Advances in Clinical and Experimental Medicine

Title abbreviation: Adv Clin Exp Med
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ISSN 1899–5276 (print)
ISSN 2451-2680 (online)
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Advances in Clinical and Experimental Medicine

2021, vol. 30, nr 10, October, p. 1031–1041

doi: 10.17219/acem/137914

Publication type: original article

Language: English

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Wang T, Lu H. Ganoderic acid A inhibits ox-LDL-induced THP-1-derived macrophage inflammation and lipid deposition via Notch1/PPARγ/CD36 signaling. Adv Clin Exp Med. 2021;30(10):1031–1041. doi:10.17219/acem/137914

Ganoderic acid A inhibits ox-LDL-induced THP-1-derived macrophage inflammation and lipid deposition via Notch1/PPARγ/CD36 signaling

Tao Wang1,A,B,C,D,E,F, Huihe Lu1,A,B,C,E,F

1 Department of Cardiology, Second Affiliated Hospital of Nantong University, China

Abstract

Background. Atherosclerosis (AS), a chronic inflammatory disease, is a major contributor to deaths worldwide. Ganoderic acid A (GAA) has been widely applied for various diseases due to its excellent anti-inflammatory properties.

Objectives. To investigate the underlying mechanism of GAA inhibition of inflammation and lipid deposition in human monocyte (THP-1) cells.

Materials and methods. The Cell Counting Kit-8 (CCK-8) assay was used to assess the potential effect of GAA on the viability of THP-1 cells. The release of inflammatory cytokines and oxidative stress was measured using enzyme-linked immunosorbent assay (ELISA) and the corresponding kit, respectively. The levels of lipid deposition and total cholesterol (TC) were also evaluated. Next, the scavenger receptors and proteins in Notch1/PPARγ/CD36 signaling were measured with western blot. As Notch1 was overexpressed in the THP-1 cells induced by oxidized low-density lipoprotein (ox-LDL), the above assays were performed again to confirm the underlying mechanism.

Results. Ganoderic acid A suppressed ox-LDL-induced inflammation and oxidative stress in THP-1 cells. At the same time, it inhibited the TC level and lipid deposition. The effects of GAA on alleviating inflammation, oxidative stress and lipid accumulation were relieved after the overexpression of Notch1 in the treated cells, and the effects of GAA on alleviating inflammation, oxidative stress and lipid accumulation were diminished. The PPARγ activator also weakened the effects of GAA on relieving inflammation, oxidative stress and lipid accumulation in ox-LDL-induced THP-1 cells.

Conclusions. Ganoderic acid A inhibits ox-LDL-induced macrophage inflammation and lipid deposition in THP-1 cells through Notch1/PPARγ/CD36 signaling, which may provide theoretical guidance for the clinical applications of GAA in AS treatment.

Key words: inflammation, Notch1, PPARγ, ganoderic acid A, lipid deposition

Background

Atherosclerosis (AS), a chronic inflammatory disease, is a leading cause of death worldwide.1 The loading of cholesterol in macrophages of the artery walls contributes to lipid deposition, which is believed to induce the occurrence and development of AS.2 Therefore, AS is considered to have a close relationship with lipid deposition. Apart from lipid deposition and long-term inflammation, immune activation and the stimulation of inflammatory mediators are also AS characteristics. Therapies targeting anti-inflammatory agents are thought to be useful methods for the treatment of AS, but investigation and studies of agents that possess anti-inflammatory effects for the resolution of AS occurrence are limited. Thus, there is a desperate need to study and develop new agents focusing on the inhibition of inflammation for the effective treatment of AS.

