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1.
Front Genet ; 12: 792991, 2021.
Article in English | MEDLINE | ID: mdl-35154246

ABSTRACT

An increasing attention is being given to treat fruits with ultraviolet C (UV-C) irradiation to extend shelf-life, senescence, and protection from different diseases during storage. However, the detailed understanding of the pathways and key changes in gene expression and metabolite accumulation related to UV-C treatments are yet to be explored. This study is a first attempt to understand such changes in banana peel irradiated with UV-C. We treated Musa nana Laur. with 0.02 KJ/m2 UV-C irradiation for 0, 4, 8, 12, 15, and 18 days and studied the physiological and quality indicators. We found that UV-C treatment reduces weight loss and decay rate, while increased the accumulation of total phenols and flavonoids. Similarly, our results demonstrated that UV-C treatment increases the activity of defense and antioxidant system related enzymes. We observed that UV-C treatment for 8 days is beneficial for M. nana peels. The peels of M. nana treated with UV-C for 8 days were then subjected to combined transcriptome and metabolome analysis. In total, there were 425 and 38 differentially expressed genes and accumulated metabolites, respectively. We found that UV-C treatment increased the expression of genes in secondary metabolite biosynthesis related pathways. Concomitant changes in the metabolite accumulation were observed. Key pathways that were responsive to UV-C irradiation include flavonoid biosynthesis, phenylpropanoid bios6ynthesis, plant-pathogen interaction, MAPK signaling (plant), and plant hormone signal transduction pathway. We concluded that UV-C treatment imparts beneficial effects on banana peels by triggering defense responses against disease, inducing expression of flavonoid and alkaloid biosynthesis genes, and activating phytohormone and MAPK signaling pathways.

2.
Brain Dev ; 38(10): 915-927, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27591118

ABSTRACT

OBJECTIVE: To describe clinical features of reversible splenial lesion syndrome (RESLES) in children. METHODS: Retrospectively analyzed clinical features of RESLES in children and compared differences between severe and non-severe group, classified by clinical global impression-scale; summarized clinical features of children with mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) from case series. RESULTS: 16 episodes of RESLES occurring in 15 Chinese children were analyzed, with 13 episodes having MERS and 3 episodes with epilepsy. 10 episodes were associated with various pathogens including rotavirus (n=5), adenovirus (n=1), influenza A (n=1), mycoplasma (n=2), and jejunum campylobacter (n=1). The common neurological symptoms included seizure, behavioral changes, altered consciousness and motor deterioration. The lesions of splenium of corpus callosum (SCC), extra-SCC (n=2) or extra-CC (n=1) showed T2-weight and FLAIR hyper-intensity, with the corresponding reduced diffusion. All had complete resolution of radiological changes except 1 episode with small residual. 8 episodes had EEG abnormalities, while elevated white blood count, increased hs-CRP, and hyponatremia were commonly revealed. 7 episodes were given steroid plus therapy, while 3 episodes were treated with antiepileptic drugs. Compared with non-severe group, the number of patients with altered consciousness, EEG abnormalities, motor deterioration, or extra-SCC lesions in severe group was significantly increased. The patients in severe group tended to need longer hospital stay interval. No case caused neurological sequelae, except 1 patient in severe group with recurrent episode and extra-CC lesions having intellectual disability (ID). Five pediatric MERS case series were summarized, including 67 episodes (40 male and 27 female; age ranging 10 m∼13y) from 65 patients, with 33 episodes in Japan, 27 in China, and 7 in Caucasian Australian children, and all patients have a good prognosis except 1 patient with ID (current study). CONCLUSION: Although RESLES in children tend to be a good outcome, the prognosis of patient in severe group, especially with extra-CC lesions, might have neurological sequelae.


Subject(s)
Brain Diseases/diagnosis , Adolescent , Brain/diagnostic imaging , Brain/physiopathology , Brain Diseases/diagnostic imaging , Brain Diseases/epidemiology , Brain Diseases/physiopathology , Child , Child, Preschool , Electroencephalography , Female , Humans , Infant , Magnetic Resonance Imaging , Male , Retrospective Studies , Severity of Illness Index , Syndrome
3.
J Biomed Mater Res B Appl Biomater ; 100(8): 2167-77, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22915482

