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骨骼与软骨中的河马信号通路:对发育和疾病的影响

The Hippo pathway in bone and cartilage: implications for development and disease.

作者信息

Shao Chenwei, Chen Hao, Liu Tingting, Pan Chun

机构信息

Institute of Translational Medicine, Yangzhou University, Yangzhou, Jiangsu, China.

Department of Orthopedics, Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu, China.

出版信息

PeerJ. 2025 Apr 22;13:e19334. doi: 10.7717/peerj.19334. eCollection 2025.

DOI:10.7717/peerj.19334
PMID:40292098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12024444/
Abstract

Bone is the main structure of the human body; it mainly plays a supporting role and participates in metabolic processes. The Hippo signaling pathway is composed of a series of protein kinases, including the mammalian STE20-like kinase MST1/2 and the large tumor suppressor LATS1/2, which are widely involved in pathophysiological processes, including cell proliferation, differentiation, apoptosis and death, especially those related to biomechanical transduction . However, the role of it in regulating skeletal system development and the evolution of bone-related diseases remains poorly understood. The pathway can intervene in and regulate the physiological activities of bone-related cells such as osteoclasts and chondrocytes through its own or other bone-related signaling pathways, such as the Wnt pathway, the Notch pathway, and receptor activator of nuclear factor-κB ligand (RANKL), thereby affecting the occurrence and development of bone diseases. This article discusses the role of the Hippo signaling pathway in bone development and disease to provide new insights into the treatment of bone-related diseases by targeting the Hippo signaling pathway.

摘要

骨骼是人体的主要结构;它主要起支撑作用并参与代谢过程。Hippo信号通路由一系列蛋白激酶组成,包括哺乳动物STE20样激酶MST1/2和大肿瘤抑制因子LATS1/2,其广泛参与病理生理过程,包括细胞增殖、分化、凋亡和死亡,尤其是那些与生物力学转导相关的过程。然而,其在调节骨骼系统发育及骨相关疾病演变中的作用仍知之甚少。该信号通路可通过自身或其他骨相关信号通路(如Wnt通路、Notch通路和核因子κB受体活化因子配体(RANKL))干预和调节破骨细胞、软骨细胞等骨相关细胞的生理活动,从而影响骨疾病的发生发展。本文探讨Hippo信号通路在骨骼发育和疾病中的作用,旨在为通过靶向Hippo信号通路治疗骨相关疾病提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba56/12024444/08922e9548b7/peerj-13-19334-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba56/12024444/5106b64cc56c/peerj-13-19334-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba56/12024444/7e3e1f216e45/peerj-13-19334-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba56/12024444/08922e9548b7/peerj-13-19334-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba56/12024444/5106b64cc56c/peerj-13-19334-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba56/12024444/7e3e1f216e45/peerj-13-19334-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba56/12024444/08922e9548b7/peerj-13-19334-g003.jpg

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本文引用的文献

1
Mesenchymal stromal cells-derived extracellular vesicles in cartilage regeneration: potential and limitations.间充质基质细胞衍生的细胞外囊泡在软骨再生中的作用:潜力与局限
Stem Cell Res Ther. 2025 Jan 23;16(1):11. doi: 10.1186/s13287-025-04135-6.
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Estrogen and estrogen receptors mediate the mechanobiology of bone disease and repair.雌激素及其受体介导骨疾病和修复的力学生物学。
Bone. 2024 Nov;188:117220. doi: 10.1016/j.bone.2024.117220. Epub 2024 Aug 5.
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Lumbar instability remodels cartilage endplate to induce intervertebral disc degeneration by recruiting osteoclasts via Hippo-CCL3 signaling.
腰椎不稳通过 Hippo-CCL3 信号招募破骨细胞重塑软骨终板,从而诱导椎间盘退变。
Bone Res. 2024 May 30;12(1):34. doi: 10.1038/s41413-024-00331-x.
4
The Hippo signalling pathway in bone homeostasis: Under the regulation of mechanics and aging.Hippo 信号通路在骨稳态中的作用:力学和衰老的调节。
Cell Prolif. 2024 Oct;57(10):e13652. doi: 10.1111/cpr.13652. Epub 2024 May 3.
5
The Hippo signaling pathway in development and regeneration.发育与再生过程中的河马信号通路。
Cell Rep. 2024 Mar 26;43(3):113926. doi: 10.1016/j.celrep.2024.113926. Epub 2024 Mar 7.
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Natural compound library screening to identify berberine as a treatment for rheumatoid arthritis.天然化合物文库筛选鉴定小檗碱治疗类风湿关节炎。
Clin Rheumatol. 2024 Mar;43(3):959-969. doi: 10.1007/s10067-024-06871-1. Epub 2024 Feb 2.
7
Adipose-derived mesenchymal stem cells (MSCs) are a superior cell source for bone tissue engineering.脂肪来源的间充质干细胞是骨组织工程的优质细胞来源。
Bioact Mater. 2023 Dec 14;34:51-63. doi: 10.1016/j.bioactmat.2023.12.003. eCollection 2024 Apr.
8
SEPHS1 attenuates intervertebral disc degeneration by delaying nucleus pulposus cell senescence through the Hippo-Yap/Taz pathway.SEPHS1 通过 Hippo-Yap/Taz 通路延缓髓核细胞衰老来减轻椎间盘退变。
Am J Physiol Cell Physiol. 2024 Feb 1;326(2):C386-C399. doi: 10.1152/ajpcell.00571.2023. Epub 2023 Dec 18.
9
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Phytomedicine. 2024 Jan;123:155243. doi: 10.1016/j.phymed.2023.155243. Epub 2023 Dec 2.
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