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Expression of Oncofetal Antigen 5T4 in Murine Taste Papillae

Background: Multicellular taste buds located within taste papillae on the tongue mediate taste sensation. In taste papillae, taste bud cells (TBCs), such as taste receptor cells and taste precursor cells, and the surrounding lingual epithelium including epithelial progenitors (also called taste stem...

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Autores principales: Takahashi, Yuka, Takahashi, Hiroo, Stern, Peter L., Kirita, Tadaaki, Tsuboi, Akio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685444/
https://www.ncbi.nlm.nih.gov/pubmed/31417363
http://dx.doi.org/10.3389/fncel.2019.00343
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author Takahashi, Yuka
Takahashi, Hiroo
Stern, Peter L.
Kirita, Tadaaki
Tsuboi, Akio
author_facet Takahashi, Yuka
Takahashi, Hiroo
Stern, Peter L.
Kirita, Tadaaki
Tsuboi, Akio
author_sort Takahashi, Yuka
collection PubMed
description Background: Multicellular taste buds located within taste papillae on the tongue mediate taste sensation. In taste papillae, taste bud cells (TBCs), such as taste receptor cells and taste precursor cells, and the surrounding lingual epithelium including epithelial progenitors (also called taste stem/progenitor cells) are maintained by continuous cell turnover throughout life. However, it remains unknown how the cells constituting taste buds proliferate and differentiate to maintain taste bud tissue. Based on in situ hybridization (ISH) screening, we demonstrated that the oncofetal antigen 5T4 (also known as trophoblast glycoprotein: TPBG) gene is expressed in the adult mouse tongue. Results: In immunohistochemistry of coronal tongue sections, 5T4 protein was detected at a low level exclusively in the basal part of the lingual epithelium in developing and adult mice, and at a high level particularly in foliate papillae and circumvallate papillae (CVPs). Furthermore, immunohistochemistry of the basal part of CVPs indicated that the proliferation marker PCNA (proliferating cell nuclear antigen) co-localized with 5T4. 5T4 was strongly expressed in Krt5(+) epithelial progenitors and Shh(+) taste precursor cells, but weakly in mature taste receptor cells. The number of proliferating cells in the CVP was higher in 5T4-knockout mice than in wild-type (WT) mice, while neither cell differentiation nor the size of taste buds differed between these two groups of mice. Notably, X-ray irradiation enhanced cell proliferation more in 5T4-knockout mice than in WT mice. Conclusion: Our results suggest that 5T4, expressed in epithelial progenitors (taste stem/progenitor cells), and taste precursor cells, may influence the maintenance of taste papillae under both normal and injury conditions.
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spelling pubmed-66854442019-08-15 Expression of Oncofetal Antigen 5T4 in Murine Taste Papillae Takahashi, Yuka Takahashi, Hiroo Stern, Peter L. Kirita, Tadaaki Tsuboi, Akio Front Cell Neurosci Neuroscience Background: Multicellular taste buds located within taste papillae on the tongue mediate taste sensation. In taste papillae, taste bud cells (TBCs), such as taste receptor cells and taste precursor cells, and the surrounding lingual epithelium including epithelial progenitors (also called taste stem/progenitor cells) are maintained by continuous cell turnover throughout life. However, it remains unknown how the cells constituting taste buds proliferate and differentiate to maintain taste bud tissue. Based on in situ hybridization (ISH) screening, we demonstrated that the oncofetal antigen 5T4 (also known as trophoblast glycoprotein: TPBG) gene is expressed in the adult mouse tongue. Results: In immunohistochemistry of coronal tongue sections, 5T4 protein was detected at a low level exclusively in the basal part of the lingual epithelium in developing and adult mice, and at a high level particularly in foliate papillae and circumvallate papillae (CVPs). Furthermore, immunohistochemistry of the basal part of CVPs indicated that the proliferation marker PCNA (proliferating cell nuclear antigen) co-localized with 5T4. 5T4 was strongly expressed in Krt5(+) epithelial progenitors and Shh(+) taste precursor cells, but weakly in mature taste receptor cells. The number of proliferating cells in the CVP was higher in 5T4-knockout mice than in wild-type (WT) mice, while neither cell differentiation nor the size of taste buds differed between these two groups of mice. Notably, X-ray irradiation enhanced cell proliferation more in 5T4-knockout mice than in WT mice. Conclusion: Our results suggest that 5T4, expressed in epithelial progenitors (taste stem/progenitor cells), and taste precursor cells, may influence the maintenance of taste papillae under both normal and injury conditions. Frontiers Media S.A. 2019-07-31 /pmc/articles/PMC6685444/ /pubmed/31417363 http://dx.doi.org/10.3389/fncel.2019.00343 Text en Copyright © 2019 Takahashi, Takahashi, Stern, Kirita and Tsuboi. http://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 Neuroscience
Takahashi, Yuka
Takahashi, Hiroo
Stern, Peter L.
Kirita, Tadaaki
Tsuboi, Akio
Expression of Oncofetal Antigen 5T4 in Murine Taste Papillae
title Expression of Oncofetal Antigen 5T4 in Murine Taste Papillae
title_full Expression of Oncofetal Antigen 5T4 in Murine Taste Papillae
title_fullStr Expression of Oncofetal Antigen 5T4 in Murine Taste Papillae
title_full_unstemmed Expression of Oncofetal Antigen 5T4 in Murine Taste Papillae
title_short Expression of Oncofetal Antigen 5T4 in Murine Taste Papillae
title_sort expression of oncofetal antigen 5t4 in murine taste papillae
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685444/
https://www.ncbi.nlm.nih.gov/pubmed/31417363
http://dx.doi.org/10.3389/fncel.2019.00343
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