• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

STAT3 介导的骨质疏松症中的成骨和破骨作用。

STAT3-mediated osteogenesis and osteoclastogenesis in osteoporosis.

机构信息

School of Public Health, North China University of Science and Technology, Caofeidian Dis, Bohai Road 21, Tangshan, 063210, People's Republic of China.

出版信息

Cell Commun Signal. 2022 Jul 25;20(1):112. doi: 10.1186/s12964-022-00924-1.

DOI:10.1186/s12964-022-00924-1
PMID:35879773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9310501/
Abstract

Osteoporosis is a common skeletal disease with marked bone loss, deterioration of the bone microstructure and bone fragility. An abnormal bone remodelling cycle with relatively increased bone resorption is the crucial pathophysiological mechanism. Bone remodelling is predominantly controlled by osteoblasts and osteoclasts, which are specialized cell types that are regulated by a variety of osteogenic and osteoclastic factors, including cytokines expressed within the bone microenvironment under local or systemic inflammatory conditions. Signal transducer and activator of transcription 3 (STAT3) plays a prominent role in the communication between cytokines and kinases by binding downstream gene promotors and is involved in a wide range of biological or pathological processes. Emerging evidence suggests that STAT3 and its network participate in bone remodelling and the development of osteoporosis, and this factor may be a potent target for osteoporosis treatment. This review focuses on the role and molecular mechanism of the STAT3 signalling pathway in osteogenesis, osteoclastogenesis and osteoporosis, particularly the bone-related cytokines that regulate the osteoblastic differentiation of bone marrow stromal cells and the osteoclastic differentiation of bone marrow macrophages by initiating STAT3 signalling. This review also examines the cellular interactions among immune cells, haematopoietic cells and osteoblastic/osteoclastic cells. Video abstract.

摘要

骨质疏松症是一种常见的骨骼疾病,其特征是明显的骨丢失、骨微观结构恶化和骨脆弱。异常的骨重塑周期,伴有相对增加的骨吸收,是关键的病理生理机制。骨重塑主要由成骨细胞和破骨细胞控制,这是两种专门的细胞类型,受多种成骨和破骨因子的调节,包括在局部或全身炎症条件下骨微环境中表达的细胞因子。信号转导子和转录激活子 3(STAT3)通过结合下游基因启动子,在细胞因子和激酶之间的通讯中发挥重要作用,并参与广泛的生物学或病理过程。新出现的证据表明,STAT3 及其网络参与骨重塑和骨质疏松症的发生,该因子可能是骨质疏松症治疗的有效靶点。本综述重点介绍 STAT3 信号通路在成骨、破骨和成骨 疏松症中的作用和分子机制,特别是通过启动 STAT3 信号通路调节骨髓基质细胞成骨分化和骨髓巨噬细胞破骨分化的骨相关细胞因子。本综述还研究了免疫细胞、造血细胞和成骨细胞/破骨细胞之间的细胞相互作用。视频摘要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/7aaeabeebf94/12964_2022_924_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/5625dd9955ee/12964_2022_924_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/7ce3be381aef/12964_2022_924_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/542c5612e260/12964_2022_924_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/4a1f89084c5a/12964_2022_924_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/7aaeabeebf94/12964_2022_924_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/5625dd9955ee/12964_2022_924_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/7ce3be381aef/12964_2022_924_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/542c5612e260/12964_2022_924_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/4a1f89084c5a/12964_2022_924_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897f/9310501/7aaeabeebf94/12964_2022_924_Fig5_HTML.jpg

