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Preparation of a High-quality Primary Cell Culture from Fish Pituitaries.
Ager-Wick, Eirill; Hodne, Kjetil; Fontaine, Romain; von Krogh, Kristine; Haug, Trude M; Weltzien, Finn-Arne.
Affiliation
  • Ager-Wick E; Department of Basic Sciences and Aquatic Medicine, Faculty of Veterinary Medicine, Norwegian University of Life Sciences.
  • Hodne K; Department of Basic Sciences and Aquatic Medicine, Faculty of Veterinary Medicine, Norwegian University of Life Sciences.
  • Fontaine R; Department of Basic Sciences and Aquatic Medicine, Faculty of Veterinary Medicine, Norwegian University of Life Sciences.
  • von Krogh K; Department of Basic Sciences and Aquatic Medicine, Faculty of Veterinary Medicine, Norwegian University of Life Sciences.
  • Haug TM; Department of Oral Biology, Faculty of Dentistry, University of Oslo.
  • Weltzien FA; Department of Basic Sciences and Aquatic Medicine, Faculty of Veterinary Medicine, Norwegian University of Life Sciences; finn-arne.weltzien@nmbu.no.
J Vis Exp ; (138)2018 08 28.
Article in En | MEDLINE | ID: mdl-30222142
ABSTRACT
Primary cell culture is a powerful tool commonly used by scientists to study cellular properties and mechanisms of isolated cells in a controlled environment. Despite vast differences in the physiology between mammals and fish, primary cell culture protocols from fish are often based on mammalian culture conditions, often with only minor modifications. The environmental differences affect not only body temperature, but also blood serum parameters such as osmolality, pH, and pH buffer capacity. As cell culture media and similar working solutions are meant to mimic characteristics of the extracellular fluid and/or blood serum to which a cell is adapted, it is crucial that these parameters are adjusted specifically to the animal in question. The current protocol describes optimized primary culture conditions for medaka (Oryzias latipes). The protocol provides detailed steps on how to isolate and maintain healthy dissociated pituitary cells for more than one week and includes the following

steps:

1. the adjustment of the osmolality to the values found in medaka blood plasma, 2. the adjustment of the incubation temperature to normal medaka temperature (here in the aquarium facility), and 3. the adjustment of the pH and bicarbonate buffer to values comparable to other fish species living at similar temperatures. The results presented using the described protocol promote physiologically meaningful results for medaka and can be used as a reference guide by scientists making primary cell cultures from other non-mammalian species.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Pituitary Gland, Anterior / Primary Cell Culture Limits: Animals Language: En Year: 2018 Type: Article

Full text: 1 Database: MEDLINE Main subject: Pituitary Gland, Anterior / Primary Cell Culture Limits: Animals Language: En Year: 2018 Type: Article