کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2077392 1079705 2014 14 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Expandable Megakaryocyte Cell Lines Enable Clinically Applicable Generation of Platelets from Human Induced Pluripotent Stem Cells
ترجمه فارسی عنوان
خطوط سلولهای مگاکاریوسیت قابل انعطاف باعث تولید پلاکت های بالینی از سلول های بنیادی پلوروپتوژن منجر به انسداد بالینی می شود
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوتکنولوژی یا زیست‌فناوری
چکیده انگلیسی


• Expandable megakaryocyte progenitors were established from human PSCs
• BMI1 and BCL-XL suppress senescence and apoptosis induced by c-MYC in imMKCLs
• imMKCLs differentiate into mature megakaryocytes and release functional platelets
• Rapid and efficient platelet yield provides key advantages for clinical application

SummaryThe donor-dependent supply of platelets is frequently insufficient to meet transfusion needs. To address this issue, we developed a clinically applicable strategy for the derivation of functional platelets from human pluripotent stem cells (PSCs). This approach involves the establishment of stable immortalized megakaryocyte progenitor cell lines (imMKCLs) from PSC-derived hematopoietic progenitors through the overexpression of BMI1 and BCL-XL to respectively suppress senescence and apoptosis and the constrained overexpression of c-MYC to promote proliferation. The resulting imMKCLs can be expanded in culture over extended periods (4–5 months), even after cryopreservation. Halting the overexpression of c-MYC, BMI1, and BCL-XL in growing imMKCLs led to the production of CD42b+ platelets with functionality comparable to that of native platelets on the basis of a range of assays in vitro and in vivo. The combination of robust expansion capacity and efficient platelet production means that appropriately selected imMKCL clones represent a potentially inexhaustible source of hPSC-derived platelets for clinical application.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: - Volume 14, Issue 4, 3 April 2014, Pages 535–548
نویسندگان
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