Immortalization of common marmoset-derived fibroblasts via expression of cell cycle regulators using the piggyBac transposon
Tissue and Cell, ISSN: 0040-8166, Vol: 77, Page: 101848
2022
- 4Citations
- 8Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations4
- Citation Indexes4
- CrossRef3
- Captures8
- Readers8
Article Description
Common marmosets are non-human primate models used in biomedical research and genome editing technology. This study aimed to establish cell lines from common marmosets and evaluate their characteristics. We obtained normal fibroblasts derived from muscle tissues of two common marmosets and immortalized them with the introduction of a mutat form of cyclin-dependent kinase 4 ( CDK4 R24C ), Cyclin D1, and telomere reverse transcriptase ( TERT ) using the piggyBac transposon. Compared to parental cells, the immortalized cell lines (named K4DT cells) showed telomerase activity and an accelerated cell proliferation rate. To our knowledge, this is the first study describing the successful establishment of immortalized common marmoset-derived fibroblasts using piggyBac transposition of CDK4 R24C, Cyclin D1, and TERT. Our generated cell lines might be a beneficial tool for future studies on disease modeling and targeted gene therapies.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0040816622001203; http://dx.doi.org/10.1016/j.tice.2022.101848; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85131967477&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/35714414; https://linkinghub.elsevier.com/retrieve/pii/S0040816622001203; https://dx.doi.org/10.1016/j.tice.2022.101848
Elsevier BV
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