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1.
Biotechnol Bioeng ; 114(1): 208-216, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27345768

RESUMO

Bioprinting as an advanced enabling technology has the capacity to construct tissues with respective anatomical structures. In order to maintain the precise printing resolution for anatomical tissue printing, cell seeding density in bioink is limited. Bone marrow derived mesenchymal stem cells (MSCs) are widely used for cartilage tissue engineering. However, the approach of ideal chondrogenic differentiation of MSCs without hypertrophy still remains elusive. Here, we reported NR2F2 plays a crucial role in MSC chondrogenesis in bioprinted cartilage. NR2F2 over-expressed MSCs showed significantly enhanced chondrogenesis and NR2F2 knockdown cells demonstrated the exactly opposite behavior. We evaluated the cells cultured in monolayer, 3D pellet, and bioprinted 3D scaffold. All observations were consistent among gene expression, biochemical analysis, histological assay, and biomechanical evaluation. The data also revealed possible involvement of NR2F2 in mechanism of MSC chondrogenic differentiation under hypoxic culture condition. Biotechnol. Bioeng. 2017;114: 208-216. © 2016 Wiley Periodicals, Inc.


Assuntos
Bioimpressão/métodos , Fator II de Transcrição COUP/metabolismo , Condrogênese/fisiologia , Células-Tronco Mesenquimais/metabolismo , Engenharia Tecidual/métodos , Animais , Fator II de Transcrição COUP/análise , Fator II de Transcrição COUP/genética , Cartilagem , Diferenciação Celular/fisiologia , Hipóxia Celular , Condrócitos/citologia , Condrócitos/metabolismo , Técnicas de Silenciamento de Genes , Humanos , Masculino , Células-Tronco Mesenquimais/citologia , Camundongos , Camundongos Endogâmicos C57BL
2.
Int J Clin Exp Pathol ; 8(6): 7112-21, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26261604

RESUMO

OBJECTIVE: In order to evaluate whether the role of chicken ovalbumin upstream promoter transcription factor II (COUP-TF II) could sever as a predictor to stratify risk of human colorectal cancer (CRC) patients, and to elucidate the preliminary molecular mechanisms of COUP-TF II involved in the development and advancement of CRC reflected by investigating the relationship of COUP-TF II with PTEN, Smad4. METHODS: 112 cases tissue microarray and immunohistochemical SP method were used to detect the expression of COUP-TF II, PTEN and Smad4 in CRC tissues and adjacent non-tumorous tissues. The clinical relevance and prognosis of COUP-TF II, PTEN, Smad4 in CRC patients were analyzed. Furthermore, Cox proportional hazards model was performed to indicate the independent prognostic factors for CRC patients using various clinicopathological parameters and COUP-TF II, PTEN and Smad4. RESULTS: COUP-TF II proteins were positively expressed in 65.2% of CRC tissues and 15.5% paired non-CRC tissues, respectively. The expression of COUP-TF II was significantly correlated with TNM stage and lymph node metastasis and a negative correlation with Smad4 expression. Patients bearing higher levels of COUP-TF II expression showed lower DFS and OS. Most importantly, Cox proportional hazards regression analyses showed COUP-TF II positive/Smad4 negative status (DFS, P=0.001; OS, P=0.005) were independent prognostic factors for CRC patients. CONCLUSION: Positive COUP-TF II expression levels has significant value in determining CRC stage and metastasis and cooperates with negative Smad4 expression contributing to assess prognosis in patients with colorectal cancer, suggesting Smad4 may be involved in the above regulation progress probably.


Assuntos
Biomarcadores Tumorais/análise , Fator II de Transcrição COUP/análise , Neoplasias Colorretais/química , Proteína Smad4/análise , Adulto , Idoso , Neoplasias Colorretais/patologia , Neoplasias Colorretais/cirurgia , Regulação para Baixo , Feminino , Humanos , Imuno-Histoquímica , Estimativa de Kaplan-Meier , Metástase Linfática , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Estadiamento de Neoplasias , PTEN Fosfo-Hidrolase/análise , Valor Preditivo dos Testes , Modelos de Riscos Proporcionais , Fatores de Risco , Análise Serial de Tecidos , Resultado do Tratamento , Regulação para Cima
3.
Neuroendocrinology ; 82(5-6): 233-44, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16721029

RESUMO

Chicken ovalbumin upstream promoter transcription factors (COUP-TF)-II (NR2F2) and EAR-2 (NR2F6) are structurally related orphan members of the nuclear receptors superfamily. There are growing evidences that these factors play important roles during processes of differentiation and proliferation of several tissues. To better understand their role in the differentiated adult rat pituitary gland, we cloned COUP-TFII and EAR-2 cDNAs from an anterior pituitary cDNA library. Subsequently, we raised and characterized specific antibodies to the N-terminal domain of both nuclear receptors. We next examined their cellular and subcellular distribution in the pituitary gland and determined their regulation during pregnancy. COUP-TFII and EAR-2 pituitary genes display, respectively, 90 and 100% homologies with their human and mouse homologues. Cellular expression of both nuclear receptors was mainly detected in the lactotropes of male and female rats, with a prominent distribution in the nuclear compartment for EAR-2, and interestingly both proteins were significantly upregulated in pituitaries of pregnant vs. cycling female rats. Thus, our results have characterized cloning of rat pituitary COUP-TFII and EAR-2 genes, demonstrated that they are both specifically expressed in lactotropes, and strongly suggested that they may play an important role in modulating prolactin (PRL) gene expression during pregnancy.


Assuntos
Fator II de Transcrição COUP/análise , Fator II de Transcrição COUP/genética , Adeno-Hipófise/química , Adeno-Hipófise/metabolismo , Receptores de Esteroides/análise , Receptores de Esteroides/genética , Fatores de Transcrição/análise , Fatores de Transcrição/genética , Sequência de Aminoácidos , Animais , Western Blotting , Fator II de Transcrição COUP/imunologia , Fator II de Transcrição COUP/fisiologia , Diferenciação Celular/fisiologia , Proliferação de Células , Clonagem Molecular , DNA Complementar/análise , DNA Complementar/genética , Eletroforese em Gel de Poliacrilamida , Feminino , Regulação da Expressão Gênica/fisiologia , Imuno-Histoquímica , Masculino , Dados de Sequência Molecular , Adeno-Hipófise/citologia , Adeno-Hipófise/fisiologia , Gravidez , Prenhez/genética , Prenhez/fisiologia , Prolactina/análise , Prolactina/genética , Prolactina/fisiologia , Ratos , Ratos Wistar , Receptores de Esteroides/imunologia , Receptores de Esteroides/fisiologia , Fatores de Transcrição/imunologia , Fatores de Transcrição/fisiologia
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