Ganoderma lucidum has been widely used in traditional Chinese medicine for the treatment of inflammatory diseases, cancers and immunological diseases.3 It has been applied for thousands of years due to its remarkable physiological and pharmacological activities. Ganoderic acid A (GAA) is one of the major triterpenoids in Ganoderma lucidum. Many experts have confirmed that GAA plays an important role in treating cancers because of its efficacy in preventing proliferation and enhancing apoptosis of multiple cancer cells.4, 5 The anti-inflammatory and anti-oxidant roles of GAA cannot be neglected because rats injected with GAA have been shown to be protected from liver injury and lung injury induced by various factors.6, 7 The latest findings show that GAA has great potential to inhibit Notch1 protein expression, which is believed to enhance the stability of peroxisome proliferator-activated receptor gamma (PPARγ) and increase the level of CD36 in human monocyte (THP-1)-derived macrophages stimulated by interleukin (IL)-4.8, 9 Lipid deposition in macrophage foam cells can contribute to the formation of plaques and exacerbate the development of AS. Inflammation is a critical risk factor for the occurrence of AS.10 Therefore, we speculated that GAA may alleviate the symptoms of AS by inhibiting inflammation and lipid deposition in THP-1-derived macrophages via the Notch1 signal.

A large quantity of low-density lipoprotein (LDL) is modified to oxidized low-density lipoprotein (ox-LDL), which aggregates in the vascular internal wall and triggers atherosclerotic plaque development.11 Therefore, the present study used ox-LDL to induce an AS model.

Objectives

The present study aimed to investigate the effects of GAA on an in vitro AS model as well as its underlying mechanism, which may provide theoretical guidance for the clinical application of GAA in the treatment of AS.

Materials and methods

Cell culture and treatments

Human monocytes (THP-1) were purchased from the American Type Culture Collection (ATCC, Manassas, USA) and cultured in RPMI 1640 medium (Sigma–Aldrich, St. Louis, USA) containing 10% fetal bovine serum (FBS) and antibiotics (100 U/mL of penicillin A and streptomycin) at 37°C in a humidified atmosphere containing 5% CO2. A total of 1 × 105 THP-1 cells were collected and cultivated with 100 nM phorbol-12-myristate13-acetate (PMA; Sigma–Aldrich) for 48 h to stimulate differentiation into macrophages. The harvested macrophages were subsequently cultured in serum-free medium containing ox-LDL (100 ng/mL; Sigma–Aldrich) for 24 h to induce foam cell formation. The GAA was purchased from YuanYe Biotechnology Co., Ltd (Shanghai, China). The cells were then treated with various concentrations of GAA (20 µm, 50 µm or 70 µm) or co-treated with a PPARγ activator. The transfection of THP-1 cells with the overexpression plasmid of Notch1 was performed using Lipofectamine 2000 (Invitrogen, Carlsbad, USA).

CCK-8

A total of 2 × 104 cells were plated into 96-well plates. After the indicated treatment, the Cell Counting Kit-8 (CCK-8; Glpbio, Montclair, USA) reagent was mixed in the culture medium and added to the 96-well plates. These cells were then incubated for 1 h. Next, the absorbance of the cells was measured using a spectrophotometer (Thermo Fisher Scientific, Waltham, USA). The absorbance at 450 nm was measured with a microplate reader (Thermo Fisher Scientific).

ELISA

The levels of tumor necrosis factor-α (TNF-α), IL-1β and IL-6 in the macrophages were evaluated using commercial enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturer’s recommendations (Abcam, Cambridge, UK).

Western blot

Total proteins were extracted from TPC-1 cells with RIPA buffer (Beyotime, Shanghai, China) and the protein concentration was measured using the BCA Protein Assay Kit (Merck Millipore, Burlington, USA). Next, 40 µg of protein in each group was separated using sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to polyvinylidene fluoride (PVDF) membranes (Merck Millipore). The membranes were blocked with 5% skimmed milk. These blots were then incubated with diluted primary antibodies for the target proteins at 4°C overnight, and then secondary antibodies (Santa Cruz Biotechnology, Santa Cruz, USA) were added to the membranes and incubated. ImageJ software (National Institutes of Health, Bethesda, USA) was used to determine the intensities. The expression of protein was normalized to GAPDH levels to correct for loading.

