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1.
Yi Chuan ; 40(11): 977-987, 2018 Nov 20.
Artigo em Chinês | MEDLINE | ID: mdl-30465530

RESUMO

The chromatin accessibility and 3D high-order structure play an important role in gene expression and regulation, and are involved in numerous cellular processes such as differentiation, development and tumorigenesis. It is currently one of the hottest research fields in epigenetics. The animal embryonic development initiates from the terminally differentiated mature eggs, which are fertilized by sperms to establish totipotent zygotes. During this complex process, the epigenome encompassing chromatin accessibility and high-order structures changes dramatically, undergoes inheritance, reprogramming and re-establishment, so that the zygote could eventually develop into a new multicellular and multi-tissue organism. In this review, we summarize the research methods and technology for chromatin accessibility and 3D high-order structures, the dynamics of chromatin structures during the animal embryonic development and how to regulate early embryogenesis, the relationship between chromatin structure and other epigenetic information such as methylation and histone modification. We hope that this review may shed light on the research of epigenome regulating embryo development.


Assuntos
Cromatina/química , Embrião de Mamíferos/metabolismo , Animais , Diferenciação Celular , Cromatina/genética , Cromatina/metabolismo , Embrião de Mamíferos/embriologia , Regulação da Expressão Gênica no Desenvolvimento
2.
Nan Fang Yi Ke Da Xue Xue Bao ; 31(6): 1090-2, 2011 Jun.
Artigo em Chinês | MEDLINE | ID: mdl-21690077

RESUMO

OBJECTIVE: To investigate the effects of methylprednisolone pretreatment on pulmonary lung permeability index and the content of the pulmonary surfactant dipalmitoylphosphatidylcholine (DPPC) in a rabbit model of reexpansion pulmonary edema. METHODS: Twenty-one male New Zealand white rabbits were randomly divided into control group, reexpansion, and reexpansion+methylprednisolone pretreatment groups. The rabbit model of reexpansion pulmonary edema was established using Sakaos method. A bolus dosage of methylprednisolone (3 mg/kg) in reexpansion+methylprednisolone group group or 2.0 ml/kg normal saline in the other two groups was administered intravenously 20 min before reexpansion pulmonary edema. Bronchoalveolar lavage fluid (BALF) and arterial blood samples were collected for measurement of the total protein (TP) and DPPC contents 4 h after reexpansion, and the pulmonary permeability index was calculated. RESULTS: The pulmonary permeability index in methylprednisolone pretreatment group was significantly lower than that in the reexpansion group (0.007∓0.002 vs 0.177∓0.004, P<0.05). Methylprednisolone pretreatment significantly increased DPPC concentration in the BALF as compared with saline treatment in the reexpansion group (61.815∓28.307 vs 101.955∓24.544 µg/ml, P<0.05). CONCLUSION: Methylprednisolone pretreatment can increase pulmonary surfactant content and improve pulmonary permeability in the rabbit model of reexpansion pulmonary edema.


Assuntos
Metilprednisolona/farmacologia , Edema Pulmonar/metabolismo , Edema Pulmonar/fisiopatologia , Surfactantes Pulmonares/metabolismo , 1,2-Dipalmitoilfosfatidilcolina/análise , Animais , Líquido da Lavagem Broncoalveolar , Permeabilidade Capilar/efeitos dos fármacos , Masculino , Permeabilidade , Coelhos
3.
Cell Res ; 13(2): 69-81, 2003 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12737516

RESUMO

During mitosis, the parent cell distributes its genetic materials equally into two daughter cells through chromosome segregation, a complex movements orchestrated by mitotic kinases and its effector proteins. Faithful chromosome segregation and cytokinesis ensure that each daughter cell receives a full copy of genetic materials of parent cell. Defects in these processes can lead to aneuploidy or polyploidy. Aurora/Ipl1p family, a class of conserved serine/threonine kinases, plays key roles in chromosome segregation and cytokinesis. This article highlights the function and regulation of Aurora/Ipl1p family in mitosis and provides potential links between aberrant regulation of Aurora/Ipl1p kinases and pathogenesis of human cancer.


Assuntos
Segregação de Cromossomos/fisiologia , Células Eucarióticas/enzimologia , Mitose/fisiologia , Proteínas Quinases/metabolismo , Proteínas Serina-Treonina Quinases/metabolismo , Proteínas de Saccharomyces cerevisiae , Aneuploidia , Animais , Aurora Quinases , Divisão Celular/fisiologia , Transformação Celular Neoplásica/genética , Humanos , Peptídeos e Proteínas de Sinalização Intracelular , Proteínas Quinases/genética , Proteínas Serina-Treonina Quinases/genética
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