Department of Orthopaedics, Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases, Shanghai Institute of Traumatology and Orthopaedics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin 2nd Road, Shanghai, 200025, P. R. China.
Department of Spine Surgery, Renji Hospital, Shanghai Jiao Tong University School of Medicine, 160 Pujian Road, Shanghai, 200127, P. R. China.
Adv Mater. 2024 Feb;36(5):e2306105. doi: 10.1002/adma.202306105. Epub 2023 Dec 6.
Inflammaging is deeply involved in aging-related diseases and can be destructive during aging. The maintenance of pH balance in the extracellular microenvironment can alleviate inflammaging and repair aging-related tissue damage. In this study, the hydrogen ion capturing hydrogel microsphere (GMNP) composed of mineralized transforming growth factor-β (TGF-β) and catalase (CAT) nanoparticles is developed via biomimetic mineralization and microfluidic technology for blocking the NLRP3 cascade axis in inflammaging. This GMNP can neutralize the acidic microenvironment by capturing excess hydrogen ions through the calcium carbonate mineralization layer. Then, the subsequent release of encapsulated TGF-β and CAT can eliminate both endogenous and exogenous stimulus of NLRP3, thus suppressing the excessive activation of inflammaging. In vitro, GMNP can suppress the excessive activation of the TXNIP/NLRP3/IL-1β cascade axis and enhance extracellular matrix (ECM) synthesis in nucleus pulposus cells. In vivo, GMNP becomes a sustainable and stable niche with microspheres as the core to inhibit inflammaging and promote the regeneration of degenerated intervertebral discs. Therefore, this hydrogen ion-capturing hydrogel microsphere effectively reverses inflammaging by interfering with the excessive activation of NLRP3 in the degenerated tissues.
炎症衰老与衰老相关疾病密切相关,并可能在衰老过程中对组织造成破坏。维持细胞外微环境的 pH 值平衡可以减轻炎症衰老并修复与衰老相关的组织损伤。在这项研究中,通过仿生矿化和微流控技术开发了由矿化转化生长因子-β(TGF-β)和过氧化氢酶(CAT)纳米颗粒组成的氢离子捕获水凝胶微球(GMNP),用于阻断炎症衰老中的 NLRP3 级联轴。这种 GMNP 可以通过碳酸钙矿化层捕获多余的氢离子来中和酸性微环境。然后,包封的 TGF-β和 CAT 的随后释放可以消除 NLRP3 的内源性和外源性刺激,从而抑制炎症衰老的过度激活。在体外,GMNP 可以抑制过度激活 TXNIP/NLRP3/IL-1β 级联轴,并增强核髓核细胞的细胞外基质(ECM)合成。在体内,GMNP 以微球为核心,形成一个可持续且稳定的小生境,抑制炎症衰老并促进退化的椎间盘再生。因此,这种氢离子捕获水凝胶微球通过干扰退变组织中 NLRP3 的过度激活,有效逆转了炎症衰老。