quantitative analysis of the effect of cancer invasiveness and collagen concentration on 3d matrix remodeling定量分析的影响癌症侵袭性和胶原蛋白浓度在3 d矩阵重构.pdfVIP

quantitative analysis of the effect of cancer invasiveness and collagen concentration on 3d matrix remodeling定量分析的影响癌症侵袭性和胶原蛋白浓度在3 d矩阵重构.pdf

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quantitative analysis of the effect of cancer invasiveness and collagen concentration on 3d matrix remodeling定量分析的影响癌症侵袭性和胶原蛋白浓度在3 d矩阵重构

Quantitative Analysis of the Effect of Cancer Invasiveness and Collagen Concentration on 3D Matrix Remodeling Dewi Harjanto, Joseph S. Maffei, Muhammad H. Zaman* Department of Biomedical Engineering, Boston University, Boston, Massachusetts, United States of America Abstract Extracellular matrix (ECM) remodeling is a key component of cell migration and tumor metastasis, and has been associated with cancer progression. Despite the importance of matrix remodeling, systematic and quantitative studies on the process have largely been lacking. Furthermore, it remains unclear if the disrupted tensional homeostasis characteristic of malignancy is due to initially altered ECM and tissue properties, or to the alteration of the tissue by tumor cells. To explore these questions, we studied matrix remodeling by two different prostate cancer cell lines in a three-dimensional collagen system. Over one week, we monitored structural changes in gels of varying collagen content using confocal reflection microscopy and quantitative image analysis, tracking metrics of fibril fraction, pore size, and fiber length and diameter. Gels that were seeded with no cells (control), LNCaP cells, and DU-145 cells were quantitatively compared. Gels with higher collagen content initially had smaller pore sizes and higher fibril fractions, as expected. However, over time, LNCaP- and DU- 145-populated matrices showed different structural properties compared both to each other and to the control gels, with LNCaP cells appearing to favor microenvironments with lower collagen fiber fractions and larger pores than DU-145 cells. We posit that the DU-145 cells’ preference for denser matrices is due to their higher invasiveness and proteolytic capabilities. Inhibition of matrix proteases resulted in reduced fibr

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