ABSTRACT
Toll-like receptors (TLRs) are pattern recognition receptors that sense a variety of pathogens, initiate innate immune responses, and direct adaptive immunity. All TLRs except TLR3 recruit the adaptor MyD88 to ultimately elicit inflammatory gene expression, whereas TLR3 and internalized TLR4 use TIR-domain-containing adaptor TRIF for the induction of type I interferon and inflammatory cytokines. Here, we identify the WD repeat and FYVE-domain-containing protein WDFY1 as a crucial adaptor protein in the TLR3/4 signaling pathway. Overexpression of WDFY1 potentiates TLR3- and TLR4-mediated activation of NF-κB, interferon regulatory factor 3 (IRF3), and production of type I interferons and inflammatory cytokines. WDFY1 depletion has the opposite effect. WDFY1 interacts with TLR3 and TLR4 and mediates the recruitment of TRIF to these receptors. Our findings suggest a crucial role for WDFY1 in bridging the TLR-TRIF interaction, which is necessary for TLR signaling.
Subject(s)
Adaptor Proteins, Vesicular Transport/genetics , Nuclear Proteins/genetics , Toll-Like Receptor 3/genetics , Toll-Like Receptor 4/genetics , Transcription Factors/genetics , Adaptor Proteins, Signal Transducing , Adaptor Proteins, Vesicular Transport/immunology , Amino Acid Motifs , Cytokines/genetics , Cytokines/immunology , Gene Expression Regulation , HEK293 Cells , Humans , Interferon Inducers/pharmacology , Interferon Regulatory Factor-3/genetics , Interferon Regulatory Factor-3/immunology , Interferon Type I/genetics , Interferon Type I/immunology , Molecular Sequence Data , Myeloid Differentiation Factor 88/genetics , Myeloid Differentiation Factor 88/immunology , NF-kappa B/genetics , NF-kappa B/immunology , Nuclear Proteins/antagonists & inhibitors , Nuclear Proteins/immunology , Plasmids/chemistry , Plasmids/immunology , Poly I-C/pharmacology , RNA, Small Interfering/genetics , RNA, Small Interfering/metabolism , Signal Transduction , Toll-Like Receptor 3/immunology , Toll-Like Receptor 4/immunology , Transcription Factors/antagonists & inhibitors , Transcription Factors/immunology , TransfectionABSTRACT
Viral infection causes activation of the transcription factor IRF3, which is critical for production of type I interferons (IFNs) and innate antiviral immune response. How virus-induced type I IFN signaling is controlled is not fully understood. Here we identified the transcription factor FoxO1 as a negative regulator for virus-triggered IFN-ß induction. Overexpression of FoxO1 inhibited virus-triggered ISRE activation, IFN-ß induction as well as cellular antiviral response, whereas knockdown of FoxO1 had opposite effects. FoxO1 interacted with IRF3 in a viral infection-dependent manner and promoted K48-linked polyubiquitination and degradation of IRF3 in the cytosol. Furthermore, FoxO1-mediated degradation of IRF3 was independent of the known E3 ubiquitin ligases for IRF3, including RBCK1 and RAUL. Our findings thus suggest that FoxO1 negatively regulates cellular antiviral response by promoting IRF3 ubiquitination and degradation, providing a previously unknown mechanism for control of type I IFN induction and cellular antiviral response.
