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Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L

Organogenesis and tissue development occur through sequential stepwise processes leading to increased lineage restriction and loss of pluripotency. An exception to this appears in the adult human breast, where rare variant epithelial cells exhibit pluripotency and multilineage differentiation potent...

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Autores principales: Breindel, Jerrica L., Skibinski, Adam, Sedic, Maja, Wronski-Campos, Ania, Zhou, Wenhui, Keller, Patricia J., Mills, Joslyn, Bradner, James, Onder, Tamer, Kuperwasser, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599181/
https://www.ncbi.nlm.nih.gov/pubmed/28781076
http://dx.doi.org/10.1016/j.stemcr.2017.06.019
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author Breindel, Jerrica L.
Skibinski, Adam
Sedic, Maja
Wronski-Campos, Ania
Zhou, Wenhui
Keller, Patricia J.
Mills, Joslyn
Bradner, James
Onder, Tamer
Kuperwasser, Charlotte
author_facet Breindel, Jerrica L.
Skibinski, Adam
Sedic, Maja
Wronski-Campos, Ania
Zhou, Wenhui
Keller, Patricia J.
Mills, Joslyn
Bradner, James
Onder, Tamer
Kuperwasser, Charlotte
author_sort Breindel, Jerrica L.
collection PubMed
description Organogenesis and tissue development occur through sequential stepwise processes leading to increased lineage restriction and loss of pluripotency. An exception to this appears in the adult human breast, where rare variant epithelial cells exhibit pluripotency and multilineage differentiation potential when removed from the signals of their native microenvironment. This phenomenon provides a unique opportunity to study mechanisms that lead to cellular reprogramming and lineage plasticity in real time. Here, we show that primary human mammary epithelial cells (HMECs) lose expression of differentiated mammary epithelial markers in a manner dependent on paracrine factors and epigenetic regulation. Furthermore, we demonstrate that HMEC reprogramming is dependent on gene silencing by the DNA methyltransferase DNMT3A and loss of histone transcriptional marks following downregulation of the methyltransferase DOT1L. These results demonstrate that lineage commitment in adult tissues is context dependent and highlight the plasticity of somatic cells when removed from their native tissue microenvironment.
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spelling pubmed-55991812017-09-21 Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L Breindel, Jerrica L. Skibinski, Adam Sedic, Maja Wronski-Campos, Ania Zhou, Wenhui Keller, Patricia J. Mills, Joslyn Bradner, James Onder, Tamer Kuperwasser, Charlotte Stem Cell Reports Article Organogenesis and tissue development occur through sequential stepwise processes leading to increased lineage restriction and loss of pluripotency. An exception to this appears in the adult human breast, where rare variant epithelial cells exhibit pluripotency and multilineage differentiation potential when removed from the signals of their native microenvironment. This phenomenon provides a unique opportunity to study mechanisms that lead to cellular reprogramming and lineage plasticity in real time. Here, we show that primary human mammary epithelial cells (HMECs) lose expression of differentiated mammary epithelial markers in a manner dependent on paracrine factors and epigenetic regulation. Furthermore, we demonstrate that HMEC reprogramming is dependent on gene silencing by the DNA methyltransferase DNMT3A and loss of histone transcriptional marks following downregulation of the methyltransferase DOT1L. These results demonstrate that lineage commitment in adult tissues is context dependent and highlight the plasticity of somatic cells when removed from their native tissue microenvironment. Elsevier 2017-08-03 /pmc/articles/PMC5599181/ /pubmed/28781076 http://dx.doi.org/10.1016/j.stemcr.2017.06.019 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Breindel, Jerrica L.
Skibinski, Adam
Sedic, Maja
Wronski-Campos, Ania
Zhou, Wenhui
Keller, Patricia J.
Mills, Joslyn
Bradner, James
Onder, Tamer
Kuperwasser, Charlotte
Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L
title Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L
title_full Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L
title_fullStr Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L
title_full_unstemmed Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L
title_short Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L
title_sort epigenetic reprogramming of lineage-committed human mammary epithelial cells requires dnmt3a and loss of dot1l
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599181/
https://www.ncbi.nlm.nih.gov/pubmed/28781076
http://dx.doi.org/10.1016/j.stemcr.2017.06.019
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