ABSTRACT

Surface modification of dental implants with biomolecules is of particularly interest recently. To mimic the structure and function of native extracellular matrix (ECM), a derivative of hyaluronic acid (HA), HA-GRGDSP, was synthesized, Arg-Gly-Asp (RGD)-containing collagen (Col)/HA multilayer polyelectrolyte films (MPFs) coating was fabricated on titanium (Ti) through alternate deposition of Col and HA-GRGDSP with 4.5 assembly cycles; moreover, bioactive molecule, basic fibroblast growth factor (bFGF), was also incorporated into such coating. This coating was then carefully characterized using scanning electronic microscope (SEM) and scanning force microscopy (SFM); bFGF release from the coating was also evaluated. (Col + bFGF)/HA-RGD coating was successfully deposited on Ti surface, and about 300 pg of bFGF could be slowly released from this coating for a week. This coating significantly promoted the initial cell attachment of human gingival fibroblasts (HGFs) compared with other groups (p < 0.05), and HGFs adhered and spread better on this coating than other groups (p < 0.05). Regarding cell proliferation and differentiation of HGFs, they were greatly stimulated when cultured on this coating (p < 0.05). These results indicated that surface modification of Ti using biomolecules might improve the sealing between the neck section of a dental implant and the soft tissue.


Subject(s)
Cell Differentiation , Cell Proliferation , Coated Materials, Biocompatible/chemistry , Collagen/chemistry , Fibroblasts/metabolism , Gingiva/metabolism , Hyaluronic Acid/chemistry , Oligopeptides/chemistry , Titanium/chemistry , Adult , Cell Adhesion , Cells, Cultured , Fibroblasts/cytology , Gingiva/cytology , Humans , Male , Materials Testing
4.
Zhonghua Er Ke Za Zhi ; 50(4): 255-60, 2012 Apr.
Article in Chinese | MEDLINE | ID: mdl-22801224

ABSTRACT

OBJECTIVE: To explore the development and prognosis of the acute flaccid paralysis (AFP) associated with enterovirus 71 (EV71) infection through clinical follow-up study for clinical and magnetic resonance imaging (MRI) features based on the research progress of virology and pathology. METHOD: Sixteen children with HFMD associated with AFP in hospital from May 1, 2011 to August 31, 2011 were investigated and the patients received intensive rehabilitation training. The 16 cases were divided into two groups (the recovery or the sequela) by if the muscle strength recovered to level 4 after intensive rehabilitation. The MRI findings of 15 children were analyzed and among them, 6 patients were reexamined after one month. The clinical markers were compared between groups including course of disease, WBC, WBC in cerebrospinal fluid (CSF), ventilator support, therapy, the worst muscle strength, the initial tendon reflex, the muscle atrophy, and multi-limb paralysis. The data were analyzed by t test and χ2 test with SPSS10.0. RESULT: All the 16 children were infected with enterovirus 71 (EV71). The myodynamia of 7 children were level 0, 4 children had serious upper limbs paralysis. The neck muscle in 3 cases and the brain stem motor ruckus in 4 cases were involved. The ankle clonus of non-completely paralyzed limbs in 14 cases occurred during rehabilitation. Eight children had the better prognosis, the other 8 children had sequela. 0 level muscle strength (0 case vs. 7 cases, χ2=12.4), the initial tendon reflex (2 cases vs. 8 cases, χ2=9.6), obvious muscle atrophy (0 case vs. 8 cases, χ2=16), were significantly different in the children with the recovery when compared to the sequela (P<0.01). The severe upper limbs paralysis had the worse prognosis than the severe lower limbs paralysis. MR imaging showed signs of spinal nerve root inflammation and the bilateral hyperintense lesions, symmetrical in the posterior portions of the medulla, pons, and asymmetrical in the ventral horns of cervical spinal cord. Signal enhancement occurred only in the early MRI examination. CONCLUSION: In the evolution of AFP due to EV71 infection, the upper motor neuron damage is common, the prognosis is related with the severity of early paralysis and neuron damage. MR imaging is helpful to understand the pathological mechanism of AFP.


