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1.
Calcif Tissue Int ; 115(2): 101-116, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38833001

ABSTRACT

Primary failure of eruption (PFE) is a rare disorder that is characterized by the inability of a molar tooth/teeth to erupt to the occlusal plane or to normally react to orthodontic force. This condition is related to hereditary factors and has been extensively researched over many years. However, the etiological mechanisms of pathogenesis are still not fully understood. Evidence from studies on PFE cases has shown that PFE patients may carry parathyroid hormone 1 receptor (PTH1R) gene mutations, and genetic detection can be used to diagnose PFE at an early stage. PTH1R variants can lead to altered protein structure, impaired protein function, and abnormal biological activities of the cells, which may ultimately impact the behavior of teeth, as observed in PFE. Dental follicle cells play a critical role in tooth eruption and root development and are regulated by parathyroid hormone-related peptide (PTHrP)-PTH1R signaling in their differentiation and other activities. PTHrP-PTH1R signaling also regulates the activity of osteoblasts, osteoclasts and odontoclasts during tooth development and eruption. When interference occurs in the PTHrP-PTH1R signaling pathway, the normal function of dental follicles and bone remodeling are impaired. This review provides an overview of PTH1R variants and their correlation with PFE, and highlights that a disruption of PTHrP-PTH1R signaling impairs the normal process of tooth development and eruption, thus providing insight into the underlying mechanisms related to PTH1R and its role in driving PFE.


Subject(s)
Receptor, Parathyroid Hormone, Type 1 , Tooth Eruption , Receptor, Parathyroid Hormone, Type 1/genetics , Receptor, Parathyroid Hormone, Type 1/metabolism , Humans , Tooth Eruption/genetics , Tooth Eruption/physiology , Mutation , Tooth, Unerupted/genetics , Animals , Tooth Diseases
2.
Mol Med ; 27(1): 109, 2021 09 16.
Article in English | MEDLINE | ID: mdl-34530740

ABSTRACT

BACKGROUND: Recently, the role of several microRNAs (miRNAs or miRs) in pulmonary diseases has been described. The molecular mechanisms by which miR-214 is possibly implicated in bronchopulmonary dysplasia (BPD) have not yet been addressed. Hence, this study aimed to investigate a putative role of miR-214 in alveolarization among preterm neonates with BPD. METHODS: Microarray-based gene expression profiling data from BPD was employed to identify differentially expressed genes. A BPD neonatal rat model was induced by hyperoxia. Pulmonary epithelial cells were isolated from rats and exposed to hyperoxia to establish cell injury models. Gain- and loss-of-function experiments were performed in BPD neonatal rats and hyperoxic pulmonary epithelial cells. MiR-214 and PlGF expression in BPD neonatal rats, and eNOS, Bcl-2, c-myc, Survivin, α-SMA and E-cadherin expression in hyperoxic pulmonary epithelial cells were measured using RT-qPCR and Western blot analysis. The interaction between PlGF and miR-214 was identified using dual luciferase reporter gene and RIP assays. IL-1ß, TNF-a, IL-6, ICAM-1 and Flt-1 expression in the rat models was measured using ELISA. RESULTS: The lung tissues of neonatal rats with BPD showed decreased miR-214 expression with elevated PlGF expression. PlGF was found to be a target of miR-214, whereby miR-214 downregulated PlGF to inactivate the STAT3 pathway. miR-214 overexpression or PlGF silencing decreased the apoptosis of hyperoxic pulmonary epithelial cells in vitro and restored alveolarization in BPD neonatal rats. CONCLUSION: Overall, the results demonstrated that miR-214 could facilitate alveolarization in preterm neonates with BPD by suppressing the PlGF-dependent STAT3 pathway.


Subject(s)
Bronchopulmonary Dysplasia/genetics , Bronchopulmonary Dysplasia/metabolism , Gene Expression Regulation , Membrane Proteins/metabolism , MicroRNAs/genetics , Placenta Growth Factor/metabolism , STAT3 Transcription Factor/metabolism , Signal Transduction , Animals , Animals, Newborn , Apoptosis , Biomarkers , Bronchopulmonary Dysplasia/diagnosis , Computational Biology/methods , Disease Models, Animal , Disease Susceptibility , Gene Expression Profiling , Immunohistochemistry , Pulmonary Alveoli/metabolism , Pulmonary Alveoli/pathology , Pulmonary Alveoli/ultrastructure , Rats
3.
Mol Med ; 26(1): 99, 2020 11 03.
Article in English | MEDLINE | ID: mdl-33143661

