Adapting Drosophila melanogaster Cell Lines to Serum-Free Culture Conditions
Successful cell culture relies on media containing xenogenic components such as fetal bovine serum to support continuous cell proliferation. Here, we report a serum-free culture condition that supports the growth and proliferation of S2R+ and Kc167 cell lines. Importantly, the gradual adaptation of...
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Published in | G3 : genes - genomes - genetics Vol. 10; no. 12; pp. 4541 - 4551 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Genetics Society of America
01.12.2020
Oxford University Press |
Subjects | |
Online Access | Get full text |
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Summary: | Successful
cell culture relies on media containing xenogenic components such as fetal bovine serum to support continuous cell proliferation. Here, we report a serum-free culture condition that supports the growth and proliferation of
S2R+ and Kc167 cell lines. Importantly, the gradual adaptation of S2R+ and Kc167 cells to a media lacking serum was supported by supplementing the media with adult
soluble extract, commonly known as fly extract. The utility of these adapted cells lines is largely unchanged. The adapted cells exhibited robust proliferative capacity and a transfection efficiency that was comparable to control cells cultured in serum-containing media. Transcriptomic data indicated that the S2R+ cells cultured with fly extract retain their hemocyte-specific transcriptome profile, and there were no global changes in the transcriptional output of cell signaling pathways. Our metabolome studies indicate that there were very limited metabolic changes. In fact, the cells were likely experiencing less oxidative stress when cultured in the serum-free media supplemented with fly extract. Overall, the
cell culture conditions reported here consequently provide researchers with an alternative and physiologically relevant resource to address cell biological research questions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contributed equally. |
ISSN: | 2160-1836 2160-1836 |
DOI: | 10.1534/g3.120.401769 |