Subject(s)
Forkhead Transcription Factors/metabolism , Interferon Regulatory Factor-3/metabolism , Interferon-beta/metabolism , Proteolysis , Ubiquitination , Vesiculovirus/metabolism , Animals , Forkhead Box Protein O1 , Forkhead Transcription Factors/genetics , Gene Knockdown Techniques , HEK293 Cells , Humans , Interferon Regulatory Factor-3/genetics , Interferon-beta/genetics , Mice , Rhabdoviridae Infections/genetics , Rhabdoviridae Infections/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism , Ubiquitin-Protein Ligases/genetics , Ubiquitin-Protein Ligases/metabolism , Vesiculovirus/geneticsABSTRACT
Current evidence suggests that porcine circovirus type 2 (PCV2) infection induces immunosuppression in piglets. Sophora subprostrate polysaccharide (SSP) exhibits various pharmacological activities, including immunoregulatory, anti-inflammatory, antiviral, and antioxidant properties. However, the acts of lncRNAs in regulating the therapeutic effects of SSP on PCV2-infected RAW264.7 cells remains poorly understood. This study aimed to investigate the molecular mechanisms by which lncRNAs regulate PCV2-induced immunosuppression during SSP treatment. Our findings revealed that 1699 mRNAs, 373 lncRNAs, and 129 miRNAs were differentially expressed in PCV2-infected RAW264.7 cells. Additionally, 359 mRNAs, 271 lncRNAs, and 79 miRNAs exhibited differential expression in SSP-treated PCV2-infected RAW264.7 cells. GO and KEGG analyses indicated that the candidate genes were enriched in the TNF/NF-κB signaling pathway. Furthermore, based on GO and KEGG pathway analysis, a ceRNA network involving chemokine (C-X-C motif) ligand 2 (CXCL2), miR-217-x, and MSTRG.5823.1 was constructed. We demonstrated that lncRNA MSTRG.5823.1 localized to the cytoplasm. Moreover, we found that silencing or overexpressing lncRNA MSTRG.5823.1 significantly modulated PCV2-induced immunosuppression by regulating the activation of the TNF/NF-κB signaling pathway. Specifically, lncRNA MSTRG.5823.1 overexpression increased the expression of TNF/NF-κB signaling pathway-related genes and proteins in PCV2-infected RAW264.7 cells. Conversely, silencing lncRNA MSTRG.5823.1 decreased their expression. Rescue assays further revealed that the suppressive effects of miR-217-x overexpression on TNF/NF-κB signaling pathway-related genes and proteins could be reversed by MSTRG.5823.1 overexpression. These findings highlight the critical role of lncRNA MSTRG.5823.1 in PCV2 infection progression and suggest a new strategy for the prevention and treatment of PCV2 infection.
Subject(s)
Circoviridae Infections , Circovirus , NF-kappa B , Polysaccharides , RNA, Long Noncoding , Signal Transduction , Sophora , Animals , Mice , Circovirus/immunology , NF-kappa B/metabolism , RNA, Long Noncoding/genetics , RNA, Long Noncoding/metabolism , RAW 264.7 Cells , Signal Transduction/drug effects , Circoviridae Infections/immunology , Polysaccharides/pharmacology , Swine , Tumor Necrosis Factor-alpha/metabolism , Tumor Necrosis Factor-alpha/genetics , MicroRNAs/genetics , MicroRNAs/metabolism , Immune Tolerance/drug effectsABSTRACT
OBJECTIVE: To study the toxic effects of aqueous extract of Crotalariae Assamicae Semen (CAS), one of the pyrrolizidine alkaloid-containing Chinese herbal medicines, in rats and the possible mechanism in association with liver damage. METHOD: The aqueous extract of CAS (CASE) was prepared by the conventional water extracting-alcohol precipitating method. The LD50 value of CASE in rats was determined by Kärber method. Rats were randomly divided into four groups in which three groups were orally administered with different doses of the CASE and one group with distilled water as control. Toxic effects were assessed by morphological, biochemical and histopathological changes. Moreover, in vitro metabolism using rat liver microsomes was also conducted and applied for the exploration of the underlying mechanism of liver damage. RESULT: The LD50 value of CASE in Wistar rats was (2.36 +/- 0.26) g x kg(-1). The toxic effects were found in all groups of rats dosed with CASE, in which serum levels of ALT and AST were significantly elevated, and the obvious and dose-dependent damages in liver and lung were observed by histopathological examination. Moreover, the liver tissue-bound pyrroles were detected and generated in a dose-dependent manner, and the pyrrole metabolites observed in the in vitro microsomal metabolism. All the evidences suggested a strong correlation between metabolism and toxicity of CASE in rats. CONCLUSION: CASE could induce the acute toxicity in rats, of which liver and lung were the major targets. Toxic effects were strongly correlated with pyrrolizidine alkaloids in CAS. The possible mechanism for its liver toxicity may be related to the formation of pyrrole metabolites as well as the corresponding tissue-binding products.
