• 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

破骨细胞与整合素

Osteoclasts and integrins.

作者信息

Teitelbaum Steven L

机构信息

Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Ann N Y Acad Sci. 2006 Apr;1068:95-9. doi: 10.1196/annals.1346.017.

DOI:10.1196/annals.1346.017
PMID:16831909
Abstract

The osteoclast is the unique bone resorptive cell that accomplishes its mission by forming an isolated acidified microenvironment between itself and the bone surface. Creation of this compartment is the first step in bone degradation and establishes that an intimate physical relationship must exist between the osteoclast and bone. Thus, identification of the mechanisms by which the osteoclast attaches to bone is essential to understanding how the cell degrades skeletal tissue. Our studies have investigated whether absence of the alphavbeta3 integrin modifies the ability of c-Fms to induce Rho GTPases, and the implications for formation of the osteoclast cytoskeleton.

摘要

破骨细胞是独特的骨吸收细胞,它通过在自身与骨表面之间形成一个孤立的酸化微环境来完成其使命。创建这个区室是骨降解的第一步,并表明破骨细胞与骨之间必须存在密切的物理关系。因此,确定破骨细胞附着于骨的机制对于理解该细胞如何降解骨骼组织至关重要。我们的研究调查了αvβ3整合素的缺失是否会改变c-Fms诱导Rho GTP酶的能力,以及对破骨细胞细胞骨架形成的影响。

相似文献

1
Osteoclasts and integrins.破骨细胞与整合素
Ann N Y Acad Sci. 2006 Apr;1068:95-9. doi: 10.1196/annals.1346.017.
2
Immunolocalization of beta 3 subunit of integrins in osteoclast membrane.整合素β3亚基在破骨细胞膜中的免疫定位
Boll Soc Ital Biol Sper. 1989 Nov;65(11):1031-7.
3
Bone remodeling and the osteoclast.骨重塑与破骨细胞
J Bone Miner Res. 1993 Dec;8 Suppl 2:S523-5. doi: 10.1002/jbmr.5650081318.
4
Integrin-mediated signaling in the regulation of osteoclast adhesion and activation.整合素介导的信号传导在破骨细胞黏附与激活调节中的作用
Front Biosci. 1998 Aug 1;3:d757-68. doi: 10.2741/A319.
5
The Rho GTPase Wrch1 regulates osteoclast precursor adhesion and migration.Rho GTP酶Wrch1调节破骨细胞前体的黏附与迁移。
Int J Biochem Cell Biol. 2009 Jun;41(6):1391-401. doi: 10.1016/j.biocel.2008.12.007. Epub 2008 Dec 24.
6
Rho GTPases in osteoclasts: orchestrators of podosome arrangement.破骨细胞中的Rho GTP酶:足体排列的协调者
Eur J Cell Biol. 2008 Sep;87(8-9):469-77. doi: 10.1016/j.ejcb.2008.03.002. Epub 2008 Apr 23.
7
M-CSF, c-Fms, and signaling in osteoclasts and their precursors.巨噬细胞集落刺激因子、原癌基因c-Fms与破骨细胞及其前体细胞中的信号传导
Ann N Y Acad Sci. 2006 Apr;1068:110-6. doi: 10.1196/annals.1346.014.
8
Baicalein inhibits osteoclast differentiation and induces mature osteoclast apoptosis.黄芩素抑制破骨细胞分化并诱导成熟破骨细胞凋亡。
Food Chem Toxicol. 2008 Nov;46(11):3375-82. doi: 10.1016/j.fct.2008.08.016. Epub 2008 Aug 26.
9
Blockade of osteoclast-mediated bone resorption through occupancy of the integrin receptor: a potential approach to the therapy of osteoporosis.通过占据整合素受体阻断破骨细胞介导的骨吸收:一种治疗骨质疏松症的潜在方法。
J Cell Biochem. 1994 Nov;56(3):323-30. doi: 10.1002/jcb.240560308.
10
Osteoclast-osteoblast communication.破骨细胞-成骨细胞通讯
Arch Biochem Biophys. 2008 May 15;473(2):201-9. doi: 10.1016/j.abb.2008.03.027. Epub 2008 Mar 29.

