# Engineering Immortalized Bovine Granulosa Cells Using a Triple‐Gene Approach: Mutant CDK4, Cyclin D1, and TERT

**Authors:** Lanlan Bai, Minami Takahashi, Jin Kobayashi, Takahiro Eitsuka, Himari Matsusaka, Taku Ozaki, Eriko Sugano, Hiroshi Tomita, Yuan Xu, Kazuhiro Kawamura, Kiyotaka Nakagawa, Tohru Kiyono, Tomokazu Fukuda

PMC · DOI: 10.1002/cbin.70126 · Cell Biology International · 2026-01-21

## TL;DR

Scientists created long-living bovine granulosa cells using three genes to study cattle reproduction and improve livestock breeding.

## Contribution

A novel triple-gene approach to immortalize bovine granulosa cells for reproductive research.

## Key findings

- Immortalized cells (bGCs-K4DT) showed over 100 population doublings without senescence.
- Cells retained key bGC marker aromatase and exhibited higher telomerase activity.
- The model supports studying platelet-rich plasma effects on follicular development.

## Abstract

Advancing reproductive technologies in livestock is essential to improve both productivity and genetic potential of cattle. Despite this importance, application of reproductive biotechnologies in cattle breeding remains limited. Bovine granulosa cells (bGCs), which are key components of the ovarian follicle, are critical in female reproduction as they produce steroid hormones and growth factors necessary for oocyte development. However, primary bGCs exhibit restricted proliferative capacity in vitro, limiting their utility in large‐scale studies on mechanisms related to follicular development. To address this limitation, we attempted to immortalize bGCs by co‐expressing human mutant cyclin‐dependent kinase 4 (CDK4R24C), cyclin D1, and telomerase reverse transcriptase (TERT) using lentiviral vectors. The resulting immortalized cells (bGCs‐K4DT) displayed extended proliferative lifespans, surpassing 100 population doublings without exhibiting signs of senescence. The transduced cells demonstrated a more active cell cycle profile and higher telomerase activity relative to parental bGCs. Importantly, they retained the bGC‐specific marker, aromatase, albeit at reduced expression levels. This immortalized bGC offers a promising model for investigating the role of bioactive components of platelet‐rich plasma (PRP) in follicular activation and growth, thereby supporting innovations in livestock reproductive technologies.

## Linked entities

- **Genes:** ccnd1.S (cyclin D1 S homeolog) [NCBI Gene 379161], TERT (telomerase reverse transcriptase) [NCBI Gene 7015], Cyp19a1 (cytochrome P450, family 19, subfamily a, polypeptide 1) [NCBI Gene 25147]

## Full-text entities

- **Genes:** CDK4 (cyclin dependent kinase 4) [NCBI Gene 510618], CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 281740] {aka CYP19, CYP19P1}, CCND1 (cyclin D1) [NCBI Gene 524530], TERT (telomerase reverse transcriptase) [NCBI Gene 518884]
- **Chemicals:** steroid hormones (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12821082/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12821082/full.md

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Source: https://tomesphere.com/paper/PMC12821082