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1.
CNS Neurosci Ther ; 25(9): 951-964, 2019 09.
Artigo em Inglês | MEDLINE | ID: mdl-31486601

RESUMO

AIMS: The objective of this study was to analyze the efficacy of polypyrrole/polylactic acid (PPy/PLA) nanofibrous scaffold cotransplanted with bone marrow stromal cells (BMSCs) in promoting the functional recovery in a rat spinal cord injury (SCI). METHODS: Female Sprague-Dawley rats were randomly divided into three groups (n = 18/group): control group, PPy/PLA group, and PPy/PLA/BMSCs group. The SCI was induced in all rats. Consequently, rats in PPy/PLA/BMSCs group were transplanted with 1 × 105 BMSCs after implantation of PPy/PLA, while those in the PPy/PLA group were implanted with PPy/PLA only; no implantation was performed in the control group. Six weeks after surgery, immunofluorescence microscopy, electron microscope, and polymerase chain reaction (PCR) techniques were performed to assess the changes in the injured spinal cord tissues. RESULTS: Electrophysiology and locomotor function testing suggested that PPy/PLA nanofibrous scaffold cotransplanted with BMSCs could promote the functional recovery of the spinal cord. Six weeks after the operation, lower amount of scar tissue was found in the PPy/PLA group compared with the control group. Abundant neurofilament (NF) and neuron-specific marker (NeuN) positive staining, and myelin formations were detected in the injured area. In addition, the transplantation of BMSCs not only improved the efficacy of PPy/PLA but also managed to survive well and was differentiated into neural and neuroglial cells. CONCLUSIONS: The implantation of PPy/PLA nanofibrous scaffold and BMSCs has a great potential to restore the electrical conduction and to promote functional recovery by inhibiting the scar tissue formation, promoting axon regeneration, and bridging the gap lesion.


Assuntos
Transplante de Células-Tronco Mesenquimais/métodos , Células-Tronco Mesenquimais/fisiologia , Nanofibras/administração & dosagem , Recuperação de Função Fisiológica/fisiologia , Traumatismos da Medula Espinal/terapia , Alicerces Teciduais , Animais , Células Cultivadas , Feminino , Poliésteres/administração & dosagem , Polímeros/administração & dosagem , Pirróis/administração & dosagem , Distribuição Aleatória , Ratos , Ratos Sprague-Dawley , Recuperação de Função Fisiológica/efeitos dos fármacos , Traumatismos da Medula Espinal/fisiopatologia
2.
Aging (Albany NY) ; 11(2): 523-535, 2019 01 17.
Artigo em Inglês | MEDLINE | ID: mdl-30654331

RESUMO

Vascular calcification/aging is common in diabetes and is associated with increased morbidity and mortality of patients. MiR-34c-5p, not miR-34c-3p, was suppressed significantly in calcification/senescence of human aorta vascular smooth muscle cells (HA-VSMCs) induced by high glucose, which was proven by the formation of mineralized nodules and staining of senescence associated-ß-galactosidase staining (SA ß-gal) positive cells. Overexpression of miR-34c-5p alleviated calcification/senescence of HA-VSMCs, whereas inhibition of miR-34c-5p received the opposite results. Bcl-2 modifying factor (BMF) was a functional target of miR-34c-5p and it was involved in the process of calcification/senescence of HA-VSMCs. Besides, lncRNA-ES3 acted as a competing endogenous RNAs (ceRNA) of miR-34c-5p to enhance BMF expression. Further, lncRNA-ES3 inhibited miR-34c-5p expression by direct interaction and its knockdown suppressed the calcification/senescence of HA-VSMCs. Our results showed for the first time that the calcification/senescence of VSMCs was regulated by lncRNA-ES3 /miR-34c-5p/BMF axis.


Assuntos
Proteínas Adaptadoras de Transdução de Sinal/metabolismo , Senescência Celular/efeitos dos fármacos , Glucose/toxicidade , MicroRNAs/metabolismo , Músculo Liso Vascular/citologia , Miócitos de Músculo Liso/metabolismo , Proteínas Adaptadoras de Transdução de Sinal/genética , Calcinose/induzido quimicamente , Regulação da Expressão Gênica/efeitos dos fármacos , Humanos , MicroRNAs/genética , Músculo Liso Vascular/patologia , Miócitos de Músculo Liso/patologia , RNA Longo não Codificante/genética
3.
Guang Pu Xue Yu Guang Pu Fen Xi ; 36(4): 1116-20, 2016 Apr.
Artigo em Chinês | MEDLINE | ID: mdl-30052010