ABSTRACT

BACKGROUND: The incidence of bronchopulmonary dysplasia (BPD), a chronic lung disease of newborns, has been paradoxically rising despite medical advances. Histone deacetylase 3 (Hdac3) has been reported to be a crucial regulator in alveologenesis. Hence, this study aims to investigate the mechanism of Hdac3 in the abnormal pulmonary angiogenesis and alveolarization of BPD. METHODS: A hyperoxia-induced BPD model of was developed in newborn mice, and primary lung fibroblasts were isolated from adult mice. Hdac3 was knocked out in vivo and knocked down in vitro, while microRNA (miR)-17 was downregulated in vivo and in vitro to clarify their roles in abnormal pulmonary angiogenesis and alveolarization. Mechanistic investigations were performed on the interplay of Hdac3, miR-17-92 cluster, enhancer of zeste homolog 1 (EZH1), p65 and placental growth factor (Pgf). RESULTS: Hdac3 was involved in abnormal alveolarization and angiogenesis in BPD mice. Further, the expression of the miR-17-92 cluster in BPD mice was downregulated by Hdac3. miR-17 was found to target EZH1, and Hdac3 rescued the inhibited EZH1 expression by miR-17 in lung fibroblasts. Additionally, EZH1 augmented Pgf expression by recruiting p65 thus enhancing the progression of BPD. Hdac3 augmented the recruitment of p65 in the Pgf promoter region through the miR-17/EZH1 axis, thus enhancing the transcription and expression of Pgf, which elicited abnormal angiogenesis and alveolarization of BPD mice. CONCLUSIONS: Altogether, the present study revealed that Hdac3 activated the EZH1-p65-Pgf axis through inhibiting miR-17 in the miR-17-92 cluster, leading to accelerated abnormal pulmonary angiogenesis and alveolarization of BPD mice.


Subject(s)
Bronchopulmonary Dysplasia/genetics , Bronchopulmonary Dysplasia/metabolism , Gene Expression Regulation, Developmental , Histone Deacetylases/genetics , MicroRNAs/genetics , Multigene Family , Animals , Biomarkers , Bronchopulmonary Dysplasia/diagnosis , Disease Models, Animal , Disease Progression , Fibroblasts/metabolism , Genetic Association Studies/methods , Genetic Predisposition to Disease , Histone Deacetylases/metabolism , Humans , Hyperoxia/genetics , Hyperoxia/metabolism , Mice , Phenotype , RNA Interference , Signal Transduction
4.
Cryobiology ; 97: 110-122, 2020 12.
Article in English | MEDLINE | ID: mdl-33011172

ABSTRACT

The present study analyzed the relationship between bovine oocytes developmental competence and mRNA expression of apoptotic and mitochondrial genes following the change of vitrification temperatures (VTs) and cryoprotectant agent concentrations (CPAs). Cumulus oocyte complexes were randomly divided into five groups: control, vitrified in liquid nitrogen (LN; -196 °C) with 5.6 M CPAs (LN 5.6 M), LN with 6.6 M CPAs (LN 6.6 M), liquid helium (LHe; -269 °C) with 5.6 M CPAs (LHe 5.6 M), and LHe with 6.6 M CPAs (LHe 6.6 M). After vitrification and warming, oocytes of vitrified and control groups were subjected to in vitro maturation (IVM), in vitro fertilization and in vitro culture. The blastocyst rate in LHe 5.6 M group was the highest among the four vitrified groups (13.7% vs. 9.4%, 1.3%, and 8.4%; P < 0.05). The mRNA expression level of 8 apoptotic- and 12 mitochondria-related genes were detected through qRT-PCR after IVM. Lower VT (LHe, -269 °C) positively affected the mRNA expression levels of apoptotic genes (BAD, BID, BTK, TP53, and TP53I3) and mitochondrial genes (COX6B1, DERA, FIS1, NDUFA1, NDUFA4, PRDX2, SLC25A5, TFB1M, and UQCRB), and reduced oxidative stress from freezing. Decreased CPAs (5.6 M) positively affected mRNA expression levels of apoptotic genes (BAD, BCL2A1, BID, and CASP3) in LHe vitrification but negatively affected apoptotic genes (BAD, BAX, BID, BTK, and BCL2A1) in LN vitrification. In conclusion, decreased VTs and CPAs in LHe vitrification may increase the blastocyst rate by changing the mRNA expression levels of these apoptotic and mitochondrial genes for the vitrified oocytes.