Detection of reactive oxygen species and malondialdehyde

The detection of reactive oxygen species (ROS) was conducted using a commercially available ROS kit (Jiancheng Bioengineering Institute, Shanghai, China), while the detection of malondialdehyde (MDA) was conducted using the corresponding MDA kit from Jiancheng Bioengineering Institute (Nanjing, China) in line with the manufacturer’s instructions.

Oil red O staining of macrophages

The treated macrophages were collected, fixed in 10% formaldehyde solution for 20 min, washed with phosphate-buffered saline (PBS) and stained using oil red O (Amresco, Solon, USA) solution (in 60% isopropanol) for 10 min. Afterwards, the stained macrophages were counterstained with hematoxylin for 3 min. The lipid-stained areas of the slides and cross-sections were observed and photographed using an inverted microscope (Olympus Corp., Tokyo, Japan) at a ×200 magnification. With the application of Image-Pro Plus image analysis software v. 6.0 (Media Cybernetics Inc., Rockville, USA), the lipid droplet content was analyzed.

Measurement of total cholesterol

Total cholesterol (TC) levels were assayed using the Amplex Red Cholesterol Assay Kit (Invitrogen) according to the manufacturer’s protocols.

RT-qPCR

Trizol reagent (Invitrogen) was used to separate the total RNA from THP-1 cells according to the manufacturer’s specifications. Before the real-time quantitative polymerase chain reaction (RT-qPCR) was performed for gene amplification using the SYBR Premix Ex TaqTM GC (TaKaRa, Tokyo, Japan) protocol on a 7900 real-time PCR system (Applied Biosystems, Foster City, USA), the complementary DNA (cDNA) was synthesized from quantified RNA with the use of a PrimeScript TM RT reagent Kit. Relative gene expression was measured using the 2−ΔΔCt method. The ratio for the mRNA of interest was normalized to GAPDH. The primers used in this study are as follows: LOX-1 forward: 5’-TTGCCTGGGATTAGTAGTGACC-3’. reverse: 5’- GCTTGCTCTTGTGTTAGGAGGT-3; SR-A forward: 5’-GCAGTGGGATCACTTTCACAA-3’, reverse: 5’-AGCTGTCATTGAGCGAGCATC-3’; Notch1 forward 5’-GAGGCGTGGCAGACTATGC-3’: reverse 5’-CTTGTACTCCGTCAGCGTGA-3’; PPARγ forward: 5’-GGGATCAGCTCCGTGGATCT-3’ reverse: 5’-TGCACTTTGGTACTCTTGAAGTT-3’; CD36 forward: 5’-GGCTGTGACCGGAACTGTG-3’, and reverse: 5’-AGGTCTCCAACTGGCATTAGAA-3’.

Statistical analyses

The results were analyzed using GraphPad Prism software v. 5.01 (GraphPad Software, San Diego, USA). All data are presented as the mean ± standard deviation (SD). One-way analysis of variance (ANOVA) was utilized to compare differences among multiple groups, followed by Tukey’s post hoc test for comparison between 2 groups. Value of p < 0.05 was considered to be statistically significant.

Results

GAA suppresses ox-LDL-induced inflammation and oxidative stress
in THP-1 cells

To confirm the effects of GAA on THP-1 cells induced by ox-LDL, the toxicity of GAA to macrophages was first assessed. The THP-1 cells were treated with different concentrations of GAA (10 µM, 20 µM, 50 µM, and 70 µM) for 24 h. The analysis showed that GAA had no toxic effect on macrophages (Figure 1A). After 100 nM of PMA treatment of THP-1 cells for 48 h, THP-1 cells were induced to differentiate into macrophages. Next, the macrophages were subjected to ox-LDL stimulation for 24 h. As shown in Figure 1B, inflammation was induced by ox-LDL through significant elevation of the levels of TNF-α, IL-1β, IL-6, and NF-κB p65 protein. However, GAA decreased their levels in a dose-dependent manner (Figure 1C). The high expression of ROS and MDA triggered by ox-LDL was gradually inhibited by increasing the dose of GAA, demonstrating that the possible alteration of oxidative stress status induced by ox-LDL in THP-1 cells was alleviated by increasing the dose of GAA (Figure 1D). Taken together, these findings show that GAA suppresses ox-LDL-induced inflammation and oxidative stress in THP-1 cells.

