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10.2147/IJN.S214363

http://scihub22266oqcxt.onion/10.2147/IJN.S214363
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31413570!6662177!31413570
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suck abstract from ncbi

pmid31413570      Int+J+Nanomedicine 2019 ; 14 (?): 5697-5711
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  • The relative effects of Ca and Mg ions on MSC osteogenesis in the surface modification of microrough Ti implants #MMPMID31413570
  • Park JW; Hanawa T; Chung JH
  • Int J Nanomedicine 2019[]; 14 (?): 5697-5711 PMID31413570show ga
  • PURPOSE: Calcium (Ca) and magnesium (Mg) ions have been used as promising bioactive ions in the surface chemistry modification of titanium (Ti) bone implants to increase bone regeneration capacity. However, it is not clear which (Ca or Mg) plays the more important role in the early osteogenic differentiation of mesenchymal stem cells (MSCs) when applied to the surface of commercially available microstructured Ti implants. This study investigated the relative effect of these two ions on the early osteogenic functionality of primary mouse bone marrow MSCs in order to obtain insights into the surface design of Ti implants with enhanced early osteogenic capacity. METHODS AND RESULTS: Wet chemical treatment was performed to modify a microrough Ti implant surface using Ca or Mg ions. Both the Ca and Mg-incorporated surfaces accelerated early cellular events and the subsequent osteogenic differentiation of MSCs compared with an unmodified microrough Ti surface. Surface Mg modification exhibited a more potent osteoblast differentiation-promoting effect than the Ca modification. Surface Mg incorporation markedly inhibited the phosphorylation of beta-catenin. CONCLUSION: These results indicate that alteration of the surface chemistry of microstructured Ti implants by wet chemical treatment with Mg ions exerts a more effect on promoting the early osteogenic differentiation of MSCs than Ca ions by enhancing early cellular functions, including focal adhesion development and stabilization of intracellular beta-catenin.
  • |*Prostheses and Implants[MESH]
  • |Animals[MESH]
  • |Calcium/*pharmacology[MESH]
  • |Cations, Divalent/pharmacology[MESH]
  • |Cell Adhesion/drug effects[MESH]
  • |Cell Differentiation/drug effects[MESH]
  • |Cell Proliferation/drug effects[MESH]
  • |Cell Shape/drug effects[MESH]
  • |Focal Adhesions/drug effects[MESH]
  • |Ions[MESH]
  • |Magnesium/*pharmacology[MESH]
  • |Mesenchymal Stem Cells/*cytology/drug effects/ultrastructure[MESH]
  • |Mice[MESH]
  • |Osteogenesis/*drug effects[MESH]
  • |Phosphorylation/drug effects[MESH]
  • |RNA, Messenger/genetics/metabolism[MESH]
  • |Surface Properties[MESH]
  • |Titanium/*pharmacology[MESH]
  • |Water/chemistry[MESH]
  • |X-Ray Diffraction[MESH]


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