Subject(s)
Genes, Mitochondrial , Vitrification , Animals , Cattle , Cryopreservation/methods , Oocytes , RNA, Messenger/genetics , Temperature
5.
BMC Med Educ ; 20(1): 280, 2020 Aug 24.
Article in English | MEDLINE | ID: mdl-32838782

ABSTRACT

BACKGROUND: Evidence-based practice (EBP) education or training are considered fundamental to building and strengthening an EBP culture, as well as to encouraging evidence-based academic and clinical practice in the nursing community. However, few valid and reliable instruments are available for the assessment of EBP teaching and learning in clinical nurses in China. Translation, reliability, and validity testing of the English Evidence-Based Practice Profile Questionnaire (EBP2Q), which has strong psychometric properties, may encourage evaluation and promote the implementation of EBP in Mainland China. METHODS: Based on established guidelines for the development of questionnaires, the English EBP2Q was translated and cross-culturally adapted. The Chinese version of the EBP2Q (EBP2Q-C) was validated using a sample of 543 nurses. Structural validity was evaluated through exploratory factor analysis and confirmatory factor analysis, and the questionnaire was tested for convergent and criterion validity. The internal consistency and test-retest reliability were also evaluated. RESULTS: The content validity index demonstrated good content validity (≥0.98). An eight-factor structure was obtained in the exploratory factor analysis, and verified by a three-order factor model from the confirmatory factor analysis (χ2/df = 2.001; RMSEA = 0.065; SRMR = 0.077; and CFI = 0.884). The Spearman's rank correlation analysis of the EBP2Q-C with the Evidence-Based Practice Questionnaire showed moderate correlations for Practice (0.58) and Confidence (0.68) and a low correlation for Sympathy (0.32). Criterion validity was demonstrated by significant differences in terms of nurses' highest education, present position, EBP training, involvement in research programs, and level of understanding of English. Both the overall Cronbach's α and the Cronbach's α for the domains exceeded 0.70. The intraclass correlation coefficients for the domains ranged between 0.75 and 0.96, indicating satisfactory repeatability. CONCLUSIONS: Except for the convergent validity of the Sympathy domain, the EBP2Q-C provided evidence of validity and reliability. Therefore, it can be applied in EBP education or training assessment in Mainland China.


Subject(s)
Evidence-Based Practice , Translations , China , Humans , Psychometrics , Reproducibility of Results , Surveys and Questionnaires
6.
Mol Vis ; 24: 471-477, 2018.
Article in English | MEDLINE | ID: mdl-30078984

ABSTRACT

Purpose: To identify disease-causing gene mutations in 21 northern Chinese families with congenital cataracts. Methods: Medical record collection and ophthalmologic examinations were conducted for 21 families with congenital cataracts. A volume of 5 ml of peripheral blood was drawn from each participant for genomic DNA isolation. Thirty-four known candidate genes for congenital cataracts were analyzed in the probands of 21 families with targeted next-generation sequencing (NGS). Bioinformatics analysis of the sequence variants was performed through computational predictive programs. Sanger sequencing was used to perform the cosegregation analysis. Genotyping and haplotype analyses were performed in two patients with a p.V44M mutation in the GJA8 gene. Results: Twelve disease-causing mutations were detected in 13 of the 21 patients, and the mutation detection rate was 61.9%. The 12 gene mutations included one nonsense, one splice site, seven missense, and three insert and deletion (INDELs) mutations. Four mutations were novel. Of the 13 patients with pathogenic gene mutations, five (38.5%) were affected by mutations in lens crystallin genes, three (23%) were affected by mutations in connexin genes, three (23%) were affected by mutations in transcription factor genes, one (7.7%) was affected by a mutation in a transmembrane transporter gene, and one (7.7%) was affected by a mutation in a chromatin-modifying protein gene. Two families carried the p.V44M mutation in the GJA8 gene. Haplotype analysis revealed a chromosome region of 475 kb containing the mutation in the GJA8 gene was harbored by two families. Conclusions: Compared with traditional Sanger sequencing, targeted NGS for genetic testing of congenital cataracts markedly increases the mutation detection rate and is cost-effective. The p.V44M mutation in the GJA8 gene was the most common mutation and was due to a founder effect within the Chinese cohort studied. The results of this study expand the gene mutation spectrum of congenital cataracts.


