4.4 Article

Development of an in vitro culture system for immature oocytes of red swamp crayfish (Procambarus clarkii)

期刊

ANIMAL REPRODUCTION SCIENCE
卷 243, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.anireprosci.2022.107005

关键词

Procambarus clarkii; Ovarian tissue; Oocytes; In vitro culture; 17-OHP

资金

  1. Central Public-interest Scientific Institution Basal Research Fund, Freshwater Fisheries Research Center CAFS [2021JBFM05]
  2. Agriculture Breeding Project by Jiangsu Provincial Department of Agriculture and Rural Affairs [PZCZ201746]
  3. Central Public-interest Scientific Institution Basal Research Fund CAFS [2022XT0102]

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The present study assessed general strategies for the isolation and in vitro culture of immature ovary-derived cells (oocytes) in red swamp crayfish (Procambarus clarkii). The effects of different digestive enzymes on cell retrieval were examined to facilitate efficient oocyte isolation. Furthermore, the study demonstrated that the exogenous hormone 17-OHP could induce oocyte maturation in vitro.
The present study assessed general strategies for the isolation and in vitro culture of immature ovary-derived cells (oocytes) in red swamp crayfish (Procambarus clarkii). In phase 1 of this study, the effects of different digestive enzymes on cell retrieval from developing ovarian tissues were examined to facilitate efficient oocyte isolation. Subsequently, the ovary-derived cells/oocytes were cultured under various conditions to evaluate the effects of basal media and supplement concentrations. Collagenase I treatment at 26 celcius for 25 min was more effective (approx. 95 %) in oocytes isolation from ovarian tissues than other treatments. Furthermore, DMEM media with HEPES (DMEM-H) were more effective than L15 for oocyte culture (72.4 % survival rate), while oocyte survival improved to 90.6 % using a 10 % fetal bovine serum supplement. In phase 2, the top-performing media were used in immature oocyte culture to assess 17 alpha-Hydroxyprogesterone (17-OHP) induction in vitro. An up-regulated expression of maturity-related genes, i.e., cyclin B, cdc2, ef1 alpha, after 12 h of incubation was evident in qPCR results, demonstrating that the exogenous hormone 17-OHP could induce P. clarkii oocyte maturation in vitro. These results may provide a basis for developing an in vitro system for P. clarkii germline cell culture, which may ultimately lead to the genetic improvement of this species.

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