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前颗粒蛋白在代谢性疾病中的分子机制及靶向治疗

Molecular mechanisms and targeted therapy of progranulin in metabolic diseases.

作者信息

Wang Xiaxia, Liang Yonglin, Yang Fan, Shi Yangyang, Shao Ruiwen, Jing Ruge, Yang Tong, Chu Qiao, An Dong, Zhou Qi, Song Jiayi, Chen Haolan, Liu Chun

机构信息

School of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, Gansu, China.

School of Traditional Chinese and Western Medicine, Gansu University of Chinese Medicine, Lanzhou, Gansu, China.

出版信息

Front Endocrinol (Lausanne). 2025 Apr 11;16:1553794. doi: 10.3389/fendo.2025.1553794. eCollection 2025.

DOI:10.3389/fendo.2025.1553794
PMID:40290306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12021630/
Abstract

Progranulin (PGRN) is a secreted glycoprotein with cytokine-like properties, exerting tripartite mechanisms of inflammation suppression, tissue repair promotion, and metabolic regulation. This multifaceted functionality positions PGRN as a potential "multi-effect therapeutic strategy" for metabolic disorders characterised by cartilage degradation and imbalanced bone remodelling, potentially establishing it as a novel therapeutic target for such conditions. Osteoarthritis, rheumatoid arthritis, intervertebral disc degeneration, osteoporosis, periodontitis, and diabetes-related complications-representing the most prevalent metabolic diseases-currently lack effective treatments due to incomplete understanding of their precise pathogenic mechanisms. Recent studies have revealed that PGRN expression levels are closely associated with the onset and progression of these metabolic disorders. However, the exact regulatory role of PGRN in these diseases remains elusive, partly owing to its tissue-specific actions and context-dependent dual roles (anti-inflammatory vs. pro-inflammatory). In this review, we summarise the structure and functions of PGRN, explore its involvement in neurological disorders, immune-inflammatory diseases, and metabolic conditions, and specifically focus on its molecular mechanisms in metabolic diseases. Furthermore, we consolidate advances in targeting PGRN and the application of its engineered derivative, Atsttrin, in metabolic bone disorders. We also discuss potential unexplored mechanisms through which PGRN may exert influence within this field or other therapeutic domains. Collectively, this work aims to provide a new framework for elucidating PGRN's role in disease pathogenesis and advancing strategies for the prevention and treatment of metabolic disorders.

摘要

颗粒蛋白前体(PGRN)是一种具有细胞因子样特性的分泌型糖蛋白,发挥着抑制炎症、促进组织修复和调节代谢的三方机制。这种多方面的功能使PGRN成为治疗以软骨降解和骨重塑失衡为特征的代谢紊乱的潜在“多效治疗策略”,有可能将其确立为这类病症的新型治疗靶点。骨关节炎、类风湿性关节炎、椎间盘退变、骨质疏松症、牙周炎以及糖尿病相关并发症——代表了最常见的代谢性疾病——由于对其确切致病机制了解不全面,目前缺乏有效的治疗方法。最近的研究表明,PGRN的表达水平与这些代谢紊乱的发生和发展密切相关。然而,PGRN在这些疾病中的确切调节作用仍然难以捉摸,部分原因是其组织特异性作用和依赖于背景的双重作用(抗炎与促炎)。在这篇综述中,我们总结了PGRN的结构和功能,探讨了其在神经疾病、免疫炎症性疾病和代谢状况中的作用,并特别关注其在代谢性疾病中的分子机制。此外,我们整合了靶向PGRN的研究进展及其工程衍生物Atsttrin在代谢性骨病中的应用。我们还讨论了PGRN可能在该领域或其他治疗领域发挥影响的潜在未探索机制。总的来说,这项工作旨在为阐明PGRN在疾病发病机制中的作用以及推进代谢紊乱的预防和治疗策略提供一个新的框架。

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本文引用的文献

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Executive Summary: Treatment of Osteoporosis and Osteoarthritis in the Oldest Old.执行摘要:高龄老年人骨质疏松症和骨关节炎的治疗
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Progranulin Protects Against Osteoporosis by Regulating Osteoclast and Osteoblast Balance via TNFR Pathway.颗粒蛋白前体通过肿瘤坏死因子受体(TNFR)途径调节破骨细胞与成骨细胞平衡来预防骨质疏松症。
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Progranulin deficiency associates with postmenopausal osteoporosis via increasing ubiquitination of estrogen receptor α.
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Genes Dis. 2024 Jan 28;12(1):101221. doi: 10.1016/j.gendis.2024.101221. eCollection 2025 Jan.
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Selective neuronal expression of progranulin is sufficient to provide neuroprotective and anti-inflammatory effects after traumatic brain injury.选择性神经元表达颗粒蛋白前体足以提供创伤性脑损伤后的神经保护和抗炎作用。
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Understanding the relationship between inflammation, apoptosis, and diabetes osteoporosis: A bioinformatics approach and experimental verification.探讨炎症、细胞凋亡与糖尿病性骨质疏松症的关系:生物信息学方法与实验验证。
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MiRNA-based therapeutic potential in multiple sclerosis.基于微小RNA的多发性硬化症治疗潜力
Front Immunol. 2024 Aug 29;15:1441733. doi: 10.3389/fimmu.2024.1441733. eCollection 2024.
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Ammonia-induced lysosomal and mitochondrial damage causes cell death of effector CD8 T cells.氨诱导的溶酶体和线粒体损伤导致效应性 CD8 T 细胞死亡。
Nat Cell Biol. 2024 Nov;26(11):1892-1902. doi: 10.1038/s41556-024-01503-x. Epub 2024 Sep 11.
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Progranulin mediates the onset of pristane induced systemic lupus erythematosus.颗粒蛋白前体介导了 pristane 诱导的系统性红斑狼疮的发病。
Adv Rheumatol. 2024 Sep 9;64(1):67. doi: 10.1186/s42358-024-00405-8.
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TRPA1 aggravates osteoclastogenesis and osteoporosis through activating endoplasmic reticulum stress mediated by SRXN1.TRPA1 通过激活由 SRXN1 介导的内质网应激加重破骨细胞生成和骨质疏松症。
Cell Death Dis. 2024 Aug 27;15(8):624. doi: 10.1038/s41419-024-07018-5.
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Medicina (Kaunas). 2024 Jul 19;60(7):1165. doi: 10.3390/medicina60071165.