Subject(s)
Aquaporins/genetics , Cataract/genetics , Connexins/genetics , Endosomal Sorting Complexes Required for Transport/genetics , Eye Proteins/genetics , Forkhead Transcription Factors/genetics , Heat Shock Transcription Factors/genetics , Mutation , Adolescent , Adult , Asian People , Cataract/congenital , Cataract/ethnology , Cataract/pathology , Child , Child, Preschool , Cohort Studies , DNA Mutational Analysis , Family , Female , Founder Effect , Gene Expression , Haplotypes , High-Throughput Nucleotide Sequencing , Humans , Lens, Crystalline/metabolism , Lens, Crystalline/pathology , Male , Middle Aged , Pedigree
7.
Br J Cancer ; 117(5): 675-684, 2017 Aug 22.
Article in English | MEDLINE | ID: mdl-28683467

ABSTRACT

BACKGROUND: The transforming growth factor-ß (TGF-ß) pathway plays a vital role in driving cancer cell epithelial-mesenchymal transition (EMT). Zonula occludens-1 (ZO-1), which is downregulated in response to TGF-ß, is able to control endothelial cell-cell tension, cell migration, and barrier formation. However, the molecular mechanism of how TGF-ß regulates ZO-1 expression remains unclear. METHODS: Breast cancer cells were treated with TGF-ß to induce an EMT progress. Chromatin immunoprecipitation and dual-luciferase reporter assay were performed to investigate direct relationship between Snail and RNA binding motif protein 38 (RBM38). The RNA immunoprecipitation combined with RNA electrophoretic mobility shift assay and dual-luciferase reporter assay were conducted to testify direct relationship between RBM38 and ZO-1. The ZO-1 siRNA was transfected to breast cancer cells that overexpress RBM38 and the control, followed by transwell and Matrigel invasion assays to examine cell migratory and invasive ability. RESULTS: Transforming growth factor-ß induced a remarkable downregulation of RBM38 in breast cancer that was directly regulated by transcription repressor Snail targeting the E-box elements in promoter region of RBM38 gene. Additionally, RBM38 positively regulated ZO-1 transcript via directly binding to AU/U-rich elements in its mRNA 3'-UTR. Moreover, by magnifying RBM38 expression, cell migration and invasion mediated by knockdown of ZO-1 in breast cancer were reversed. CONCLUSIONS: All the results clarified a linear regulation relationship among Snail, RBM38, and ZO-1, implicating RBM38 as a pivotal mediator in TGF-ß-induced EMT in breast cancer.


Subject(s)
Epithelial-Mesenchymal Transition , RNA, Messenger/metabolism , RNA-Binding Proteins/genetics , RNA-Binding Proteins/metabolism , Zonula Occludens-1 Protein/genetics , Zonula Occludens-1 Protein/metabolism , 3' Untranslated Regions , Benzamides/pharmacology , Breast Neoplasms/chemistry , Cell Movement/drug effects , Cell Movement/genetics , Dioxoles/pharmacology , Down-Regulation , E-Box Elements/genetics , Epithelial-Mesenchymal Transition/drug effects , Female , Gene Expression , Humans , MCF-7 Cells , Promoter Regions, Genetic , Protein Serine-Threonine Kinases/antagonists & inhibitors , RNA, Small Interfering/genetics , RNA-Binding Proteins/analysis , Receptor, Transforming Growth Factor-beta Type I , Receptors, Transforming Growth Factor beta/antagonists & inhibitors , Snail Family Transcription Factors/genetics , Transfection , Transforming Growth Factor beta/pharmacology , Zonula Occludens-1 Protein/analysis
8.
BMC Ophthalmol ; 17(1): 115, 2017 Jul 04.
Article in English | MEDLINE | ID: mdl-28676040

ABSTRACT

BACKGROUND: This study evaluates patients with congenital aniridia and cataract who underwent phacoemulsification, capsular tension ring placement, and foldable intraocular lens implantation. METHODS: In this prospective case series, 10 patients (17 eyes) underwent cataract surgery via a 3.2 mm clear corneal incision. A continuous circular capsulorhexis with <6 mm diameter was employed. A capsular tension ring and HOYA yellow foldable posterior chamber intraocular lens was implanted. All patients wore color contact lenses postoperatively. Paired t test was used to compare visual acuity, intraocular pressure, and corneal endothelial changes before and after surgery. RESULTS: A single surgeon performed all surgeries. The best-corrected visual acuity improved from value 1.03 ± 0.27LogMAR preoperatively to value 0.78 ± 0.26LogMAR postoperatively (p = 0.000). The photophobic symptoms improved significantly after surgery. The mean corneal endothelial cell density before and after surgery was 3280 ± 473 cells/mm2 and 2669 ± 850 cells/mm2, respectively (p = 0.006). None of the patients developed corneal endothelial decompensation or secondary glaucoma after surgery. CONCLUSIONS: Treatment of congenital aniridia and coexistent cataract by phacoemulsification, posterior chamber foldable lens implantation, capsular tension ring placement was safe and effective. Use of colored contact lenses in the postoperative period can reduce photophobic symptoms in this group of patients. TRIAL REGISTRATION: ChiCTR-OOC-17011638 (retrospectively registered at 12,June,2017).


