4.5 Article

Synthetic Extracellular Matrices for 3D Culture of Schwann Cells, Hepatocytes, and HUVECs

Journal

BIOENGINEERING-BASEL
Volume 9, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/bioengineering9090453

Keywords

hydrogel; polyisocyanides; adhesive peptide; 3D culture

Funding

  1. National Key Research and Development Program of China [2021YFA0719303]
  2. National Natural Science Foundation of China [81901058, 81900686]
  3. Natural Science Foundation of Guangdong Province [2022A1515010952]
  4. Shenzhen Fundamental Research Foundation [JCYJ20210324115814040]

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This study demonstrates the use of synthetic hydrogels from polyisocyanides (PIC) to support the growth and maintenance of cells from different germ layers. Schwann cells and hepatocytes formed multicellular spheroids and maintained their properties, while endothelial cells only spread and formed a cell network in hydrogels containing specific adhesive peptides.
Synthetic hydrogels from polyisocyanides (PIC) are a type of novel thermoreversible biomaterials, which can covalently bind biomolecules such as adhesion peptides to provide a suitable extracellular matrix (ECM)-like microenvironment for different cells. Although we have demonstrated that PIC is suitable for three-dimensional (3D) culture of several cell types, it is unknown whether this hydrogel sustains the proliferation and passaging of cells originating from different germ layers. In the present study, we propose a 3D culture system for three representative cell sources: Schwann cells (ectoderm), hepatocytes (endoderm), and endothelial cells (mesoderm). Both Schwann cells and hepatocytes proliferated into multicellular spheroids and maintained their properties, regardless of the amount of cell-adhesive RGD motifs in long-term culture. Notably, Schwann cells grew into larger spheroids in RGD-free PIC than in PIC-RGD, while HL-7702 showed the opposite behavior. Endothelial cells (human umbilical vein endothelial cells, HUVECs) spread and formed an endothelial cell (EC) network only in PIC-RGD. Moreover, in a hepatocyte/HUVEC co-culture system, the characteristics of both cells were well kept for a long period in PIC-RGD. In all, our work highlights a simple ECM mimic that supports the growth and phenotype maintenance of cells from all germ layers in the long term. Our findings might contribute to research on biological development, organoid engineering, and in vitro drug screening.

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