Development of novel apoptosis-assisted lung tissue decellularization methods

• Published in: bioRxiv
• Main Authors: Song, Young Hye, Maynes, Mark, Hlavac, Nora, Visosevic, Daniel, Daramola, Kaitlyn, Porvasnik, Stacy L, Schmidt, Christine E
• Format: Paper
• Language: English
• Published: Cold Spring Harbor Cold Spring Harbor Laboratory Press 25.05.2020
• Subjects: Apoptosis; Camptothecin; Cell culture; Detergents; Epithelial cells; Extracellular matrix; Hydrogels; Immunological tolerance; Lungs; Nerves; Preservation; Regenerative medicine; Transplantation
• DOI: 10.1101/2020.05.21.109173

Decellularized tissues hold great potential for both regenerative medicine and disease modeling applications. The acellular extracellular matrix (ECM)-enriched scaffolds can be recellularized with patient-derived cells prior to transplantation, or digested to create thermally-gelling hydrogels for 3D cell culture. Current methods of decellularization clear cellular components using detergents, which can result in loss of ECM proteins and tissue architectural integrity. Recently, an alternative approach utilizing apoptosis to decellularize excised murine sciatic nerves resulted in superior ECM preservation, cell removal, and immune tolerance in vivo. However, this apoptosis-assisted decellularization approach has not been optimized for other tissues with a more complex geometry, such as lungs. To this end, we developed an apoptosis-assisted lung tissue decellularization method using a combination of camptothecin and sulfobetaine-10 (SB-10) to induce apoptosis and facilitate gentle and effective removal of cell debris, respectively. Importantly, combination of the two agents resulted in superior cell removal and ECM preservation compared to either of the treatments alone, presumably because of pulmonary surfactants. In addition, our method was superior in cell removal compared to a previously established detergent-based decellularization protocol. Furthermore, thermally-gelling lung ECM proteins supported high viability of rat lung epithelial cells for up to 2 weeks in culture. This work demonstrates that apoptosis-based lung tissue decellularization is a superior technique that warrants further utilization for both regenerative medicine and disease modeling applications. Competing Interest Statement The authors have declared no competing interest.