Evidence map›Paper›PMID 42015225›Full record

ArticleBMC veterinary research2026

Establishment and identification of immortalized sheep ovarian granulosa cells.

Hao Chen, Yue Yuan, Rui Xiao, Xiaona Ding, Zhijie Zhao, Pinshen Li, Bingzhu Zhao, Taojie Zhang, Yingpai Zhaxi, Shengdong Huo

Abstract read
In one paragraph

Article in BMC veterinary research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Hao ChenCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Yue YuanCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Rui XiaoCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Xiaona DingCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Zhijie ZhaoCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Pinshen LiCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Bingzhu ZhaoCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Taojie ZhangCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Yingpai ZhaxiCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China.
Shengdong HuoCollege of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, 730030, China. huoshd@xbmu.edu.cn.

Funding

Lanzhou Science and Technology Plan Project [No. 2022-2--44]National Natural Science Foundation of China [32460907]Plateau Animal Disease Innovation Team [20240036]
6 · The paper itself

Abstract

backgroundFollicular granulosa cells (GCs) are an important cellular resource for studying animal reproductive functions.

resultsThis study aimed to investigate SV40T lentiviral vector-mediated gene transfection in sheep ovarian granulosa cells (GCs) and systematically validate their biological characteristics and functions after immortalization. By optimizing infection conditions (MOI = 10), efficient transfection of the GFP-tagged SV40T gene was successfully achieved (approximately 90% efficiency), leading to the establishment of an immortalized sheep granulosa cell line (GCs-SV40T-GFP). This cell line could be stably passaged for over 50 generations while maintaining consistent cellular morphology and stable fluorescence expression. Compared to primary cells, the immortalized cells exhibited significantly accelerated proliferation, with flow cytometry revealing a marked increase in the proportion of cells in S and G1 phases (P < 0.05). Functional assays confirmed that these cells continuously secreted estradiol (P < 0.05). Further experiments demonstrated that even at the 50th passage, the immortalized cells still highly expressed key granulosa cell functional markers, FSHR and CYP19A1. Karyotype analysis confirmed the maintenance of a normal chromosomal karyotype across different passages (primary, 10th, 25th, and 50th). Additionally, the cells exhibited a dose-dependent functional response to hormonal stimulation, with FSHR protein expression significantly upregulated in response to increasing concentrations of exogenous estradiol (P < 0.05). In vivo safety evaluation showed that GCs-SV40T-GFP cells did not induce tumor formation in mice.

conclusionsIn this study, a functionally stable immortalized sheep granulosa cell model was successfully constructed. At the same time, it also provides an important tool for animal reproductive function research and hormone regulation mechanism exploration.

Indexed as

Granulosa CellsAnimalsAromataseCell LineCell ProliferationEstradiolFemaleLentivirusReceptors, FSHSheepTransfectionAromataseEstradiolReceptors, FSHGranulosa cellsImmortalizationSV40T lentiviral vector

Identifiers

PMID42015225
PMCPMC13255389

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.