کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8456947 | 1548787 | 2017 | 13 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Stromal PDGFR-α Activation Enhances Matrix Stiffness, Impedes Mammary Ductal Development, and Accelerates Tumor Growth
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کلمات کلیدی
ECMAFMTFMCAFsLSLH&E - H & EHyaluronic acid - اسید هیالورونیکCancer-associated fibroblasts - فیبروبلاست های مرتبط با سرطانExtracellular matrix - ماتریکس خارج سلولیatomic force microscopy - میکروسکوپ نیروی اتمیTraction force microscopy - میکروسکوپ نیروی کششیHematoxylin and Eosin - هماتوکسیلین و ائوزین
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
تحقیقات سرطان
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
The extracellular matrix (ECM) is critical for mammary ductal development and differentiation, but how mammary fibroblasts regulate ECM remodeling remains to be elucidated. Herein, we used a mouse genetic model to activate platelet derived growth factor receptor-alpha (PDGFRα) specifically in the stroma. Hyperactivation of PDGFRα in the mammary stroma severely hindered pubertal mammary ductal morphogenesis, but did not interrupt the lobuloalveolar differentiation program. Increased stromal PDGFRα signaling induced mammary fat pad fibrosis with a corresponding increase in interstitial hyaluronic acid (HA) and collagen deposition. Mammary fibroblasts with PDGFRα hyperactivation also decreased hydraulic permeability of a collagen substrate in an in vitro microfluidic device assay, which was mitigated by inhibition of either PDGFRα or HA. Fibrosis seen in this model significantly increased the overall stiffness of the mammary gland as measured by atomic force microscopy. Further, mammary tumor cells injected orthotopically in the fat pads of mice with stromal activation of PDGFRα grew larger tumors compared to controls. Taken together, our data establish that aberrant stromal PDGFRα signaling disrupts ECM homeostasis during mammary gland development, resulting in increased mammary stiffness and increased potential for tumor growth.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neoplasia - Volume 19, Issue 6, June 2017, Pages 496-508
Journal: Neoplasia - Volume 19, Issue 6, June 2017, Pages 496-508
نویسندگان
Anisha M. Hammer, Gina M. Sizemore, Vasudha C. Shukla, Alex Avendano, Steven T. Sizemore, Jonathan J. Chang, Raleigh D. Kladney, Maria C. Cuitiño, Katie A. Thies, Quinn Verfurth, Arnab Chakravarti, Lisa D. Yee, Gustavo Leone, Jonathan W. Song,