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本文引用的文献

1
Matrix metalloproteinase-driven endochondral fracture union proceeds independently of osteoclast activity.基质金属蛋白酶驱动的软骨内骨折愈合过程独立于破骨细胞活性。
J Bone Miner Res. 2013 Jul;28(7):1550-60. doi: 10.1002/jbmr.1889.
2
Patient-related risk factors for fracture-healing complications in the United Kingdom General Practice Research Database.英国普通实践研究数据库中与患者相关的骨折愈合并发症风险因素。
Acta Orthop. 2012 Dec;83(6):653-60. doi: 10.3109/17453674.2012.747054. Epub 2012 Nov 9.
3
MMP9 regulates the cellular response to inflammation after skeletal injury.MMP9 调节骨骼损伤后炎症细胞的反应。
Bone. 2013 Jan;52(1):111-9. doi: 10.1016/j.bone.2012.09.018. Epub 2012 Sep 23.
4
Human macrophage regulation via interaction with cardiac adipose tissue-derived mesenchymal stromal cells.通过与心脏脂肪组织来源的间充质基质细胞相互作用调节人巨噬细胞。
J Cardiovasc Pharmacol Ther. 2013 Jan;18(1):78-86. doi: 10.1177/1074248412453875. Epub 2012 Aug 15.
5
Classical macrophage activation up-regulates several matrix metalloproteinases through mitogen activated protein kinases and nuclear factor-κB.经典的巨噬细胞激活通过丝裂原活化蛋白激酶和核因子-κB 上调几种基质金属蛋白酶。
PLoS One. 2012;7(8):e42507. doi: 10.1371/journal.pone.0042507. Epub 2012 Aug 3.
6
Monocytes induce STAT3 activation in human mesenchymal stem cells to promote osteoblast formation.单核细胞诱导人骨髓间充质干细胞中 STAT3 的激活,促进成骨细胞的形成。
PLoS One. 2012;7(7):e39871. doi: 10.1371/journal.pone.0039871. Epub 2012 Jul 3.
7
Chondroclasts are mature osteoclasts which are capable of cartilage matrix resorption.软骨细胞是成熟的破骨细胞,能够吸收软骨基质。
Virchows Arch. 2012 Aug;461(2):205-10. doi: 10.1007/s00428-012-1274-3. Epub 2012 Jul 11.
8
Current insights on the regenerative potential of the periosteum: molecular, cellular, and endogenous engineering approaches.目前对骨膜再生潜力的认识:分子、细胞和内源性工程方法。
J Orthop Res. 2012 Dec;30(12):1869-78. doi: 10.1002/jor.22181. Epub 2012 Jul 9.
9
CCR2 recruits an inflammatory macrophage subpopulation critical for angiogenesis in tissue repair.CCR2 招募了一个炎症性巨噬细胞亚群,该亚群对于组织修复中的血管生成至关重要。
Blood. 2012 Jul 19;120(3):613-25. doi: 10.1182/blood-2012-01-403386. Epub 2012 May 10.
10
Macrophage plasticity and polarization: in vivo veritas.巨噬细胞的可塑性和极化:体内的真实情况。
J Clin Invest. 2012 Mar;122(3):787-95. doi: 10.1172/JCI59643. Epub 2012 Mar 1.

解析巨噬细胞对骨修复的作用。

Unraveling macrophage contributions to bone repair.

作者信息

Wu Andy C, Raggatt Liza J, Alexander Kylie A, Pettit Allison R

机构信息

Mater Research, Translational Research Institute , Woolloongabba, Queensland, Australia ; UQ-Centre for Clinical Research, Royal Brisbane and Women's Hospital, The University of Queensland , Herston, Queensland, Australia.

Mater Research, Translational Research Institute , Woolloongabba, Queensland, Australia.

出版信息

Bonekey Rep. 2013 Jun 26;2:373. doi: 10.1038/bonekey.2013.107. eCollection 2013.

DOI:10.1038/bonekey.2013.107
PMID:25035807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4098570/
Abstract

Macrophages have reemerged to prominence with widened understanding of their pleiotropic contributions to many biologies and pathologies. This includes clear advances in revealing their importance in wound healing. Here we have focused on the current state of knowledge with respect to bone repair, which has received relatively little scientific attention compared with its soft-tissue counterparts. Our detailed characterization of resident tissue macrophages residing in bone-lining tissues (osteomacs), including their pro-anabolic function, exposed a more prominent role for these cells in bone biology than previously anticipated. Recent studies have confirmed the importance of macrophages in early inflammatory processes that establish the healing cascade after bone fracture. Emerging data support that macrophage influence extends into both anabolic and catabolic phases of repair, suggesting that these cells have prolonged and diverse functions during fracture healing. More research is needed to clarify macrophage phase-specific contributions, temporospatial subpopulation variance and macrophage specific-molecular mediators. There is also clear motivation for determining whether macrophage alterations underlie compromised fracture healing. Overall, there is strong justification to pursue strategies targeting macrophages and/or their products for improving normal bone healing and overcoming failed repair.

摘要

随着对巨噬细胞在多种生物学和病理学中多效性作用的深入了解,它们再次成为研究热点。这包括在揭示其在伤口愈合中的重要性方面取得的明显进展。在此,我们聚焦于骨修复方面的当前知识状态,相较于软组织修复,骨修复受到的科学关注相对较少。我们对驻留在骨衬组织中的组织巨噬细胞(骨巨噬细胞)进行了详细表征,包括它们的促合成代谢功能,结果表明这些细胞在骨生物学中的作用比之前预期的更为突出。最近的研究证实了巨噬细胞在早期炎症过程中的重要性,这些炎症过程启动了骨折后的愈合级联反应。新出现的数据支持巨噬细胞的影响延伸至修复的合成代谢和分解代谢阶段,这表明这些细胞在骨折愈合过程中具有长期且多样的功能。需要更多研究来阐明巨噬细胞在不同阶段的具体作用、时空亚群差异以及巨噬细胞特异性分子介质。确定巨噬细胞的改变是否是骨折愈合受损的基础也具有明确的研究意义。总体而言,有充分的理由探索针对巨噬细胞和/或其产物的策略,以促进正常骨愈合并克服修复失败的问题。