Subject(s)
Aniridia/diagnosis , Cataract/complications , Lenses, Intraocular , Phacoemulsification/methods , Visual Acuity , Adolescent , Adult , Aniridia/complications , Aniridia/surgery , Cataract/diagnosis , Cataract/physiopathology , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Prospective Studies , Tomography, Optical Coherence , Young Adult
10.
Bioorg Med Chem Lett ; 26(5): 1391-6, 2016 Mar 01.
Article in English | MEDLINE | ID: mdl-26848110

ABSTRACT

Eight new isocoumarin glycosides (1-8) were obtained from the solid culture of the wetland soil-derived fungus Metarhizium anisopliae (No. DTH12-10). Their chemical structures were elucidated by analyses of HR ESI-TOF MS, (1)H, (13)C NMR, (1)H-(1)H COSY, HSQC, and HMBC spectra. The absolute configurations were determined by single crystal X-ray diffraction, circular dichroism (CD) spectrum, and chemical derivatization methods. In addition, inhibition of the biofilm formation and the secretion of virulence factor of the new isocoumarin glycosides against Pseudomonas aeruginosa strain PAOA (clinical isolates) were evaluated. The result revealed that compound 1 showed antibacterial activity comparable with (Z)-4-bromo-5-(bromomethylene)-2(5H)-furanone (BF).


Subject(s)
Anti-Bacterial Agents/pharmacology , Glycosides/pharmacology , Isocoumarins/pharmacology , Metarhizium/chemistry , Pseudomonas aeruginosa/drug effects , Wetlands , Anti-Bacterial Agents/chemistry , Biofilms/drug effects , Biofilms/growth & development , Dose-Response Relationship, Drug , Glycosides/chemistry , Isocoumarins/chemistry , Molecular Structure , Structure-Activity Relationship
11.
Transfus Apher Sci ; 54(2): 235-41, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26780991

ABSTRACT

OBJECTIVE: To investigate the impacts of perioperative blood transfusion on the immune function and prognosis in colorectal cancer (CC) patients. METHODS: A retrospective analysis was conducted in 1404 CC patients, including 1223 sporadic colorectal cancer (SCC) patients and 181 hereditary colorectal cancer (HCC) patients. Among them, 701 SCC and 102 HCC patients received perioperative blood transfusion. The amount of T lymphocyte subsets and natural killer (NK) cells was measured. All patients received a 10-year follow-up and relapse, metastasis and curative conditions were recorded. RESULTS: In SCC group, mortality, local recurrence and distant metastasis rate of transfused patients were significantly higher than non-transfused patients (all P <0.05). In HCC group, mortality was apparently higher in transfused patients than non-transfused patients (P = 0.002). SCC patients transfused with ≥3 U of blood had significantly higher mortality than patients transfused with <3 U (P = 0.006). The amount of T lymphocyte subsets and NK cells showed statistical differences before and after perioperative blood transfusion in SCC and HCC patients (all P <0.05). Also, there existed statistical differences in CD4+/CD8+ ratio among SCC patients before and after the perioperative blood transfusion (P <0.05). CC patients who received perioperative blood transfusion had markedly lower 10-year survival rates as compared with those who did not receive (both P <0.05). SCC patients transfused with ≥3 U of blood had remarkably lower survival rates compared with SCC patients transfused with <3 U (P = 0.002). CONCLUSIONS: Perioperative blood transfusion could impact immune function, increased postoperative mortality, local recurrence rate and distant metastasis rate in CC patients; and survival rate of CC patients is negatively related to blood transfusion volume.