GAA suppresses lipid deposition
in ox-LDL-induced THP-1 cells

Abnormal lipid metabolism is an important risk factor for the development of AS.12 Therefore, the level of lipid accumulation was measured with oil red O staining. Compared with the control group, ox-LDL-induced THP-1 cells exhibited markedly higher levels of lipid deposition, which were gradually relieved by GAA treatment (Figure 2A). Meanwhile, the TC level of THP-1 cells was markedly ele­vated by ox-LDL. Nevertheless, as the dose of GAA increased, the TC level of THP-1 cells treated by ox-LDL decreased (Figure 2B). The scavenger receptors that play an important part in lipid uptake have a close relationship with the pathogenesis of AS.13 Various scavenger receptors (SR) like SR class A (SR-A), SR class B (CD36) and lectin-like oxidized LDL 1 receptor (LOX-1) can recognize and bind to modified LDL. The uptake of modified lipoproteins by these SRs makes great contributions to foam cell formation.14 Therefore, RT-qPCR and western blot were adopted to measure the expression of SR-A and CD36. The reduced expression of SR-A and CD36 in ox-LDL-induced THP-1 cells treated with GAA implied the inhibitory role of GAA in lipid uptake (Figure 3A,B). Thus, the conclusion can be drawn that GAA suppresses lipid deposition in ox-LDL-induced THP-1 cells.

GAA suppresses expression
of Notch1/PPARγ/CD36 signaling
in ox-LDL-induced THP-1 cells

The effects of GAA on the expression of Notch1, PPARγ and CD36 in ox-LDL-induced THP-1 cells were measured. As seen in Figure 4, compared with the control group, the expression of Notch1, PPARγ and CD36 increased in the ox-LDL group. Notably, the levels of Notch1, PPARγ and CD36 in ox-LDL-induced THP-1 cells were reduced by GAA. Thus, GAA suppresses the expression of Notch1/PPARγ/CD36 in ox-LDL-induced THP-1 cells.

GAA suppresses inflammation and oxidative stress in ox-LDL-induced THP-1 cells via Notch1/PPARγ/CD36 signaling

Next, the expression of Notch1 was increased to a relatively high level to allow detection of its downstream effectors (Figure 5A). The overexpression of Notch1 increased the expression of PPARγ and CD36, indicating a positive relationship between Notch1 and its downstream effectors (Figure 5B). Compared with ox-LDL-induced THP-1 cells with GAA treatment, the expression of inflammatory cytokines and NF-KB p65 was higher in ox-LDL-induced THP-1 cells with combined GAA and the overexpression plasmid of Notch1 (Ov-Notch1) treatment (Figure 6A,B). Similarly, pretreatment with troglitazone (10 µM), which is a PPARγ activator, in ox-LDL-induced THP-1 cells upon GAA challenge for 2 h led to an increased level of inflammatory cytokines. Treatment with Ov-Notch1 and PPARγ activator resulted in higher levels of ROS and MDA, respectively, in ox-LDL-induced THP-1 cells with GAA treatment (Figure 6C). Therefore, GAA suppresses inflammation and oxidative stress in ox-LDL-induced THP-1 cells via Notch1/PPARγ/CD36 signaling.

