# A New Cardiac Decellularized Extracellular Matrix (dECM)-Based Hydrogel: From Its Development with a Standardized Myocardial Decellularization Procedure to In Vitro Model Applications

**Authors:** Giacomo Bernava, Martina Boaron, Golnar Abdalvand, Massimo Marchesan, Francesco Tona, Giovanni Civieri, Isabella Bondani, Gianluca Bacchiega, Laura Iop

PMC · DOI: 10.3390/gels12020115 · Gels · 2026-01-28

## TL;DR

A new hydrogel made from pig heart tissue is developed to better mimic the heart's environment for studying diseases and testing drugs.

## Contribution

A novel cardiac dECM-based hydrogel is developed using a standardized decellularization procedure with reproducible properties and biocompatibility.

## Key findings

- The dECM hydrogel preserved extracellular matrix proteins and effectively removed cellular components.
- The hydrogel supported high cell viability and proliferation in both 2.5D and 3D in vitro models.
- It is a promising platform for cardiac tissue engineering and cardiotoxicity screening.

## Abstract

Cardiovascular diseases remain the leading cause of mortality worldwide, underscoring the urgent need for reliable in vitro models that recapitulate the complexity of the native myocardium. Conventional two-dimensional (2D) cultures lack structural and biochemical complexity, whereas in vivo models are costly, raise ethical concerns, and have poor translational potential. In this study, we developed a novel hydrogel scaffold derived from decellularized porcine ventricular myocardium (dECM). A newly optimized decellularization strategy effectively removed cellular and nuclear components while preserving essential extracellular matrix proteins. The dECM-based hydrogel exhibited reproducible self-crosslinking, gelation kinetics, and stability. Cytocompatibility assays using human bone marrow-derived mesenchymal stem cells demonstrated excellent viability and proliferation upon contact with the biomaterial. Multidimensional hydrogel applications (2.5D and 3D) in vitro revealed higher cell densities than those observed under 2D conditions. Moreover, using human umbilical vein endothelial cells, the dECM-based hydrogel proved to be a valid tool for fabricating cardiovascular in vitro models. As such, this cardiac dECM-based hydrogel is a structurally preserved, biocompatible platform that supports both short- and long-term cell culture. The scaffold has the potential to serve promising applications in cardiac tissue engineering, disease modeling, and cardiotoxicity screening by offering a closer mimicry of the native myocardial environment.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** MYL2 (myosin light chain 2) [NCBI Gene 4633] {aka CMH10, MFM12, MLC-2, MLC-2s/v, MLC-2v, MLC2}, GJA1 (gap junction protein alpha 1) [NCBI Gene 2697] {aka AVSD3, CMDR, CX43, EKVP, EKVP3, GJAL}, MMRN1 (multimerin 1) [NCBI Gene 22915] {aka ECM, EMILIN4, GPIa*, MMRN}, ELN (elastin) [NCBI Gene 2006] {aka ADCL1, SVAS, WBS, WS}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, MYL12B (myosin light chain 12B) [NCBI Gene 103910] {aka MLC-B, MRLC2}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, ACTN1 (actinin alpha 1) [NCBI Gene 87] {aka BDPLT15}, TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}, AGRN (agrin) [NCBI Gene 375790] {aka AGRIN, CMS8, CMSPPD}
- **Diseases:** cardiac disease (MESH:D006331), heart failure (MESH:D006333), Cytotoxicity (MESH:D064420), cerebrovascular disease (MESH:D002561), dECM (MESH:C535509), Cardiovascular disease (MESH:D002318), heart attack (MESH:D009203), death (MESH:D003643), hypertension (MESH:D006973), cardiotoxic (MESH:D066126), stroke (MESH:D020521), angina (MESH:D000787), Hydrogel swelling (MESH:D004487), coronary heart disease (MESH:D003327), muscle relaxant (MESH:D019042), inflammatory (MESH:D007249), injury to (MESH:D014947)
- **Chemicals:** DAPI (MESH:C007293), DMSO (MESH:D004121), valsartan (MESH:D000068756), PBS (MESH:D007854), Eosin (MESH:D004801), Heparin (MESH:D006493), sucrose (MESH:D013395), paraformaldehyde (MESH:C003043), polylactic acid (MESH:C033616), L-glutamine (MESH:D005973), CO2 (MESH:D002245), Tris (MESH:D014325), carbon nanotubes (MESH:D037742), Hematoxylin (MESH:D006416), penicillin (MESH:D010406), bosentan (MESH:D000077300), CellTiter 96  Aqueous One (-), hyaluronic acid (MESH:D006820), NaOH (MESH:D012972), HCl (MESH:D006851), acetic acid (MESH:D019342), SDS (MESH:D012967), Ascorbic Acid (MESH:D001205), 2,3-Butanedione monoxime (MESH:C004717), water (MESH:D014867), TERGITOL (MESH:D011060), Triton X-100 (MESH:D017830), streptomycin (MESH:D013307), nitrogen (MESH:D009584), polyethylene glycol (MESH:D011092), EDTA (MESH:D004492), Hydrocortisone (MESH:D006854), chitosan (MESH:D048271), Phalloidin (MESH:D010590), alginate (MESH:D000464), MgCl2 (MESH:D015636), OCT (MESH:C051883), NaCl (MESH:D012965), gold (MESH:D006046)
- **Species:** Homo sapiens (human, species) [taxon 9606], Sus scrofa (pig, species) [taxon 9823]
- **Cell lines:** HUVEC — Homo sapiens (Human), Finite cell line (CVCL_2959)

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940387/full.md

## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940387/full.md

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Source: https://tomesphere.com/paper/PMC12940387