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Role of cytoskeleton in regulating fusion of nucleoli: a study using the activated mouse oocyte model.
Lian, Hua-Yu; Jiao, Guang-Zhong; Wang, Hui-Li; Tan, Xiu-Wen; Wang, Tian-Yang; Zheng, Liang-Liang; Kong, Qiao-Qiao; Tan, Jing-He.
Afiliación
  • Lian HY; College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China.
  • Jiao GZ; College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China.
  • Wang HL; College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China.
  • Tan XW; College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China.
  • Wang TY; College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China.
  • Zheng LL; College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China.
  • Kong QQ; College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China.
  • Tan JH; College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China tanjh@sdau.edu.cn.
Biol Reprod ; 91(3): 56, 2014 Sep.
Article en En | MEDLINE | ID: mdl-25061094
ABSTRACT
Although fusion of nucleoli was observed during pronuclear development of zygotes and the behavior of nucleoli in pronuclei has been suggested as an indicator of embryonic developmental potential, the mechanism for nucleolar fusion is unclear. Although both cytoskeleton and the nucleolus are important cellular entities, there are no special reports on the relationship between the two. Role of cytoskeleton in regulating fusion of nucleoli was studied using the activated mouse oocyte model. Mouse oocytes were cultured for 6 h in activating medium (Ca²âº-free CZB medium containing 10 mM SrCl2) supplemented with or without inhibitors for cytoskeleton or protein synthesis before pronuclear formation, nucleolar fusion, and the activity of maturation-promoting factor (MPF) were examined. Whereas treatment with microfilament inhibitor cytochalasin D or B or intermediate filament inhibitor acrylamide suppressed nucleolar fusion efficiently, treatment with microtubule inhibitor demecolcine or nocodazole or protein synthesis inhibitor cycloheximide had no effect. The cytochalasin D- or acrylamide-sensitive temporal window coincided well with the reported temporal window for nucleolar fusion in activated oocytes. Whereas a continuous incubation with demecolcine prevented pronuclear formation, pronuclei formed normally when demecolcine was excluded during the first hour of activation treatment when the MPF activity dropped dramatically. The results suggest that 1) microfilaments and intermediate filaments but not microtubules support nucleolar fusion, 2) proteins required for nucleolar fusion including microfilaments and intermediate filaments are not de novo synthesized, and 3) microtubule disruption prevents pronuclear formation by activating MPF.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oocitos / Oogénesis / Citoesqueleto / Nucléolo Celular / Factor Promotor de Maduración Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biol Reprod Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oocitos / Oogénesis / Citoesqueleto / Nucléolo Celular / Factor Promotor de Maduración Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biol Reprod Año: 2014 Tipo del documento: Article