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Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes

Immortalized cell lines are valuable resources to expand the molecular characterization of major histocompatibility complex genes and their presented antigens. We generated a panel of immortalized cell lines by transfecting human telomerase reverse transcriptase (hTERT) into primary fibroblast cells...

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Autores principales: Le, Quy Van Chanh, Youk, SeungYeon, Choi, Munjeong, Jeon, Hyoim, Kim, Won-Il, Ho, Chak-Sum, Park, Chankyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8859410/
https://www.ncbi.nlm.nih.gov/pubmed/35198008
http://dx.doi.org/10.3389/fgene.2022.815328
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author Le, Quy Van Chanh
Youk, SeungYeon
Choi, Munjeong
Jeon, Hyoim
Kim, Won-Il
Ho, Chak-Sum
Park, Chankyu
author_facet Le, Quy Van Chanh
Youk, SeungYeon
Choi, Munjeong
Jeon, Hyoim
Kim, Won-Il
Ho, Chak-Sum
Park, Chankyu
author_sort Le, Quy Van Chanh
collection PubMed
description Immortalized cell lines are valuable resources to expand the molecular characterization of major histocompatibility complex genes and their presented antigens. We generated a panel of immortalized cell lines by transfecting human telomerase reverse transcriptase (hTERT) into primary fibroblast cells prepared from ear, fetal, and lung tissues of 10 pigs from five breeds and successfully cultured them for 30–45 passages. The cell growth characteristic of the immortalized fibroblasts was similar to that of primary fibroblast, which was unable to form colonies on soft agar. The genotypes of major swine leukocyte antigen (SLA) genes, including three classical class I (SLA-1, -2, and -3) and three class II genes (DQB1, DRB1, and DQA), were determined using high-resolution typing. A total of 58 alleles, including a novel allele for SLA-2, were identified. Each cell line was unique. A cell line derived from a National Institutes of Health miniature pig was homozygous across the six major SLA genes. The expression levels of SLA classical class I genes varied among the cell lines and were slightly upregulated in the immortalized compared to the primary cells based on semiquantitative reverse transcription polymerase chain reaction. The immortalized porcine fibroblast cell lines with diverse SLA haplotypes that were developed in this study have potential to be applied in studies regarding the molecular characteristics and genetic structure of SLA genes and epitope–major histocompatibility complex interactions in pigs.
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spelling pubmed-88594102022-02-22 Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes Le, Quy Van Chanh Youk, SeungYeon Choi, Munjeong Jeon, Hyoim Kim, Won-Il Ho, Chak-Sum Park, Chankyu Front Genet Genetics Immortalized cell lines are valuable resources to expand the molecular characterization of major histocompatibility complex genes and their presented antigens. We generated a panel of immortalized cell lines by transfecting human telomerase reverse transcriptase (hTERT) into primary fibroblast cells prepared from ear, fetal, and lung tissues of 10 pigs from five breeds and successfully cultured them for 30–45 passages. The cell growth characteristic of the immortalized fibroblasts was similar to that of primary fibroblast, which was unable to form colonies on soft agar. The genotypes of major swine leukocyte antigen (SLA) genes, including three classical class I (SLA-1, -2, and -3) and three class II genes (DQB1, DRB1, and DQA), were determined using high-resolution typing. A total of 58 alleles, including a novel allele for SLA-2, were identified. Each cell line was unique. A cell line derived from a National Institutes of Health miniature pig was homozygous across the six major SLA genes. The expression levels of SLA classical class I genes varied among the cell lines and were slightly upregulated in the immortalized compared to the primary cells based on semiquantitative reverse transcription polymerase chain reaction. The immortalized porcine fibroblast cell lines with diverse SLA haplotypes that were developed in this study have potential to be applied in studies regarding the molecular characteristics and genetic structure of SLA genes and epitope–major histocompatibility complex interactions in pigs. Frontiers Media S.A. 2022-02-07 /pmc/articles/PMC8859410/ /pubmed/35198008 http://dx.doi.org/10.3389/fgene.2022.815328 Text en Copyright © 2022 Le, Youk, Choi, Jeon, Kim, Ho and Park. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Le, Quy Van Chanh
Youk, SeungYeon
Choi, Munjeong
Jeon, Hyoim
Kim, Won-Il
Ho, Chak-Sum
Park, Chankyu
Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes
title Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes
title_full Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes
title_fullStr Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes
title_full_unstemmed Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes
title_short Development of an Immortalized Porcine Fibroblast Cell Panel With Different Swine Leukocyte Antigen Genotypes
title_sort development of an immortalized porcine fibroblast cell panel with different swine leukocyte antigen genotypes
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8859410/
https://www.ncbi.nlm.nih.gov/pubmed/35198008
http://dx.doi.org/10.3389/fgene.2022.815328
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