Silicon dioxide nanoparticles induce insulin resistance through endoplasmic reticulum stress and generation of reactive oxygen species
Silicon dioxide nanoparticles (SiO2 NPs) are one of the most widely utilized NPs in various food sectors. However, the potential endocrine toxicity of SiO2 NPs has not been characterized.
In the present study, mice were orally administered a series of doses of SiO2 NPs. All doses of SiO2 NPs were absorbed into the blood, liver, and pancreas of the mice. Administration of 100 mg/kg bw (body weight) of SiO2 NPs significantly increased blood glucose levels in mice. However, the same dose of SiO2 fine-particles (FPs) did not result in altered blood glucose. Whole-genome analysis showed that SiO2 NPs affected the expression of genes associated with reactive oxygen species (ROS) production and endoplasmic reticulum (ER) stress. In addition, we showed that SiO2 NPs activated xenobiotic metabolism, resulting in ER stress. Endoplasmic reticulum stress resulted in increased ROS production, which activated the NF-κB pathway leading to expression of inflammatory cytokines. Increased inflammatory cytokine expression resulted in serine phosphorylation of IRS1, which induced insulin resistance (IR). Furthermore these inflammatory cytokines activated the MAPK pathway, which further promoted the serine phosphorylation of IRS1. Insulin resistance resulted in elevated blood glucose. The ER stress inhibitor 4-phenylbutyric acid (4-PBA) inhibited SiO2 NP-induced ROS production. The ROS scavenger N-acetylcysteine (NAC) did not affect SiO2 NP-induced ER stress, but inhibited SiO2 NP-induced activation of the NF-κB and MAPK pathways, expression of inflammatory cytokines, SiO2 NP-induced serine phosphorylation of IRS1, and SiO2 NP-induced elevations of blood glucose.
Silicon dioxide NPs induced IR through ER stress and generation of ROS, but SiO2 FPs did not. Therefore, lifelong exposure of humans to SiO2 NPs may result in detrimental effects on blood glucose. The results of this study strongly suggested that non-nanoformed SiO2 should be used as food additives.
KeywordsSilicon dioxide nanoparticles RNA-sequencing Endoplasmic reticulum stress Blood glucose Mice
- B H Pvalue
Benjamin Hochberg adjust Pvalue
dynamic light scattering
energy dispersive X-ray analysis
extracellular regulated kinase
inductively coupled plasma-mass spectrometry
inductively coupled plasma-optical emission spectrometry
insulin receptor substrate
c-Jun activating kinase
mitogen-activated protein kinase
nuclear factor E2-related factor 2
Oral Glucose Tolerance Test
reactive oxygen species
scanning electron microscopy
Silicon dioxide nanoparticles
terminal deoxynucleotidyl transferase-mediated dUDP nick end-labeling
Particles between 1 and 100 nm in size are characterized as nanoparticles (NPs) . Amorphous silicon dioxide (SiO2) NPs have been widely used for various applications, such as coatings, paints, adhesives, composites, cosmetics, food additives, and for drug delivery and diagnostics. The conventional form of amorphous silica is used as a food additive [1, 2]. Studies have estimated the typical doses intake of SiO2 NPs at 124 mg per day based on consumption of food products that contain SiO2 NPs. The major sources of SiO2 NPs are noodles, soups, rubs, and coffee creamers [3, 4]. However, the potential toxicity of SiO2 NPs has not been addressed. In cells, exposure to SiO2 NPs resulted in glutathione depletion and DNA damage, and activation of the MAPK/ERK1/2 and Nrf2/ARE pathways [5, 6]. Inductively coupled plasma-mass spectrometry (ICP-MS) analysis showed that rats exposed to 2500 mg/kg body weight (bw) SiO2 NPs per day for 84 days by oral administration had SiO2 NPs distributed in the lungs, kidneys, and spleen. Although no silicon was detected in the liver, histopathological analysis and gene expression studies showed evidence of liver fibrosis after 84 days of exposure . In BALB/c mice exposed to 50 nm SiO2 NPs, histopathological analysis showed lung thrombosis, cardiac wall fibrosis and calcifications, brain infarctions with necrotizing inflammatory response, retinal injuries with calcification, and focal gliosis . In addition, blood biochemical parameters such as albumin, cholesterol, triglycerides, total protein, urea, high-density lipoprotein (HDL), and low-density lipoprotein (LDL), and alkaline phosphatase (ALP) and aspartate aminotransferase (AST) activities, were significantly increased in mice administered SiO2 NPs . These studies showed that SiO2 NPs can induce wide-ranging systemic effects. However, the