# Engineering Multilayered Hepatic Cell Sheet Model Using Oxygen-Supplying MeHA/CPO Hydrogel

**Authors:** Kyungsook Kim, So Hee Han, Jiyoen Oh, Delger Bayarsaikhan, Moon Suk Kim, Dayoen Kim, Teruo Okano, Bonghee Lee

PMC · DOI: 10.3390/bioengineering12101132 · Bioengineering · 2025-10-21

## TL;DR

A new hydrogel that supplies oxygen helps create multilayered liver-like tissues, improving cell survival and function for potential use in liver regeneration and drug testing.

## Contribution

A novel oxygen-releasing hydrogel is developed to support multilayered hepatic tissue engineering with improved viability and function.

## Key findings

- The MeHA/CPO hydrogel enhanced structural integrity and supported multilayered iHep sheet formation.
- Double-layered iHep sheets with the hydrogel showed increased expression of paracrine factors and improved albumin secretion.
- The oxygen-releasing system alleviated hypoxic stress and preserved hepatocyte identity.

## Abstract

Three-dimensional (3D) hepatic tissue engineering holds great potential for liver regeneration, disease modeling, and drug screening. These applications require densely layered hepatic tissues that mimic native 3D liver architecture. However, limited oxygen supply and reduced cell viability in densely layered hepatic constructs remain key challenges. To overcome this, this study developed a photo-crosslinkable, oxygen-releasing hydrogel composed of methacrylated hyaluronic acid (MeHA) and calcium peroxide (CPO). The MeHA/CPO hydrogel exhibited favorable rheological properties and sustained oxygen release. Induced pluripotent stem cell-derived hepatocyte (iHep) sheets were cultured with or without MeHA/CPO hydrogel in single- and double-layer formats. The hydrogel enhanced structural integrity and supported the formation of a multilayer (~33 µm). Double-layered iHep sheets with MeHA/CPO showed the significantly increased expression of paracrine factors (HGF, VEGF, Alb) and improved albumin secretion without loss of hepatocyte identity (AFP, HNF4α). This oxygen-releasing system effectively alleviates hypoxic stress, supporting the structural and functional viability of multilayered iHep sheets. Our platform provides a promising approach for engineering metabolically active hepatic tissues and may serve as a foundation for 3D hepatic tissue engineering.

## Linked entities

- **Genes:** HGF (hepatocyte growth factor) [NCBI Gene 3082], VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422], ALB (albumin) [NCBI Gene 213], AFP (alpha fetoprotein) [NCBI Gene 174], HNF4A (hepatocyte nuclear factor 4 alpha) [NCBI Gene 3172]
- **Chemicals:** calcium peroxide (PubChem CID 14779)

## Full-text entities

- **Genes:** HNF4A (hepatocyte nuclear factor 4 alpha) [NCBI Gene 3172] {aka FRTS4, HNF4, HNF4a7, HNF4a8, HNF4a9, HNF4alpha}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, HGF (hepatocyte growth factor) [NCBI Gene 3082] {aka DFNB39, F-TCF, HGFB, HPTA, SF}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}
- **Diseases:** hypoxic (MESH:D002534)
- **Chemicals:** Oxygen (MESH:D010100), MeHA (-), CPO (MESH:C403632), hyaluronic acid (MESH:D006820)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12561752/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12561752/full.md

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Source: https://tomesphere.com/paper/PMC12561752