• 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

利用内源性细胞机制促进骨修复。

Harnessing Endogenous Cellular Mechanisms for Bone Repair.

作者信息

Lo Sicco Claudia, Tasso Roberta

机构信息

Department of Experimental Medicine, University of Genoa, Genoa, Italy.

Ospedale Policlinico San Martino, Istituto di Ricovero e Cura a Carattere Scientifico per l'Oncologia, Genoa, Italy.

出版信息

Front Bioeng Biotechnol. 2017 Sep 4;5:52. doi: 10.3389/fbioe.2017.00052. eCollection 2017.

DOI:10.3389/fbioe.2017.00052
PMID:28929099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5591576/
Abstract

Although autologous tissue transplantation represents a valid approach for bone repair, it has encountered crucial barriers in therapeutic translation, not least the invasive process necessary for stem cell isolation. In recent years, the scientific community has made significant strides for identifying new treatment options, and great emphasis has been placed on the tight interaction between skeletal and immune system in modulating the outcome of bone repair. Within the context of specific injury environmental cues, the cross talk among inflammatory cells and tissue resident and/or circulating progenitor cells is crucial to finely coordinate repair and remodeling processes. The appropriate modulation of the inflammatory response can now be considered a new trend in the field of regenerative medicine, as it raises the attracting possibility to enhance endogenous progenitor cell functions, finally leading to tissue repair. Therefore, new treatment options have been developed considering the wide spectrum of bone-inflammation interplay, considering in particular the cell intrinsic cues responsible for the modulation of the injured environment. In this review, we will provide a panoramic overview focusing on novel findings developed to uphold endogenous bone repair.

摘要

尽管自体组织移植是骨修复的一种有效方法,但它在治疗转化过程中遇到了关键障碍,尤其是干细胞分离所需的侵入性过程。近年来,科学界在确定新的治疗选择方面取得了重大进展,并且高度重视骨骼与免疫系统在调节骨修复结果中的紧密相互作用。在特定损伤环境线索的背景下,炎症细胞与组织驻留和/或循环祖细胞之间的相互作用对于精细协调修复和重塑过程至关重要。现在,适当调节炎症反应可被视为再生医学领域的一个新趋势,因为它带来了增强内源性祖细胞功能的诱人可能性,最终导致组织修复。因此,考虑到骨与炎症相互作用的广泛范围,特别是考虑到负责调节损伤环境的细胞内在线索,已经开发了新的治疗选择。在这篇综述中,我们将提供一个全景概述,重点关注为支持内源性骨修复而取得的新发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ea/5591576/582393bdf6a4/fbioe-05-00052-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ea/5591576/582393bdf6a4/fbioe-05-00052-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3ea/5591576/582393bdf6a4/fbioe-05-00052-g001.jpg

相似文献

1
Harnessing Endogenous Cellular Mechanisms for Bone Repair.利用内源性细胞机制促进骨修复。
Front Bioeng Biotechnol. 2017 Sep 4;5:52. doi: 10.3389/fbioe.2017.00052. eCollection 2017.
2
Stem Cell Therapy in Brain Trauma: Implications for Repair and Regeneration of Injured Brain in Experimental TBI Models脑外伤中的干细胞治疗:对实验性创伤性脑损伤模型中受损脑修复和再生的影响
3
Modulation of the Activity of Stem and Progenitor Cells by Immune Cells.免疫细胞对干细胞和祖细胞活性的调节。
Stem Cells Transl Med. 2022 Mar 31;11(3):248-258. doi: 10.1093/stcltm/szab022.
4
At the interface of the immune system and the nervous system: how neuroinflammation modulates the fate of neural progenitors in vivo.
Ernst Schering Res Found Workshop. 2005(53):83-114. doi: 10.1007/3-540-27626-2_6.
5
Influence of Platelet-Rich and Platelet-Poor Plasma on Endogenous Mechanisms of Skeletal Muscle Repair/Regeneration.富血小板血浆和贫血小板血浆对骨骼肌修复/再生内源性机制的影响。
Int J Mol Sci. 2019 Feb 5;20(3):683. doi: 10.3390/ijms20030683.
6
Implementation of Endogenous and Exogenous Mesenchymal Progenitor Cells for Skeletal Tissue Regeneration and Repair.内源性和外源性间充质祖细胞在骨骼组织再生与修复中的应用
Bioengineering (Basel). 2020 Aug 4;7(3):86. doi: 10.3390/bioengineering7030086.
7
Regenerative pharmacology for the treatment of acute kidney injury: Skeletal muscle stem/progenitor cells for renal regeneration?用于治疗急性肾损伤的再生药理学:骨骼肌干/祖细胞用于肾脏再生?
Pharmacol Res. 2016 Nov;113(Pt B):802-807. doi: 10.1016/j.phrs.2016.03.014. Epub 2016 Mar 18.
8
Ambivalence of progenitor cells in vascular repair and plaque stability.祖细胞在血管修复和斑块稳定性中的矛盾性。
Curr Opin Lipidol. 2008 Oct;19(5):491-7. doi: 10.1097/MOL.0b013e32830dfe33.
9
Homing of endogenous stem/progenitor cells for in situ tissue regeneration: Promises, strategies, and translational perspectives.内源性干细胞/祖细胞的归巢用于原位组织再生:前景、策略和转化视角。
Biomaterials. 2011 Apr;32(12):3189-209. doi: 10.1016/j.biomaterials.2010.12.032.
10
Genesis of myocardial repair with cardiac progenitor cells and tissue engineering.心脏祖细胞与组织工程促进心肌修复的机制
Heart Asia. 2010 Sep 18;2(1):109-11. doi: 10.1136/ha.2009.001651. eCollection 2010.

