Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Histol Histopathol ; 26(4): 433-42, 2011 04.
Artigo em Inglês | MEDLINE | ID: mdl-21360436

RESUMO

Wound repair is a complex process that involves inflammation, proliferation, extracellular matrix deposition/remodeling and apoptosis. Autoimmune diseases profoundly affect the healing process. We have used histological parameters to characterize the recruitment of mast cells and the proliferative activity and apoptosis in the fibrovascular tissue induced by subcutaneous polyether-polyurethane sponge implants in lupus-prone New Zealand White (NZW) and in control Balb/c mouse strains at days 10 and 21 post implantation. Fibrovascular tissue infiltration (hematoxylin and eosin staining), mast cell number (Dominici staining) and cellular proliferation (AgNOR staining) peaked early (day 10) but collagen deposition (picrosirius red staining) and apoptosis remained high in implants of NZW mice during the experimental period. In contrast, implants of Balb/c animals showed a progressive increase in mast cell recruitment and cellular proliferation but apoptosis fell from day 10 to 21 post-implantation. This divergent response early mast cells recruitment, excessive collagen deposition and disturbed removal of apoptotic cells from the site of injury in NZW mice implies that the genotype trait of NZW mice is a determining factor in abnormal healing response.


Assuntos
Apoptose/fisiologia , Reação a Corpo Estranho/patologia , Implantes Experimentais/efeitos adversos , Lúpus Eritematoso Sistêmico/patologia , Paniculite de Lúpus Eritematoso/patologia , Animais , Antígenos Nucleares/fisiologia , Proliferação de Células , Colágeno/metabolismo , Modelos Animais de Doenças , Reação a Corpo Estranho/imunologia , Reação a Corpo Estranho/metabolismo , Lúpus Eritematoso Sistêmico/imunologia , Lúpus Eritematoso Sistêmico/metabolismo , Masculino , Mastócitos/patologia , Camundongos , Camundongos Endogâmicos BALB C , Paniculite de Lúpus Eritematoso/imunologia , Paniculite de Lúpus Eritematoso/metabolismo , Especificidade da Espécie , Cicatrização/imunologia
2.
Mol Hum Reprod ; 17(6): 392-8, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21297155

RESUMO

The oocyte's meiotic spindle is a dynamic structure that relies on microtubule organization and regulation by centrosomes. Disorganization of centrosomal proteins, including the nuclear mitotic apparatus (NuMA) protein and the molecular motor complex dynein/dynactin, can lead to chromosomal instability and developmental abnormalities. The present study reports the distribution and function of these proteins in human oocytes, zygotes and early embryos. A total of 239 oocytes, 90 zygotes and discarded embryos were fixed and analyzed with confocal microscopy for NuMA and dynactin distribution together with microtubules and chromatin. Microtubule-associated dynein-dependent transport functions were explored by inhibiting phosphatase and ATPase activity with sodium-orthovanadate (SOV). At germinal vesicle (GV) stages, NuMA was dispersed across the nucleoplasm. After GV breaks down, NuMA became cytoplasmic before localizing at the spindle poles in metaphase I and II oocytes. Aberrant NuMA localization patterns were found during oocyte in vitro maturation. After fertilization, normal and abnormal pronuclear stage zygotes and embryos displayed translocation of NuMA to interphase nuclei. SOV treatment for up to 2 h induced lower maturation rates with chromosomal scattering and ectopic localization of NuMA. Accurate distribution of NuMA is important for oocyte maturation, zygote and embryo development in humans. Proper assembly of NuMA is likely necessary for bipolar spindle organization and human oocyte developmental competence.


Assuntos
Antígenos Nucleares , Embrião de Mamíferos/metabolismo , Proteínas Associadas à Matriz Nuclear , Oócitos/metabolismo , Fuso Acromático/metabolismo , Feto Abortado , Adenosina Trifosfatases/antagonistas & inibidores , Adenosina Trifosfatases/metabolismo , Adulto , Antígenos Nucleares/fisiologia , Proteínas de Ciclo Celular , Núcleo Celular/metabolismo , Núcleo Celular/ultraestrutura , Centrossomo/metabolismo , Centrossomo/ultraestrutura , Cromossomos , Complexo Dinactina , Dineínas/fisiologia , Embrião de Mamíferos/embriologia , Embrião de Mamíferos/ultraestrutura , Desenvolvimento Embrionário , Feminino , Fertilização , Humanos , Metáfase , Microscopia Confocal , Proteínas Associadas aos Microtúbulos/fisiologia , Microtúbulos/efeitos dos fármacos , Microtúbulos/metabolismo , Microtúbulos/ultraestrutura , Proteínas Associadas à Matriz Nuclear/fisiologia , Oócitos/crescimento & desenvolvimento , Oócitos/ultraestrutura , Monoéster Fosfórico Hidrolases/antagonistas & inibidores , Monoéster Fosfórico Hidrolases/metabolismo , Gravidez , Fuso Acromático/ultraestrutura , Tubulina (Proteína)/fisiologia , Vanadatos/farmacologia , Zigoto
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA