Regulation of osteoclast polarization
- PMID: 17660975
- DOI: 10.1007/s10266-007-0071-y
Regulation of osteoclast polarization
Abstract
Osteoclast function consists of several processes: recognition of mineralized tissues, development of ruffled borders and sealing zones, secretion of acids and proteolytic enzymes into the space beneath the ruffled border, and incorporation and secretion of bone degradation products using the transcytosis system. One of the most important questions concerning osteoclast function is how osteoclasts recognize bone and polarize. During the past decade, new approaches have been taken to investigate the regulation of osteoclast polarization. Attachment of osteoclasts to some proteins containing the Arg-Gly-Asp sequence motif through vitronectin receptors is the first step in inducing the polarization of osteoclasts. Physical properties of bone such as hardness or roughness are also required to induce osteoclast polarity. Osteoclasts cultured even on plastic dishes secrete protons toward the dish surface, suggesting that osteoclasts recognize plastic as a mineralized matrix and secrete protons. This notion was supported by the recent findings that bisphosphonates and reveromycin A were specifically incorporated into polarized osteoclasts cultured even on plastic dishes. On the other hand, a sealing zone, defined as a thick band of actin, is induced in osteoclasts adherent only on an apatite-containing mineralized matrix. These results suggest that osteoclasts recognize physical properties of the mineralized tissue to secrete protons, and also sense apatite itself or components of apatite to form the sealing zone. Here, we review recent findings on the regulation of osteoclast polarization. We also discuss how osteoclasts recognize mineralized tissues to form the sealing zone.
Similar articles
-
Osteoclast integrin alphaVbeta3 is present in the clear zone and contributes to cellular polarization.Cell Tissue Res. 1996 Dec;286(3):507-15. doi: 10.1007/s004410050720. Cell Tissue Res. 1996. PMID: 8929353
-
Apatite-mediated actin dynamics in resorbing osteoclasts.Mol Biol Cell. 2004 Dec;15(12):5231-41. doi: 10.1091/mbc.e04-06-0522. Epub 2004 Sep 15. Mol Biol Cell. 2004. PMID: 15371537 Free PMC article.
-
Osteoclast polarization is not required for degradation of bone matrix in rachitic FGF23 transgenic mice.Bone. 2008 Jun;42(6):1111-21. doi: 10.1016/j.bone.2008.01.019. Epub 2008 Feb 13. Bone. 2008. PMID: 18346951
-
Intracellular membrane trafficking in bone resorbing osteoclasts.Microsc Res Tech. 2003 Aug 15;61(6):496-503. doi: 10.1002/jemt.10371. Microsc Res Tech. 2003. PMID: 12879417 Review.
-
[Osteoclasts in bone metabolism].Kaibogaku Zasshi. 1991 Aug;66(4):215-25. Kaibogaku Zasshi. 1991. PMID: 1759556 Review. Japanese.
Cited by
-
The Actin-Binding Protein PPP1r18 Regulates Maturation, Actin Organization, and Bone Resorption Activity of Osteoclasts.Mol Cell Biol. 2018 Jan 29;38(4):e00425-17. doi: 10.1128/MCB.00425-17. Print 2018 Feb 15. Mol Cell Biol. 2018. PMID: 29158294 Free PMC article.
-
Non-invasive optical detection of cathepsin K-mediated fluorescence reveals osteoclast activity in vitro and in vivo.Bone. 2009 Feb;44(2):190-8. doi: 10.1016/j.bone.2008.10.036. Epub 2008 Oct 22. Bone. 2009. PMID: 19007918 Free PMC article.
-
Osteoclasts' Ability to Generate Trenches Rather Than Pits Depends on High Levels of Active Cathepsin K and Efficient Clearance of Resorption Products.Int J Mol Sci. 2020 Aug 18;21(16):5924. doi: 10.3390/ijms21165924. Int J Mol Sci. 2020. PMID: 32824687 Free PMC article.
-
Puerarin specifically disrupts osteoclast activation via blocking integrin-β3 Pyk2/Src/Cbl signaling pathway.J Orthop Translat. 2022 Feb 16;33:55-69. doi: 10.1016/j.jot.2022.01.003. eCollection 2022 Mar. J Orthop Translat. 2022. PMID: 35228997 Free PMC article.
-
Cellular biology of fracture healing.J Orthop Res. 2019 Jan;37(1):35-50. doi: 10.1002/jor.24170. Epub 2018 Nov 30. J Orthop Res. 2019. PMID: 30370699 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous