Cargando…

From Single Cells to Tissues: Interactions between the Matrix and Human Breast Cells in Real Time

BACKGROUND: Mammary gland morphogenesis involves ductal elongation, branching, and budding. All of these processes are mediated by stroma - epithelium interactions. Biomechanical factors, such as matrix stiffness, have been established as important factors in these interactions. For example, epithel...

Descripción completa

Detalles Bibliográficos
Autores principales: Barnes, Clifford, Speroni, Lucia, Quinn, Kyle P., Montevil, Mael, Saetzler, Kurt, Bode-Animashaun, Gbemisola, McKerr, George, Georgakoudi, Irene, Downes, C. Stephen, Sonnenschein, Carlos, Howard, C. Vyvyan, Soto, Ana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972096/
https://www.ncbi.nlm.nih.gov/pubmed/24691468
http://dx.doi.org/10.1371/journal.pone.0093325
_version_ 1782309547029823488
author Barnes, Clifford
Speroni, Lucia
Quinn, Kyle P.
Montevil, Mael
Saetzler, Kurt
Bode-Animashaun, Gbemisola
McKerr, George
Georgakoudi, Irene
Downes, C. Stephen
Sonnenschein, Carlos
Howard, C. Vyvyan
Soto, Ana M.
author_facet Barnes, Clifford
Speroni, Lucia
Quinn, Kyle P.
Montevil, Mael
Saetzler, Kurt
Bode-Animashaun, Gbemisola
McKerr, George
Georgakoudi, Irene
Downes, C. Stephen
Sonnenschein, Carlos
Howard, C. Vyvyan
Soto, Ana M.
author_sort Barnes, Clifford
collection PubMed
description BACKGROUND: Mammary gland morphogenesis involves ductal elongation, branching, and budding. All of these processes are mediated by stroma - epithelium interactions. Biomechanical factors, such as matrix stiffness, have been established as important factors in these interactions. For example, epithelial cells fail to form normal acinar structures in vitro in 3D gels that exceed the stiffness of a normal mammary gland. Additionally, heterogeneity in the spatial distribution of acini and ducts within individual collagen gels suggests that local organization of the matrix may guide morphogenesis. Here, we quantified the effects of both bulk material stiffness and local collagen fiber arrangement on epithelial morphogenesis. RESULTS: The formation of ducts and acini from single cells and the reorganization of the collagen fiber network were quantified using time-lapse confocal microscopy. MCF10A cells organized the surrounding collagen fibers during the first twelve hours after seeding. Collagen fiber density and alignment relative to the epithelial surface significantly increased within the first twelve hours and were a major influence in the shaping of the mammary epithelium. The addition of Matrigel to the collagen fiber network impaired cell-mediated reorganization of the matrix and increased the probability of spheroidal acini rather than branching ducts. The mechanical anisotropy created by regions of highly aligned collagen fibers facilitated elongation and branching, which was significantly correlated with fiber organization. In contrast, changes in bulk stiffness were not a strong predictor of this epithelial morphology. CONCLUSIONS: Localized regions of collagen fiber alignment are required for ductal elongation and branching suggesting the importance of local mechanical anisotropy in mammary epithelial morphogenesis. Similar principles may govern the morphology of branching and budding in other tissues and organs.
format Online
Article
Text
id pubmed-3972096
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-39720962014-04-04 From Single Cells to Tissues: Interactions between the Matrix and Human Breast Cells in Real Time Barnes, Clifford Speroni, Lucia Quinn, Kyle P. Montevil, Mael Saetzler, Kurt Bode-Animashaun, Gbemisola McKerr, George Georgakoudi, Irene Downes, C. Stephen Sonnenschein, Carlos Howard, C. Vyvyan Soto, Ana M. PLoS One Research Article BACKGROUND: Mammary gland morphogenesis involves ductal elongation, branching, and budding. All of these processes are mediated by stroma - epithelium interactions. Biomechanical factors, such as matrix stiffness, have been established as important factors in these interactions. For example, epithelial cells fail to form normal acinar structures in vitro in 3D gels that exceed the stiffness of a normal mammary gland. Additionally, heterogeneity in the spatial distribution of acini and ducts within individual collagen gels suggests that local organization of the matrix may guide morphogenesis. Here, we quantified the effects of both bulk material stiffness and local collagen fiber arrangement on epithelial morphogenesis. RESULTS: The formation of ducts and acini from single cells and the reorganization of the collagen fiber network were quantified using time-lapse confocal microscopy. MCF10A cells organized the surrounding collagen fibers during the first twelve hours after seeding. Collagen fiber density and alignment relative to the epithelial surface significantly increased within the first twelve hours and were a major influence in the shaping of the mammary epithelium. The addition of Matrigel to the collagen fiber network impaired cell-mediated reorganization of the matrix and increased the probability of spheroidal acini rather than branching ducts. The mechanical anisotropy created by regions of highly aligned collagen fibers facilitated elongation and branching, which was significantly correlated with fiber organization. In contrast, changes in bulk stiffness were not a strong predictor of this epithelial morphology. CONCLUSIONS: Localized regions of collagen fiber alignment are required for ductal elongation and branching suggesting the importance of local mechanical anisotropy in mammary epithelial morphogenesis. Similar principles may govern the morphology of branching and budding in other tissues and organs. Public Library of Science 2014-04-01 /pmc/articles/PMC3972096/ /pubmed/24691468 http://dx.doi.org/10.1371/journal.pone.0093325 Text en © 2014 Barnes et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Barnes, Clifford
Speroni, Lucia
Quinn, Kyle P.
Montevil, Mael
Saetzler, Kurt
Bode-Animashaun, Gbemisola
McKerr, George
Georgakoudi, Irene
Downes, C. Stephen
Sonnenschein, Carlos
Howard, C. Vyvyan
Soto, Ana M.
From Single Cells to Tissues: Interactions between the Matrix and Human Breast Cells in Real Time
title From Single Cells to Tissues: Interactions between the Matrix and Human Breast Cells in Real Time
title_full From Single Cells to Tissues: Interactions between the Matrix and Human Breast Cells in Real Time
title_fullStr From Single Cells to Tissues: Interactions between the Matrix and Human Breast Cells in Real Time
title_full_unstemmed From Single Cells to Tissues: Interactions between the Matrix and Human Breast Cells in Real Time
title_short From Single Cells to Tissues: Interactions between the Matrix and Human Breast Cells in Real Time
title_sort from single cells to tissues: interactions between the matrix and human breast cells in real time
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972096/
https://www.ncbi.nlm.nih.gov/pubmed/24691468
http://dx.doi.org/10.1371/journal.pone.0093325
work_keys_str_mv AT barnesclifford fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT speronilucia fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT quinnkylep fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT montevilmael fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT saetzlerkurt fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT bodeanimashaungbemisola fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT mckerrgeorge fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT georgakoudiirene fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT downescstephen fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT sonnenscheincarlos fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT howardcvyvyan fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime
AT sotoanam fromsinglecellstotissuesinteractionsbetweenthematrixandhumanbreastcellsinrealtime