Subject(s)
Crotalaria/chemistry , Drugs, Chinese Herbal/toxicity , Liver/drug effects , Alanine Transaminase/metabolism , Animals , Drugs, Chinese Herbal/administration & dosage , Lethal Dose 50 , Liver/enzymology , Liver/injuries , Male , Microsomes, Liver/drug effects , Microsomes, Liver/enzymology , Pyrrolizidine Alkaloids/administration & dosage , Pyrrolizidine Alkaloids/toxicity , Rats , Rats, WistarABSTRACT
The nano/micron sized-fluticasone propionate inhalable suspension (FPs) is used for asthma treatment, and this study aimed to elucidate the effects of particle size on the absorption of FPs by various pulmonary cells and the subsequent therapeutic efficacy for asthma. FPs of 727, 1136 and 1612 nm were prepared, and an increase in diameter diminished the endocytosis and macropinocytosis of FPs by alveolar epithelial cells (A549 and Calu-3 cells) but facilitated their uptake by M2-like macrophages; results about the transport across Calu-3 monolayer showed the mucus layer was the main rate-limiting step for the uptake of FPs by epithelial cells; the animal tests showed that although a decrease in diameter improved the pulmonary absorption of FPs, the particle size did not affect the lung distribution of FPs; a further detection revealed that larger FPs were taken more effectively by alveolar macrophages and lymphocytes and exerted a better therapeutic effect on asthma than the smaller ones. This study showed that the particle size of FPs had a significant impact on their absorption, elimination and cellular distribution in the lung after inhalation and further on their effectiveness in asthma treatment, and the particle size of the nano/micron sized-FPs should be designed and optimized for asthma treatment on the premise of meeting the requirements of inhalation preparations.
Subject(s)
Androstadienes , Asthma , Animals , Fluticasone/pharmacology , Fluticasone/therapeutic use , Particle Size , Androstadienes/therapeutic use , Asthma/drug therapy , Lung , Administration, InhalationABSTRACT
OBJECTIVE: The aim of this study was to load Verapamil Hydrochloride to carboxylated multi-walled carbon nanotubes( c-CNTs) and discuss the mechanism of drug release which could act as an effective basis for c-MWNTs used as drug carriers of controlled and sustained release delivery system. METHODS: Raw CNTs were treated with mixed strong acid to obtain c-CNTs. Raman, IR, SEM and HR-TEM were used to characterize the CNTs and investigate the loading sites for drugs. The release behavior of the drug delivery system in vitro and the release model were studied. RESULTS: The raw CNTs were successfully grafted with carboxyl group by acid treatment. The water-soluble ability of c-CNTs was greatly improved. The length of c-CNTs was 200-300nm. Meanwhile, the ends of c-CNTs were opened. The results of the drug loading experiment showed that the more adding drugs, the larger loading content of drugs. Most of the drugs were loaded into the inner pores of c-CNTs when adding drugs was no more than 0.1 as quantity as c-CNTs. As the quantity of adding drugs increased, the drugs were loaded both in the inner pores and on the out-wall of c-CNTs. The release results in vitro showed release mechanism had something with the quantity of adding drugs. CONCLUSION: C-CNTs can be used as carriers of sustained and controlled release delivery system. Ideal release behavior of drugs can be achieved by choosing appropriate formula.
Subject(s)
Drug Carriers/chemistry , Nanotubes, Carbon/chemistry , Verapamil/administration & dosage , Verapamil/chemistry , Delayed-Action Preparations , Feasibility Studies , Hydrogen-Ion Concentration , Microscopy, Electron, Transmission , Nanotechnology/methods , Nanotubes, Carbon/ultrastructure , Solubility , Temperature , Verapamil/metabolismABSTRACT
In this work, the kinetic mechanisms of pyrolysis of cellulose with different physical structures were illustrated. The crystalline cellulose showed better thermal stability and required higher energy for decomposition with more concentrated reactions due to the highly ordered structure. The crystallinity of the ball milling and ionic liquid pretreated cellulose decreased and the structure was relatively loose and disordered, thereby reducing the thermal stability, so the global activation energy of both samples decreased and the intensive reaction caused by the collapse of structure was alleviated. In fast pyrolysis, crystalline cellulose favored fast pyrolytic saccharification, and the highest levoglucosan yield reached 64.3 wt% at 400 °C. This research was helpful to deduce the influence of physical structure on the pyrolytic product distribution of cellulose, thereby providing useful information to promote the development of pyrolytic saccharification.
ABSTRACT
Background: The clearance of nanomaterials (NMs) from the liver is essential for clinical safety, and their hepatic clearance is primarily determined by the co-disposition process of various types of hepatic cells. Studies of this process and the subsequent clearance routes are urgently needed for organic NMs, which are used as drug carriers more commonly than the inorganic ones. Materials and methods: In this study, the co-disposition of chitosan-based nanoparticles (CsNps) by macrophages and hepatocytes at both the cellular and animal levels as well as their subsequent biological elimination were investigated. RAW264.7 and Hepa1-6 cells were used as models of Kupffer cells and hepatocytes, respectively. Results: The cellular studies showed that CsNps released from RAW264.7 cells could enter Hepa1-6 cells through both clathrin- and caveolin-mediated endocytosis. The transport from Kupffer cells to hepatocytes was also studied in mice, and it was observed that most CsNps localized to the hepatocytes after intravenous injection. Following the distribution in hepatocytes, the hepatobiliary-fecal excretion route was shown to be the primary elimination route for CsNps, besides the kidney-urinary excretion route. The elimination of CsNps in mice was a lengthy process, with a half time of about 2 months. Conclusion: The demonstration in this study of the transport of CsNps from macrophages to hepatocytes and the subsequent hepatobiliary-fecal excretion provides basic information for the future development and clinical application of NMs.