引用本文的文献

1
Progress in Dentin-Derived Bone Graft Materials: A New Xenogeneic Dentin-Derived Material with Retained Organic Component Allows for Broader and Easier Application.牙本质衍生骨移植材料的研究进展:一种新型保留有机成分的异种牙本质衍生材料,具有更广泛和更容易的应用前景。
Cells. 2024 Oct 31;13(21):1806. doi: 10.3390/cells13211806.
2
Implications of siRNA Therapy in Bone Health: Silencing Communicates.小干扰RNA疗法对骨骼健康的影响:沉默进行交流。
Biomedicines. 2024 Jan 1;12(1):90. doi: 10.3390/biomedicines12010090.
3
From Free Tissue Transfer to Hydrogels: A Brief Review of the Application of the Periosteum in Bone Regeneration.

本文引用的文献

1
Bone fracture healing is delayed in splenectomic rats.脾切除大鼠的骨折愈合延迟。
Life Sci. 2017 Mar 15;173:55-61. doi: 10.1016/j.lfs.2016.12.005. Epub 2016 Dec 10.
2
Fracture healing physiology and the quest for therapies for delayed healing and nonunion.骨折愈合生理学以及对延迟愈合和骨不连治疗方法的探索。
J Orthop Res. 2017 Feb;35(2):213-223. doi: 10.1002/jor.23460. Epub 2016 Dec 19.
3
Resting and injury-induced inflamed periosteum contain multiple macrophage subsets that are located at sites of bone growth and regeneration.
从游离组织移植到水凝胶:骨膜在骨再生中应用的简要综述
Gels. 2023 Sep 21;9(9):768. doi: 10.3390/gels9090768.
4
Extracellular Matrices to Modulate the Innate Immune Response and Enhance Bone Healing.细胞外基质调节固有免疫反应和增强骨愈合。
Front Immunol. 2019 Sep 20;10:2256. doi: 10.3389/fimmu.2019.02256. eCollection 2019.
5
Editorial: Vascularization for Regenerative Medicine.社论:再生医学中的血管化
Front Bioeng Biotechnol. 2018 Nov 21;6:175. doi: 10.3389/fbioe.2018.00175. eCollection 2018.
6
Circulating healing (CH) cells expressing BST2 are functionally activated by the injury-regulated systemic factor HGFA.循环修复 (CH) 细胞表达 BST2,可被损伤调节的系统性因子 HGFA 激活。
Stem Cell Res Ther. 2018 Nov 8;9(1):300. doi: 10.1186/s13287-018-1056-1.
静息和损伤诱导炎症的骨膜含有多种巨噬细胞亚群,这些亚群位于骨骼生长和再生部位。
Immunol Cell Biol. 2017 Jan;95(1):7-16. doi: 10.1038/icb.2016.74. Epub 2016 Nov 15.
4
Highly Dynamic Transcriptional Signature of Distinct Macrophage Subsets during Sterile Inflammation, Resolution, and Tissue Repair.无菌性炎症、消退和组织修复过程中不同巨噬细胞亚群的高度动态转录特征
J Immunol. 2016 Jun 1;196(11):4771-82. doi: 10.4049/jimmunol.1502490. Epub 2016 Apr 29.
5
Inhibition of IL-1R1/MyD88 signalling promotes mesenchymal stem cell-driven tissue regeneration.抑制白细胞介素-1受体1/髓样分化因子88信号通路可促进间充质干细胞驱动的组织再生。
Nat Commun. 2016 Mar 22;7:11051. doi: 10.1038/ncomms11051.
6
Abdominal aortic calcification: A reappraisal of epidemiological and pathophysiological data.腹主动脉钙化:流行病学和病理生理学数据的重新评估。
Bone. 2016 Mar;84:25-37. doi: 10.1016/j.bone.2015.12.004. Epub 2015 Dec 10.
7
Identification of a New Cell Population Constitutively Circulating in Healthy Conditions and Endowed with a Homing Ability Toward Injured Sites.鉴定一种在健康状态下持续循环且具有向损伤部位归巢能力的新细胞群体。
Sci Rep. 2015 Nov 12;5:16574. doi: 10.1038/srep16574.
8
Atorvastatin Reduces Circulating Osteoprogenitor Cells and T-Cell RANKL Expression in Osteoporotic Women: Implications for the Bone-Vascular Axis.阿托伐他汀可减少骨质疏松症女性循环中的骨祖细胞及T细胞RANKL表达:对骨-血管轴的影响
Cardiovasc Ther. 2016 Feb;34(1):13-20. doi: 10.1111/1755-5922.12163.
9
Exposure to a youthful circulaton rejuvenates bone repair through modulation of β-catenin.暴露于年轻的循环系统中可通过调节β-连环蛋白来促进骨修复。
Nat Commun. 2015 May 19;6:7131. doi: 10.1038/ncomms8131.
10
Identification and specification of the mouse skeletal stem cell.小鼠骨骼干细胞的鉴定与特性研究
Cell. 2015 Jan 15;160(1-2):285-98. doi: 10.1016/j.cell.2014.12.002.