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Engineering large-scale hiPSC-derived vessel-integrated muscle-like lattices for enhanced volumetric muscle regeneration. | LitMetric

AI Article Synopsis

  • Engineering tissue implants using human induced pluripotent stem cells (hiPSCs) shows potential for repairing large tissue losses but faces challenges in survival and integration.* -
  • The study introduces scalable vessel-integrated muscle-like lattices (VMLs) that feature dense hiPSC-derived myofibers and vessel-like microchannels, enhancing myofiber maturation and host integration.* -
  • This advanced bioprinting technology allows for the creation of larger, prevascularized muscle tissues, which successfully restore muscle function and promote healing in volumetric muscle loss injury models.*

Article Abstract

Engineering biomimetic tissue implants with human induced pluripotent stem cells (hiPSCs) holds promise for repairing volumetric tissue loss. However, these implants face challenges in regenerative capability, survival, and geometric scalability at large-scale injury sites. Here, we present scalable vessel-integrated muscle-like lattices (VMLs), containing dense and aligned hiPSC-derived myofibers alongside passively perfusable vessel-like microchannels inside an endomysium-like supporting matrix using an embedded multimaterial bioprinting technology. The contractile and millimeter-long myofibers are created in mechanically tailored and nanofibrous extracellular matrix-based hydrogels. Incorporating vessel-like lattice enhances myofiber maturation in vitro and guides host vessel invasion in vivo, improving implant integration. Consequently, we demonstrate successful de novo muscle formation and muscle function restoration through a combinatorial effect between improved graft-host integration and its increased release of paracrine factors within volumetric muscle loss injury models. The proposed modular bioprinting technology enables scaling up to centimeter-sized prevascularized hiPSC-derived muscle tissues with custom geometries for next-generation muscle regenerative therapies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11625013PMC
http://dx.doi.org/10.1016/j.tibtech.2024.08.001DOI Listing

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