Recent studies regarding neuronal differentiation of mesenchymal stem cells （MSCs） have primarily focused on induction methods and transplantation in vivo. However, knowledge about the intrinsic regulatory mechanism...Recent studies regarding neuronal differentiation of mesenchymal stem cells （MSCs） have primarily focused on induction methods and transplantation in vivo. However, knowledge about the intrinsic regulatory mechanisms underlying neuronal induction of MSCs remains limited and unclear. OBJECTIVE： To elucidate the role of JAK-STAT3 signaling pathway during neuronal differentiation of MSCs using a combination of the JAK-STAT3 signaling inhibitor AG490 and growth factors. DESIGN, TIME AND SETTING： Neural, molecular, biomedical, in vitro experiment was performed at the Laboratory of Pharmacology, School of Pharmacy, Nanjing Medical University between March and December 2008 MATERIALS： An inhibitor of the JAK-STAT3 signaling pathway was purchased from Calbiochem, USA. Antibody kit for total and phosphorylated STAT3 was purchased from Cell Signaling, USA. METHODS： MSCs from passage 3 were assigned to non-induced, growth factor, and AG490 groups. MAIN OUTCOME MEASURE： The number of cells expressing neuron-specific enolase, microtubule-associated protein, and glial fibrillary acidic protein were determined by immunocytochemistry. Total and phosphorylated （Tyr705） expression levels of STAT3 protein were measured by Western blot analysis. RESULTS： MSCs were transdifferentiated into neuronal- and astrocyte-like phenotypes through the induction of epidermal growth factor, basic fibroblast growth factor, and brain-derived neurotrophic factor. In addition, the JAK-STAT3 signaling pathway was significantly activated during neural differentiation. Expression of phosphorylated （Tyr705） STAT3 was inhibited with AG490 （5 pmol/L） prior to neural induction with epidermal growth factor, basic fibroblast growth factor, and brain-derived neurotrophic factor; proportion of astrocyte-like cells was significantly reduced （P 〈 0.01）, and the proportion of neuronal-like phenotypes was significantly increased （P〈 0.01）. CONCLUSION： JAK-STAT3 signaling pathway was shown to regulate neuronal induction of bone marrow MSCs. The proportion of MSC-induced neuronal-like cells was increased following treatment with the JAK-STAT3 signaling inhibitor AG490.展开更多
[Objectives] To optimize the preparation process of 5-methyl-2-(2,4,4,7-tetramethylchromanyl) phenol(impurity C) and the liquid phase determination method of the impurity, and to provide an important basis for the est...[Objectives] To optimize the preparation process of 5-methyl-2-(2,4,4,7-tetramethylchromanyl) phenol(impurity C) and the liquid phase determination method of the impurity, and to provide an important basis for the establishment of material methods and quality control of thymol. [Methods] The 4,7-dimethylcoumarin as the starting material was hydrolyzed by potassium hydroxide to obtain the substance II 5-methyl-2-(1-propylene-2-yl) phenol, and then purified and treated with hydrochloric acid to obtain a pale yellow solid. High-purity main peak was obtained by high-performance liquid phase method, and it was identified as impurity C by ~1H-NMR measurement and spectrum analysis. [Results] After the method was optimized, the synthesis route to the impurity C was simple, and the purity of impurity C was high. The obtained impurity C was confirmed by ~1H-NMR to be a compound 5-methyl-2-(2,4,4,7-tetramethylchromanyl) phenol. The liquid phase detection method was successfully established to identify the compound. [Conclusions] The optimized method is easy to control and the impurity C has high purity and it is expected to provide quality assurance for the study of related substances in the quality control of thymol.展开更多
Silver nanowires （NWs） coated with platinum （Pt） nanoparticles were synthesized via a galvanic partial replacement of Ag NWs in an aqueous K2PtC16 solution at room temperature. The products were char- acterized us...Silver nanowires （NWs） coated with platinum （Pt） nanoparticles were synthesized via a galvanic partial replacement of Ag NWs in an aqueous K2PtC16 solution at room temperature. The products were char- acterized using a combination of electron microscopies, selected area electron diffraction, energy- dispersive X-ray mapping and X-ray diffraction. The surface morphology and Pt/Ag composition ratios are controlled by adjusting the K2PtC16 concentration. Different concentrations result in various surface morphologies including rough nanoparticle coating, porous and relatively smooth surfaces. The forma- tion mechanism was discussed based on the lattice constants＇ difference, concentration driven nucleation, consumption of Ag NWs, and stoichiometry of the replacement reaction. The effects of the bimetallic interface on the catalytic activity toward the reduction of 4-nitrophenol by sodium borohydride were studied. The activity of Ag-Pt NWs is highly enhanced over monometallic nanostructures, and opti- mized by a low Pt loading of 1.34 at.%, which indicates a catalytic role of the inter-metallic interface for the elecrrnn transfer.展开更多
基金the National Nature Science Foundation of China, No. 30973092"Xingwei" Project Medical Emphasis Grant from Jiangsu Province, No. RC2007062