Subject(s)
Chitosan/pharmacology , Hepatocytes/cytology , Hepatocytes/metabolism , Nanoparticles/chemistry , Animals , Biological Transport , Cell Line, Tumor , Drug Carriers/metabolism , Exocytosis , Hepatocytes/drug effects , Kinetics , Liver/metabolism , Macrophages/metabolism , Mice , Nanoparticles/ultrastructure , PhotonsABSTRACT
In this study, ball milling and ionic liquid pretreatments were utilized to alter cellulose structure prior to fast pyrolysis and enzymatic hydrolysis. The variations in the products distribution of cellulose fast pyrolysis, and their dependence on the structure of cellulose, and the temperature of fast pyrolysis were illustrated. Fast pyrolysis of pretreated cellulose yielded more levoglucosan than crystalline cellulose (14.7%) at 300⯰C. Nevertheless, the levoglucosan achieved higher yield (64.3%) from crystalline cellulose at 400⯰C. At last, a comparison between fast pyrolysis and enzymatic hydrolysis for cellulose saccharifaction was made. Fast pyrolysis was a promising alternative to liberate levoglucosan from cellulose. Further investigation and development were required to maximize the levoglucosan production.
Subject(s)
Cellulose/metabolism , Glucose/analogs & derivatives , Biomass , Fermentation , Glucose/biosynthesis , Hydrolysis , Pyrolysis , Temperature , Time FactorsABSTRACT
BACKGROUND: Salt stress is an important factor that limits rice yield. We identified a novel, strongly salt tolerant rice landrace called Changmaogu (CMG) collected from a coastal beach of Zhanjiang, Guangdong Province, China. The salt tolerance of CMG was much better than that of the international recognized salt tolerant rice cultivar Pokkali in the germination and seedling stages. RESULTS: To understand the molecular basis of salt tolerance in CMG, we performed BSA-seq for two extreme bulks derived from the cross between CMG and a cultivar sensitive to salt, Zhefu802. Transcriptomic sequencing was conducted for CMG at the germination and young seedling stages. Six candidate regions for salt tolerance were mapped on Chromosome 1 by BSA-seq using the extreme populations. Based on the polymorphisms identified between both parents, we detected 32 genes containing nonsynonymous coding single nucleotide polymorphisms (SNPs) and frameshift mutations in the open reading frame (ORF) regions. With transcriptomic sequencing, we detected a large number of differentially expressed genes (DEGs) at the germination and seedling stages under salt stress. KEGG analysis indicated two of 69 DEGs shared at the germination and seedling stages were significantly enriched in the pathway of carotenoid biosynthesis. Of the 169 overlapping DEGs among three sample points at the seedling stage, 13 and six DEGs were clustered into the pathways of ABA signal transduction and carotenoid biosynthesis, respectively. Of the 32 genes carrying sequence variation, only OsPP2C8 (Os01g0656200) was differentially expressed in the young seedling stage under salt stress and also showed sequence polymorphism in the ORFs between CMG and Zhefu802. CONCLUSION: OsPP2C8 was identified as the target candidate gene for salinity tolerance in the seedling stage. This provides an important genetic resource for the breeding of novel salt tolerant rice cultivars.
ABSTRACT
Lasers with spherical or cylindrical dielectric resonators supported by whispering gallery modes (WGM) have attracted much interest due to their microscopic size, high cavity Q factor, and low lasing threshold. Cylindrical microcavity lasers based on the gain only in the evanescent field region of whispering gallery modes have been demonstrated in our recent works. The gain was excited by the evanescent wave of longitudinal optical pumping along the optical fiber. To well understand the obtained lasing spectra, the mode assignment is required. The explicit asymptotic formulas for the position and mode-interval of whispering gallery modes were obtained from the characteristic equation of whispering gallery modes in a cylindrical micro-cavity. The formulas were used to analyze the lasing spectra emitting from cylindrical microcavies which were evanescent-wave-gain pumped. The lasing spectra were found to be transverse magnetic modes(TM), and then the spectra were mode assigned with two integers, i.e., radial quantum numbers (1) and angular momentum numbers (n). Based on the explicit asymptotic formulas, all of the spectra from five optical fibers with a diameter ranging from 215 to 328 mm were well mode assigned. In the match between experimental spectral data and the asymptotic formula, only two matched parameters (l, n) were used, and the wavelength deviation in the match was less than 0.05 nm, which indicated that the mode assignment was reliable and precise. The spectral mode-assignment of cylindrical micro-cavity is important for computing the spatial distribution of mode intensity and is crucial for the applications of frequency-shift biosensor built in cylindrical micro-cavities. The method introduced in this paper can also be used to measure the diameters and refractive indexes of cylindrical micro-cavies precisely.
