کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2070810 1544568 2016 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Engineered heart tissues and induced pluripotent stem cells: Macro- and microstructures for disease modeling, drug screening, and translational studies
ترجمه فارسی عنوان
بافت های قلب مهندسی شده و سلول های بنیادی پلورپوفتون القا شده: ماکرو و ریزساختار برای مدل سازی بیماری ها، غربالگری دارو و مطالعات ترجمه
کلمات کلیدی
بیماری قلب و عروقی، مدل سازی بیماری، غربالگری مواد مخدر، سلول های بنیادی پلوروپتوژن منجر شده، مهندسی بافت
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوتکنولوژی یا زیست‌فناوری
چکیده انگلیسی

Engineered heart tissue has emerged as a personalized platform for drug screening. With the advent of induced pluripotent stem cell (iPSC) technology, patient-specific stem cells can be developed and expanded into an indefinite source of cells. Subsequent developments in cardiovascular biology have led to efficient differentiation of cardiomyocytes, the force-producing cells of the heart. iPSC-derived cardiomyocytes (iPSC-CMs) have provided potentially limitless quantities of well-characterized, healthy, and disease-specific CMs, which in turn has enabled and driven the generation and scale-up of human physiological and disease-relevant engineered heart tissues. The combined technologies of engineered heart tissue and iPSC-CMs are being used to study diseases and to test drugs, and in the process, have advanced the field of cardiovascular tissue engineering into the field of precision medicine. In this review, we will discuss current developments in engineered heart tissue, including iPSC-CMs as a novel cell source. We examine new research directions that have improved the function of engineered heart tissue by using mechanical or electrical conditioning or the incorporation of non-cardiomyocyte stromal cells. Finally, we discuss how engineered heart tissue can evolve into a powerful tool for therapeutic drug testing.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Advanced Drug Delivery Reviews - Volume 96, 15 January 2016, Pages 234–244
نویسندگان
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