Aminated 3D Printed Polystyrene Maintains Stem Cell Proliferation and Osteogenic Differentiation

• Published in: Tissue engineering. Part C, Methods Vol. 26; no. 2; p. 118
• Main Authors: Lerman, Max J, Smith, Brandon T, Gerald, Anushka G, Santoro, Marco, Fookes, James A, Mikos, Antonios G, Fisher, John P
• Format: Journal Article
• Language: English
• Published: United States 01.02.2020
• Subjects: Cell Differentiation; Cell Proliferation; Cells, Cultured; Humans; Mesenchymal Stem Cells - cytology; Osteoblasts - cytology; Osteogenesis; Polystyrenes - chemistry; Printing, Three-Dimensional - instrumentation; Tissue Engineering - methods; Tissue Scaffolds - chemistry; mesenchymal stem cell; plasma treatment; scaffold; osteogenic differentiation; surface modification; bioreactor; 3D printing
• ISSN: 1937-3392
• DOI: 10.1089/ten.tec.2019.0217

As 3D printing becomes more common and the technique is used to build culture platforms, it is imperative to develop surface treatments for specific responses. The advantages of aminating and oxidizing polystyrene (PS) for human mesenchymal stem cell (hMSC) proliferation and osteogenic differentiation are investigated. We find that ammonia (NH ) plasma incorporates amines while oxygen plasma adds carbonyl and carboxylate groups. Across 2D, 3D, and 3D dynamic culture, we find that the NH - treated surfaces encouraged cell proliferation. Our results show that the NH -treated scaffold was the only treatment allowing dynamic proliferation of hMSCs with little evidence of osteogenic differentiation. With osteogenic media, particularly in 3D culture, we find the NH treatment encouraged greater and earlier expression of RUNX2 and ALP. The NH -treated PS scaffolds support hMSC proliferation without spontaneous osteogenic differentiation in static and dynamic culture. This work provides an opportunity for further investigations into shear profiling and coculture within the developed culture system toward developing a bone marrow niche model.