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. 2024 May 2;76(4):483–502. doi: 10.1007/s10616-024-00630-5

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — Composition of different cardiac models, co-culture variations and the endpoint analyses used in the study. Cardiomyocyte controls were plated as 2D monoculture on top of thin 0.1% gelatin coating or as 3D monoculture on top of gellan gum-gelatin hydrogel. Vascular co-cultures (ASC + EC), cardiovascular multiculture (ASC + CM + EC) and myocardial co-culture (ASC + CM) were formed in 3D in gellan gum-gelatin hydrogel