effects of SiO2 NPs on the endocrine system are unknown. Diabetes is a multifactorial endocrine disease in which both genetic predisposition and environmental factors contribute to disease onset and progression . Diabetes is the fifth leading cause of death in the United States, and the number of people with diabetes in the world is expected to double from 2000 to 2030 . Food additives are considered important pathogenic factors for diabetes [10, 12]. For example, the relationship between iron and glucose metabolism has been demonstrated. Excess iron can induce insulin resistance (IR) and diabetes through increased oxidative stress . Excessive reactive oxygen species (ROS) production is a hallmark of oxidative damage in many diseases, and can lead to mitochondrial dysfunction, cellular aging, and apoptosis . Reactive oxygen species can contribute to development of diabetes through induction of apoptosis in the pancreas and insulin resistance (IR) in the liver. Previous studies have demonstrated that SiO2 NPs induced cytotoxicity through excessive ROS production [6, 8]. Therefore, further investigation of the role of SiO2 NPs in food additives in the development and progression of diabetes is of importance. The mechanisms by which SiO2 NPs increase ROS levels in animals have not been characterized. Recent studies showed that ROS generation is closely linked to endoplasmic reticulum (ER) stress [14, 15]. ER stress is defined as an imbalance between the protein folding capacity of the ER, and the functional demand that is placed on this organelle. To restore ER homeostasis, cells trigger the ER stress response, also known as the unfolded protein response (UPR) [15, 16]. ER stress can either activate or deactivate the expression of vital genes associated with ROS generation, such as those in the mitochondrial respiratory chain, arachidonic acid metabolism pathway, cytochrome P450 (CYP) family, glucose oxidase, amino acid oxidases, xanthine oxidase, NADPH/NADPH oxidases, and NO synthases [16, 17]. In addition, the transcriptional factor nuclear factor E2-related factor 2 (Nrf2), a downstream effector of ER stress, is an important endogenous antioxidant pathway that protects against oxidative stress [15, 18]. However, whether ER stress is involved in ROS production in response to SiO2 NPs has not been reported. In this study, we evaluated the effects of dietary SiO2 NPs on blood glucose homeostasis. Silicon dioxide NPs were administered orally to mice, and blood glucose was measured. RNA sequencing was used to evaluate the whole-transcriptome response of the mice, and the genome-wide pathways affected by SiO2 NPs in mice were further investigated, particularly those related to blood glucose homeostasis.
Characterization and absorption of SiO2 NPs
Effects of SiO2 NPs on blood glucose
RNA sequencing and transcriptome characterization of mice following oral administration of SiO2 NPs
SiO2 NPs increased blood glucose in mice from week 10
SiO2 NPs increased ROS levels in mice starting at week eight
SiO2 NPs induced ER stress in mice from week six
SiO2 NPs activated the NF-κB and MAPK pathways in mice
SiO2 NPs have been used for many years in food applications, such as for clearing of beers and wines, as anticaking agents to maintain flow properties in powder products, and to thicken pastes [1, 2]. The daily human intake of SiO2 NPs may be as high as 124 mg [3, 4]. In most in vivo toxicity studies, SiO2 NPs exhibit higher rates of absorption and more extensive organ distribution when administered orally than when delivered via other routes of administration [7, 9]. In addition, the acute toxicity and subacute toxicity after single or repeated doses via ingestion have been investigated, showing that SiO2 NPs affected nearly all organ systems [8, 9]. However, the toxicological effects of SiO2 NPs on blood glucose levels have not been studied. In this study, SiO2 NPs were administered orally to mice, and blood glucose was measured. Reports have shown that SiO2 NPs can be absorbed into the blood from the digestive system and accumulate in the liver, kidney, and spleen [7, 8, 19]. In the present study, oral administration of 25, 50, 100, and 200 mg/kg bw of fumed SiO2 NPs resulted in absorption and accumulation in the liver, pancreas, spleen, kidney, and small intestine of mice. Furthermore, fumed SiO2 NPs significantly increased blood glucose in mice at a dose of 100 mg/kg bw of SiO2 NPs or higher starting at week 10. Brun showed that the average intestinal surface area in humans is approximately 250 m2, and the average