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Effect of germ cell Wdr1 deletion on the ovarian function of mice / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 819-823, 2018.
Artigo em Chinês | WPRIM | ID: wpr-775829
ABSTRACT
OBJECTIVE@#To study the effect of Wdr1 deletion in germ cells on ovarian function of mice.@*METHODS@#Oocyte-specific gene knockout mouse model was constructed by crossing Wdr1female mice with Cre recombinase transgenic male mice which was driven by a germ cell-specific promoter. Wdr1; Ddx4-Cre mice and control mice were sacrificed at 14 days, 28 days and 4 months after birth, whose ovaries were subjected to photography, paraffin sectioning and Hematoxylin-Eosin (HE) staining. The ovarian volume and follicular numbers were recorded at various time points.@*RESULTS@#The ovarian volume of Wdr1 ; Ddx4-Cre mice was slightly lower than that of the controls at 14 days. HE staining showed that primordial follicles, primary follicles and secondary follicles were slightly reduced compared with the control mice at 14 days. The ovarian volume of Wdr1 ; Ddx4-Cre mice was significantly lower than that of the control mice at 28 days and 4 months. HE staining showed that all developmental follicles were significantly reduced compared with the control mice.@*CONCLUSION@#Wdr1 gene deletion in germ cells can influence early ovarian function of mice and lead to premature ovarian failure.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Oócitos / Camundongos Transgênicos / Camundongos Knockout / Genética / Células Germinativas / Folículo Ovariano / Proteínas dos Microfilamentos Limite: Animais Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2018 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Oócitos / Camundongos Transgênicos / Camundongos Knockout / Genética / Células Germinativas / Folículo Ovariano / Proteínas dos Microfilamentos Limite: Animais Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2018 Tipo de documento: Artigo