Increased extracellular matrix density decreases MCF10A breast cell acinus formation in 3D culture conditions. (12th February 2013)

• Record Type: Journal Article
• Authors: Lance, Amanda; Yang, Chih‐Chao; Swamydas, Muthulekha; Dean, Delphine; Deitch, Sandy; Burg, Karen J. L.; Dréau, Didier
• Is Part Of: Journal of tissue engineering and regenerative medicine. Volume 10:Number 1(2016)
• Page Start: 71
• Page End: 80
• Publication Date: 2013-02-12
• Subjects: acinus -- ß‐casein -- breast -- collagen -- density -- E‐cadherin -- extracellular matrix -- laminin -- MMP14 -- tensile strength; Tissue engineering -- Periodicals; Regeneration (Biology) -- Periodicals; 610.28
• DOI: 10.1002/term.1675
• Languages: English
• ISSNs: 1932-6254

Abstract

Abstract: The extracellular matrix (ECM) contributes to the generation and dynamic of normal breast tissue, in particular to the generation of polarized acinar and ductal structures. In vitro 3D culture conditions, including variations in the composition of the ECM, have been shown to directly influence the formation and organization of acinus‐like and duct‐like structures. Furthermore, the density of the ECM appears to also play a role in the normal mammary tissue and tumour formation. Here we show that the density of the ECM directly influences the number, organization and function of breast acini. Briefly, non‐malignant human breast MCF10A cells were incubated in increasing densities of a Matrigel®–collagen I matrix. Elastic moduli near and distant to the acinus structures were measured by atomic force microscopy, and the number of acinus structures was determined. Immunochemistry was used to investigate the expression levels of E‐cadherin, laminin, matrix metalloproteinase‐14 and ß ‐casein in MCF10A cells. The modulus of the ECM was significantly increased near the acinus structures and the number of acinus structures decreased with the increase in Matrigel–collagen I density. As evaluated by the expression of laminin, the organization of the acinus structures present was altered as the density of the ECM increased. Increases in both E‐cadherin and MMP14 expression by MCF10A cells as ECM density increased were also observed. In contrast, MCF10A cells expressed lower ß ‐casein levels as the ECM density increased. Taken together, these observations highlight the key role of ECM density in modulating the number, organization and function of breast acini. Copyright © 2013 John Wiley & Sons, Ltd.