GAA inhibits lipid deposition
in ox-LDL-induced THP-1 cells
via Notch1/PPARγ/CD36 signaling

To further confirm the role of the Notch1/PPARγ/CD36 signal in lipid deposition in the AS model, the level of lipid accumulation was detected in ox-LDL-induced THP-1 cells with different treatments. As Figure 7A shows, lipid accumulation reached the highest level in ox-LDL-induced THP-1 cells without any other treatment. The GAA greatly relieved lipid accumulation in ox-LDL-induced THP-1 cells. Furthermore, the addition of Ov-Notch1 or PPARγ activator promoted the formation of oil droplets. Notch signaling is recognized to regulate PPARγ protein stability in human macrophages.15 In our study, the TC content, which was reduced by GAA, increased by Notch1 overexpression or PPARγ activator (Figure 7B). The changes in the expression levels of LOX-1 and SR-A demonstrate the same alteration as the abovementioned results (Figure 8A,B). Therefore, the conclusion that GAA inhibits lipid deposition in ox-LDL-induced THP-1 cells via Notch1/PPARγ/CD36 signaling can be drawn. However, Ov-Notch1 and PPARγ activator can partly reverse the suppressive effects of GAA on lipid deposition in ox-LDL-induced THP-1 cells. Together, these results demonstrate that Notch1/PPARγ/CD36 signaling pathway is involved in the effects of GAA on lipid deposition.

Discussion

Macrophages play a critical role in innate immunity and diseases of high prevalence, including cancer, obesity and AS.16 When monocytes arrive at an injury site, they transform into macrophages, the activation of which can respond to signals in damaged tissues.17 Macrophages are thought to play a pathogenic role in the formation of atherosclerotic plaques. The roles of macrophages in AS are tied to its polarization. Polarized macrophages are divided into 2 phenotypes: M1 and M2.2 Activated M1 macrophages can be induced by lipopolysaccharides (LPS), while M2 macrophages are activated after exposure to various cytokines, including IL-4, IL-13 and IL-10.

It was previously reported that pro-inflammatory factors, including IL-1β, IL-6 and TNF-α, are critical contributors to the progression of AS. Thus, it is of great value to find novel targets for the suppression of inflammation related to AS lesions.3 Together with the decrease in the level of NF-KB p65, which is a transcription factor involved in the regulation of inflammation, the inhibition of these cytokines by GAA in THP-1 cells under ox-LDL conditions potently implies the role of GAA in blocking the inflammatory response.18 Consistent with our results, a previous report suggested that GAA caused decreased levels of IL-1β, IL-6 and TNF-α in mice with lung injury.7 Anti-oxidant therapy is considered an effective method for the prevention and treatment of AS because the inflammatory changes triggering the occurrence of AS can be inhibited by suppressing oxidized lipoprotein and lipid formation and oxidative stress.19 Due to the remarkable effects of GAA on alleviating inflammation in multiple injuries and blocking the development of cancers, GAA was hypothesized to play a critical role in AS. We identified that GAA was able to suppress the release of inflammatory factors and oxidative stress in ox-LDL-induced THP-1 cells. Furthermore, lipid deposition induced by ox-LDL in THP-1 cells was relieved by GAA.

