Cargando…
Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia
In the mammary gland, epithelial cells are embedded in a ‘soft' environment and become functionally differentiated in culture when exposed to a laminin-rich extracellular matrix gel. Here, we define the processes by which mammary epithelial cells integrate biochemical and mechanical extracellul...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2569873/ https://www.ncbi.nlm.nih.gov/pubmed/18843297 http://dx.doi.org/10.1038/emboj.2008.206 |
_version_ | 1782160087998005248 |
---|---|
author | Alcaraz, Jordi Xu, Ren Mori, Hidetoshi Nelson, Celeste M Mroue, Rana Spencer, Virginia A Brownfield, Doug Radisky, Derek C Bustamante, Carlos Bissell, Mina J |
author_facet | Alcaraz, Jordi Xu, Ren Mori, Hidetoshi Nelson, Celeste M Mroue, Rana Spencer, Virginia A Brownfield, Doug Radisky, Derek C Bustamante, Carlos Bissell, Mina J |
author_sort | Alcaraz, Jordi |
collection | PubMed |
description | In the mammary gland, epithelial cells are embedded in a ‘soft' environment and become functionally differentiated in culture when exposed to a laminin-rich extracellular matrix gel. Here, we define the processes by which mammary epithelial cells integrate biochemical and mechanical extracellular cues to maintain their differentiated phenotype. We used single cells cultured on top of gels in conditions permissive for β-casein expression using atomic force microscopy to measure the elasticity of the cells and their underlying substrata. We found that maintenance of β-casein expression required both laminin signalling and a ‘soft' extracellular matrix, as is the case in normal tissues in vivo, and biomimetic intracellular elasticity, as is the case in primary mammary epithelial organoids. Conversely, two hallmarks of breast cancer development, stiffening of the extracellular matrix and loss of laminin signalling, led to the loss of β-casein expression and non-biomimetic intracellular elasticity. Our data indicate that tissue-specific gene expression is controlled by both the tissues' unique biochemical milieu and mechanical properties, processes involved in maintenance of tissue integrity and protection against tumorigenesis. |
format | Text |
id | pubmed-2569873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-25698732008-11-07 Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia Alcaraz, Jordi Xu, Ren Mori, Hidetoshi Nelson, Celeste M Mroue, Rana Spencer, Virginia A Brownfield, Doug Radisky, Derek C Bustamante, Carlos Bissell, Mina J EMBO J Article In the mammary gland, epithelial cells are embedded in a ‘soft' environment and become functionally differentiated in culture when exposed to a laminin-rich extracellular matrix gel. Here, we define the processes by which mammary epithelial cells integrate biochemical and mechanical extracellular cues to maintain their differentiated phenotype. We used single cells cultured on top of gels in conditions permissive for β-casein expression using atomic force microscopy to measure the elasticity of the cells and their underlying substrata. We found that maintenance of β-casein expression required both laminin signalling and a ‘soft' extracellular matrix, as is the case in normal tissues in vivo, and biomimetic intracellular elasticity, as is the case in primary mammary epithelial organoids. Conversely, two hallmarks of breast cancer development, stiffening of the extracellular matrix and loss of laminin signalling, led to the loss of β-casein expression and non-biomimetic intracellular elasticity. Our data indicate that tissue-specific gene expression is controlled by both the tissues' unique biochemical milieu and mechanical properties, processes involved in maintenance of tissue integrity and protection against tumorigenesis. Nature Publishing Group 2008-11-05 2008-10-09 /pmc/articles/PMC2569873/ /pubmed/18843297 http://dx.doi.org/10.1038/emboj.2008.206 Text en Copyright © 2008, European Molecular Biology Organization http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits distribution, and reproduction in any medium, provided the original author and source are credited. This licence does not permit commercial exploitation or the creation of derivative works without specific permission. |
spellingShingle | Article Alcaraz, Jordi Xu, Ren Mori, Hidetoshi Nelson, Celeste M Mroue, Rana Spencer, Virginia A Brownfield, Doug Radisky, Derek C Bustamante, Carlos Bissell, Mina J Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia |
title | Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia |
title_full | Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia |
title_fullStr | Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia |
title_full_unstemmed | Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia |
title_short | Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia |
title_sort | laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2569873/ https://www.ncbi.nlm.nih.gov/pubmed/18843297 http://dx.doi.org/10.1038/emboj.2008.206 |
work_keys_str_mv | AT alcarazjordi lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT xuren lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT morihidetoshi lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT nelsoncelestem lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT mrouerana lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT spencervirginiaa lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT brownfielddoug lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT radiskyderekc lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT bustamantecarlos lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia AT bissellminaj lamininandbiomimeticextracellularelasticityenhancefunctionaldifferentiationinmammaryepithelia |