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1.
Asian Pacific Journal of Tropical Medicine ; (12): 165-168, 2012.
Artigo em Inglês | WPRIM | ID: wpr-819805

RESUMO

Liver failure is the end stage of hepatopathy with unfavorable prognosis. In two patients with liver failure, viable primary human hepatocytes, obtained from resected liver tissue of patients with hepatolithiasis, were transplanted into the spleen by interventional therapy through femoral arterial cannula. After transplantation, the patients' clinical symptoms and liver function were significantly improved. However, their bilirubin increased within six days following transplantation. One suffered from hepatic coma and give up treatment and the other patient died fourteen days after transplantation. It is technically safe to treat liver failure by intrasplenic transplantation of adult hepatocytes and the clinical efficacy has been confirmed. How to make transplanted hepatic cells proliferate and functionally survive is the key point to maintain continuous improvement of the recipient's hepatic function.


Assuntos
Adulto , Humanos , Masculino , Bilirrubina , Metabolismo , Evolução Fatal , Encefalopatia Hepática , Patologia , Hepatócitos , Transplante , Falência Hepática , Metabolismo , Patologia , Cirurgia Geral , Testes de Função Hepática , Baço , Patologia , Falha de Tratamento
2.
Journal of Central South University(Medical Sciences) ; (12): 167-173, 2006.
Artigo em Chinês | WPRIM | ID: wpr-813741

RESUMO

OBJECTIVE@#To screen the inflammatory mediators genes regulated by HSF1, and explore the mechanism of downstream genes regulated by HSF1.@*METHODS@#HSF-/- and HSF1+/+ mice were injected with 15 mg/kg LPS intraperitoneally (ip), respectively, and were treated as previous after HSR. The total RNA of lung tissues were extracted and filtrated by SuperArray gene Microarry. The promoter of candidate genes were analyzed by transcription element search software to search for heat shock element (HSE). Select the suppressor of cytokine signaling 3 (SOCS3) with HSE. Macrophage cells were stimulated with 400 ng/mL LPS, and were treated as previous after HSR, then the total RNA was extracted respectively. RT-PCR and northern blot assay were performed to detect the expression levels of SOCS3 mRNA.@*RESULTS@#Fifteen genes were repressed by HSF1, including 9 genes with complete HSE. Eleven genes were accelerated by HSF1 possibly, including 8 genes with complete HSE. The promoter of SOCS3 gene contained one complete HSE. LPS stimulation obviously increased the levels of SOCS3 mRNA in macrophages of RAW264.7 mice, which was inhibited by HSR and over-expression of HSF1.@*CONCLUSION@#HSR or HSF1 inhibits LPS induced expression of SOCS3 mRNA; HSF1 might inhibit LPS-induced expression of SOCS3 mRNA by binding to HSE in the promoter of SOCS3 gene.


Assuntos
Animais , Camundongos , Proteínas de Ligação a DNA , Genética , Farmacologia , Endotoxemia , Genética , Fatores de Transcrição de Choque Térmico , Proteínas de Choque Térmico , Genética , Inflamação , Genética , Lipopolissacarídeos , Macrófagos , Metabolismo , Camundongos Endogâmicos BALB C , Camundongos Knockout , Mutação , RNA Mensageiro , Genética , Transdução de Sinais , Proteína 3 Supressora da Sinalização de Citocinas , Proteínas Supressoras da Sinalização de Citocina , Genética , Fatores de Transcrição , Genética , Farmacologia
3.
Journal of Central South University(Medical Sciences) ; (12): 32-37, 2005.
Artigo em Chinês | WPRIM | ID: wpr-813480

RESUMO

OBJECTIVE@#To observe whether HSP70 could protect against H2O2-induced apoptosis in C2C12 myogenic cells by inhibiting Smac release from the mitochondria.@*METHODS@#HSP70 gene and full length Smac gene was transiently transfected in C2C12 myogenic cells by lipofectamine and the protein levels of HSP70 and Smac were analysed by Western blotting. Hoechst 33 258 staining was used to examine cell morphological changes and to calculate percentage of apoptotic nuclei. DNA ladder pattern on agarose gel electrophoresis was used to observe the DNA fragmentation. Activities of caspase-3 and caspase-9 were assayed with Western blotting. The release of Smac from the mitochondria to the cytoplasm was observed by immunofluorescence.@*RESULTS@#H2O2 ( 0.5 mmol/L ) activated caspase-3, caspase-9 8 h after the treatment and specific morphological changes of apoptosis 12 h after the treatment, and overexpression of Smac significantly promoted H2O2-induced activation of caspase-3, caspase-9 and apoptosis in C2C12 myogenic cells. HSP70 overexpression significantly inhibited H2O2-induced and Smac-promoted apoptosis, as shown by no specific DNA ladder pattern in agarose gel electrophoresis, decrease of percentage of apoptotic nuclei, and marked inactivation of caspase-3 and caspase-9. HSP70 could inhibit the release of Smac from the mitochondria to the cytoplasm 2 h after the treatment by H2O2.@*CONCLUSION@#HSP70 inhibits Smac release from the mitochondria and protects against H2O2-induced apoptosis in C2C12 myogenic cells.


Assuntos
Humanos , Apoptose , Proteínas Reguladoras de Apoptose , Células Cultivadas , Proteínas de Choque Térmico HSP70 , Farmacologia , Peróxido de Hidrogênio , Peptídeos e Proteínas de Sinalização Intracelular , Metabolismo , Mitocôndrias Cardíacas , Metabolismo , Proteínas Mitocondriais , Metabolismo , Mioblastos , Metabolismo , Miócitos Cardíacos , Metabolismo
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