Subject(s)
Enterovirus A, Human/pathogenicity , Hand, Foot and Mouth Disease/pathology , Paralysis/diagnosis , Paralysis/virology , Child, Preschool , Female , Follow-Up Studies , Hand, Foot and Mouth Disease/diagnosis , Hand, Foot and Mouth Disease/virology , Humans , Infant , Magnetic Resonance Imaging , Male , Paralysis/pathology , Prognosis
5.
Med Sci Monit ; 18(7): BR265-72, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22739726

ABSTRACT

BACKGROUND: Surface chemistry of dental implant plays an important role in osseointegration. Heat treatment might alter surface chemistry and result in different biological response. The aim of this study was to investigate the roles of heat treatment of H2O2/HCl-treated Ti implants in cell attachment, proliferation and osteoblastic differentiation. MATERIAL/METHODS: Sandblasted, dual acid-etched and H2O2/HCl heat-treated discs were set as the control group and sandblasted, dual acid-etched H2O2/HCl-treated discs were the test group. Both groups' discs were sent for surface characterization. MC3T3-E1 cells were seeded on these 2 groups' discs for 3 hours to 14 days, and then cell attachment, cell proliferation and cell differentiation were evaluated. RESULTS: Scanning electron microscope analysis revealed that the titanium discs in the 2 groups shared the same surface topography, while x-ray diffraction examination showed an anatase layer in the control group and titanium hydride diffractions in the test group. The cell attachment of the test group was equivalent to that of the control group. Cell proliferation was slightly stimulated at all time points in the control group, but the alkaline phosphatase (ALP) activity and osteocalcin (OC) production increased significantly in the test group compared with those in the control group at every time point investigated (p<0.05 or p<0.01). Moreover, the osteoblastic differentiation-related genes AKP-2, osteopontin (OPN) and OC were greatly up-regulated in the test group (p<0.05 or p<0.01). CONCLUSIONS: The results implied that surface chemistry played an important role in cell response, and H2O2/HCl etched titanium surface without subsequent heat treatment might improve osseointegration response.


Subject(s)
Acid Etching, Dental , Dental Implants , Hot Temperature , Hydrochloric Acid/pharmacology , Hydrogen Peroxide/pharmacology , Titanium/chemistry , Titanium/pharmacology , Alkaline Phosphatase/metabolism , Animals , Cell Adhesion/drug effects , Cell Differentiation/drug effects , Cell Differentiation/genetics , Cell Line , Cell Proliferation/drug effects , Gene Expression Regulation/drug effects , Intracellular Space/drug effects , Intracellular Space/enzymology , Mice , Microscopy, Electron, Scanning , Osteoblasts/cytology , Osteoblasts/drug effects , Osteoblasts/enzymology , Osteoblasts/ultrastructure , Osteocalcin/genetics , Osteocalcin/metabolism , Osteogenesis/drug effects , Osteogenesis/genetics , Surface Properties/drug effects , X-Ray Diffraction
6.
Arch Oral Biol ; 57(5): 460-8, 2012 May.
Article in English | MEDLINE | ID: mdl-22054726

ABSTRACT

OBJECTIVE: There is no certain conclusion on the effect of recombinant human Osteogenic Protein-1 (OP-1, BMP-7) on the proliferation of the osteoblast-like cell line, MC3T3-E1. Furthermore, the optimal dose of rhOP-1 on cell differentiation still needs to be elucidated. This investigation aims to delineate the biofunctional characteristics of rhOP-1 in inducing osteoblastogenesis of MC3T3-E1 through in vitro time-course and dose-response studies. DESIGN: MC3T3-E1 cells were cultured for 1, 4, 7 days with the addition of different rhOP-1 concentrations (0, 10, 20, 50, 100, 200, 400 ng/ml), and cell proliferation and cell differentiation were examined. RESULTS: MC3T3-E1 cell proliferation was stimulated by rhOP-1 in a dose-dependent manner (0-400 ng/ml) on day 1, whereas on day 4 and 7, it was still stimulated at low concentrations (10, 20, 50 ng/ml) but inhibited at high ones (200, 400 ng/ml). The alkaline phosphatase (ALP) activity, osteocalcin (OC) production, collagen deposition and extracellular matrix mineralization were dramatically elevated by rhOP-1 treatment, as a function of culture time and rhOP-1 concentration, and all of them reached a plateau at the concentration of 200 ng/ml. Real-time quantitative RT-PCR results showed Runx2, AKP-2, OC and Nog mRNA expressions increased in a dose- and time-dependent manner, and their expressions were significantly higher at high rhOP-1 concentrations than that of low ones. No significant differences were found between the effects of 200 ng/ml rhOP-1 and 400 ng/ml rhOP-1 on the differentiation of MC3T3-E1 cells, except the expression of Nog mRNA, whose expression level was much higher at 400 ng/ml than that at 200 ng/ml. CONCLUSIONS: These results suggest that cell proliferation of MC3T3-E1 is depended on culture time and rhOP-1 concentration, rhOP-1 could stimulate the differentiation of MC3T3-E1 cells and the optimal concentration could be 200 ng/ml.


