Laminin and biomimetic extracellular elasticity enhance functional differentiation in mammary epithelia

• Jordi Alcaraz ^[1] ; Ren Xu ^[1] ; Hidetoshi Mori ^[1] ; Celeste M Nelson ^[1] ; Rana Mroue ^[1] ; Virginia A Spencer ^[1] ; Doug Brownfield ^[1] ; Derek C Radisky ^[1] ; Carlos Bustamante ^[2] ; Mina J Bissell ^[1]
  1. [1] Lawrence Berkeley National Laboratory

     Lawrence Berkeley National Laboratory

     Estados Unidos

     
  2. [2] Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA; Department of Physics, University of California, Berkeley, CA, USA; Howard Hughes Medical Institute, University of California, Berkeley, CA, USA
• Localización: EMBO journal: European Molecular Biology Organization, ISSN 0261-4189, Vol. 27, Nº. 21, 2008, págs. 2829-2838
• Idioma: inglés
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• Resumen

  • 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.