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通过胆碱能-钙信号传导拯救不愈合的退化唾液腺。

Rescue of non-healing, degenerative salivary glands by cholinergic-calcium signaling.

作者信息

Li Jianlong, Sun Bo, Tan Li Xuan, Griffin Nathan, Niknezhad Seyyed Vahid, Yu Chieh, Berthoin Lionel, Cruz-Pacheco Noel, Mohabbat Seayar, Sinada Hanan, Efraim Yael, Chen Feeling Yu Ting, An Luye, Gaylord Eliza A, Bahney Chelsey S, Lombaert Isabelle M A, Knox Sarah M

机构信息

Department of Cell and Tissue Biology, School of Dentistry, University of California San Francisco, San Francisco, California, USA; School of Health and Life Sciences, University of Health and Rehabilitation Sciences, Qingdao, China.

These authors contributed equally.

出版信息

bioRxiv. 2025 Feb 28:2024.12.31.630834. doi: 10.1101/2024.12.31.630834.

Abstract

Chronic degenerative wounds are often deemed irreparable, directing research efforts to focus predominantly on acute tissue injury regeneration while leaving endogenous repair mechanisms for chronically damaged tissues largely unexplored. In this study, we demonstrate that non-healing, severely degenerated salivary gland tissues can be fundamentally restored through first-line treatment with muscarinic agonists. This approach rescues tissue structure and function, returning it to a homeostatic-like state, and reactivates endogenous regeneration processes to drive new cell expansion that persists for months post-treatment. Furthermore, neuromimetic activation profoundly depletes radiation-induced DNA damage and re-establishes the nerve-acinar relationship, ultimately restoring the tissues physiological capacity to maintain homeostasis, even in the absence of treatment. We show that full recovery of organ function, comparable to uninjured controls, is primarily mediated by the re-differentiation of aberrantly de-differentiated epithelial acinar cells and the restoration of mitochondrial function via a muscarinic-calcium signaling pathway. These findings challenge the prevailing notion that chronic organ degeneration is irreversible and propose a readily testable therapeutic strategy for epithelial restoration with potential applications across a spectrum of chronic injuries.

摘要

慢性退行性伤口通常被认为无法修复,这使得研究工作主要集中在急性组织损伤的再生上,而慢性受损组织的内源性修复机制在很大程度上未得到探索。在本研究中,我们证明,通过毒蕈碱激动剂的一线治疗,无法愈合、严重退化的唾液腺组织可从根本上得到恢复。这种方法挽救了组织结构和功能,使其恢复到类似稳态的状态,并重新激活内源性再生过程,以驱动新细胞增殖,这种增殖在治疗后持续数月。此外,神经模拟激活能显著减少辐射诱导的DNA损伤,并重建神经-腺泡关系,最终恢复组织维持稳态的生理能力,即使在没有治疗的情况下也是如此。我们表明,与未受伤的对照组相当的器官功能完全恢复,主要是由异常去分化的上皮腺泡细胞重新分化以及通过毒蕈碱-钙信号通路恢复线粒体功能介导的。这些发现挑战了慢性器官退化是不可逆的这一普遍观念,并提出了一种易于测试的上皮修复治疗策略,该策略可能适用于一系列慢性损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7701/11874919/3c7b085cf1a4/nihpp-2024.12.31.630834v2-f0001.jpg

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