Subject(s)
Blood Transfusion , Colorectal Neoplasms , Killer Cells, Natural/immunology , Perioperative Care , T-Lymphocyte Subsets/immunology , Adult , Aged , Colorectal Neoplasms/immunology , Colorectal Neoplasms/mortality , Colorectal Neoplasms/surgery , Disease-Free Survival , Female , Follow-Up Studies , Humans , Male , Middle Aged , Retrospective Studies , Survival Rate
12.
Graefes Arch Clin Exp Ophthalmol ; 254(11): 2247-2255, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27460281

ABSTRACT

PURPOSE: To investigate the influence of daily activities on myopic refractive change and myopic onset in Chinese urban students. METHODS: The Beijing Myopia Progression Study was a 3-year cohort study. Cycloplegic refraction and a daily activity questionnaire were assessed at baseline and at follow-up examinations. Refractive change was defined as the difference in cycloplegic spherical equivalent (SE) between the final follow-up and baseline. 386 students were initially enrolled in the baseline study. RESULTS: At the final follow-up, 222 students (57.5 %) with completed refractive error and daily activity data were analyzed. These students spent 0.32 ± 2.33 h/day more on near work (p = 0.04), and 0.21 ± 1.31 h/day less on outdoor leisure (p = 0.02), than they did at baseline. In the multivariate analysis, the younger among the secondary students (ß = 0.06, p < 0.001), and those with more near work hours at baseline (ß = -0.028, p = 0.033), exhibited more myopic refractive change. However, myopic refractive change was not found to be significantly associated with near work hours in the primary students, or with time spent outdoors, in either school level. After stratifying the activity hours into quartile groups, students with a greater near work load at baseline (trend P = 0.03) exhibited a greater myopic refractive change and had a higher risk to develop myopia (hazard ratio, 95 % confidence interval: 5.19, 1.49-18.13), after adjusting for the confounders. However, no significant association was found related to outdoor activity. CONCLUSIONS: In this cohort, children with a greater near work load at baseline exhibited more myopic refractive change and were also more likely to develop myopia. The protective effect of outdoor activity on myopic refractive change was not observed.


Subject(s)
Myopia/physiopathology , Refraction, Ocular/physiology , Schools , Students , Urban Population , Activities of Daily Living , Adolescent , Age of Onset , Child , China/epidemiology , Disease Progression , Female , Follow-Up Studies , Humans , Incidence , Male , Myopia/epidemiology , Retrospective Studies , Surveys and Questionnaires , Time Factors , Vision Tests
13.
Biomed Environ Sci ; 29(2): 127-36, 2016 02.
Article in English | MEDLINE | ID: mdl-27003170

ABSTRACT

OBJECTIVE: Cr(VI) removal from industrial effluents and sediments has attracted the attention of environmental researchers. In the present study, we aimed to isolate bacteria for Cr(VI) bioremediation from sediment samples and to optimize parameters of biodegradation. METHODS: Strains with the ability to tolerate Cr(VI) were obtained by serial dilution and spread plate methods and characterized by morphology, 16S rDNA identification, and phylogenetic analysis. Cr(VI) was determined using the 1,5-diphenylcarbazide method, and the optimum pH and temperature for degradation were studied using a multiple-factor mixed experimental design. Statistical analysis methods were used to analyze the results. RESULTS: Fifty-five strains were obtained, and one strain (Sporosarcina saromensis M52; patent application number: 201410819443.3) having the ability to tolerate 500 mg Cr(VI)/L was selected to optimize the degradation conditions. M52 was found be able to efficiently remove 50-200 mg Cr(VI)/L in 24 h, achieving the highest removal efficiency at pH 7.0-8.5 and 35 °C. Moreover, M52 could completely degrade 100 mg Cr(VI)/L at pH 8.0 and 35 °C in 24 h. The mechanism involved in the reduction of Cr(VI) was considered to be bioreduction rather than absorption. CONCLUSION: The strong degradation ability of S. saromensis M52 and its advantageous functional characteristics support the potential use of this organism for bioremediation of heavy metal pollution.


Subject(s)
Chromium/metabolism , Geologic Sediments/microbiology , RNA, Ribosomal, 16S/genetics , Sporosarcina/isolation & purification , Biodegradation, Environmental , China , Sporosarcina/genetics , Sporosarcina/metabolism
14.
Guang Pu Xue Yu Guang Pu Fen Xi ; 36(9): 2732-5, 2016 Sep.
Article in Zh | MEDLINE | ID: mdl-30084586

ABSTRACT

Terahertz frequency resolution is an important factor affecting substance identification, but the presence of the device reflection within the terahertz time domain spectroscopy systems, causes the presence of a plurality of reflection peaks in the reference and measurement signals with low frequency resolution, because of the length truncation of time domain signal. In order to remove the influence of the reflection peak, this paper proposes a method based on empirical mode decomposition to remove the time domain reflection peak, to improve the terahertz frequency resolution. The time domain reflection peaks are positioned by correlation with the real terahertz peak, calculating the reflection peak upper and lower envelope and an average, obtaining intrinsic mode functions, and alternating reflection peaks with intrinsic mode functions, the effective length of the time domain signal is increased to improve the terahertz frequency resolution. Water vapor in the air terahertz transmission spectroscopy results show that this method can self adaptively remove a plurality of reflection peaks and has good repairing effect on the terahertz time-domain signal; the frequency resolution is increased by 12 times; and the useful information of absorption spectrum is not lost; the absorption peak position and the number is consistent with real spectrum; the terahertz spectrum ability to identify is well preserved.

