Fabrication of a novel 3D-printed perfusion bioreactor for complex cell culture models

We introduce a novel fabrication method for developing a 3D-printed perfusion bioreactor (3D-PBR) to facilitate the in situ growth and differentiation of human bone marrow (BM)-derived mesenchymal stem cells (MSCs) while enabling coculture with vascular cells. To recapitulate human physiology, in vitro platforms must incorporate several key features of their native target organ. This often entails a supportive 3D architecture for growing and differentiating multiple human cell types in situ under perfusion. Other essential characteristics include reproducibility, ease of customization, and biocompatibility. Our 3D-PBR combines these features and was fabricated using a biocompatible resin-based polymer, which was 3D-printed, followed by the addition of a permeable membrane to create a coculture microenvironment. MSCs were encapsulated in a collagen-fibrin gel alongside human endothelium within the 3D-PBR. The physical cues that our 3D-PBR provided facilitated the differentiation of MSCs into specific lineages, such as adipocytes and osteoblasts. Immunohistochemistry images demonstrated that cells grown in the 3D-PBR exhibited more physiologically relevant BM perivascular niche markers compared to static culture models. Our method utilizes emerging 3D printing techniques and alternative materials, departing from traditional PDMS-based soft lithography. These advancements in fabrication further enhance in vitro platforms for diverse cell culture models and vascular permeability assays.

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Publication Details

Journal
Scientific Reports
Published
2025-03-24
DOI
https://doi.org/10.1038/s41598-025-94093-z
Citations
7
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
4.72
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article

Fabrication of a novel 3D-printed perfusion bioreactor for complex cell culture models

Jennifer Foster Harris, David J. Ross, Brian H. Jun, Brian M. Patterson et al.
7 citations
Scientific Reports
3D Printing in Biomedical Research
4.72
article

Fabrication of a novel 3D-printed perfusion bioreactor for complex cell culture models

Jennifer Foster Harris, David J. Ross, Brian H. Jun, Brian M. Patterson, Katie L. Davis, Arasely M. Rodriguez, Mohammad O. Ishak, Jacob E. Torrez
article en
7 citations

Abstract

We introduce a novel fabrication method for developing a 3D-printed perfusion bioreactor (3D-PBR) to facilitate the in situ growth and differentiation of human bone marrow (BM)-derived mesenchymal stem cells (MSCs) while enabling coculture with vascular cells. To recapitulate human physiology, in vitro platforms must incorporate several key features of their native target organ. This often entails a supportive 3D architecture for growing and differentiating multiple human cell types in situ under perfusion. Other essential characteristics include reproducibility, ease of customization, and biocompatibility. Our 3D-PBR combines these features and was fabricated using a biocompatible resin-based polymer, which was 3D-printed, followed by the addition of a permeable membrane to create a coculture microenvironment. MSCs were encapsulated in a collagen-fibrin gel alongside human endothelium within the 3D-PBR. The physical cues that our 3D-PBR provided facilitated the differentiation of MSCs into specific lineages, such as adipocytes and osteoblasts. Immunohistochemistry images demonstrated that cells grown in the 3D-PBR exhibited more physiologically relevant BM perivascular niche markers compared to static culture models. Our method utilizes emerging 3D printing techniques and alternative materials, departing from traditional PDMS-based soft lithography. These advancements in fabrication further enhance in vitro platforms for diverse cell culture models and vascular permeability assays.

Scientific ReportsVol. 15(1)
Los Alamos National Laboratory (US), University of New Mexico (US)
Openalex Percentile: Top 5%
3D Printing in Biomedical Research
4.72
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Fabrication of a novel 3D-printed perfusion bioreactor for complex cell culture models — Jennifer Foster Harris, David J. Ross, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS