(366ae) Elastin-Based Coatings for Long-Term Organoid Culture of Human Stem Cells | AIChE

(366ae) Elastin-Based Coatings for Long-Term Organoid Culture of Human Stem Cells

Research Interests: My focus is on enhancing in vitro adipose cell culture models to mimic progressive adiposity. Specifically, I work on creating aminated-ELP based coating that could support long-term culture of adipocyte to capture progressing adiposity. I investigate the effects of RGD-containing elastin-like polypeptide-polyethyleneimine (ELP-PEI) coatings on adipocyte morphology and differentiation within 3D clusters of adipose-derived stem cells (ASCs). By assessing the impact of these coatings over extended culture periods, my research aims to refine adipose cell culture models for applications such as drug screening and tissue engineering.

Objective: Current in vitro adipose cell culture models do not replicate progressive adiposity due to limitations in facilitating the gradual intracellular fat buildup in 3D clusters of adipose-derived stem cells (ASCs) over extended periods. Previously, we cultured human ASCs as 3D spheroids on elastin-like polypeptide-polyethyleneimine (ELP-PEI) coatings and ELP-PEI coatings containing Arginine-Glycine-Aspartic Acid (RGD) residues. We observed that adding three RGD residues to the C-terminus of ELP showed superior spheroid retention. In this study, we qualitatively and quantitatively assessed the impact of the RGD-containing ELP-PEI coating on adipocyte morphology and differentiation over an eight-week culture period.

Materials and Methods: ELP conjugated with RGD was produced from genetically modified Escherichia coli bacteria via suspension culture. These ELP-RGD molecules were conjugated with PEI (MW= 800 Da) via carbodiimide chemistry. 5 mg/mL of 5 mol% ELP-(RGD)3-PEI conjugates were adsorbed onto 24-well tissue culture polystyrene (TCPS) plates by placing 200 µL solution in each well. 50,000 human ASCs per well were cultured for 3 days on coated plates to form 3D spheroids. The spheroids were differentiated along the adipogenic lineage for 3 days and matured for 8 weeks.

Results: We observed several dynamic changes in cell morphology over the cell culture period. Initially, on Day 3, the cells aggregated to form spheroids and maintained the spheroid morphology after 3 days of differentiation. After 7 days of maturation in adipogenic media, it was observed that the spheroids were surrounded by a monolayer of 2D cells. By day 14, there was a shift toward a predominantly 2D morphology, although with scattered cell clusters. Interestingly, by day 28, there was a reformation of spheroids, indicating a cyclic pattern of spheroid formation and dispersal within the culture period. The spheroids then continued to increase in size till day 56.

Conclusion: This observation underscored the dynamic nature of cell-surface interactions of the human stem cells with the elastin-based coatings containing RGD. We will further probe these results by measuring the adipocyte gene expression and integrin binding.