ABSTRACT
High-frequency gating InGaAs/InP single-photon detectors (SPDs) are widely used for applications requiring single-photon detection in the near-infrared region such as quantum key distribution. Reducing SPD size is highly desired for practical use, which is favorable to the implementation of further system integration. Here we present, to the best of our knowledge, the most compact high-frequency sine wave gating (SWG) InGaAs/InP SPD. We design and fabricate an InGaAs/InP single-photon avalanche diode (SPAD) with optimized semiconductor structure and then encapsulate the SPAD chip and a mini-thermoelectric cooler inside a butterfly package with a size of 12.5 mm × 22 mm × 10 mm. Moreover, we implement a monolithic readout circuit for the SWG SPD in order to replace the quenching electronics that is previously designed with board-level integration. Finally, the components of SPAD, the monolithic readout circuit, and the affiliated circuits are integrated into a single module with a size of 13 cm × 8 cm × 4 cm. Compared with the 1.25 GHz SWG InGaAs/InP SPD module (25 cm × 10 cm × 33 cm) designed in 2012, the volume of our miniaturized SPD is reduced by 95%. After the characterization, the SPD exhibits excellent performance with a photon detection efficiency of 30%, a dark count rate of 2.0 kcps, and an afterpulse probability of 8.8% under the conditions of 1.25 GHz gating rate, 100 ns hold-off time, and 243 K. Also, we perform the stability test over one week, and the results show the high reliability of the miniaturized SPD module.
ABSTRACT
Mediator of IRF3 activation (MITA), also known as stimulator of interferon genes (STING), plays a vital role in the innate immune responses to cytosolic dsDNA. The trafficking of MITA from the ER to perinuclear vesicles is necessary for its activation of the downstream molecules, which lead to the production of interferons and pro-inflammatory cytokines. However, the exact mechanism of MITA activation remains elusive. Here, we report that transmembrane emp24 protein transport domain containing 2 (TMED2) potentiates DNA virus-induced MITA signaling. The suppression or deletion of TMED2 markedly impairs the production of type I IFNs upon HSV-1 infection. TMED2-deficient cells harbor greater HSV-1 load than the control cells. Mechanistically, TMED2 associates with MITA only upon viral stimulation, and this process potentiates MITA activation by reinforcing its dimerization and facilitating its trafficking. These findings suggest an essential role of TMED2 in cellular IFN responses to DNA viruses.
Subject(s)
DNA Viruses/physiology , Interferons/metabolism , Membrane Proteins/metabolism , Protein Multimerization , COP-Coated Vesicles/metabolism , Cytosol/metabolism , DNA/metabolism , Endoplasmic Reticulum/metabolism , Golgi Apparatus/metabolism , HEK293 Cells , Herpesvirus 1, Human/physiology , Humans , Immunity, Innate , Protein Transport , Signal Transduction , THP-1 Cells , Vesicular Transport ProteinsABSTRACT
Interferon-induced transmembrane protein 3 (IFITM3) is a restriction factor that can be induced by viral infection and interferons (IFNs). It inhibits the entry and replication of many viruses, which are independent of receptor usage but dependent on processes that occur in endosomes. In this study, we demonstrate that IFITM3 plays important roles in regulating the RNA-virus-triggered production of IFN-ß in a negative-feedback manner. Overexpression of IFITM3 inhibited Sendai virus-triggered induction of IFN-ß, whereas knockdown of IFITM3 had the opposite effect. We also showed that IFITM3 was constitutively associated with IRF3 and regulated the homeostasis of IRF3 by mediating the autophagic degradation of IRF3. These findings suggest a novel inhibitory function of IFITM3 on the RNA-virus-triggered production of type I IFNs and cellular antiviral responses.
