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2.
Mol Endocrinol ; 19(12): 3023-37, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16020483

RESUMO

Uterine decidualization is characterized by stromal cell proliferation and differentiation, which are controlled by ovarian hormones estradiol and progesterone. Here we report that the proliferative response of UIII rat uterine stromal cells to a short treatment with progestins requires active progesterone receptor (PR) and estrogen receptor beta (ERbeta) as well as a rapid and transient activation of Erk1-2 and Akt signaling. The optimal R5020 concentration for the proliferative response as well as for activation of the signaling cascades was between 10 and 100 pm. UIII cells are negative for ERalpha and have low levels of ERbeta and PR located mainly in the cytoplasm. Upon progestin treatment PR translocated to the cell nucleus where it colocalized with activated Erk1-2. Neither progestins nor estradiol transactivated the corresponding transfected reporter genes, suggesting that endogenous PR and ERbeta are transcriptionally incompetent. A fraction of endogenous PR and ERbeta form a complex as demonstrated by coimmunoprecipitation. Taken together, our results suggest that the proliferative response of uterine stromal cells to picomolar concentrations of progestins does not require direct transcriptional effects and is mediated by activation of the Erk1-2 and Akt signaling pathways via cross talk between PR and ERbeta.


Assuntos
Endométrio/efeitos dos fármacos , Receptor beta de Estrogênio/metabolismo , Progestinas/farmacologia , Receptores de Progesterona/metabolismo , Transporte Ativo do Núcleo Celular , Animais , Núcleo Celular/química , Núcleo Celular/metabolismo , Proliferação de Células , Citoplasma/química , Citoplasma/metabolismo , Endométrio/citologia , Ativação Enzimática , Receptor alfa de Estrogênio/genética , Receptor beta de Estrogênio/antagonistas & inibidores , Feminino , Genes Reporter , Genoma , Proteína Quinase 1 Ativada por Mitógeno/análise , Proteína Quinase 1 Ativada por Mitógeno/metabolismo , Proteína Quinase 3 Ativada por Mitógeno/análise , Proteína Quinase 3 Ativada por Mitógeno/metabolismo , Mutação , Promegestona/farmacologia , Proteínas Proto-Oncogênicas c-akt/análise , Proteínas Proto-Oncogênicas c-akt/metabolismo , Ratos , Receptores de Progesterona/análise , Transdução de Sinais , Células Estromais/efeitos dos fármacos , Transcrição Gênica , Ativação Transcricional
3.
Curr Protoc Mol Biol ; 116: 28.7.1-28.7.14, 2016 10 10.
Artigo em Inglês | MEDLINE | ID: mdl-27723084

RESUMO

Cell line establishment of somatic cells is a valuable resource to preserve genetic material of rare, difficult-to-find, endangered and giant species like Jaguar (Panthera onca), the largest South American felid. This unit focuses on the isolation and culture of fibroblasts from Jaguar skin and muscle biopsies, and ear cartilage dissection immediately after death to preserve one of the several endangered species in this biome. These culture techniques enabled us to contribute 570 samples from 45 autochthonous and endangered species, including Jaguar. The fibroblasts obtained are a part of the Genetic Bank of Buenos Aires Zoo with the 6700 samples, including tissues such as muscle, ovarian, testicular, blood, fibroblast cultures, sperm, hair, and fluids and cells from 450 individuals of 87 different species. © 2016 by John Wiley & Sons, Inc.


Assuntos
Técnicas de Cultura de Células/métodos , Separação Celular/métodos , Espécies em Perigo de Extinção , Fibroblastos/citologia , Panthera , Animais , Cartilagem/citologia , Células Cultivadas , Criopreservação/métodos , Músculos/citologia , Panthera/metabolismo , Pele/citologia
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