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

利用 hiPSC 构建大规模血管整合的肌肉样网格,以增强肌肉体积再生

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作者:Lee Myung Chul, Jodat Yasamin A, Endo Yori, Rodríguez-delaRosa Alejandra, Zhang Ting, Karvar Mehran, Al Tanoury Ziad, Quint Jacob, Kamperman Tom, Kiaee Kiavash, Ochoa Sofia Lara, Shi Kun, Huang Yike, Rosales Montserrat Pineda, Arnaout Adnan, Lee Hyeseon, Kim Jiseong, Ceron Eder Luna, Reyes Isaac Garcia, Panayi Adriana C, Martinez Angel Flores Huidobro, Wang Xichi, Kim Ki-Tae, Moon Jae-I, Park Seung Gwa, Lee Kangju, Calabrese Michelle A, Hassan Shabir, Lee Junmin, Tamayol Ali, Lee Luke, Pourquié Olivier, Kim Woo-Jin, Sinha Indranil, Shin Su Ryon
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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