Subject(s)
Autophagosomes/metabolism , Interferon Regulatory Factor-3/immunology , Interferon Type I/immunology , Membrane Proteins/immunology , Proteolysis , RNA Virus Infections/immunology , RNA Viruses/immunology , RNA-Binding Proteins/immunology , HEK293 Cells , HeLa Cells , Humans , Interferon Regulatory Factor-3/genetics , Interferon Type I/genetics , Membrane Proteins/genetics , RNA Virus Infections/genetics , RNA Virus Infections/pathology , RNA Viruses/genetics , RNA-Binding Proteins/geneticsABSTRACT
OBJECTIVE: To study matrix metalloproteinase 2 (MMP-2) effects on transforming growth factor-beta1 (TGF-beta1) activation status and downstream signaling during arterial aging. METHODS AND RESULTS: Western blotting and immunostaining showed that latent and activated TGF-beta1 are markedly increased within the aorta of aged Fisher 344 cross-bred Brown Norway (30 months of age) rats compared with adult (8 months of age) rats. Aortic TGF-beta1-type II receptor (TbetaRII), its downstream molecules p-similar to mad-mother against decapentaplegic (SMAD)2/3 and SMAD4, fibronectin, and collagen also increased with age. Moreover, TGF-beta1 staining is colocalized with that of activated MMP-2 within the aged arterial wall and vascular smooth muscle cell (VSMC) in vitro, and this physical association was confirmed by coimmunoprecipitation. Incubation of young aortic rings ex vivo or VSMCs in vitro with activated MMP-2 enhanced active TGF-beta1, collagen, and fibronectin expression to the level of untreated old counterparts, and this effect was abolished via inhibitors of MMP-2. Interestingly, in old untreated rings or VSMCs, the increased TGF-beta1, fibronectin, and collagen were also substantially reduced by inhibition of MMP-2. CONCLUSIONS: Active TGF-beta1, its receptor, and receptor-mediated signaling increase within the aortic wall with aging. TGF-beta1 activation is dependent, in part at least, by a concomitant age-associated increase in MMP-2 activity. Thus, MMP-2-activated TGF-beta1, and subsequently TbetaRII signaling, is a novel molecular mechanism for arterial aging.
Subject(s)
Aging/physiology , Aorta/physiology , Matrix Metalloproteinase 2/physiology , Receptors, Transforming Growth Factor beta/metabolism , Signal Transduction/physiology , Transforming Growth Factor beta/metabolism , Aging/metabolism , Animals , Aorta/metabolism , Biomarkers/metabolism , Collagen/biosynthesis , Endothelium, Vascular/metabolism , Fibronectins/biosynthesis , Muscle, Smooth, Vascular/cytology , Muscle, Smooth, Vascular/metabolism , Myocytes, Smooth Muscle/metabolism , Protein Serine-Threonine Kinases , RNA, Messenger/metabolism , Rats , Rats, Inbred F344 , Receptor, Transforming Growth Factor-beta Type II , Smad Proteins/metabolism , Tissue Distribution , Transforming Growth Factor beta/genetics , Transforming Growth Factor beta1ABSTRACT
Biodegradable nanomaterials have been widely used in numerous medical fields. To further improve such efforts, this study focused on the intracellular disposition of chitosan nanoparticles (CsNPs) in macrophages, a primary cell of the mononuclear phagocyte system (MPS). Such interactions with the MPS determine the nanoparticle retention time in the body and consequently play a significant role in their own clinical safety. In this study, various dye-labeled CsNPs (about 250 nm) were prepared, and a murine macrophage cell line (RAW 264.7) was selected as a model macrophage. The results showed two mechanisms of macrophage incorporation of CsNPs, ie, a clathrin-mediated endocytosis pathway (the primary) and phagocytosis. Following internalization, the particles partly dissociated in the cells, indicating cellular digestion of the nanoparticles. It was proved that, after intracellular uptake, a large proportion of CsNPs were exocytosed within 24 h; this excretion induced a decrease in fluorescence intensity in cells by 69%, with the remaining particles possessing difficulty being cleared. Exocytosis could be inhibited by both wortmannin and vacuolin-1, indicating that CsNP uptake was mediated by lysosomal and multivesicular body pathways, and after exocytosis, the reuptake of CsNPs by neighboring cells was verified by further experiments. This study, thus, elucidated the fate of CsNPs in macrophages as well as identified cellular disposition mechanisms, providing the basis for how CsNPs are recognized by the MPS; such information is crucial to numerous medical applications of CsNPs.
