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.
Laura Paz-ArtigasSandra González-LanaNicolás PoloPedro VicentePilar Montero-CalleMiguel A MartínezGregorio RábagoMargarida SerraFelipe PrósperManuel M MazoArantxa GonzálezIgnacio OchoaJose Luis PedrazPublished in: ACS biomaterials science & engineering (2024)
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.
Keyphrases
- induced pluripotent stem cells
- left ventricular
- endothelial cells
- induced apoptosis
- high glucose
- ischemia reperfusion injury
- healthcare
- primary care
- stem cells
- cell cycle arrest
- neuropathic pain
- systemic sclerosis
- high throughput
- emergency department
- idiopathic pulmonary fibrosis
- pluripotent stem cells
- heart failure
- cell death
- cerebral ischemia
- endoplasmic reticulum stress
- cell proliferation
- subarachnoid hemorrhage
- atrial fibrillation
- human health
- brain injury