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Common lizard primary oviduct cell culture: A model system for the genetic and cellular basis of oviparity and viviparity.
Smout, John Laurence; Bain, Maureen M; McLaughlin, Mark; Elmer, Kathryn R.
Affiliation
  • Smout JL; School of Biodiversity, One Health and Veterinary Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, Scotland, G12 8QQ, UK.
  • Bain MM; School of Biodiversity, One Health and Veterinary Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, Scotland, G12 8QQ, UK.
  • McLaughlin M; School of Biodiversity, One Health and Veterinary Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, Scotland, G12 8QQ, UK.
  • Elmer KR; School of Biodiversity, One Health and Veterinary Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, Scotland, G12 8QQ, UK. Electronic address: kathryn.elmer@glasgow.ac.uk.
Exp Cell Res ; 442(1): 114196, 2024 Aug 06.
Article in En | MEDLINE | ID: mdl-39117090
ABSTRACT
Reproduction by egg-laying (oviparity) or live-bearing (viviparity) is a genetically determined trait fundamental to the biology of amniotes. Squamates are an emerging model for the genetics of reproductive mode yet lack cell culture models valuable for exploring molecular mechanisms. Here, we report a novel primary culture model for reproductive biology cell cultures derived from the oviduct tissues (infundibulum, uterus and vagina) of oviparous and viviparous common lizards (Lacertidae Zootoca vivipara). We maintained and expanded these cultures for over 100 days, including repeated subculturing and successful revival of cryopreserved cells. Immunocytochemical investigation suggested expression of both epithelial and fibroblast-like proteins, and RNA sequencing of cultured cells as compared to in vivo oviduct tissue showed changes in gene expression in response to the cell culture environment. Despite this, we confirmed the maintenance of distinct gene expression patterns in viviparous and oviparous cells after 60+ days of cell culture, finding 354 differentially expressed genes between viviparous and oviparous cells. Furthermore, we confirmed the expression of 15 viviparity-associated candidate genes in cells maintained for 60+ days in culture. Our study demonstrates the feasibility and utility of oviduct cell culture for molecular analysis of reproductive mode and provides a tool for future genetic experiments.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Exp Cell Res Year: 2024 Document type: Article Affiliation country: United kingdom Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Exp Cell Res Year: 2024 Document type: Article Affiliation country: United kingdom Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA