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Transcriptional and Histological Analyses of the Thymic Developmental Process in the Fetal Pig
The humanized pig model, in which human cells or tissues can be functionally maintained in pigs, can be an invaluable tool for human medical research. Although the recent development of immunodeficient pigs has opened the door for the development of such a model, the efficient engraftment and differ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Association for Laboratory Animal Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160976/ https://www.ncbi.nlm.nih.gov/pubmed/24770647 http://dx.doi.org/10.1538/expanim.63.215 |
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author | Suzuki, Shunichi Suzuki, Misae Nakai, Michiko Sembon, Shoichiro Fuchimoto, Daiichiro Onishi, Akira |
author_facet | Suzuki, Shunichi Suzuki, Misae Nakai, Michiko Sembon, Shoichiro Fuchimoto, Daiichiro Onishi, Akira |
author_sort | Suzuki, Shunichi |
collection | PubMed |
description | The humanized pig model, in which human cells or tissues can be functionally maintained in pigs, can be an invaluable tool for human medical research. Although the recent development of immunodeficient pigs has opened the door for the development of such a model, the efficient engraftment and differentiation of human cells may be difficult to achieve. The transplantation of human cells into fetal pigs, whose immune system is immature, will ameliorate this problem. Therefore, we examined the development of porcine fetal thymus, which is critical for the establishment of the immune system. We first analyzed the levels of mRNA expression of genes that are relevant to the function of thymic epithelial cells or thymocytes in whole thymi from 35 to 85 days of gestation (DG) and at 2 days postpartum (DP) by quantitative RT-PCR. In addition, immunohistochemical analyses of thymic epithelial cells from DG35 to DG55 and DP2 were performed. These analyses showed that the thymic cortex was formed as early as DG35, and thymic medulla gradually developed from DG45 to DG55. These findings suggested that, at least before DG45, the thymus do not differentiate to form fully functional T cells. |
format | Online Article Text |
id | pubmed-4160976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Japanese Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41609762014-10-21 Transcriptional and Histological Analyses of the Thymic Developmental Process in the Fetal Pig Suzuki, Shunichi Suzuki, Misae Nakai, Michiko Sembon, Shoichiro Fuchimoto, Daiichiro Onishi, Akira Exp Anim Original The humanized pig model, in which human cells or tissues can be functionally maintained in pigs, can be an invaluable tool for human medical research. Although the recent development of immunodeficient pigs has opened the door for the development of such a model, the efficient engraftment and differentiation of human cells may be difficult to achieve. The transplantation of human cells into fetal pigs, whose immune system is immature, will ameliorate this problem. Therefore, we examined the development of porcine fetal thymus, which is critical for the establishment of the immune system. We first analyzed the levels of mRNA expression of genes that are relevant to the function of thymic epithelial cells or thymocytes in whole thymi from 35 to 85 days of gestation (DG) and at 2 days postpartum (DP) by quantitative RT-PCR. In addition, immunohistochemical analyses of thymic epithelial cells from DG35 to DG55 and DP2 were performed. These analyses showed that the thymic cortex was formed as early as DG35, and thymic medulla gradually developed from DG45 to DG55. These findings suggested that, at least before DG45, the thymus do not differentiate to form fully functional T cells. Japanese Association for Laboratory Animal Science 2014-04-26 2014 /pmc/articles/PMC4160976/ /pubmed/24770647 http://dx.doi.org/10.1538/expanim.63.215 Text en ©2014 Japanese Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Original Suzuki, Shunichi Suzuki, Misae Nakai, Michiko Sembon, Shoichiro Fuchimoto, Daiichiro Onishi, Akira Transcriptional and Histological Analyses of the Thymic Developmental Process in the Fetal Pig |
title | Transcriptional and Histological Analyses of the Thymic Developmental Process
in the Fetal Pig |
title_full | Transcriptional and Histological Analyses of the Thymic Developmental Process
in the Fetal Pig |
title_fullStr | Transcriptional and Histological Analyses of the Thymic Developmental Process
in the Fetal Pig |
title_full_unstemmed | Transcriptional and Histological Analyses of the Thymic Developmental Process
in the Fetal Pig |
title_short | Transcriptional and Histological Analyses of the Thymic Developmental Process
in the Fetal Pig |
title_sort | transcriptional and histological analyses of the thymic developmental process
in the fetal pig |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160976/ https://www.ncbi.nlm.nih.gov/pubmed/24770647 http://dx.doi.org/10.1538/expanim.63.215 |
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