intestinal surface area of mice is 2.5 m2 . Therefore, the average intestinal surface area of humans is 100-fold greater than that in mice. Human intake of 124 mg of SiO2 NPs (i.e., 0.5 mg/m2 intestine) corresponds to a 41.3 mg daily intake of a 0.03 kg mouse (1.25 mg/mouse, i.e., 0.5 mg/m2 intestine). A dose of 100 mg/kg bw (3 mg/mouse, i.e. 1.2 mg/m2 intestine), which increased blood glucose in mice in this study, corresponds to 2.5-fold the daily intake of humans. Whether a lifelong exposure of humans to SiO2 NPs can induce increased blood glucose should be evaluated further. Lifelong exposure of humans to SiO2 NPs likely results in accumulation of these nanoparticles, which is likely to lead to increased blood glucose. In this study, Stober SiO2 NPs were also absorbed from the digestive system, leading to increased blood glucose in mice starting at week 10. However, fumed SiO2 FPs and Stober SiO2 FPs were not absorbed from the digestive system and did not affect blood glucose levels in mice. Therefore, the main factor in SiO2 NPs effects on blood glucose was particle size. The World Health Organization uses the OGTT and ITT for diagnosis of diabetes types . In this study, the OGTTs and ITTs were conducted in weeks 10 and 18, respectively. The results showed that the primary mechanism of SiO2 NP-induced hyperglycemia in both the early and late stages was IR. Hyperglycemia is the main characteristic of both diabetes subtypes [10, 22]. Type 1 diabetes is an autoimmune disease characterized by destruction of pancreatic β-cells, resulting in absolute insulin deficiency . Insulin resistance, a feature of type 2 diabetes, is characterized by reduced activity of insulin despite increased insulin concentrations . Insulin resistance leads to increased blood glucose, and high levels of blood glucose then induce the loss of β-cell mass, resulting in loss of function [23, 24]. In this study, SiO2 NPs did not induce apoptosis of β-cells, and thus did not affect insulin secretion. However, the mice exhibited reduced insulin sensitivity at weeks 10 and 18. Compared with SiO2 NPs, SiO2 FPs did not affect insulin secretion and did not induce IR in mice. The liver is the classical insulin-responsive organ, and is closely associated with IR . In this study we evaluated the liver transcriptome to explore the mechanisms of SiO2 NP toxicity. Our results showed that SiO2 NPs affected several GO terms associated with ROS generation (GO-ID: 0055114, 16,491, 16,705, 4497, etc.) and ER stress (GO-ID: 34976, 6986, 34,620, 30,968, etc.). Reactive oxygen species production is a hallmark of oxidative damage in many diseases, and can lead to mitochondrial dysfunction, cellular aging, and apoptosis . Reactive oxygen species also contribute to diabetes through induction of apoptosis in the pancreas, and induction of IR in liver. Silicon dioxide NPs have been reported to produce excessive ROS, resulting in consumption of endogenous antioxidants such as SOD and GSH, and damage to biological macromolecules such as nucleic acids, lipids, and proteins through lipid peroxidation [6, 8].. However, the mechanisms by which SiO2 NPs increase ROS levels in animals remains unclear. In this study, whole-genome network results showed that ROS generation was closely associated with ER stress. The ER is the cellular organelle responsible for synthesis and folding of secreted and membrane-bound proteins. A variety of stimuli can lead to accumulation of unfolded proteins, a condition called ER stress [14, 15]. PERK, IRE1, and ATF6 are important sensory elements and major injury pathway initiation factors of ER stress. When ER stress occurs, these proteins are separated from GRP78 to activate downstream signaling pathways, such as phosphorylation of eIF2α, mRNA and protein expression of CHOP, sheared-XBP1 (resulting in increased mRNA and protein ratios of sheared-XBP1/total XBP1 (XBP1-s/t)) and ATF6. Restoration of ER homeostasis occurs by reducing protein translation and promoting chaperone production [14, 16]. In addition, the resulting intermediates of ER stress can either activate or deactivate the expression of vital genes associated with ROS generation, such as those in the mitochondrial respiratory chain, the arachidonic acid pathway, the cytochrome P450 (CYP) family, glucose oxidase, amino acid oxidases, xanthine oxidase, NADPH/NADPH oxidases, and NO synthases [16, 17]. Furthermore, ROS can also cause ER stress. For example, CYP-derived peroxynitrite can react with H2O2 to generate singlet oxygen in the ER, resulting in ER stress [17, 25]. In this