Bio-3D printing with smooth muscle cells derived from human iPSCs via neural crest and its application for the tracheal regeneration.

Hashimoto, Shintaro; Taniguchi, Daisuke; Doi, Ryoichiro; Obata, Tomohiro; Shiraishi, Toshio; Matsumoto, Takamune; Maruta, Hiroshi; Akao, Keiko et al. · Biofabrication · 2025

basic_science · Level V

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Abstract

Smooth muscle cells (SMCs) derived from induced pluripotent stem cells (iPSCs) have been used for scaffold-free structures; however, their use in regenerated organs is rare and not well established. The induction of mesenchymal stem cells (MSCs) via neural crest cells (NCCs) from iPSCs offers advantages such as a large-scale cell stock. While research has progressed on the chondrogenic differentiation and regenerative medicine applications of cartilage derived from human iPSC-derived MSCs via a NCCs lineage (iNC), studies on smooth muscle, a critical tracheal component alongside cartilage, remain limited. In this study, we aimed to establish a method for generating airway smooth muscle tissue constructs using human iNCMSCs, assess their contractile function, and evaluate their regenerative potential in tracheal cartilage defects. iNCMSCs were cultured for 28 d in Dulbecco's Modified Eagle Medium (DMEM) with fetal bovine serum (FBS), with one group receiving transforming growth factor beta 1 (TGF<i>β</i>1, DMEM-TGF<i>β</i>1 group) and the other group without TGF<i>β</i>1 (DMEM group). SMCs markers was assessed using immunofluorescence staining. The tissue constructs were bio-3D printed using spheroids from the DMEM-TGF<i>β</i>1 group and transplanted as smooth muscle patches into full-thickness defects in the rats' tracheas. The DMEM-TGF<i>β</i>1 group showed strong expression of SMCs markers such as<i>α</i>-smooth muscle actin, calponin, and myosin heavy chain. After 28 d post-transplant, histological evaluation confirmed graft engraftment, adequate blood flow, and epithelial layer extensions from the recipient tissues, along with well-maintained tracheal structures. This study demonstrated the feasibility of using iPSC-derived iNCMSCs to generate bio-3D printed smooth muscle constructs for tracheal regeneration. Our findings support the potential of this strategy as a novel approach for airway reconstruction, offering a scaffold-free cell-based platform for future clinical applications in tissue engineering for airway regeneration.

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