Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/173110
Título: Generation of Self-Induced Myocardial Ischemia in Large-Sized Cardiac Spheroids without Alteration of Environmental Conditions Recreates Fibrotic Remodeling and Tissue Stiffening Revealed by Constriction Assays
Autor: Paz-Artigas, Laura
González-Lana, Sandra
Polo, Nicolás
Vicente, Pedro
Montero-Calle, Pilar
Martínez, Miguel A.
Rábago, Gregorio
Serra, Margarida
Prósper, Felipe
Mazo, Manuel M.
González, Arantxa
Ochoa, Ignacio
Ciriza, Jesús
Palavras-chave: cardiac spheroid
fibrosis
hiPCS-CM
myocardial ischemia
stiffness
Biomaterials
Biomedical Engineering
Data: 17-Jan-2024
Resumo: A combination of human-induced pluripotent stem cells (hiPSCs) and 3D microtissue culture techniques allows the generation of models that recapitulate the cardiac microenvironment for preclinical research of new treatments. In particular, spheroids represent the simplest approach to culture cells in 3D and generate gradients of cellular access to the media, mimicking the effects of an ischemic event. However, previous models required incubation under low oxygen conditions or deprived nutrient media to recreate ischemia. Here, we describe the generation of large spheroids (i.e., larger than 500 μm diameter) that self-induce an ischemic core. Spheroids were generated by coculture of cardiomyocytes derived from hiPSCs (hiPSC-CMs) and primary human cardiac fibroblast (hCF). In the proper medium, cells formed aggregates that generated an ischemic core 2 days after seeding. Spheroids also showed spontaneous cellular reorganization after 10 days, with hiPSC-CMs located at the center and surrounded by hCFs. This led to an increase in microtissue stiffness, characterized by the implementation of a constriction assay. All in all, these phenomena are hints of the fibrotic tissue remodeling secondary to a cardiac ischemic event, thus demonstrating the suitability of these spheroids for the modeling of human cardiac ischemia and its potential application for new treatments and drug research.
Descrição: Funding Information: This work has been supported by the European Union’s H2020 research and innovation programme under grant agreements No 829010 (PRIME H2020-FETOPEN-2018-2019-2020-01), 778354 (CISTEM H2020-MSCA-RISE-201), 874827 (BRAV∃), and 848109 (CRUCIAL); Instituto de Salud Carlos III cofinanced by European Regional Development Fund-FEDER “A way to make Europe” PI19/01350, PI21/00946 and CB16/11/00483; MCIN/AEI/10.13039/501100011033/ADVANCE (PID2022-139859OB-I00) and MCIN CARDIOPRINT (PLEC2021-008127); Gobierno de Navarra Proyectos Estratégicos IMPRIMED (0011-1411-2021-000096) and BIOHEART (0011-1411-2022-000071) and Gobierno de Navarra Proyectos Colaborativos BIOGEN (PC020-021-022). The regional Government of Aragon provided L.P. studentship. Publisher Copyright: © 2024 The Authors. Published by American Chemical Society.
Peer review: yes
URI: http://hdl.handle.net/10362/173110
DOI: https://doi.org/10.1021/acsbiomaterials.3c01302
ISSN: 2373-9878
Aparece nas colecções:Home collection (ITQB)

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