引用本文的文献

1
Overexpression of miR17 ~ 92 in Myeloid Cells in Mice Increased Bone Mass Through Reduced Bone Resorption and Increased Bone Formation in Sex-Dependent Manner.小鼠骨髓细胞中miR17 ~ 92的过表达通过减少骨吸收和增加骨形成以性别依赖的方式增加骨量。
Calcif Tissue Int. 2025 Jan 3;116(1):9. doi: 10.1007/s00223-024-01325-x.
2
Imaging of Bone Metastases in Breast Cancer.乳腺癌骨转移的影像学表现。
Semin Nucl Med. 2022 Sep;52(5):531-541. doi: 10.1053/j.semnuclmed.2022.01.005. Epub 2022 Feb 27.
3
Decreased Trabecular Bone Mass in -Deficient Mice.
- 缺乏症小鼠的骨小梁骨量减少。
Cells. 2021 Nov 4;10(11):3020. doi: 10.3390/cells10113020.
4
Imaging with radiolabelled bisphosphonates.放射性标记双膦酸盐的影像学检查。
Bone. 2020 Aug;137:115372. doi: 10.1016/j.bone.2020.115372. Epub 2020 Apr 28.
5
Bone morphogenetic proteins: Their role in regulating osteoclast differentiation.骨形态发生蛋白:它们在调节破骨细胞分化中的作用。
Bone Rep. 2019 May 5;10:100207. doi: 10.1016/j.bonr.2019.100207. eCollection 2019 Jun.
6
Engineering of L-Plastin Peptide-Loaded Biodegradable Nanoparticles for Sustained Delivery and Suppression of Osteoclast Function In Vitro.负载L-肌动蛋白肽的可生物降解纳米颗粒的工程设计用于体外持续递送和抑制破骨细胞功能
Int J Cell Biol. 2019 May 5;2019:6943986. doi: 10.1155/2019/6943986. eCollection 2019.
7
A novel miR17/protein tyrosine phosphatase-oc/EphA4 regulatory axis of osteoclast activity.一种新型的 miR17/蛋白酪氨酸磷酸酶-oc/EphA4 调节破骨细胞活性的轴。
Arch Biochem Biophys. 2018 Jul 15;650:30-38. doi: 10.1016/j.abb.2018.05.014. Epub 2018 May 17.
8
Functional and Hybrid Imaging of Bone Metastases.骨转移的功能与混合成像
J Bone Miner Res. 2018 Jun;33(6):961-972. doi: 10.1002/jbmr.3444. Epub 2018 May 23.
9
Imaging αβ integrin expression in skeletal metastases with Tc-maraciclatide single-photon emission computed tomography: detection and therapy response assessment.Tc-马卡瑞肽单光子发射计算机断层扫描显示骨骼转移中 αβ 整合素的表达:检测和治疗反应评估。
Eur J Nucl Med Mol Imaging. 2018 Jun;45(6):898-903. doi: 10.1007/s00259-017-3926-7. Epub 2018 Feb 2.
10
Conditional Disruption of in Osteoclasts Led to Activation of Osteoclasts and Loss of Trabecular Bone In Part Through Suppression of the miR17-Mediated Downregulation of Protein-Tyrosine Phosphatase-oc in Mice.破骨细胞中[具体基因]的条件性破坏导致破骨细胞活化和骨小梁骨丢失,部分原因是通过抑制miR17介导的小鼠蛋白酪氨酸磷酸酶-oc的下调。
JBMR Plus. 2017 Oct;1(2):73-85. doi: 10.1002/jbm4.10014. Epub 2017 Aug 1.