Cargando…
Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing
Aging is closely associated with increased susceptibility to breast cancer, yet there have been limited systematic studies of aging-induced alterations in the mammary gland. Here, we leverage high-throughput single-cell RNA sequencing to generate a detailed transcriptomic atlas of young and aged mur...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898263/ https://www.ncbi.nlm.nih.gov/pubmed/33378681 http://dx.doi.org/10.1016/j.celrep.2020.108566 |
_version_ | 1783653828855332864 |
---|---|
author | Li, Carman Man-Chung Shapiro, Hana Tsiobikas, Christina Selfors, Laura M. Chen, Huidong Rosenbluth, Jennifer Moore, Kaitlin Gupta, Kushali P. Kenneth Gray, G. Oren, Yaara Steinbaugh, Michael J. Guerriero, Jennifer L. Pinello, Luca Regev, Aviv Brugge, Joan S. |
author_facet | Li, Carman Man-Chung Shapiro, Hana Tsiobikas, Christina Selfors, Laura M. Chen, Huidong Rosenbluth, Jennifer Moore, Kaitlin Gupta, Kushali P. Kenneth Gray, G. Oren, Yaara Steinbaugh, Michael J. Guerriero, Jennifer L. Pinello, Luca Regev, Aviv Brugge, Joan S. |
author_sort | Li, Carman Man-Chung |
collection | PubMed |
description | Aging is closely associated with increased susceptibility to breast cancer, yet there have been limited systematic studies of aging-induced alterations in the mammary gland. Here, we leverage high-throughput single-cell RNA sequencing to generate a detailed transcriptomic atlas of young and aged murine mammary tissues. By analyzing epithelial, stromal, and immune cells, we identify age-dependent alterations in cell proportions and gene expression, providing evidence that suggests alveolar maturation and physiological decline. The analysis also uncovers potential pro-tumorigenic mechanisms coupled to the age-associated loss of tumor suppressor function and change in microenvironment. In addition, we identify a rare, age-dependent luminal population co-expressing hormone-sensing and secretory-alveolar lineage markers, as well as two macrophage populations expressing distinct gene signatures, underscoring the complex heterogeneity of the mammary epithelia and stroma. Collectively, this rich single-cell atlas reveals the effects of aging on mammary physiology and can serve as a useful resource for understanding aging-associated cancer risk. |
format | Online Article Text |
id | pubmed-7898263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-78982632021-02-22 Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing Li, Carman Man-Chung Shapiro, Hana Tsiobikas, Christina Selfors, Laura M. Chen, Huidong Rosenbluth, Jennifer Moore, Kaitlin Gupta, Kushali P. Kenneth Gray, G. Oren, Yaara Steinbaugh, Michael J. Guerriero, Jennifer L. Pinello, Luca Regev, Aviv Brugge, Joan S. Cell Rep Article Aging is closely associated with increased susceptibility to breast cancer, yet there have been limited systematic studies of aging-induced alterations in the mammary gland. Here, we leverage high-throughput single-cell RNA sequencing to generate a detailed transcriptomic atlas of young and aged murine mammary tissues. By analyzing epithelial, stromal, and immune cells, we identify age-dependent alterations in cell proportions and gene expression, providing evidence that suggests alveolar maturation and physiological decline. The analysis also uncovers potential pro-tumorigenic mechanisms coupled to the age-associated loss of tumor suppressor function and change in microenvironment. In addition, we identify a rare, age-dependent luminal population co-expressing hormone-sensing and secretory-alveolar lineage markers, as well as two macrophage populations expressing distinct gene signatures, underscoring the complex heterogeneity of the mammary epithelia and stroma. Collectively, this rich single-cell atlas reveals the effects of aging on mammary physiology and can serve as a useful resource for understanding aging-associated cancer risk. 2020-12-29 /pmc/articles/PMC7898263/ /pubmed/33378681 http://dx.doi.org/10.1016/j.celrep.2020.108566 Text en This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Carman Man-Chung Shapiro, Hana Tsiobikas, Christina Selfors, Laura M. Chen, Huidong Rosenbluth, Jennifer Moore, Kaitlin Gupta, Kushali P. Kenneth Gray, G. Oren, Yaara Steinbaugh, Michael J. Guerriero, Jennifer L. Pinello, Luca Regev, Aviv Brugge, Joan S. Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing |
title | Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing |
title_full | Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing |
title_fullStr | Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing |
title_full_unstemmed | Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing |
title_short | Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing |
title_sort | aging-associated alterations in mammary epithelia and stroma revealed by single-cell rna sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898263/ https://www.ncbi.nlm.nih.gov/pubmed/33378681 http://dx.doi.org/10.1016/j.celrep.2020.108566 |
work_keys_str_mv | AT licarmanmanchung agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT shapirohana agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT tsiobikaschristina agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT selforslauram agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT chenhuidong agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT rosenbluthjennifer agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT moorekaitlin agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT guptakushalip agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT kennethgrayg agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT orenyaara agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT steinbaughmichaelj agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT guerrierojenniferl agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT pinelloluca agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT regevaviv agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing AT bruggejoans agingassociatedalterationsinmammaryepitheliaandstromarevealedbysinglecellrnasequencing |