study, fumed SiO2 NPs induced ER stress (from week 6), which was followed by increased ROS (from week 8), and increased blood glucose in mice (from week 10). These results indicated that ROS did not induce ER stress in this study. Whole-genome results showed that SiO2 NPs increased the expression of Cyp2b9 and Cyp2a4. Cytochrome P450 enzymes, specifically CYP families 1–3, play a pivotal role in drug and xenobiotic metabolism [17, 25]. Overexpression of CYP enzymes in yeast and HepGH2 cells has been shown to induce responses involved in the URP and ER stress [16, 26]. In this study, SiO2 NPs increased the gene expression of Cyp2b9 earlier than fumed SiO2 NPs induced ER stress, which indicated that fumed SiO2 NPs activated xenobiotic metabolism, resulting in ER stress. Endoplasmic reticulum stress and ROS generation were each blocked by specific inhibitors. 4-phenylbutyric acid is a low molecular weight compound that stabilizes protein conformation, improves the folding capacity of the ER, and facilitates trafficking of mutant proteins to suppress ER stress . In this study, 4-PBA inhibited fumed SiO2 NP-induced ER stress and inhibited ROS generation in mice, which suggested that fumed SiO2 NPs increased ROS production through ER stress. The transcriptional factor nuclear factor E2-related factor 2 (Nrf2), localized downstream of the PERK pathway, mediates antioxidant enzymes, resulting in augmentation of intracellular ROS production [15, 27]. In this study, whole-genome results showed that fumed SiO2 NP-induced ER stress affected the Nrf2 pathway by affecting the expression of Nrf2, Nqo-1, and HO-1, resulting in increased ROS production in mice. Stober NPs also affected the expression of Cyp2b9, ER stress, and ROS generation, but Fumed FPs and Stober FPs did not induce these effects. N-acetyl cysteine is a ROS scavenger . However, NAC inhibited SiO2 NP-induced ROS production, but not ER stress. However, NAC inhibited increased blood glucose. These results showed that fumed SiO2 NPs induced ER stress, ER stress increased ROS production, and ROS induced blood glucose elevation. The major pathway of insulin receptor signal transduction is the insulin receptor substrate (IRS)-phosphatidylinositol 3-kinase (PI3K)-Akt (also known as PKB) pathway . IRS1 isoforms are intracellular adaptor proteins that are recruited to the activated insulin receptor. Dephosphorylation of these isoforms on serine/threonine residues by the insulin receptor initiates the recruitment and activation of PI3K. Activated PI3K phosphorylates serine/threonine moieties of Akt. Akt acts as a central node in regulation of the biological effects of insulin [22, 29]. In this study, fumed SiO2 NP-induced ROS production inhibited dephosphorylation of the serine residues of IRS1 and inhibited phosphorylation of the serine residues of Akt, resulting in IR. In addition, fumed SiO2 NP-induced ROS production resulted in activation of the NF-κB and MAPK pathways, resulting in serine phosphorylation of IRS1. NF-κB is a family of transcription factors that plays a critical role in inflammation. Reactive oxygen species have been reported to induce NF-κB activation due to phosphorylation of IκB, which results in NF-κB translocation to the nucleus and phosphorylation of p65 [18, 27]. NF-κB induces the expression of inflammatory cytokines such as TNF-α and IL-6, which can result in phosphorylation of IRS1 [30, 31], resulting in activation of different mitogen-activated protein kinase (MAPK) cascades, leading to activation of p38 MAPK, extracellular regulated kinase (ERK), and c-Jun N-terminal kinase (JNK) [18, 29]. JNK and p38-MAPK also contribute to phosphorylation of IRS1 [22, 29]. Similar to Fumed NPs, Stober NPs also activated the NF-κB and MAPK pathways, resulting in IRS1 phosphorylation, and induction of IR in mice. In contrast, Fumed FPs and Stober FPs did not induce these effects.
Preparation and characterization of SiO2 NPs
Fumed SiO2 NPs and FPs were obtained from Sigma Co., Ltd. (Product No. S5130, S5505, Roedermark, Germany). Stober SiO2 NPs were obtained from Zhongkeleiming Technology Co., Ltd. (Product No. DKSIO050, DKSIO300, Beijing, China). The primary particle sizes and morphology were measured using TEM and SEM (FEI Co., Ltd., OR, USA). The hydrodynamic size and zeta potential of nanoparticles in PBS were measured using DLS (Zetasizer, Malvern Instruments Ltd., Worcestershire, UK). Endotoxin analysis was performed using the Limulus Amoebocyte Lysate (LAL) assay and the Pyros Kinetix instrument from Associates of Cape Co., Ltd. (East Falmouth, MA).