Subject(s)
Bone Morphogenetic Proteins/administration & dosage , Bone Morphogenetic Proteins/pharmacology , Cell Differentiation/drug effects , Cell Proliferation/drug effects , Osteoblasts/cytology , Osteoblasts/drug effects , Alkaline Phosphatase/metabolism , Analysis of Variance , Animals , Carrier Proteins/metabolism , Cell Line , Cells, Cultured , Collagen/metabolism , Core Binding Factor Alpha 1 Subunit/metabolism , DNA Primers , Dose-Response Relationship, Drug , Extracellular Matrix/metabolism , In Vitro Techniques , Mice , Osteocalcin/metabolism , Real-Time Polymerase Chain Reaction , Staining and Labeling , Time Factors
7.
Article in English | MEDLINE | ID: mdl-19716504

ABSTRACT

The purpose of the present study was to evaluate the bioactivity of chemical treatment of titanium alloy (Ti-6Al-4V) in vitro. Smooth-surface discs of Ti-6Al-4V were used in this study. Sandblasted, dual acid-etched and H(2)O(2)/HCl heat-treated discs were set as test group, and sandblasted, dual acid-etched discs as control group. SEM and XRD analysis revealed a porous anatase gel layer on rough surface in the test group and a rough surface in the control group. Mouse pre-osteoblasts (MC3T3-E1 cells) were cultured on these 2 group discs, and then cell proliferation and differentiation were examined 4 days, 7 days, and 14 days after cell seeding. Cell proliferation was greatly stimulated at all time points when cultured in test group (P < .05). The alkaline phosphatase (ALP) activity and osteocalcin (OC) production were much higher in the test group compared with the control group at every time point investigated (P < .05). Furthermore, in the test group, the expressions of alkaline phosphatase-2, osteocalcin, and collagen type I alpha 1 mRNAs were significantly up-regulated as compared with those in the control group (P < .05 or P < .01). The results suggested that H(2)O(2)/HCl and heat-treatment might facilitate better integration of Ti-6Al-4V implants with bone.


Subject(s)
Acid Etching, Dental/methods , Biocompatible Materials/chemistry , Dental Alloys/chemistry , Hydrochloric Acid/chemistry , Hydrogen Peroxide/chemistry , Osteoblasts/cytology , Oxidants/chemistry , Titanium/chemistry , 3T3 Cells , Actins/analysis , Alkaline Phosphatase/analysis , Alloys , Animals , Biomarkers/analysis , Carbon Compounds, Inorganic/chemistry , Cell Differentiation , Cell Proliferation , Dental Etching/methods , Mice , Microscopy, Electron, Scanning , Osteocalcin/analysis , Porosity , Silicon Compounds/chemistry , Surface Properties , Time Factors , Up-Regulation , X-Ray Diffraction
8.
Acta Crystallogr Sect E Struct Rep Online ; 64(Pt 5): m649-50, 2008 04 10.
Article in English | MEDLINE | ID: mdl-21202197

ABSTRACT

The title complex, [Er(C(5)H(5)NO)(C(2)O(4))(H(2)O)](n), is a new erbium polymer based on oxalate and 4-oxidopyridinium ligands. The Er(II) center is coordinated by six O atoms from three oxalate ligands, one O atom from a 4-oxidopyridinium ligand and one water mol-ecule, and displays a distorted square-anti-prismatic coordination geometry. The oxalate ligands are both chelating and bridging, and link Er(II) ions, forming Er-oxalate layers in which the attached water and 4-oxidopyridinium units point alternately up and down. A mirror plane passes through the Er atom, one C, the oxide O and two oxalate O atoms. The layers are assembled into a three-dimensional supra-molecular network via inter-molecular hydrogen bonding and π-π stacking inter-actions [centroid-centroid distances of 3.587 (2) Šbetween parallel pyridinium rings]. Both the water mol-ecule and the 4-oxidopyridinium ligand are disordered over two sites in a 1:1 ratio.

9.
Acta Crystallogr Sect E Struct Rep Online ; 64(Pt 12): e34, 2008 Nov 13.
Article in English | MEDLINE | ID: mdl-21581104

ABSTRACT

The chemical name in the title, the formula and the scheme of the paper by Gu, Hao, Song, Lin & Ma [Acta Cryst. (2008), E64, m649-m650] are corrected.[This corrects the article DOI: 10.1107/S1600536808009380.].

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