文摘Recent studies regarding neuronal differentiation of mesenchymal stem cells （MSCs） have primarily focused on induction methods and transplantation in vivo. However, knowledge about the intrinsic regulatory mechanisms underlying neuronal induction of MSCs remains limited and unclear. OBJECTIVE： To elucidate the role of JAK-STAT3 signaling pathway during neuronal differentiation of MSCs using a combination of the JAK-STAT3 signaling inhibitor AG490 and growth factors. DESIGN, TIME AND SETTING： Neural, molecular, biomedical, in vitro experiment was performed at the Laboratory of Pharmacology, School of Pharmacy, Nanjing Medical University between March and December 2008 MATERIALS： An inhibitor of the JAK-STAT3 signaling pathway was purchased from Calbiochem, USA. Antibody kit for total and phosphorylated STAT3 was purchased from Cell Signaling, USA. METHODS： MSCs from passage 3 were assigned to non-induced, growth factor, and AG490 groups. MAIN OUTCOME MEASURE： The number of cells expressing neuron-specific enolase, microtubule-associated protein, and glial fibrillary acidic protein were determined by immunocytochemistry. Total and phosphorylated （Tyr705） expression levels of STAT3 protein were measured by Western blot analysis. RESULTS： MSCs were transdifferentiated into neuronal- and astrocyte-like phenotypes through the induction of epidermal growth factor, basic fibroblast growth factor, and brain-derived neurotrophic factor. In addition, the JAK-STAT3 signaling pathway was significantly activated during neural differentiation. Expression of phosphorylated （Tyr705） STAT3 was inhibited with AG490 （5 pmol/L） prior to neural induction with epidermal growth factor, basic fibroblast growth factor, and brain-derived neurotrophic factor; proportion of astrocyte-like cells was significantly reduced （P 〈 0.01）, and the proportion of neuronal-like phenotypes was significantly increased （P〈 0.01）. CONCLUSION： JAK-STAT3 signaling pathway was shown to regulate neuronal induction of bone marrow MSCs. The proportion of MSC-induced neuronal-like cells was increased following treatment with the JAK-STAT3 signaling inhibitor AG490.
文摘[Objectives] To optimize the preparation process of 5-methyl-2-(2,4,4,7-tetramethylchromanyl) phenol(impurity C) and the liquid phase determination method of the impurity, and to provide an important basis for the establishment of material methods and quality control of thymol. [Methods] The 4,7-dimethylcoumarin as the starting material was hydrolyzed by potassium hydroxide to obtain the substance II 5-methyl-2-(1-propylene-2-yl) phenol, and then purified and treated with hydrochloric acid to obtain a pale yellow solid. High-purity main peak was obtained by high-performance liquid phase method, and it was identified as impurity C by ~1H-NMR measurement and spectrum analysis. [Results] After the method was optimized, the synthesis route to the impurity C was simple, and the purity of impurity C was high. The obtained impurity C was confirmed by ~1H-NMR to be a compound 5-methyl-2-(2,4,4,7-tetramethylchromanyl) phenol. The liquid phase detection method was successfully established to identify the compound. [Conclusions] The optimized method is easy to control and the impurity C has high purity and it is expected to provide quality assurance for the study of related substances in the quality control of thymol.
基金supported by the National Natural Science Foundation of China(Grant Nos.51975392 and 51775360)the National Key Research and Development Program(Grant No.2021YFB3400300)+1 种基金the Natural Science Foundation of the Jiangsu Higher Education Institutions of China(Grant No.19KJA220001)the Natural Science Foundation of Jiangsu Province(Grant Nos.BK20201412 and BK20221361).
基金financial support of the project from the PAPD(No.50831004)the Fundamental Research Funds for the Central Universities(Nos.021314380019 and 1106021343)+3 种基金the Innovation Fund of Jiangsu Province(No.BY2013072-06)the Natural Science Foundation of Jiangsu Province (No.2012729)the National Natural Science Foundation of China (No.11374136)the State Key Program for Basic Research of China (No.2010CB631004)
文摘Silver nanowires （NWs） coated with platinum （Pt） nanoparticles were synthesized via a galvanic partial replacement of Ag NWs in an aqueous K2PtC16 solution at room temperature. The products were char- acterized using a combination of electron microscopies, selected area electron diffraction, energy- dispersive X-ray mapping and X-ray diffraction. The surface morphology and Pt/Ag composition ratios are controlled by adjusting the K2PtC16 concentration. Different concentrations result in various surface morphologies including rough nanoparticle coating, porous and relatively smooth surfaces. The forma- tion mechanism was discussed based on the lattice constants＇ difference, concentration driven nucleation, consumption of Ag NWs, and stoichiometry of the replacement reaction. The effects of the bimetallic interface on the catalytic activity toward the reduction of 4-nitrophenol by sodium borohydride were studied. The activity of Ag-Pt NWs is highly enhanced over monometallic nanostructures, and opti- mized by a low Pt loading of 1.34 at.%, which indicates a catalytic role of the inter-metallic interface for the elecrrnn transfer.
