Study on immortalization of Mongolian sheep fibroblast cells

This study aims to establish an immortalized fibroblast cell line from Mongolian sheep. Primary Mongolian sheep fibroblasts (SSF) were isolated using tissue explant and enzymatic digestion methods, followed by microscopic observation, growth curve plotting, and karyotype analysis. The results confir...

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Main Authors: Bin. Liu, Shichao. Wang, Fanhua. Meng, Bei. Wu, Yanru Zhang, Junwei. Cao
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:Animal Biotechnology
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Online Access:https://www.tandfonline.com/doi/10.1080/10495398.2025.2459915
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author Bin. Liu
Shichao. Wang
Fanhua. Meng
Bei. Wu
Yanru Zhang
Junwei. Cao
author_facet Bin. Liu
Shichao. Wang
Fanhua. Meng
Bei. Wu
Yanru Zhang
Junwei. Cao
author_sort Bin. Liu
collection DOAJ
description This study aims to establish an immortalized fibroblast cell line from Mongolian sheep. Primary Mongolian sheep fibroblasts (SSF) were isolated using tissue explant and enzymatic digestion methods, followed by microscopic observation, growth curve plotting, and karyotype analysis. The results confirmed the successful isolation of SSF. Human (hTERT) and sheep (sTERT) telomerase reverse transcriptase vectors were separately introduced into SSF, with cells passaged up to 36 generations following G418 selection. Microscopic examination and qRT-PCR results demonstrated that TERT transfection did not alter the morphology of SSF and led to stable, high levels of TERT expression (P < 0.01). Cell counting and flow cytometry revealed that TERT-transfected cells had higher viability and lower apoptosis rates compared to SSF (P < 0.05). Karyotype and soft agar colony formation assays indicated that hTERT and sTERT-transfected cells maintained normal characteristics without malignant transformation. β-galactosidase staining indicated that TERT transfection significantly reduced cellular senescence (P < 0.001). Additionally, sTERT-transfected cells exhibited higher TERT expression, enhanced viability, proliferation, and anti-senescence effects compared to hTERT-transfected cells (P < 0.05). In summary, the introduction of hTERT and sTERT effectively extends the lifespan of SSF, with sTERT demonstrating a more pronounced effect. This study provides critical evidence for preserving Mongolian sheep genetic resources and developing immortalized cell lines.
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spelling doaj-art-b3db61c6d3a04540a04356400d6a12e62025-08-20T03:48:15ZengTaylor & Francis GroupAnimal Biotechnology1049-53981532-23782025-12-0136110.1080/10495398.2025.2459915Study on immortalization of Mongolian sheep fibroblast cellsBin. Liu0Shichao. Wang1Fanhua. Meng2Bei. Wu3Yanru Zhang4Junwei. Cao5College of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, People’s Republic of ChinaDepartment of Medical Laboratory, Hohhot First Hospital, Hohhot, Inner Mongolia, People’s Republic of ChinaCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, People’s Republic of ChinaCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, People’s Republic of ChinaCollege of Medicine, Hainan Vocational University of Science and Technology, Haikou, Hainan, People’s Republic of ChinaCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, People’s Republic of ChinaThis study aims to establish an immortalized fibroblast cell line from Mongolian sheep. Primary Mongolian sheep fibroblasts (SSF) were isolated using tissue explant and enzymatic digestion methods, followed by microscopic observation, growth curve plotting, and karyotype analysis. The results confirmed the successful isolation of SSF. Human (hTERT) and sheep (sTERT) telomerase reverse transcriptase vectors were separately introduced into SSF, with cells passaged up to 36 generations following G418 selection. Microscopic examination and qRT-PCR results demonstrated that TERT transfection did not alter the morphology of SSF and led to stable, high levels of TERT expression (P < 0.01). Cell counting and flow cytometry revealed that TERT-transfected cells had higher viability and lower apoptosis rates compared to SSF (P < 0.05). Karyotype and soft agar colony formation assays indicated that hTERT and sTERT-transfected cells maintained normal characteristics without malignant transformation. β-galactosidase staining indicated that TERT transfection significantly reduced cellular senescence (P < 0.001). Additionally, sTERT-transfected cells exhibited higher TERT expression, enhanced viability, proliferation, and anti-senescence effects compared to hTERT-transfected cells (P < 0.05). In summary, the introduction of hTERT and sTERT effectively extends the lifespan of SSF, with sTERT demonstrating a more pronounced effect. This study provides critical evidence for preserving Mongolian sheep genetic resources and developing immortalized cell lines.https://www.tandfonline.com/doi/10.1080/10495398.2025.2459915Mongolian sheepfibroblastimmortalizationhuman telomerase reverse transcriptasesheep telomerase reverse transcriptase
spellingShingle Bin. Liu
Shichao. Wang
Fanhua. Meng
Bei. Wu
Yanru Zhang
Junwei. Cao
Study on immortalization of Mongolian sheep fibroblast cells
Animal Biotechnology
Mongolian sheep
fibroblast
immortalization
human telomerase reverse transcriptase
sheep telomerase reverse transcriptase
title Study on immortalization of Mongolian sheep fibroblast cells
title_full Study on immortalization of Mongolian sheep fibroblast cells
title_fullStr Study on immortalization of Mongolian sheep fibroblast cells
title_full_unstemmed Study on immortalization of Mongolian sheep fibroblast cells
title_short Study on immortalization of Mongolian sheep fibroblast cells
title_sort study on immortalization of mongolian sheep fibroblast cells
topic Mongolian sheep
fibroblast
immortalization
human telomerase reverse transcriptase
sheep telomerase reverse transcriptase
url https://www.tandfonline.com/doi/10.1080/10495398.2025.2459915
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