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Cell Type- and Sex-Dependent Transcriptome Profiles of Rat Anterior Pituitary Cells

Understanding the physiology and pathology of an organ composed of a variety of cell populations depends critically on genome-wide information on each cell type. Here, we report single-cell transcriptome profiling of over 6,800 freshly dispersed anterior pituitary cells from postpubertal male and fe...

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Autores principales: Fletcher, Patrick A., Smiljanic, Kosara, Maso Prévide, Rafael, Iben, James R., Li, Tianwei, Rokic, Milos B., Sherman, Arthur, Coon, Steven L., Stojilkovic, Stanko S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760010/
https://www.ncbi.nlm.nih.gov/pubmed/31620083
http://dx.doi.org/10.3389/fendo.2019.00623
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author Fletcher, Patrick A.
Smiljanic, Kosara
Maso Prévide, Rafael
Iben, James R.
Li, Tianwei
Rokic, Milos B.
Sherman, Arthur
Coon, Steven L.
Stojilkovic, Stanko S.
author_facet Fletcher, Patrick A.
Smiljanic, Kosara
Maso Prévide, Rafael
Iben, James R.
Li, Tianwei
Rokic, Milos B.
Sherman, Arthur
Coon, Steven L.
Stojilkovic, Stanko S.
author_sort Fletcher, Patrick A.
collection PubMed
description Understanding the physiology and pathology of an organ composed of a variety of cell populations depends critically on genome-wide information on each cell type. Here, we report single-cell transcriptome profiling of over 6,800 freshly dispersed anterior pituitary cells from postpubertal male and female rats. Six pituitary-specific cell types were identified based on known marker genes and characterized: folliculostellate cells and hormone-producing corticotrophs, gonadotrophs, thyrotrophs, somatotrophs, and lactotrophs. Also identified were endothelial and blood cells from the pituitary capillary network. The expression of numerous developmental and neuroendocrine marker genes in both folliculostellate and hormone-producing cells supports that they have a common origin. For several genes, the validity of transcriptome analysis was confirmed by qRT-PCR and single cell immunocytochemistry. Folliculostellate cells exhibit impressive transcriptome diversity, indicating their major roles in production of endogenous ligands and detoxification enzymes, and organization of extracellular matrix. Transcriptome profiles of hormone-producing cells also indicate contributions toward those functions, while also clearly demonstrating their endocrine function. This survey highlights many novel genetic markers contributing to pituitary cell type identity, sexual dimorphism, and function, and points to relationships between hormone-producing and folliculostellate cells.
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spelling pubmed-67600102019-10-16 Cell Type- and Sex-Dependent Transcriptome Profiles of Rat Anterior Pituitary Cells Fletcher, Patrick A. Smiljanic, Kosara Maso Prévide, Rafael Iben, James R. Li, Tianwei Rokic, Milos B. Sherman, Arthur Coon, Steven L. Stojilkovic, Stanko S. Front Endocrinol (Lausanne) Endocrinology Understanding the physiology and pathology of an organ composed of a variety of cell populations depends critically on genome-wide information on each cell type. Here, we report single-cell transcriptome profiling of over 6,800 freshly dispersed anterior pituitary cells from postpubertal male and female rats. Six pituitary-specific cell types were identified based on known marker genes and characterized: folliculostellate cells and hormone-producing corticotrophs, gonadotrophs, thyrotrophs, somatotrophs, and lactotrophs. Also identified were endothelial and blood cells from the pituitary capillary network. The expression of numerous developmental and neuroendocrine marker genes in both folliculostellate and hormone-producing cells supports that they have a common origin. For several genes, the validity of transcriptome analysis was confirmed by qRT-PCR and single cell immunocytochemistry. Folliculostellate cells exhibit impressive transcriptome diversity, indicating their major roles in production of endogenous ligands and detoxification enzymes, and organization of extracellular matrix. Transcriptome profiles of hormone-producing cells also indicate contributions toward those functions, while also clearly demonstrating their endocrine function. This survey highlights many novel genetic markers contributing to pituitary cell type identity, sexual dimorphism, and function, and points to relationships between hormone-producing and folliculostellate cells. Frontiers Media S.A. 2019-09-18 /pmc/articles/PMC6760010/ /pubmed/31620083 http://dx.doi.org/10.3389/fendo.2019.00623 Text en Copyright © 2019 Fletcher, Smiljanic, Maso Prévide, Iben, Li, Rokic, Sherman, Coon and Stojilkovic. 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 Endocrinology
Fletcher, Patrick A.
Smiljanic, Kosara
Maso Prévide, Rafael
Iben, James R.
Li, Tianwei
Rokic, Milos B.
Sherman, Arthur
Coon, Steven L.
Stojilkovic, Stanko S.
Cell Type- and Sex-Dependent Transcriptome Profiles of Rat Anterior Pituitary Cells
title Cell Type- and Sex-Dependent Transcriptome Profiles of Rat Anterior Pituitary Cells
title_full Cell Type- and Sex-Dependent Transcriptome Profiles of Rat Anterior Pituitary Cells
title_fullStr Cell Type- and Sex-Dependent Transcriptome Profiles of Rat Anterior Pituitary Cells
title_full_unstemmed Cell Type- and Sex-Dependent Transcriptome Profiles of Rat Anterior Pituitary Cells
title_short Cell Type- and Sex-Dependent Transcriptome Profiles of Rat Anterior Pituitary Cells
title_sort cell type- and sex-dependent transcriptome profiles of rat anterior pituitary cells
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760010/
https://www.ncbi.nlm.nih.gov/pubmed/31620083
http://dx.doi.org/10.3389/fendo.2019.00623
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