Subject(s)
Chitosan/pharmacokinetics , Exocytosis/drug effects , Macrophages/drug effects , Nanoparticles/chemistry , Androstadienes/pharmacology , Animals , Biological Transport/drug effects , Cell Line , Chitosan/chemistry , Chitosan/pharmacology , Endocytosis/drug effects , Fluorescent Dyes/chemistry , Fluorescent Dyes/pharmacokinetics , Heterocyclic Compounds, 4 or More Rings/pharmacology , Macrophages/metabolism , Mice , Mononuclear Phagocyte System/drug effects , Phagocytosis/drug effects , WortmanninABSTRACT
Upon binding to RNA structures from invading viruses, RIG-I and MDA5 are recruited to mitochondria to interact with VISA and initiate antiviral type I interferon (IFN) responses. How this process is mediated is less understood. In this report, we demonstrate that ECSIT is an essential scaffolding protein that mediates the association of VISA and RIG-I or MDA5. Overexpression of ECSIT potentiated virus-triggered activation of IFN-regulatory factor 3 (IRF3) and expression of IFNB1, whereas knockdown of ECSIT impaired viral infection-induced activation of IRF3 and expression of IFNB1 as well as cellular antiviral responses. Mechanistically, ECSIT was associated with VISA on mitochondria and important for bridging RIG-I and MDA5 to VISA. Our findings suggest that ECSIT mediates virus-triggered type I IFN induction by bridging RIG-I and MDA5 to the VISA complex, and provide new insights into the molecular events of innate antiviral immune responses.
Subject(s)
Adaptor Proteins, Signal Transducing/metabolism , DEAD-box RNA Helicases/metabolism , Mitochondria/metabolism , Virus Diseases/immunology , Viruses/immunology , Adaptor Proteins, Signal Transducing/genetics , Antigens, Viral/immunology , DEAD Box Protein 58 , Gene Expression Regulation, Viral , HEK293 Cells , Humans , Immunity, Innate , Interferon Regulatory Factor-3/genetics , Interferon Regulatory Factor-3/metabolism , Interferon-Induced Helicase, IFIH1 , Interferon-beta/genetics , Interferon-beta/metabolism , Protein Binding/genetics , RNA, Small Interfering/genetics , Receptors, Immunologic , Signal Transduction/genetics , Transgenes/geneticsABSTRACT
OBJECTIVES: To study the function of chymase on heart remodeling by overexpression of human chymase in the heart of transgenic mice. METHODS: Transgenic mice were produced by microinjection. The chymase mRNA levels in the heart and other tissues were assessed by competitive reverse transcriptase-polymerase chain reaction (RT-PCR). The expression of collagen I/III genes was analyzed by Northern blot hybridization. Chymase and angiotensin-converting enzyme (ACE) activities, and angiotensin II (Ang II) content in the heart were determined by radioimmunoassay (RIA). The matrix metalloprotease-9 (MMP-9) in protein and activity levels were measured by Western blot and zymogram, respectively. RESULTS: A model of transgenic mice with selective overexpression of a rat myosin light chain 2 promoter-human heart chymase (MLC(2-)-hChymase) fusion gene was produced. In MLC(2)-hChymase transgenic mice (the F(6) line), the human heart chymase gene was expressed at a high level in heart and at lower levels in skeletal muscle and kidney, while no expression was detected in the liver or lung. The heart chymase activity increased markedly in the F(6) transgenic mice versus non-transgenic mice (0.274 +/- 0.071 U/mg versus 0.152 +/- 0.021 U/mg) ( P < 0.05), with no difference in ACE activity. Heart Ang II level in the F(6) transgenic mice increased nearly threefold (1984 +/- 184 versus 568 +/- 88 pg/g protein) ( P < 0.05) but was unchanged in plasma. MMP-9 activity increased significantly in the cardiac tissue of F(6) transgenic mice ( P < 0.05), while both collagen I and the ratio of collagen I : III mRNA levels decreased significantly (both P < 0.05). The F(6) transgenic mice showed no significant changes in cardiac parameters. CONCLUSIONS: We have demonstrated selective overexpression of human chymase gene in the heart of transgenic mice, and the results support the hypothesis of a dual Ang II-forming pathway from chymase and ACE in the cardiac tissue in vivo. The results also suggest that chymase may play a role in heart remodeling by increasing Ang II formation and activating MMP-9, and the regulation of collagen I gene expression.
