1.Progress in research of relationship between heavy metal exposure and cardiovascular disease.
F LU ; F ZHAO ; J Y CAI ; L LIU ; X M SHI
Chinese Journal of Epidemiology 2018;39(1):102-106
Heavy metal is one of pollutants existed widely in the environment, its relationship with cardiovascular disease has attracted more and more attention. In this review, the concentrations of heavy metals, including lead, cadium and asenic, in the body from several national surveillance networks and the epidemiological studies on the effects of the exposure of three heavy metals on cardiovascular system were summarized. It is suggested to strengthen nationwide surveillance for body concentrations of heavy metals in general population in order to provide baseline data for quantitative evaluation of the risk of heavy metal exposure on cardiovascular disease.
Cadmium
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Cardiovascular Diseases/chemically induced*
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Environmental Exposure/adverse effects*
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Environmental Pollutants/toxicity*
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Epidemiologic Studies
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Humans
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Lead/toxicity*
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Metals, Heavy/toxicity*
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Neoplasms
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Research/trends*
2.An octamer of enolase from Streptococcus suis.
Qiong LU ; Hao LU ; Jianxun QI ; Guangwen LU ; George F GAO
Protein & Cell 2012;3(10):769-780
Enolase is a conserved cytoplasmic metalloenzyme existing universally in both eukaryotic and prokaryotic cells. The enzyme can also locate on the cell surface and bind to plasminogen, via which contributing to the mucosal surface localization of the bacterial pathogens and assisting the invasion into the host cells. The functions of the eukaryotic enzymes on the cell surface expression (including T cells, B cells, neutrophils, monocytoes, neuronal cells and epithelial cells) are not known. Streptococcus suis serotype 2 (S. suis 2, SS2) is an important zoonotic pathogen which has recently caused two large-scale outbreaks in southern China with severe streptococcal toxic shock syndrome (STSS) never seen before in human sufferers. We recently identified the SS2 enolase as an important protective antigen which could protect mice from fatal S.suis 2 infection. In this study, a 2.4-angstrom structure of the SS2 enolase is solved, revealing an octameric arrangement in the crystal. We further demonstrated that the enzyme exists exclusively as an octamer in solution via a sedimentation assay. These results indicate that the octamer is the biological unit of SS2 enolase at least in vitro and most likely in vivo as well. This is, to our knowledge, the first comprehensive characterization of the SS2 enolase octamer both structurally and biophysically, and the second octamer enolase structure in addition to that of Streptococcus pneumoniae. We also investigated the plasminogen binding property of the SS2 enzyme.
Amino Acid Sequence
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Binding Sites
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Crystallography, X-Ray
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Humans
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Models, Molecular
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Molecular Sequence Data
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Phosphopyruvate Hydratase
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chemistry
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metabolism
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Plasminogen
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metabolism
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Protein Multimerization
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Protein Structure, Quaternary
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Solutions
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Species Specificity
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Streptococcus suis
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enzymology
3.Optimization of enzymatic extraction of effective constituents from fibrous roots of Salvia miltiorrhiza by central composite design and response surface method.
Gang LU ; Guo-dong DU ; Jun-ru WANG ; Zong-suo LIANG
China Journal of Chinese Materia Medica 2008;33(16):1976-1981
The fibrous roots are the residues of production of cut crude drug of Danshen (Salvia miltiorrhiza). Enzymatic pretreatment and ultrasonic extraction are beneficial to extract effective constituents from fibrous roots more effectively. The present research was to optimize the enzymatic parameters by the central composite design and response surface method. Under the best conditions, the yields of total tanshinones and total salvianolic acids in the extracts of enzymatic pretreatment increased by 113.92% and 30.64%, comparing with the non-enzymatic extraction, respectively. TLC analysis also showed that the types of effective constituents in the two samples were not affected by enzymatic hydrolysis. Meanwhile, the complex correlation coefficients of the mathematical models were high, which provided a good prediction.
Diterpenes, Abietane
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Drugs, Chinese Herbal
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chemistry
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Phenanthrenes
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chemistry
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Plant Roots
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chemistry
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Salvia miltiorrhiza
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chemistry
6.Recent research on myositis-specific autoantibodies in juvenile dermatomyositis.
Chinese Journal of Contemporary Pediatrics 2021;23(10):1064-1068
Juvenile dermatomyositis (JDM) is an autoimmune disease manifesting as proximal muscle weakness and skin rash and can involve multiple systems and visceral organs. Myositis-specific autoantibodies (MSAs) are highly associated with various complications and prognosis in JDM. Patients with anti-Mi-2 antibodies tend to have good prognosis and typical clinical symptoms. Patients with anti-MDA5 antibodies often have diffuse interstitial lung disease and skin ulcer, with mild symptoms of myositis. Patients with anti-NXP2 antibodies often have calcinosis, and such antibodies are associated with gastrointestinal bleeding and perforation. Patients with anti-TIF1-γ antibodies have diffuse and refractory skin lesions. Anti-SAE antibodies are rarely detected in children, with few reports of such cases. This article reviews the features of clinical phenotypes in JDM children with these five types of MSAs, so as to provide a basis for the clinical treatment and follow-up management of children with JDM.
Autoantibodies
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Dermatomyositis
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Humans
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Lung Diseases, Interstitial/etiology*
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Myositis
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Prognosis
7.Establishment of a new low-density cDNA macroarray and the application in the activity of IFN against HBV.
Shi-he GUAN ; Hua-ping LIU ; Dong-liang YANG ; Meng-ji LU ; Michael ROGGENDORF ; Joerg F SCHLAAK
Chinese Journal of Experimental and Clinical Virology 2005;19(3):236-239
OBJECTIVETo investigate the expression profile of genes which are involved in IFN antiviral activity and IFN signal transduction pathway in Hep G2 and HepG2.2.15 cells.
METHODSGenes of interest were selected from the UniGene database (http://www.ncbi.nlm.gov/UniGene/Hs.Home.html). The 5'IMAGE clones with 0.5-0.8 kb length were chosen and ordered from RZPD company. The cDNA inserts were amplified by PCR and then were spotted onto the Hybond-N+ membranes. The membranes were denatured and neutralized for Macroarray analysis. HepG2.2.15 and Hep G2 cells were treated without or with IFN-alpha for 6 h, and the total cellular RNA was isolated using Trizol Reagent. Radio-labelled cDNA was generated from 20 microgram of RNA by reverse transcription using 360 units of reverse transcriptase in the presence of 30 microCi of alpha-32P dCTP. Hybridization was performed between 32P-labelled cDNA and membrane arrays. The membranes were then scanned, and the intensity of autoradiographic spots was quantitated by Cyclone Storage Phosphor System. The images were subsequently analysed by the OptiQuant Imager Analysis Software and converted into digital data.
RESULTSThe authors found that just partially IFN-inducible genes were expressed in Hep G2 and HepG2.2.15 cells, and the majority of IFN-inducible genes was lowly responsive or non-responsive to IFN-a treatment. Some interferon-stimulated genes (ISGs) were inhibited or blocked, especially in HepG2.2.15 cells. Interestingly, the authors found that the IFN signal transduction pathway (Jak-STAT) was intact and unimpaired in HepG2.2.15 cells.
CONCLUSIONDifferential gene expression profiles in response to IFN were found between Hep G2 and HepG2.2.15 cells.
Antiviral Agents ; pharmacology ; Carcinoma, Hepatocellular ; genetics ; pathology ; virology ; Cell Line, Tumor ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; drug effects ; Hepatitis B virus ; drug effects ; Humans ; Interferons ; pharmacology ; Liver Neoplasms ; genetics ; pathology ; virology ; Oligonucleotide Array Sequence Analysis ; methods ; RNA, Viral ; genetics ; metabolism ; Reverse Transcriptase Polymerase Chain Reaction
9.Expression, purification, and bio-activity analysis of fusion protein HBx-EGFP-TLM.
Xiaoyan SHI ; Yingying ZHANG ; Xiaowei ZHOU ; Jiansheng LU ; Zekun GUO ; Peitang HUANG
Chinese Journal of Biotechnology 2011;27(9):1371-1378
Hepatitis B virus X protein (HBx) has various functions and plays a crucial role in the development of hepatocellular carcinoma (HCC). However, due to different transfection efficiency levels and experimental approaches, it is difficult to correlate the exact functions of HBx to HBV-associated HCC. In this study, we constructed two prokaryotic expression vectors, pGEX-HBx-EGFP-TLM and pGEX-EGFP-TLM, which expressed HBx-EGFP-TLM and EGFP-TLM fusion proteins respectively. Both vectors contained a coding sequence of TLM transduction motif derived from the PreS2-domain of Hepatitis B Virus surface antigens. In addition, EGFP was expressed as a reporter reflecting the transduction efficiency of TLM. The fusion protein HBx-EGFP-TLM or EGFP-TLM purified from Escherichia coli BL21(DE3) by AKTA Purifier system was incubated with AML12 and SMMC-7721 cells. Both Western blotting and laser confocal results indicated that the translocation motif TLM could lead HBx-EGFP and EGFP into the cytoplasm. Dual-Luciferase Reporter Assay revealed that the activity of mEZH2 promoter could be up-regulated by the recombinant HBx. In conclusion, we expressed a cell-permeable HBx, which could provide a new method to study the functions of HBx.
Amino Acid Motifs
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genetics
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Cell-Penetrating Peptides
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biosynthesis
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genetics
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Escherichia coli
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genetics
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metabolism
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Genetic Vectors
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genetics
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Green Fluorescent Proteins
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biosynthesis
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genetics
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Hepatitis B Surface Antigens
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genetics
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Protein Precursors
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genetics
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Recombinant Fusion Proteins
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biosynthesis
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genetics
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isolation & purification
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Trans-Activators
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biosynthesis
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genetics
10.The receptors and entry of measles virus: a review.
Guangwen LU ; George F GAO ; Jinghua YAN
Chinese Journal of Biotechnology 2013;29(1):1-9
Measles virus is an enveloped virus with a non-segmented negative-sense RNA genome. Two envelope glycoproteins on the viral surface, namely hemagglutinin (H) and membrane fusion protein (F), are responsible for the virus entry into susceptible host cells. The specific interaction between H and its cellular receptors is a key step in successful virus infection, determining the infectivity and tissue tropism of the measles virus. Thus far, three H receptors have been identified, including the complement regulatory molecule CD46, the signaling lymphocyte activation molecule (SLAM) and the cell adhesion molecule Nectin-4. Here, we reviewed our molecular understanding on the recognition mechanism of these receptors by the viral H protein, aiming to promote future studies on antiviral drug design and measles virus-based oncolytic therapy.
Animals
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Antigens, CD
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metabolism
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Cell Adhesion Molecules
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metabolism
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Hemagglutinins, Viral
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metabolism
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Humans
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Measles virus
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pathogenicity
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physiology
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Membrane Cofactor Protein
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metabolism
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Membrane Fusion
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Membrane Fusion Proteins
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metabolism
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Receptors, Cell Surface
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metabolism
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Receptors, Virus
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metabolism
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Signaling Lymphocytic Activation Molecule Family Member 1