دورية أكاديمية

3D bioprinted aged human post‐infarct myocardium tissue model

التفاصيل البيبلوغرافية
العنوان: 3D bioprinted aged human post‐infarct myocardium tissue model
المؤلفون: Gozde Basara, Lara Ece Celebi, George Ronan, Victoria Discua Santos, Pinar Zorlutuna
المصدر: Health Science Reports, Vol 7, Iss 4, Pp n/a-n/a (2024)
بيانات النشر: Wiley, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
مصطلحات موضوعية: 3D bioprinting, extracellular vesicles, human induced pluripotent stem cell‐derived cardiac fibroblasts, human induced pluripotent stem cell‐derived cardiomyocyte, myocardial infarction, post‐MI models, Medicine
الوصف: Abstract Background and Aims Fibrotic tissue formed after myocardial infarction (MI) can be as detrimental as MI itself. However, current in vitro cardiac fibrosis models fail to recapitulate the complexities of post‐MI tissue. Moreover, although MI and subsequent fibrosis is most prominent in the aged population, the field suffers from inadequate aged tissue models. Herein, an aged human post‐MI tissue model, representing the native microenvironment weeks after initial infarction, is engineered using three‐dimensional bioprinting via creation of individual bioinks to specifically mimic three distinct regions: remote, border, and scar. Methods The aged post‐MI tissue model is engineered through combination of gelatin methacryloyl, methacrylated hyaluronic acid, aged type I collagen, and photoinitiator at variable concentrations with different cell types, including aged human induced pluripotent stem cell‐derived cardiomyocytes, endothelial cells, cardiac fibroblasts, and cardiac myofibroblasts, by introducing a methodology which utilizes three printheads of the bioprinter to model aged myocardium. Then, using cell‐specific proteins, the cell types that comprised each region are confirmed using immunofluorescence. Next, the beating characteristics are analyzed. Finally, the engineered aged post‐MI tissue model is used as a benchtop platform to assess the therapeutic effects of stem cell‐derived extracellular vesicles on the scar region. Results As a result, high viability (>74%) was observed in each region of the printed model. Constructs demonstrated functional behavior, exhibiting a beating velocity of 6.7 μm/s and a frequency of 0.3 Hz. Finally, the effectiveness of hiPSC‐EV and MSC‐EV treatment was assessed. While hiPSC‐EV treatment showed no significant changes, MSC‐EV treatment notably increased cardiomyocyte beating velocity, frequency, and confluency, suggesting a regenerative potential. Conclusion In conclusion, we envision that our approach of modeling post‐MI aged myocardium utilizing three printheads of the bioprinter may be utilized for various applications in aged cardiac microenvironment modeling and testing novel therapeutics.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2398-8835
العلاقة: https://doaj.org/toc/2398-8835Test
DOI: 10.1002/hsr2.1945
الوصول الحر: https://doaj.org/article/7f7295325d194ac7b3a688044a403904Test
رقم الانضمام: edsdoj.7f7295325d194ac7b3a688044a403904
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23988835
DOI:10.1002/hsr2.1945