Notch signaling is a critical transcriptional factor in the regulation of differentiation and proliferation of stem cells.20 The Notch signaling pathway is involved in interactions among cells throughout the organs of the body in a large number of diseases. It is suggested that the cellular processes of monocytes and the modulation of macrophages are determined by this signaling pathway.21, 22 In the present study, Notch signaling was induced by ox-LDL but inhibited by GAA. Furthermore, the overexpression of Notch1 relieved the inhibitory effect of GAA on the reduction of inflammatory factors and oxidative stress. PPARγ, a ligand-activated transcription factor that regulates fatty acid metabolism, plays a role in lipid deposition, cell differentiation and inflammation.23 It has been reported that ox-LDL can strongly activate PPARγ to regulate gene expression in macrophages.24 The expression of PPARγ was markedly increased after ox-LDL was used to induce THP-1 cells, suggesting successful activation of PPARγ by ox-LDL. The GAA treatment potently inhibited its expression, while the PPARγ activator, which activates the PPARγ signal, led to further inflammation and oxidative stress. Therefore, the mechanism by which GAA alleviates inflammation and oxidative stress might be related to a PPARγ-dependent signal. Internalized ox-LDL supplies rich oxidized fatty acids that serve as ligands to PPARγ, thereby inducing genes such as CD36.25 The role of CD36 in long-chain fatty acid uptake and oxidation has been deeply studied. The findings have shown that it participates in processes like apoptosis, inflammation and AS.26 CD36 has great potential in scavenging ox-LDL to protect intima from cholesterol deposits and atherosclerotic lesions.27 Knockout of CD36 is associated with enhanced symptoms in patients with atherosclerotic cardiovascular diseases.28 In this study, GAA inhibited the expression of Notch1, PPARγ and CD36 as well as lipid deposition. The expression of scavenger receptors could also be inhibited by GAA.

Limitations

There is still a lack of in vivo evidence to confirm the role and action mechanism of GAA in AS. Furthermore, how GAA affects Notch1/PPARγ/CD36 signaling requires deeper investigation.

Conclusions

Ganoderic acid A inhibits ox-LDL-induced THP-1-derived macrophage inflammation and lipid deposition via Notch1/PPARγ/CD36 signaling, which may provide theoretical guidance for the clinical application of GAA in AS treatment.

