were treated with Bay11-7082, they were able to re-polarize to the M2 phenotype. This result was determined according to higher Arg-1 and IL-1β levels and lower TNF-α and iNOS levels (Fig. 5C). Macrophages of which phenotype was reversed by Bay11-7082 treatment also promoted the proliferation, migration and invasion of Hepa1–6 cells (Fig. 5D). These results indicated that Ly108 may promote HCC progression by inhibiting the NF-κB pathway.

Discussion

SLAMF6 is an immune regulator that is expressed at the surface of hematopoietic cells. Previous studies have revealed that SLAMF6 is involved in numerous diseases, including systemic lupus erythematosus and lethal colitis (25,27). However, the role of macrophages SLAMF6 expression in HCC progression remains unknown. The present study reported increased SLAMF6 expression levels in the HCC microenvironment, which facilitated M2-polarization and promoted HCC cell migration, invasion and proliferation.

The results from the present study suggested that there was a relationship between SLAMF6 and TAM-related tumor-promoting inflammation. SLAMF6 expression level was higher in the peripheral CD14+ monocytes of patients with HCC compared with healthy donors and was associated with certain clinicopathological characteristics of patients. Furthermore, TAMs, also known as M2-like macrophages, exhibited higher SLAMF6 (Ly108 in mice) expression level compared with M1-like macrophages. In addition, the tumor microenvironment was determined to be the cause of high SLAMF6 expression and could also promote macrophage polarization. SLAMF6 expression in TAMs was able to promote HCC cell proliferation, migration and invasion, indicating the important role of SLAMF6 in HCC development.

After demonstrating that SLAMF6 was upregulated in the peripheral CD14+ monocytes of patients with HCC, our study aimed to elucidate the relationship between SLAMF6 expression level and certain clinicopathological characteristics of patients with HCC, including HBV status, AFP level, the number of tumors, the lymphatic metastasis occurrence, the distant metastasis occurrence and the different stages of tumors. Only SLAMF6 expression level in the CD14+ monocytes from patients with HCC that were HBV positive or whose serum AFP levels was >100 ng/ml was significantly higher compared with the control group. This may be due to the diversity of the patients from whom blood samples were obtained. Upregulated SLAMF6 levels were also observed in the murine HCC model, which verifies this conclusion.

Macrophages are classified into two phenotypes: The classically activated M1 phenotype and the alternatively activated M2 phenotype (8). Among these, the M2-like phenotype is considered to be a TAM, serving an important role in the promotion of tumor growth and progression and accelerating HCC cell invasion and migration, thereby worsening patient prognosis (12,13). The results from the present study revealed that TAMs had higher SLAMF6 expression levels compared with M1-like macrophages. Furthermore, these findings were in accordance with those obtained in human blood samples, indicating that the monocytes from patients with HCC may have a tendency towards the M2 phenotype and may therefore exhibit higher SLAMF6 expression level. The present study also demonstrated that the tumor microenvironment may facilitate macrophage SLAMF6 expression and polarization. The tumor microenvironment is extremely complex and its components could promote the expression of SLAMF6. However, this conclusion is difficult to verify. The results from the present study indicated that SLAMF6 silencing significantly inhibited the proliferation, migration and invasion of Hepa1–6 cells. Furthermore, SLAMF6 silencing could inhibit tumor growth in the murine HCC model. Taken together, these finding suggested a potential role of SLAMF6 in TAM-mediated HCC progression.

NF-κB is a signaling pathway that serves an important role in macrophage polarization (30). It has been reported that SLAMF6 regulates the function of Th2 cells via the NF-κB pathway (29). The results from the present study demonstrated that SLAMF6 accelerated HCC growth by inhibiting the NF-κB signaling pathway.

The findings from our study suggested that increased SLAMF6 expression levels in patients with HCC may be caused by the tumor microenvironment, which promoted HCC development via the NF-κB signaling pathway. However, further investigation is required to determine the relationship between SLAMF6 expression and the clinicopathological characteristics of patients with HCC. Furthermore, determining why SLAMF6 expression level was upregulated in M2 macrophages and elucidating the mechanisms underlying the interactions between SLAMF6 and NF-κB should be the aim of future studies.