Science advances · 2026
Dynamic adaptive coassembled sericin protein orchestrating stem cell development for nucleus pulposus regeneration.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Li Xing, Zhao Yize, Gu Peiyang, Zhao Chengkun, Fan Yujiang, Zhang Xingdong, Zhao Chao, Ma Peter X, Feng Ganjun, Sun Yong
Аннотация
The zonal structure of natural extracellular matrix (ECM) creates a dynamic microenvironment that regulates mechanical and biochemical signals to support stem cell development. Here, we engineered a dynamic adaptive protein gel by coassembling bioactive sericin with an amphiphilic tripeptide, forming a nucleus pulposus (NP)-like viscoelastic network with rapid stress relaxation. This coassembled protein gel sequentially activated integrin β3-mediated mechanotransduction, promoted cytoskeletal remodeling and Yes-associated protein nuclear translocation, and subsequently up-regulated bioactive factors and ECM synthesis to orchestrate stem cell development. Incorporation of kartogenin provided sustained chondrogenic cues, thereby promoting stem cell differentiation and preserving NP tissue integrity in vivo. Together, these findings establish a phase separation-driven, adaptive protein matrix that orchestrates both mechanical and biochemical signaling for robust intervertebral disc regeneration.
Предметные рубрики MeSH
AnimalsFemaleRabbitsRatsAnilidesCell DifferentiationDisease Models, AnimalExtracellular MatrixHydrogelsInjections, SubcutaneousIntervertebral Disc DegenerationMechanotransduction, CellularMesenchymal Stem Cell TransplantationMesenchymal Stem CellsMolecular Docking SimulationMolecular Dynamics SimulationNucleus PulposusPeptide FragmentsPhthalic AcidsProtein EngineeringRats, Sprague-DawleyRegenerationSericinsSurface-Active AgentsChondrogenesis