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

Figures


Fig. 1. The effect of GAA on the viability of THP-1 cells. A. The viability of THP-1 cells treated with GAA was assessed with the CCK-8 assay; B. The inflammatory cytokines in ox-LDL-induced THP-1 cells were detected with ELISA; C. The expression level of NF-kB p65 was measured with western blot; D. Oxidative stress-related factors were measured using the corresponding kits. Experimental data are presented as mean ±SD
*** p < 0.001 compared to ox-LDL (−), # p < 0.05, ## p < 0.01, ### p < 0.001 compared to ox-LDL (+), GAA [µM] (−). ox-LDL − oxidized low-density lipoprotein; ELISA − enzyme-linked immunosorbent assay; SD − standard deviation; CCK-8 − Cell Counting Kit-8; GAA − ganoderic acid A; THP-1 − human monocyte.
Fig. 2. GAA suppresses lipid deposition in ox-LDL-induced THP-1 cells. A. The level of lipid deposition was detected with oil red O staining; B. The TC level was assayed using the Amplex Red Cholesterol Assay Kit. Values are expressed as mean ±SD
*** p < 0.001 compared to ox-LDL (−), # p < 0.05, ### p < 0.001 compared to ox-LDL (+), GAA [µM] (−); ox-LDL − oxidized low-density lipoprotein; TC − total cholesterol; SD − standard deviation; GAA − ganoderic acid A; THP-1 − human monocyte.
Fig. 3. The expression of scavenger receptors was measured with qPCR and western blot. Experimental data are shown as mean ±SD
*** p < 0.001 compared to ox-LDL (−), ## p < 0.01, ### p < 0.001 compared to ox-LDL (+), GAA [µM] (−), #p < 0.05, ###p < 0.001 compared to ox-LDL (+), GAA [µM] (−). ox-LDL − oxidized low-density lipoprotein; SD − standard deviation; GAA − ganoderic acid A; THP-1 − human monocyte; qPCR − quantitative polymerase chain reaction.
Fig. 4. GAA suppresses the expression of Notch1/PPARγ/CD36 in ox-LDL-induced THP-1 cells. A and B. Gene and protein expression in the Notch1/PPARγ/CD36 signaling pathway was assayed using qPCR and western blot, respectively. Experimental data are shown as mean ±SD
*** p < 0.001 compared to ox-LDL (−), #p < 0.05, ##p < 0.01, ###p < 0.001 compared to ox-LDL (+) + GAA [µM] (−). ox-LDL − oxidized low-density lipoprotein; SD − standard deviation; GAA − ganoderic acid A; THP-1 − human monocyte; qPCR − quantitative polymerase chain reaction.
Fig. 5. Notch1 overexpression reversed the effects of GAA. GAA suppresses inflammation and oxidative stress in ox-LDL-induced THP-1 cells via Notch1/PPARγ/CD36 signaling pathway. A. The level of Notch1 was detected after it was overexpressed in THP-1 cells; B. Protein expression in the Notch1/PPARγ/CD36 signaling pathway was assayed using western blot. Values are expressed as mean ±SD
*** p < 0.001 compared to Ov-NC, ### p < 0.001 compared to ox-LDL (+) + GAA (−) + Ov-NC (−) + Ov-Notch1 (−), $$$ p < 0.001 compared to ox-LDL (+) + GAA (+) + Ov-NC (+) +Ov-Notch1 (−). ox-LDL − oxidized low-density lipoprotein; SD − standard deviation; GAA − ganoderic acid A; THP-1 − human monocyte.
Fig. 6. GAA suppresses inflammation and oxidative stress in ox-LDL-induced THP-1 cells via Notch1/PPARγ/CD36 signaling pathway. A. The inflammatory cytokines in ox-LDL-induced THP-1 cells were detected with ELISA; B. The expression level of NF-kB p65 was measured using western blot; C. The oxidative stress-related factors were measured using the corresponding kits. Values are expressed as mean ±SD
*** p < 0.001 compared to Ov-NC, ### p < 0.001 compared to ox-LDL (+) + GAA (−) + Ov-NC (−) + Ov-Notch1 (−), $$$ p < 0.001 compared to ox-LDL (+) + GAA (+) + Ov-NC (+) + Ov-Notch1 (−). ox-LDL − oxidized low-density lipoprotein; SD − standard deviation; ELISA - enzyme-linked immunosorbent assay; GAA − ganoderic acid A; THP-1 − human monocyte; PPARγ − peroxisome proliferator-activated receptor gamma; NC − negative control.
Fig. 7. GAA inhibits lipid deposition in ox-LDL-induced THP-1 cells via Notch1/PPARγ/CD36 signaling pathway. A. The level of lipid deposition was detected with oil red O staining; B. The TC level was assayed using the Amplex Red Cholesterol Assay Kit. Values are expressed as mean ±SD
*** p < 0.001 compared to Ov-NC, ###p < 0.001 compared to ox-LDL (+) + GAA (−) + Ov-NC (−) + Ov-Notch1 (−), $$$ p < 0.001 compared to ox-LDL (+) + GAA (+) + Ov-NC (+) + Ov-Notch1 (−). ox-LDL − oxidized low-density lipoprotein; TC − total cholesterol; SD − standard deviation; GAA − ganoderic acid A; THP-1 − human monocyte; PPARγ − peroxisome proliferator-activated receptor gamma; NC − negative control.
Fig. 8. GAA inhibits the expression of scavenger receptors in ox-LDL-induced THP-1 cells via Notch1/PPARγ/CD36 signaling pathway. The expression of scavenger receptors was measured with qPCR and western blot. Values are expressed as mean ±SD
*** p < 0.001 compared to Ov-NC, ###p < 0.001 compared to ox-LDL (+) + GAA (−) + Ov-NC (−) + Ov-Notch1 (−), $$$p < 0.001 compared to ox-LDL (+) + GAA (+) + Ov-NC (+) + Ov-Notch1 (−). ox-LDL − oxidized low-density lipoprotein; TC − total cholesterol; SD − standard deviation; GAA − ganoderic acid A; THP-1 − human monocyte; qPCR − quantitative polymerase chain reaction; PPARγ − peroxisome proliferator-activated receptor gamma; NC − negative control.

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