Animal care and exposure to SiO2 NPs
Six-week-old ICR male mice (22.97 ± 0.33 g) were obtained from Harbin Veterinary Research Institute (Harbin, China) and acclimated for 7 days after arrival at the study facility. Mice were housed in an animal room with controlled temperature (21–24 °C) and light cycle (12 h light/dark). Autoclaved water and rodent diet (Keao Co., Ltd., Beijing, China) were provided ad libitum. An ultrasonic bath (Ningbo Scientz Biotechnology Co., Ltd., Ningbo, China) at a frequency of 40 kHz with power at 400 W was used to scatter the SiO2 NPs and FPs. After ultrasonic wave stirring for 30 min, the SiO2 NP-PBS or SiO2 FP-PBS suspension was orally administered by syringe once per day, 7 days per week, for 10 or 18 weeks to each group of mice. To explore the endocrine effects of the oral administration of SiO2 NPs and determine the dose that increased blood glucose, mice were orally administered suspensions of SiO2 NPs at the doses of 25, 50, 100, and 200 mg/kg bw. The total doses the mice received were approximately 44.5, 96.7, 177.8, and 389.6 mg after 10 weeks, or approximately 86.7, 187.4, 355.3, 750.9 mg after 18 weeks. Then, in the experiment that explored the mechanism for the effect of SiO2 NPs on blood glucose, the dose of 100 mg/kg bw SiO2 NPs was selected. In addition, in the mechanism experiment, the doses of 100 mg/kg bw 4-PBA and NAC were orally administered to mice simultaneously with the oral administration of the suspension at 100 mg/kg bw SiO2 NPs. The total dose of mice received was approximately 179.7 mg after 10 weeks. The control group mice were given an equal volume of PBS.
Blood collection and analysis
Tail vein blood was collected every 2 weeks. Before the collection, mice were fasted for 16 h. The blood glucose in the tail vein blood was measured using a glucose assay kit (Wako Pure Chemical Industries, Ltd., Osaka, Japan), and the blood insulin was measured using a mouse insulin ELISA kit (Shibayagi Co., Ltd., Gunma, Japan). TNF-α and IL-6 were measured using TNF-α and IL-6 kits, respectively (R&D Systems, Minneapolis, MN, USA).
Glucose and insulin tolerance test
In OGTT, mice were fasted for 16 h and then orally administered glucose (1.5 g/kg bw). In ITT, mice were fasted for 6 h and then injected with insulin (0.4 IU/kg bw). Blood was collected for blood glucose and insulin measurement from the tail vein at 0, 30, 60, 120 min. Blood glucose and insulin were measured using each kit as above described.
Silicon content analysis
The livers and pancreases were removed from the mice, and 0.3 g of each tissue was weighed, digested, and analyzed for silicon content. Briefly, the tissues were digested in nitric acid (ultrapure grade) overnight. After the addition of 0.5 mL of H2O2, the mixed solutions were heated at approximately 160 °C using a high-pressure reaction container in an oven chamber until the samples were completely digested. Then, the solutions were heated at 120 °C to remove the remaining nitric acid and until the solutions were colorless and clear. Last, the remaining solutions were diluted to 3 mL with 2% nitric acid. ICP-OES (Optima 5300 DV, Perkin Elmer Inc., CA, USA) was used to analyze the silicon concentration in the samples. The data are expressed as micrograms per gram fresh tissue. To assess whether SiO2 particles occurred in each tissue after the oral administration of SiO2 NPs, 0.1 g of each tissue was also weighed for SEM and EDXA. The tissues were homogenized in RIPA lysis buffer, filtered to discard cell debris using a 0.45 μm filter membrane, and centrifuged for 30 min at 18000×g to precipitate the SiO2 NPs. The precipitate was resuspended in alcohol and then spread out on an aluminum sheet, sputter-coated with platinum, and observed by SEM. The surface element was analyzed by EDXA.
