Modular Bioreactor Design for Directed Tendon/Ligament Tissue Engineering

• Published in: Bioengineering (Basel) Vol. 9; no. 3; p. 127
• Main Authors: Delakowski, Axel J, Posselt, Jared D, Wagner, Christopher T
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 21.03.2022; MDPI
• Subjects: Bioengineering; bioreactor; Bioreactors; Cell culture; Collagen; Design; differentiation; Extracellular matrix; Feedback control; Gene expression; Gene regulation; Hypotheses; Joint and ligament injuries; ligament; Ligaments; Load cells; Mathematical models; Mechanical stimuli; mesenchymal cells; Mesenchyme; Modular design; Modular engineering; Modular systems; Reliability analysis; Scaffolds; Signaling; Software; Strain; Stromal cells; tendon; Tendons; Tissue engineering; Wnt protein; United States > US; tendon; differentiation; bioreactor; mesenchymal cells; extracellular matrix; ligament
• ISSN: 2306-5354; 2306-5354
• DOI: 10.3390/bioengineering9030127

Functional tissue-engineered tendons and ligaments remain to be prepared in a reproducible and scalable manner. This study evaluates an acellular 3D extracellular matrix (ECM) scaffold for tendon/ligament tissue engineering and their ability to support strain-induced gene regulation associated with the tenogenesis of cultured mesenchymal stromal cells. Preliminary data demonstrate unique gene regulation patterns compared to other scaffold forms, in particular in Wnt signaling. However, the need for a robust bioreactor system that minimizes process variation was also evident. A design control process was used to design and verify the functionality of a novel bioreactor. The system accommodates 3D scaffolds with clinically-relevant sizes, is capable of long-term culture with customizable mechanical strain regimens, incorporates in-line load measurement for continuous monitoring and feedback control, and allows a variety of scaffold configurations through a unique modular grip system. All critical functional specifications were met, including verification of physiological strain levels from 1-10%, frequency levels from 0.2-0.5 Hz, and accurate load measurement up to 50 N, which can be expanded on the basis of load cell capability. The design process serves as a model for establishing statistical functionality and reliability of investigative systems. This work sets the stage for detailed analyses of ECM scaffolds to identify critical differentiation signaling responses and essential matrix composition and cell-matrix interactions.