相似文献

1
STAT3-mediated osteogenesis and osteoclastogenesis in osteoporosis.STAT3 介导的骨质疏松症中的成骨和破骨作用。
Cell Commun Signal. 2022 Jul 25;20(1):112. doi: 10.1186/s12964-022-00924-1.
2
The loss of STAT3 in mature osteoclasts has detrimental effects on bone structure.成熟破骨细胞中 STAT3 的缺失对骨结构有不良影响。
PLoS One. 2020 Jul 30;15(7):e0236891. doi: 10.1371/journal.pone.0236891. eCollection 2020.
3
Stattic inhibits RANKL-mediated osteoclastogenesis by suppressing activation of STAT3 and NF-κB pathways.Stattic 通过抑制 STAT3 和 NF-κB 通路的激活来抑制 RANKL 介导的破骨细胞生成。
Int Immunopharmacol. 2018 May;58:136-144. doi: 10.1016/j.intimp.2018.03.021. Epub 2018 Mar 26.
4
Combinatorial Surface Roughness Effects on Osteoclastogenesis and Osteogenesis.组合表面粗糙度对破骨细胞生成和成骨的影响。
ACS Appl Mater Interfaces. 2018 Oct 31;10(43):36652-36663. doi: 10.1021/acsami.8b10992. Epub 2018 Oct 16.
5
Methylsulfonylmethane Inhibits RANKL-Induced Osteoclastogenesis in BMMs by Suppressing NF-κB and STAT3 Activities.甲基磺酰甲烷通过抑制NF-κB和STAT3活性来抑制RANKL诱导的骨髓巨噬细胞破骨细胞生成。
PLoS One. 2016 Jul 22;11(7):e0159891. doi: 10.1371/journal.pone.0159891. eCollection 2016.
6
Suppression of IRF9 Promotes Osteoclast Differentiation by Decreased Ferroptosis via STAT3 Activation.抑制 IRF9 通过激活 STAT3 减少铁死亡来促进破骨细胞分化。
Inflammation. 2024 Feb;47(1):99-113. doi: 10.1007/s10753-023-01896-1. Epub 2023 Oct 7.
7
Lumichrome inhibits osteoclastogenesis and bone resorption through suppressing RANKL-induced NFAT activation and calcium signaling.卢米酮通过抑制 RANKL 诱导的 NFAT 激活和钙信号来抑制破骨细胞生成和骨吸收。
J Cell Physiol. 2018 Nov;233(11):8971-8983. doi: 10.1002/jcp.26841. Epub 2018 Jun 15.
8
The cross-talk between osteoclasts and osteoblasts in response to strontium treatment: involvement of osteoprotegerin.成骨细胞与破骨细胞间的串扰在锶治疗中的反应:骨保护素的参与。
Bone. 2011 Dec;49(6):1290-8. doi: 10.1016/j.bone.2011.08.031. Epub 2011 Sep 9.
9
Melatonin up-regulates bone marrow mesenchymal stem cells osteogenic action but suppresses their mediated osteoclastogenesis via MT -inactivated NF-κB pathway.褪黑素通过 MT 失活 NF-κB 通路上调骨髓间充质干细胞成骨作用,但抑制其介导的破骨细胞生成。
Br J Pharmacol. 2020 May;177(9):2106-2122. doi: 10.1111/bph.14972. Epub 2020 Feb 12.
10
Loss of signal transducer and activator of transcription 3 in osteoblasts impaired the bone healing in inflammatory microenvironment.成骨细胞中信号转导子和转录激活子 3 的缺失损害了炎症微环境中的骨愈合。
Mol Oral Microbiol. 2024 Jun;39(3):136-151. doi: 10.1111/omi.12425. Epub 2023 Jun 22.

引用本文的文献

1
Modulating Proliferation, Migration and Differentiation of Mesenchymal Stem Cells Using Interleukins.利用白细胞介素调节间充质干细胞的增殖、迁移和分化
Curr Stem Cell Res Ther. 2025;20(5):546-564. doi: 10.2174/011574888X313750240524115446.
2
Outer-Membrane Vesicles Are Internalized by Human Macrophages and Promote a Pro-Inflammatory Profile.外膜囊泡被人类巨噬细胞内化并促进促炎表型。
Int J Mol Sci. 2025 Apr 11;26(8):3630. doi: 10.3390/ijms26083630.
3
Bioinformatics-Based Analysis of Ferroptosis-Related Biomarkers and the Prediction of Drugs Affecting the Adipogenic Differentiation of MSCs.

本文引用的文献

1
PIAS3/SOCS1-STAT3 axis responses to oxidative stress in hepatocellular cancer cells.PIAS3/SOCS1-STAT3轴对肝癌细胞氧化应激的反应
Am J Transl Res. 2021 Nov 15;13(11):12395-12409. eCollection 2021.
2
STAT3 is critical for skeletal development and bone homeostasis by regulating osteogenesis.STAT3 在骨骼发育和骨内稳态中起着关键作用,通过调节成骨作用。
Nat Commun. 2021 Nov 25;12(1):6891. doi: 10.1038/s41467-021-27273-w.
3
STAT3 as a mediator of oncogenic cellular metabolism: Pathogenic and therapeutic implications.STAT3 作为致癌细胞代谢的介质:发病机制和治疗意义。
基于生物信息学的铁死亡相关生物标志物分析及影响间充质干细胞成脂分化的药物预测
Biomedicines. 2025 Apr 11;13(4):940. doi: 10.3390/biomedicines13040940.
4
STAT3 Signaling Pathway in Health and Disease.健康与疾病中的信号转导和转录激活因子3(STAT3)信号通路
MedComm (2020). 2025 Mar 30;6(4):e70152. doi: 10.1002/mco2.70152. eCollection 2025 Apr.
5
The dual role of titanium particles in osteolysis: implications for gene therapy in prosthesis loosening.钛颗粒在骨溶解中的双重作用:对假体松动基因治疗的启示。
Eur J Med Res. 2025 Mar 29;30(1):216. doi: 10.1186/s40001-025-02452-3.
6
LINC00968 accelerates osteogenic differentiation of bone marrow mesenchymal stem cells via the miR-17-5p/STAT3 axis.LINC00968通过miR-17-5p/STAT3轴加速骨髓间充质干细胞的成骨分化。
J Orthop Surg Res. 2025 Mar 6;20(1):242. doi: 10.1186/s13018-025-05627-0.
7
Functionalized zeolite regulates bone metabolic microenvironment.功能化沸石调节骨代谢微环境。
Mater Today Bio. 2025 Feb 5;31:101558. doi: 10.1016/j.mtbio.2025.101558. eCollection 2025 Apr.
8
Network Pharmacology and Experimental Validation of the Therapeutic Effect of Baji Capsule on LPS-Induced Osteoporosis.八极胶囊对脂多糖诱导的骨质疏松症治疗作用的网络药理学及实验验证
Orthop Res Rev. 2025 Feb 11;17:61-81. doi: 10.2147/ORR.S488478. eCollection 2025.
9
The potential link between the development of Alzheimer's disease and osteoporosis.阿尔茨海默病的发展与骨质疏松症之间的潜在联系。
Biogerontology. 2025 Jan 20;26(1):43. doi: 10.1007/s10522-024-10181-z.
10
Loss of STAT3 in osteoblasts has detrimental and sexually dimorphic effects on skeletal development.成骨细胞中STAT3的缺失对骨骼发育具有有害的性别差异影响。
PLoS One. 2024 Dec 17;19(12):e0315078. doi: 10.1371/journal.pone.0315078. eCollection 2024.
Neoplasia. 2021 Dec;23(12):1167-1178. doi: 10.1016/j.neo.2021.10.003. Epub 2021 Oct 29.
4
LncRNA ROR/miR-145-5p axis modulates the osteoblasts proliferation and apoptosis in osteoporosis.长链非编码 RNA ROR/miR-145-5p 轴调控骨质疏松症中骨细胞的增殖和凋亡。
Bioengineered. 2021 Dec;12(1):7714-7723. doi: 10.1080/21655979.2021.1982323.
5
Incidence of osteoporosis and ambient air pollution in South Korea: a population-based retrospective cohort study.韩国骨质疏松症的发病率与环境空气污染:一项基于人群的回顾性队列研究。
BMC Public Health. 2021 Oct 6;21(1):1794. doi: 10.1186/s12889-021-11866-7.
6
Role of long non-coding RNA H19 in the development of osteoporosis.长链非编码 RNA H19 在骨质疏松症发展中的作用。
Mol Med. 2021 Sep 28;27(1):122. doi: 10.1186/s10020-021-00386-0.
7
Naringin promotes osteogenesis and ameliorates osteoporosis development by targeting JAK2/STAT3 signalling.柚皮苷通过靶向JAK2/STAT3信号通路促进成骨作用并改善骨质疏松症的发展。
Clin Exp Pharmacol Physiol. 2022 Jan;49(1):113-121. doi: 10.1111/1440-1681.13591. Epub 2021 Oct 21.
8
MiR-183 regulates the differentiation of osteoblasts in the development of osteoporosis by targeting Smad4.miR-183 通过靶向 Smad4 调节成骨细胞分化在骨质疏松症的发展中。
Acta Histochem. 2021 Oct;123(7):151786. doi: 10.1016/j.acthis.2021.151786. Epub 2021 Sep 9.
9
Emerging roles of circular RNAs in osteoporosis.环状 RNA 在骨质疏松症中的新兴作用。
J Cell Mol Med. 2021 Oct;25(19):9089-9101. doi: 10.1111/jcmm.16906. Epub 2021 Sep 6.
10
DUSP6 expression is associated with osteoporosis through the regulation of osteoclast differentiation via ERK2/Smad2 signaling.DUSP6 的表达通过 ERK2/Smad2 信号通路调节破骨细胞分化与骨质疏松症相关。
Cell Death Dis. 2021 Sep 2;12(9):825. doi: 10.1038/s41419-021-04110-y.