Reactive oxygen species assessment
ROS levels were assessed using the levels of total SOD (T-SOD), GSH and MDA. Livers were homogenized in nine volumes (1:10 w/v) of PBS. Homogenates were centrifuged at 750 g for 10 min at 4 °C to discard cell debris. The T-SOD, GSH and MDA of serum and liver supernatant were measured using each kit (Nanjing Jiancheng Bioengineering Institute, Nanjing, China).
Pancreases and livers were fixed in 4% paraformaldehyde solution for 24 h, embedded in paraffin, cut into 5 μm sections, and placed onto glass slides. The β-cell mass was identified by immunohistochemical localization of insulin with an anti-insulin antibody (Santa Cruz Biotechnology, Inc., CA, USA). For the analysis of cell apoptosis, pancreatic and liver sections were stained with the TUNEL (KeyGen Biotech. Co., Ltd., Nanjing, China). DNase I pretreated cells were used as the positive control.
RNA sequencing and data analysis
To ensure unbiased analysis of tissue response, the total RNA was isolated from random sections (10–15 mg) of liver. The RNA was isolated using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) and purified using a RNeasy Plus Mini kit (Qiagen, Mississauga, ON, Canada). Three livers of each group were sequenced, and the data were analyzed. In brief, the RNA was sequenced on one sequencing lane of an Illumina Genome Analyzer II system (Illumina). The paired-end reads were mapped to the mouse genome (version NCBIm37/mm9) using Tophat. The mapped reads were used to quantify the transcripts from the RefSeq reference database. The genes met the fold change > 2 and Benjamin Hochberg adjust Pvalue (B H Pvalue) < 0.05 were the significant differently expressed genes which were used for the following analysis. For the functional annotation analysis of genes, the BiNGO (http://apps.cytoscape.org/apps/bingo) was used. The GO terms met the B H Pvalue < 0.001 were the significant GO terms.
Real-time quantitative PCR
1 μg total RNA was used to perform reverse transcription using PrimeScript™ RT reagent Kit (TaKaRa, Tokyo, Japan). Real-time polymerase chain reaction amplification of cDNA was performed with SYBR Premix Ex Taq™ II (TaKaRa, Tokyo, Japan). Primers were listed in Table S3.
Liver tissues were resuspended in RIPA lysis buffer. Lysates were centrifuged for 15 min at 12000 g and 4 °C, and protein contents of the supernatant were determined using DC protein kit (Bio-Rad Laboratories, CA, USA). Aliquots of the proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and transferred to PVDF membranes (Bio-Rad Laboratories, CA, USA). PVDF membranes were incubated with antibodies against phospho-Eif2α, GRP78, CHOP, ATF6 (90KD), ATF6 (50KD), shear-XBP1 (XBP1-s), unshear-XBP1 (XBP1-u), Cleaved-Capsase3 (Cleaved-Casp3), phospho-IRS1 (Ser307), phospho-Akt (Ser473), IRS1, Akt, phospho-NFκB-p65, phospho-IκBα, phospho- JNK, phospho-p38-MAPK, NFκB-p65, IκBα, JNK1, p38-MAPK and β-actin. All antibodies were purchased from Cell Signaling Technology (Danvers, MA, USA).
Results were expressed as mean ± SEM and were analyzed using GraphPad Prism version 5.0 (GraphPad Software, LaJolla, CA). All calculated significances are based on the one-way analysis of variance (ANOVA) test and the post hoc Tukey’s test. A p value less than 0.05 was considered statistically significant.
NG conceived the idea. HHL and NG designed the experiments. HHL, XJW and DQY performed the in vivo experiments. HHL, QG, BYZ and XPF contributed to gene expression analysis. HHL, QG and JL contributed to protein expression analysis. NG, QW, YO, YJF, KC and LPH performed statistical analysis. HHL and NG made figures and wrote the manuscript. All authors have read and approved the final manuscript.
This work was supported by funds of the National Natural Science Foundation of China (Grant No. 21677044), the Open Project of State Key Laboratory of Urban Water Resource and Environment of Harbin Institute of Technology (Grant No. HCK201805).
Ethics approval and consent to participate
The study was reviewed and approved by the Ethics Research Committee of the School of Life Science and Technology of Harbin Institute of Technology and were conducted according to guidelines for the care and use of experimental animals approved by the Heilongjiang Province People’s Congress (http://www.nicpbp.org.cn/sydw/CL0249/2730.html).
Consent for publication
The authors declare there are no competing financial interests.
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