A simple method for ex vivo honey bee cell culture capable of in vitro gene expression analysis

• Published in: PloS one Vol. 16; no. 9; p. e0257770
• Main Authors: Watanabe, Kazuyo, Yoshiyama, Mikio, Akiduki, Gaku, Yokoi, Kakeru, Hoshida, Hiroko, Kayukawa, Takumi, Kimura, Kiyoshi, Hatakeyama, Masatsugu
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 23.09.2021; Public Library of Science (PLoS)
• Subjects: Abdomen; Antibiotics; Apis mellifera; Bees; Biological research; Biology and Life Sciences; Breeding of animals; Cell culture; Cell lines; Double-stranded RNA; Engineering and Technology; Ethanol; Fluorescence; Gene expression; Genetics; Genomes; Grasslands; Green fluorescent protein; Hemocytes; Honey; IE2 protein; Insects; Larvae; Livestock; Medicine and Health Sciences; Morphology; Research and Analysis Methods; Signal transduction; Transfection; Viral infections; Japan; United States > US
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0257770

Cultured cells are a very powerful tool for investigating biological events in vitro; therefore, cell lines have been established not only in model insect species, but also in non-model species. However, there are few reports on the establishment of stable cell lines and development of systems to introduce genes into the cultured cells of the honey bee (Apis mellifera). We describe a simple ex vivo cell culture system for the honey bee. Hemocyte cells obtained from third and fourth instar larvae were cultured in commercial Grace's insect medium or MGM-450 insect medium for more than two weeks maintaining a normal morphology without deterioration. After an expression plasmid vector bearing the enhanced green fluorescent protein (egfp) gene driven by the immediate early 2 (IE2) viral promoter was transfected into cells, EGFP fluorescence was detected in cells for more than one week from one day after transfection. Furthermore, double-stranded RNA corresponding to a part of the egfp gene was successfully introduced into cells and interfered with egfp gene expression. A convenient and reproducible method for an ex vivo cell culture that is fully practicable for gene expression assays was established for the honey bee.