TY - JOUR
T1 - Biologically-Inspired Melt Electrowriting for the Generation of Highly Biomimetic Functional Myocardium
AU - Iglesias-Garcia, Olalla
AU - Flandes-Iparraguirre, Maria
AU - Montero-Calle, Pilar
AU - Rosales, Ricardo M.
AU - Ullate-Agote, Asier
AU - Sanchez-Bueno, Andrea
AU - Larequi, Eduardo
AU - Anaut-Lusar, Ilazki
AU - Laita, Nicolas
AU - Olivan-Viguera, Aida
AU - Iglesias, Elena
AU - Abizanda, Gloria
AU - San Martin-Uriz, Patxi
AU - Aguirre-Ruiz, Paula
AU - Aranguren, Xabier L.
AU - de Yebenes, Manuel Garcia
AU - Gavira, Juan Jose
AU - Martinez, Miguel Angel
AU - Pena, Estefania
AU - Doblare, Manuel
AU - de-Juan-Pardo, Elena M.
AU - Pueyo, Esther
AU - Prosper, Felipe
AU - Vega, Manuel M. Mazo
PY - 2025/8/14
Y1 - 2025/8/14
N2 - In the heart, the specific 3D structure of myocardial layers produces an efficient ejection of blood. When myocardial infarction strikes, this architecture is disrupted, adding a disarranged contraction to the decreased availability of pumping units (cardiomyocytes, CMs). In this work, the alignment of cardiac fibers in a large animal model (pig) is characterized and employ melt electrowriting (MEW) to fabricate a bio-inspired scaffold with diamond-shaped pores. Using human-induced pluripotent stem cell-derived CMs and cardiac fibroblasts, human cardiac tissues with a biomimetic in-plane contraction are generated. MEW-diamond tissues beat macroscopically for over 1 month, with significantly faster kinetics, increased force, and higher conduction velocity than those based on square or rectangular pores. The diamond design induces a specific hiPSC-CM alignment resulting in the observed in-plane contraction. Transcriptomic analysis using bulk RNA-seq reveals diamond-MEW tissues present features of maturation as compared to traditional 2D cultures. Finally, the bio-inspired cardiac tissues are employed to treat an infarction model in athymic rats, showing a significant benefit on systolic function and remodeling, tied to the presence of large grafts of human cells remuscularizing the ventricular wall. All in all, it is demonstrated that the new design generates superior human cardiac tissues with therapeutic capacity.
AB - In the heart, the specific 3D structure of myocardial layers produces an efficient ejection of blood. When myocardial infarction strikes, this architecture is disrupted, adding a disarranged contraction to the decreased availability of pumping units (cardiomyocytes, CMs). In this work, the alignment of cardiac fibers in a large animal model (pig) is characterized and employ melt electrowriting (MEW) to fabricate a bio-inspired scaffold with diamond-shaped pores. Using human-induced pluripotent stem cell-derived CMs and cardiac fibroblasts, human cardiac tissues with a biomimetic in-plane contraction are generated. MEW-diamond tissues beat macroscopically for over 1 month, with significantly faster kinetics, increased force, and higher conduction velocity than those based on square or rectangular pores. The diamond design induces a specific hiPSC-CM alignment resulting in the observed in-plane contraction. Transcriptomic analysis using bulk RNA-seq reveals diamond-MEW tissues present features of maturation as compared to traditional 2D cultures. Finally, the bio-inspired cardiac tissues are employed to treat an infarction model in athymic rats, showing a significant benefit on systolic function and remodeling, tied to the presence of large grafts of human cells remuscularizing the ventricular wall. All in all, it is demonstrated that the new design generates superior human cardiac tissues with therapeutic capacity.
KW - Advanced function
KW - Aligned contraction
KW - Cardiac tissue engineering
KW - hiPSCs
KW - Melt electrowriting
KW - Myocardial infarction
KW - Myocardial regeneration
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=uwapure5-25&SrcAuth=WosAPI&KeyUT=WOS:001470299700001&DestLinkType=FullRecord&DestApp=WOS_CPL
UR - https://www.scopus.com/pages/publications/105005196794
U2 - 10.1002/adfm.202420106
DO - 10.1002/adfm.202420106
M3 - Article
SN - 1616-301X
VL - 35
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 33
M1 - 2420106
ER -