Subject(s)
Heart/physiology , Serine Endopeptidases/biosynthesis , Serine Endopeptidases/genetics , Angiotensin II/genetics , Angiotensin II/metabolism , Animals , Animals, Genetically Modified , Cardiac Myosins/genetics , Chymases , Collagen/biosynthesis , Collagen/genetics , Enzyme Activation/genetics , Gene Deletion , Gene Expression Regulation, Enzymologic/genetics , Matrix Metalloproteinase 9/genetics , Matrix Metalloproteinase 9/metabolism , Mice , Mice, Transgenic/genetics , Models, Animal , Models, Cardiovascular , Myocardium/cytology , Myocardium/metabolism , Myosin Light Chains/genetics , Peptidyl-Dipeptidase A/genetics , Peptidyl-Dipeptidase A/metabolism , Promoter Regions, Genetic/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats/genetics , Rats, Wistar/genetics , Reverse Transcriptase Polymerase Chain Reaction , Transcription, Genetic/geneticsABSTRACT
Calpain, a cytosolic cysteine protease, requires calcium ions for activity. It has been reported that calpain is involved in the degradation of myofibrillar and neurofilament proteins, and the activation of phosphorylase b kinase and protein kinase C. More recently, calpain was shown to participate in apoptosis. In order to understand the calpain-related signal transduction pathway and its changes during hypertrophy, and especially in hypertension, we screened a human heart cDNA library to find proteins that interact with calpain. 1) Using PCR we amplified the full-length, domain II, domain III and domain IV cDNA of calpain (calcium-activated neutral protease, CANP) I large subunit respectively. 2) Then the fragments were cloned into pGBKT7 vector, resulting in 4 bait expression constructs (pGBKT7-CANP, pGBKT7-CANP II, pGBKT7-CANP III, and pG BKT7-CANP IV). 3) After 4 bait vectors were transformed into AH109 by the lithium acetate-mediated method, AH109/pGBKT7-CANP, AH109/pGBKT7-CANP II, AH109/pGBKT7-CANP III, and AH109/pGBKT7-CANP IV were obtained, respectively. 4) After the human heart cDNA library was sequentially transformed into AH109/ pGBKT7-CANP, 1000-1200 positive clones were grown on SD/Trp-Leu-Ade-His-. Only 150 positive clones were obtained through a colony-lift filter assay to detect beta-galactosidase activity. 5) Total 105 clones among above 150 positive clones were eliminated through that the duplicate, pseudopositive and autoactive detection, respectively. 6) Finally, sequencing eliminated clones with a wrong open reading frame (ORF). Eight clones were cancelled with wrong ORF. The remaining 37 positive clones were analyzed using BLAST software available on the Internet and classified as follows: 1. enzymes or proteins related to signal transduction in the cell; 2. contraction proteins 3. matrix proteins 4. unknown proteins. 7) In order to determine which domain of the calpain I large subunit was involved in the interaction with these real clones, the 37 clones were transformed into AH109/pGBKT7-CANP II, AH109/pGBKT7-CANP III or AH109/pGBKT7-CANP IV. Among these 37 clones, 29 clones could interact with domain II, 5 clones could interact with domain III and 6 clones could interact with domain IV. Thus, we successfully constructed 4 bait expression vectors, pGBKT7-CANP, pGBKT7-CANP II, pGBKT7-CANP III and pGBKT7-CANP IV, and obtained 37 real positive clones that interacted with the calpain I large subunit by screening a human heart cDNA library using pGBKT7-CANP as bait. Among them, 29 clones could interact with domain II of the calpain I large subunit, where the active site of calpain is located. Additional studies will be needed to clarify the calpain-related signal transduction pathway in greater detail.
Subject(s)
Calpain/physiology , DNA, Complementary/genetics , Myocardium/metabolism , Proteins/physiology , Two-Hybrid System Techniques , Gene Library , Humans , Yeasts/geneticsABSTRACT
Recent years, great interest has been devoted to the conversion of biomass-derived carbohydrate into sugars, such as glucose, mannose and fructose. These are important versatile intermediate products that are easily processed into high value-added biofuels. In this work, microwave-assisted dilute sulfuric acid hydrolysis of deproteinated palm kernel cake (DPKC) was systematically studied using Response Surface Methodology. The highest mannose yield (92.11%) was achieved at the optimized condition of 148°C, 0.75N H2SO4, 10min 31s and substrate to solvent (SS) ratio (w/v) of 1:49.69. Besides that, total fermentable sugars yield (77.11%), was obtained at 170°C, 0.181N H2SO4, 6min 6s and SS ratio (w/v) of 1:40. Ridge analysis was employed to further verify the optimum conditions. Thus, this work provides fundamental data of the practical use of DPKC as low cost, high yield and environmental-friendly material for the production of mannose and other sugars.