Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Apoptosis ; 13(9): 1065-87, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18622770

RESUMO

The vertebrate ovary is an extremely dynamic organ in which excessive or defective follicles are rapidly and effectively eliminated early in ontogeny and thereafter continuously throughout reproductive life. More than 99% of follicles disappear, primarily due to apoptosis of granulosa cells, and only a minute fraction of the surviving follicles successfully complete the path to ovulation. The balance between signals for cell death and survival determines the destiny of the follicles. An abnormally high rate of cell death followed by atresia can negatively affect fertility and eventually lead irreversibly to premature ovarian failure. In this review we provide a short overview of the role of programmed cell death in prenatal differentiation of the primordial germ cells and in postnatal folliculogenesis. We also discuss the issue of neo-oogenesis. Next, we highlight molecules involved in regulation of granulosa cell apoptosis. We further discuss the potential use of scores for apoptosis in granulosa cells and characteristics of follicular fluid as prognostic markers for predicting the outcome of assisted reproduction. Potential therapeutic strategies for combating premature ovarian failure are also addressed.


Assuntos
Morfogênese , Oogênese , Folículo Ovariano/citologia , Folículo Ovariano/crescimento & desenvolvimento , Óvulo/citologia , Animais , Morte Celular , Feminino , Humanos , Técnicas de Reprodução Assistida
2.
J Morphol ; 263(2): 203-15, 2005 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15593343

RESUMO

Epidermally derived tendon cells attach the exoskeleton (cuticle) of the Branchiopod crustacean, Artemia franciscana, to underlying muscle in the hindgut, while the structurally similar transalar tendon (epithelial) cells, which also arise from the epidermis and are polarized, connect dorsal and ventral exopodite surfaces. To establish these latter attachments the transalar tendon cells interact with cuticles on opposite sides of the exopodite by way of their apical surfaces and with one another via basal regions, or the cuticle attachments may be mediated through linkages with phagocytic storage cells found in the hemolymph. In some cases, phyllopod tendon cells attach directly to muscle cells. Tendon cells in the hindgut of Artemia possess microtubule bundles, as do the transalar cells, and they extend from the basal myotendinal junction to the apical domain located near the cuticle. The bundled microtubules intermingle with thin filaments reminiscent of microfilaments, but intermediate filament-like structures are absent. Microtubule bundles converging at apical cell surfaces contact structures termed apical invaginations, composed of cytoplasmic membrane infoldings associated with electron-dense material. Intracuticular rods protrude from apical invaginations, either into the cuticle during intermolt or the molting fluid in premolt. Confocal microscopy of immunofluorescently stained samples revealed tyrosinated, detyrosinated, and acetylated tubulins, the first time posttranslationally modified isoforms of this protein have been demonstrated in crustacean tendon cells. Microfilaments, as shown by staining with phalloidin, coincided spatially with microtubule bundles. Artemia tendon cells clearly represent an interesting system for study of cytoskeleton organization within the context of cytoplasmic polarity and the results in this article indicate functional cooperation of microtubules and microfilaments. These cytoskeletal elements, either acting independently or in concert, may transmit tension from muscle to cuticle in the hindgut and resist compression when connecting exopodite cuticular surfaces.


Assuntos
Artemia/metabolismo , Epiderme/metabolismo , Microtúbulos/metabolismo , Tubulina (Proteína)/metabolismo , Animais , Artemia/citologia , Artemia/ultraestrutura , Epiderme/ultraestrutura , Microscopia Eletrônica de Transmissão , Microtúbulos/ultraestrutura , Isoformas de Proteínas/metabolismo
3.
J Morphol ; 199(1): 41-52, 1989 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29865624

RESUMO

The molting cycle of Artemia is described and subdivided in stages A-D3 according to the system of Drach. Determination of the stages is done in living animals by light microscopic observation of changes in the texture of the setal matrix of the exopodites. A parallel ultrastructural investigation of the integument was carried out to control the proposed staging scheme. The duration of each stage was calculated.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...