15.
Guang Pu Xue Yu Guang Pu Fen Xi ; 36(10): 3394-8, 2016 Oct.
Article in English | MEDLINE | ID: mdl-30246998

ABSTRACT

Complex ZnO compound material has great potential applications for optoelectronic devices. In this article, we give report to a simulation growth of a kind of special"fruiting ball"­­natural "Platanus Occidentalis" made of Al2O3, Au and ZnO. The surface of "Platanus Occidentalis " has numerous tiny Au seeds on the surface of Al2O3 ball. ZnO needles synthesized by the electrodeposition technique grow well on the Au seed layer. The obtained mono dispersive needles (or hexagonal columns) have different distribution density. The prepared sample looks like the assembled "Platanus Occidentalis" in photographs of scanning electron microscopy (SEM). Photoluminescence (PL) of samples at 6 K temperature and other characteristics are investigated. The appearance of sharp bound exciton (BE) emission line and the longitudinal optical (LO)-phonon replicas imply that the ZnO nanocolumns are of high optical quality.

16.
Biomarkers ; 20(6-7): 481-6, 2015.
Article in English | MEDLINE | ID: mdl-26616149

ABSTRACT

We investigated the effects of perioperative blood transfusion in the prognosis of hereditary and sporadic colon cancer. There are 1075 colon cancer patients, including 936 sporadic colon cancer and 139 with hereditary colon cancer undergoing surgery at our hospital. All patients underwent 10 years of follow-up. In the sporadic group, mortality, local recurrence rate and distant metastases rate of transfused patients were significantly higher than non-transfused patients. The 10-year survival rates were significantly lower in patients receiving blood transfusions compared to non-transfused patients. In the hereditary group, mortality was higher in transfused patients compared to non-transfused patients.


Subject(s)
Blood Transfusion/methods , Colonic Neoplasms/surgery , Colonic Neoplasms/therapy , Perioperative Period , Adult , Aged , Colonic Neoplasms/mortality , Combined Modality Therapy , Female , Follow-Up Studies , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Neoplasm Metastasis , Neoplasm Recurrence, Local , Outcome Assessment, Health Care/methods , Outcome Assessment, Health Care/statistics & numerical data , Prognosis , Proportional Hazards Models , Survival Rate , Time Factors
17.
J Nat Prod ; 78(6): 1221-30, 2015 Jun 26.
Article in English | MEDLINE | ID: mdl-25978520

ABSTRACT

Eight new viridins, nodulisporiviridins A-H (1-8), were isolated from the extract of an endolichenic fungal strain Nodulisporium sp. (No. 65-17-2-1) that was fermented with potato-dextrose broth. The structures were determined using spectroscopic and X-ray crystallographic analysis. Nodulisporiviridins A-D (1-4) are unique viridins with an opened ring A. The Aß42 aggregation inhibitory activities of 1-8 were evaluated using a thioflavin T (ThT) assay with epigallocatechin gallate (EGCG) as the positive control (EGCG IC50 of 0.5 µM). Nodulisporiviridin G (7) displayed potent inhibitory activity with an IC50 value of 1.2 µM, and the preliminary trend of activity of these viridins as Aß42 aggregation inhibitors was proposed. The short-term memory assay on an Aß transgenic drosophila model of Alzheimer's disease showed that all eight compounds improved the short-term memory capacity, with potencies close to that of the positive control (memantine).


Subject(s)
Androstenes/isolation & purification , Androstenes/pharmacology , Bacteriocins/isolation & purification , Bacteriocins/pharmacology , Xylariales/chemistry , Alzheimer Disease/drug therapy , Amyloid beta-Peptides/drug effects , Amyloid beta-Peptides/metabolism , Androstenes/chemistry , Animals , Bacteriocins/chemistry , Catechin/analogs & derivatives , China , Crystallography, X-Ray , Disease Models, Animal , Humans , Molecular Conformation , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Peptide Fragments
18.
Med Sci Monit ; 21: 3474-82, 2015 Nov 12.
Article in English | MEDLINE | ID: mdl-26558525

