Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell Line

The primary sheep trophoblast cells (STCs) have a finite lifespan in culture. This feature limits the scope for long-term in vitro studies with STCs. This study was an attempt to establish and characterize a telomerase-immortalized sheep trophoblast cell line. STCs were isolated and purified by usin...

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Main Authors: Yufei Zhang, Jing Shi, Shuying Liu
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2016/5808575
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spelling doaj-9b1ea616364f486b862b4ce8fad158122020-11-25T01:08:50ZengHindawi LimitedBioMed Research International2314-61332314-61412016-01-01201610.1155/2016/58085755808575Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell LineYufei Zhang0Jing Shi1Shuying Liu2College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, ChinaCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, ChinaCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, ChinaThe primary sheep trophoblast cells (STCs) have a finite lifespan in culture. This feature limits the scope for long-term in vitro studies with STCs. This study was an attempt to establish and characterize a telomerase-immortalized sheep trophoblast cell line. STCs were isolated and purified by using Percoll and specific immunoaffinity purification, respectively. The purified STCs were transfected with a plasmid carrying sequences of human telomerase reverse transcriptase (hTERT) to create immortalized sheep trophoblast cell line (hTERT-STCs). hTERT-STCs showed a stable expression of hTERT gene, serially passaged for a year, and showed active proliferation without signs of senescence. Cytokeratin 7 (CK-7), secreted human chorionic gonadotrophin subunit β (CG-β), placental lactogen (PL), and endogenous jaagsiekte sheep retrovirus (enJSRV) envelope genes were expressed in hTERT-STCs. Transwell cell invasion assay indicated that hTERT-STCs still possessed the same invasive characteristics as normal primary sheep trophoblast cells. hTERT-STCs could not grow in soft agar and did not develop into tumors in nude mice. In this study, we established a strain of immortalized sheep trophoblast cell line which could be gainfully employed in the future as an experimental model to study trophoblast cells with secretory function, invasive features, and probable biological function of enJSRV envelope genes.http://dx.doi.org/10.1155/2016/5808575
collection DOAJ
language English
format Article
sources DOAJ
author Yufei Zhang
Jing Shi
Shuying Liu
spellingShingle Yufei Zhang
Jing Shi
Shuying Liu
Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell Line
BioMed Research International
author_facet Yufei Zhang
Jing Shi
Shuying Liu
author_sort Yufei Zhang
title Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell Line
title_short Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell Line
title_full Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell Line
title_fullStr Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell Line
title_full_unstemmed Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell Line
title_sort establishment and characterization of a telomerase-immortalized sheep trophoblast cell line
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2016-01-01
description The primary sheep trophoblast cells (STCs) have a finite lifespan in culture. This feature limits the scope for long-term in vitro studies with STCs. This study was an attempt to establish and characterize a telomerase-immortalized sheep trophoblast cell line. STCs were isolated and purified by using Percoll and specific immunoaffinity purification, respectively. The purified STCs were transfected with a plasmid carrying sequences of human telomerase reverse transcriptase (hTERT) to create immortalized sheep trophoblast cell line (hTERT-STCs). hTERT-STCs showed a stable expression of hTERT gene, serially passaged for a year, and showed active proliferation without signs of senescence. Cytokeratin 7 (CK-7), secreted human chorionic gonadotrophin subunit β (CG-β), placental lactogen (PL), and endogenous jaagsiekte sheep retrovirus (enJSRV) envelope genes were expressed in hTERT-STCs. Transwell cell invasion assay indicated that hTERT-STCs still possessed the same invasive characteristics as normal primary sheep trophoblast cells. hTERT-STCs could not grow in soft agar and did not develop into tumors in nude mice. In this study, we established a strain of immortalized sheep trophoblast cell line which could be gainfully employed in the future as an experimental model to study trophoblast cells with secretory function, invasive features, and probable biological function of enJSRV envelope genes.
url http://dx.doi.org/10.1155/2016/5808575
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AT shuyingliu establishmentandcharacterizationofatelomeraseimmortalizedsheeptrophoblastcellline
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