TY - JOUR
T1 - Masticatory-Driven Piezoelectric Hydrogels with Electrical Stimulation-Triggered NPY Condensate for Mandibular Bone Regeneration
AU - Zhai, Xiaoting
AU - Cui, Yi
AU - Xu, Junwei
AU - Liu, Meijing
AU - Liu, Yanan
AU - Wang, Xiaogang
AU - Hu, Lei
N1 - Publisher Copyright:
© 2026 Wiley-VCH GmbH.
PY - 2026/4/10
Y1 - 2026/4/10
N2 - Mandibular bone defects, especially critical-sized ones, are a major challenge in oral and maxillofacial surgery. Electrical stimulation (ES) enhances bone repair, but its underlying mechanism remains elusive. This study presents a masticatory-driven piezoelectric hydrogel that converts chewing motions into endogenous-like ES, triggering on-demand NPY condensate release to enhance regeneration, validated in rat critical-sized defect models. NPY as a key mediator is identified: ES triggers its phase transition to activate osteogenic signaling. The engineered hydrogel generates >20 mV cm−1 (exceeding the ≥2 mV cm−1 threshold for NPY liquid-liquid phase separation, LLPS) under physiological chewing. ES induces NPY conformational rearrangement (N-terminus buried) to activate Y2 receptors (Y2R) on periodontal ligand-derived stromal cells (PDLSCs). Mechanistically, ES plus NPY condensate promotes osteogenic differentiation of PDLSCs through pAKT-Runx2 signaling. In vitro, the hydrogel boosts PDLSCs osteogenesis by 2-fold (p < 0.001). In 4-week and 12-week rat mandibular bone defects, it yielded greater bone volume and higher density (p < 0.01) vs. controls, with Y2R-pAKT-RUNX2 activation confirmed. This self-powered strategy leverages mastication for targeted ES, offering a mechanism-driven solution that addresses current limitations and holds clinical promise.
AB - Mandibular bone defects, especially critical-sized ones, are a major challenge in oral and maxillofacial surgery. Electrical stimulation (ES) enhances bone repair, but its underlying mechanism remains elusive. This study presents a masticatory-driven piezoelectric hydrogel that converts chewing motions into endogenous-like ES, triggering on-demand NPY condensate release to enhance regeneration, validated in rat critical-sized defect models. NPY as a key mediator is identified: ES triggers its phase transition to activate osteogenic signaling. The engineered hydrogel generates >20 mV cm−1 (exceeding the ≥2 mV cm−1 threshold for NPY liquid-liquid phase separation, LLPS) under physiological chewing. ES induces NPY conformational rearrangement (N-terminus buried) to activate Y2 receptors (Y2R) on periodontal ligand-derived stromal cells (PDLSCs). Mechanistically, ES plus NPY condensate promotes osteogenic differentiation of PDLSCs through pAKT-Runx2 signaling. In vitro, the hydrogel boosts PDLSCs osteogenesis by 2-fold (p < 0.001). In 4-week and 12-week rat mandibular bone defects, it yielded greater bone volume and higher density (p < 0.01) vs. controls, with Y2R-pAKT-RUNX2 activation confirmed. This self-powered strategy leverages mastication for targeted ES, offering a mechanism-driven solution that addresses current limitations and holds clinical promise.
KW - electrical stimulation (ES)
KW - liquid-liquid phase separation (LLPS)
KW - mandibular bone regeneration
KW - masticatory-driven piezoelectric hydrogel
KW - neuropeptide Y (NPY)
UR - https://www.scopus.com/pages/publications/105028994890
U2 - 10.1002/adhm.202504780
DO - 10.1002/adhm.202504780
M3 - 文章
C2 - 41588793
AN - SCOPUS:105028994890
SN - 2192-2640
VL - 15
JO - Advanced Healthcare Materials
JF - Advanced Healthcare Materials
IS - 14
M1 - e04780
ER -