ABSTRACT

BACKGROUND: The aim of this study was to investigate associations of 3 common polymorphisms in the VEGF gene, -2578C>A, -634C>G, and 936C>T, with risk of tetralogy of Fallot (TOF) in Chinese Han children. MATERIAL AND METHODS: From January 2010 to June 2013, a total of 400 pediatric subjects were recruited, including 160 cases with TOF (TOF group) and 240 healthy controls (control group). The genotypes of 3 common VEGF polymorphisms, -2578C>A, -634C>G, and 936C>T, were analyzed by polymerase chain reaction restriction fragment length polymorphism. All data were analyzed with SPSS 18.0 software. RESULTS: No significant differences were observed in body mass index or sex between TOF patients and controls (both P>0.05), but significant differences in age and family history of TOF were observed between the 2 groups (both P<0.05). The AA genotype in -2578C>A of VEGF was correlated with a significantly increased risk of TOF, and TOF risk in A allele carrier was 1.54-fold higher than that of C allele carrier (OR=1.54, 95%CI=1.14-2.09, P=0.005); the statistical significance was still present after Bonferroni correction (Pc=0.045). GG genotype in -634C>G of VEGF gene was also associated with an increased risk of TOF, and TOF risk in patients with G allele was 1.62-fold higher compared to patients with C allele (OR=1.62, 95%CI=1.19-2.21, P=0.002); the statistical significance was still present after Bonferroni correction (Pc=0.018). Interestingly, T allele in VEGF 936C>T polymorphism is associated with a decreased TOF risk (OR=0.65, 95%CI=0.49-0.87, P=0.003, the statistical significance was still present after Bonferroni correction (Pc=0.027). The result of logistic regression analysis revealed that -2578C>A, -634C>G, and 936C>T genotypes are independently related to the prevalence of TOF (all P<0.05). CONCLUSIONS: Our results confirmed that VEGF genetic polymorphisms, -2578C>A and -634C>G, may be associated with an increased TOF risk, while 936C>T polymorphism may be associated with decreased TOF risk.


Subject(s)
Polymorphism, Single Nucleotide , Tetralogy of Fallot/blood , Tetralogy of Fallot/genetics , Vascular Endothelial Growth Factor A/genetics , Alleles , Biomarkers/blood , Child , Child, Preschool , China , Echocardiography, Doppler , Female , Gene Frequency , Genotype , Heterozygote , Humans , Infant , Linkage Disequilibrium , Male , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Risk Factors , Software , Tetralogy of Fallot/diagnostic imaging , Tetralogy of Fallot/surgery , Vascular Endothelial Growth Factor A/blood
19.
J Asian Nat Prod Res ; 17(6): 671-5, 2015.
Article in English | MEDLINE | ID: mdl-26096303

ABSTRACT

Pericoterpenoid A (1), a new cadinane-type sesquiterpene, was isolated from an endolichenic fungal strain Periconia sp. (No. 19-4-2-1). Its structure was characterized by analyzing the spectroscopic data (IR, MS, 1D- and 2D-NMR). The antimicrobial activity against Escherichia coli, Staphylococcus aureus, Aspergillus niger, and Candida albicans was evaluated. Pericoterpenoid A showed moderate antimicrobial activity against A. niger and weak activity against C. albicans. This is the first report of the presence of cadinane-type sesquiterpene in Periconia sp.


Subject(s)
Ascomycota/chemistry , Sesquiterpenes/isolation & purification , Sesquiterpenes/pharmacology , Aspergillus niger/drug effects , Candida albicans/drug effects , Escherichia coli/drug effects , Microbial Sensitivity Tests , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Polycyclic Sesquiterpenes , Sesquiterpenes/chemistry , Staphylococcus aureus/drug effects
20.
J Asian Nat Prod Res ; 17(5): 550-8, 2015 May.
Article in English | MEDLINE | ID: mdl-26022116

ABSTRACT

Three new cyclohexenones (1-3, named sarcosones A-C) and two new isocoumarins (4 and 5), together with five known isocoumarins (6-10), were isolated from the solid cultures of an endophytic fungus Sarcosomataceae sp. NO.49-14-2-1. Their chemical structures were elucidated by analyses of HR-ESI-TOF-MS, (1)H, (13)C NMR, (1)H-(1)H COSY, HSQC, and HMBC spectra. Their absolute configurations were determined via modified Mosher's method and circular dichroism spectra method.


Subject(s)
Ascomycota/chemistry , Cyclohexanes/isolation & purification , Isocoumarins/isolation & purification , Cyclohexanes/chemistry , Isocoumarins/chemistry , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular
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