来自γδ T细胞的可溶性Sema4D通过丛蛋白b /mTOR信号传导抑制成骨细胞,参与双磷酸盐相关颌骨骨坏死的发病机制。

IF 5.6 1区 生物学 Q2 CELL BIOLOGY
Lingling Ou, Shijia Qiao, Zhuoyi Liao, Xiner Tan, Hui Huang, Zhiyan Zhou, Ruhui Luo, Weijun Zeng, Yan Yang, Zhongxuan Zhang, Jingchen Chen, Shengli Wang, Yiqin Jiang, Jianlei Hao, Yuqin Shen, Longquan Shao
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引用次数: 0

摘要

双膦酸盐相关性颌骨坏死(BRONJ)是长期接受双膦酸盐治疗的患者的严重并发症,而我们对BRONJ发病机制的了解还远远不够。γδ (γδ) T细胞主要分布于粘膜组织,在免疫调节和骨代谢中发挥重要作用;然而,γδ T细胞在BRONJ发病机制中的作用机制尚未阐明。在这里,我们通过腹腔注射唑来膦酸钠诱导野生型(WT)和t细胞受体δ缺陷(TCRδ-/-)小鼠bronj样病变。我们的研究结果表明,γδ T细胞浸润BRONJ病变抑制成骨细胞分化,而γδ T细胞缺失在TCRδ-/-小鼠中恢复成骨功能并显著降低BRONJ病变发生率。从机制上,我们发现活化的γδ T细胞分泌的基质金属蛋白酶3 (MMP3)是将膜结合的Sema4D (mSema4D)切割成可溶性Sema4D (sSema4D)的关键酶。该裂解产物与成骨细胞丛蛋白b1 /2受体结合,激活mTOR信号通路,抑制成骨分化(ALP/Runx2下调)。为了促进BRONJ病变的修复,我们设计了一种双功能复合水凝胶(Gel-BG@ab),将PLGA-PEG-PLGA与介孔生物活性玻璃(BG)和抗sema4d抗体结合在一起。这种复合水凝胶实现了持续的抗体释放,有效地中和了sSema4D,恢复了成骨细胞的活性,减少了体内bronj样病变的形成。本研究提供了MMP3-Sema4D-Plexin-B1/2/mTOR在BRONJ中串扰的证据,并引入了一种靶向生物材料策略来破坏致病反馈回路。Gel-BG@ab是免疫调节和再生医学的结合,为BRONJ的免疫-物质联合治疗提供了理论和技术上的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Soluble Sema4D From γδ T Cells Exerts Osteoblast Inhibition via Plexin-B/mTOR Signalling Contributing to Pathogenesis of Bisphosphonate-Related Osteonecrosis of the Jaws.

Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is a severe complication in patients undergoing long-term bisphosphonate therapy, while our knowledge on the pathogenesis of BRONJ is far from sufficient. Gamma delta (γδ) T cells predominantly distribute in mucosal tissues and play an important role in both immune modulation and bone metabolism; however, the mechanism of γδ T cells in the pathogenesis of BRONJ has not been elucidated. Here, we induced BRONJ-like lesions in wild-type (WT) and T-cell receptor delta-deficient (TCRδ-/-) mice via intraperitoneal zoledronate injection. Our findings revealed that γδ T cells infiltrating BRONJ lesions suppressed osteoblast differentiation, whereas γδ T cell depletion in TCRδ-/- mice restored osteogenic function and significantly reduced BRONJ lesion incidence. Mechanistically, we identified matrix metalloproteinase 3 (MMP3) secreted by activated γδ T cells as a critical enzyme cleaving membrane-bound Sema4D (mSema4D) into soluble Sema4D (sSema4D). This cleavage product bound to Plexin-B1/2 receptors on osteoblasts, activating the mTOR signalling pathway to inhibit osteogenic differentiation (ALP/Runx2 downregulation). To promote the repair of BRONJ lesions, we engineered a dual-functional composite hydrogel (Gel-BG@ab) combining PLGA-PEG-PLGA with mesoporous bioactive glass (BG) and anti-Sema4D antibodies. This composite hydrogel achieved sustained antibody release, effectively neutralising sSema4D, restoring osteoblast activity and reducing the formation of BRONJ-like lesions in vivo. This study provides evidence of MMP3-Sema4D-Plexin-B1/2/mTOR crosstalk in BRONJ and introduces a targeted biomaterial strategy to disrupt pathogenic feedback loops. The Gel-BG@ab is the integration of immunomodulation and regenerative medicine, providing both theoretical and technical insights for the immune-material combination therapy of BRONJ.

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来源期刊
Cell Proliferation
Cell Proliferation 生物-细胞生物学
CiteScore
14.80
自引率
2.40%
发文量
198
审稿时长
1 months
期刊介绍: Cell Proliferation Focus: Devoted to studies into all aspects of cell proliferation and differentiation. Covers normal and abnormal states. Explores control systems and mechanisms at various levels: inter- and intracellular, molecular, and genetic. Investigates modification by and interactions with chemical and physical agents. Includes mathematical modeling and the development of new techniques. Publication Content: Original research papers Invited review articles Book reviews Letters commenting on previously published papers and/or topics of general interest By organizing the information in this manner, readers can quickly grasp the scope, focus, and publication content of Cell Proliferation.
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