RESUMO

The spectral analysis method was applied experimentally to extract the spectral indices, measure and analyze the spectral characteristics and their difference of the mixture which are composed in soil in Central Shaanxi Plain and the diesel and motor oil respectively, aiming to provide solutions to practical difficulties in detecting, analyzing the spectral characteristics and difference between the soil leaking with equal content diesel and motor oil and predicting the leaking content of diesel in the soil. The spectral response curves of the soil leaking with different oil respectively and the soil leaking with diesel with different content were collected. Then the spectral prediction model for the leaking content of diesel in the soil was built based on the reflectance characteristics. The coefficient of the detection (R2) was introduced to evaluate the stability of the built model,and the parameter root mean squared error (RMSE) was introduced to estimate the precision and the predictability of the model built in this work. It is demonstrated that : (1) The reflectance of soil leaking with diesel is less than that of the equal content motor oil. And there is a double absorption trough of the reflectance curve of both soil leaking with diesel and motor oil at 1 740 and 2 328 nm. The spectral absorption indices and absorption depth of the soil leaking with diesel keep less than the equal content motor oil. (2) The built spectral prediction model for the leaking content of diesel in the soil demonstrates good stability with the coefficient of determination at R2=0.854, and performs favorable predictability (Root-Mean-Square Error, RMSE=0.016), which can benefit the effective prediction and quick estimation methods of the leaking content of diesel in the soil, enrich and progress the experimental method and theoretical research work of spectral prediction on soil leaking oil content and promote the application of remote sensing in safety production and environmental protection.

5.
Int J Biol Sci ; 7(6): 762-8, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21698002

RESUMO

The use of bone marrow mesenchymal stem cell- (MSC) transplantation therapy for cardiac diseases is limited due to poor survival of implanted cells. MicroRNAs (miRNAs) have been reported to be involved in regulating almost all cellular processes, including apoptosis. In this study, we found that the miRNA profile was altered during apoptosis induced by hypoxia and serum deprivation (hypoxia/SD). We further revealed that over-expression of miR-21, miR-23a and miR-210 could promote the survival of MSCs exposed to hypoxia/SD. In contrast, down-regulation of miR-21, miR-23a and miR-503 aggravated apoptosis of MSCs. It was indicated that these miRNAs may play important roles during MSC apoptosis induced by hypoxia/SD.


Assuntos
Apoptose , Hipóxia/metabolismo , Células-Tronco Mesenquimais/fisiologia , MicroRNAs/metabolismo , Animais , Regulação para Baixo , Perfilação da Expressão Gênica , Técnicas de Silenciamento de Genes , Hipóxia/fisiopatologia , Ratos , Ratos Sprague-Dawley , Regulação para Cima
6.
Zhonghua Xin Xue Guan Bing Za Zhi ; 36(8): 685-90, 2008 Aug.
Artigo em Chinês | MEDLINE | ID: mdl-19100107

RESUMO

OBJECTIVE: To investigated the effect of lovastatin on hypoxia and serum deprivation (Hypoxia/SD) induced rat MSCs apoptosis in vitro and associated signaling pathway changes. METHODS: MSCs were isolated from Sprague-Dawley rats. The anti-apoptotic effects of lovastatin were detected using Hoechst33342 and annexin V-FITC/PI binding assay by Flow cytometric analysis. The phosphorylation of Akt and ERK1/2, the cytochrome C and the cleaved caspase-3 were detected by Western blot. RESULTS: Lovastatin (0.01 - 1 micromol/L) significantly reduced Hypoxia/SD-induced MSCs apoptosis and increased Akt phosphorylation, reduced caspase-3 activation and cytochrome c release from mitochondria to cytosol in a time dependent manner. These effects could be significantly blocked by both PI3K inhibitor, LY294002 and ERK1/2 inhibitor, U0126. CONCLUSIONS: Our results showed that lovastatin protects MSCs from Hypoxia/SD-induced apoptosis via activating PI3K/Akt and ERK1/2 signaling pathways suggesting a potential role of statins as an adjunct therapeutic agent during transplanting MSCs into damaged heart after myocardial infarction.


Assuntos
Apoptose/efeitos dos fármacos , Lovastatina/farmacologia , Células-Tronco Mesenquimais/efeitos dos fármacos , Transdução de Sinais/efeitos dos fármacos , Animais , Caspase 3/metabolismo , Hipóxia Celular , Células Cultivadas , Citocromos c/metabolismo , MAP Quinases Reguladas por Sinal Extracelular/metabolismo , Células-Tronco Mesenquimais/citologia , Fosfatidilinositol 3-Quinases/metabolismo , Fosforilação , Proteínas Proto-Oncogênicas c-akt/metabolismo , Ratos , Ratos Sprague-Dawley
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