Age-Related Effects of Advanced Glycation End Products (Ages) in Bone Matrix on Osteoclastic Resorption

Verfasser / Beitragende:
[Xiao Yang, Chintan Gandhi, MD. Rahman, Mark Appleford, Lian-Wen Sun, Xiaodu Wang]
Ort, Verlag, Jahr:
2015
Enthalten in:
Calcified Tissue International, 97/6(2015-12-01), 592-601
Format:
Artikel (online)
ID: 605520577
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024 7 0 |a 10.1007/s00223-015-0042-1  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00223-015-0042-1 
245 0 0 |a Age-Related Effects of Advanced Glycation End Products (Ages) in Bone Matrix on Osteoclastic Resorption  |h [Elektronische Daten]  |c [Xiao Yang, Chintan Gandhi, MD. Rahman, Mark Appleford, Lian-Wen Sun, Xiaodu Wang] 
520 3 |a Advanced glycation end products (AGEs) accumulate in bone extracellular matrix as people age. Previous studies have shown controversial results regarding the role of in situ AGEs accumulation in osteoclastic resorption. To address this issue, this study cultured human osteoclast cells directly on human cadaveric bone slices from different age groups (young and elderly) to warrant its relevance to in vivo conditions. The cell culture was terminated on the 3rd, 7th, and 10th day, respectively, to assess temporal changes in the number of differentiated osteoclasts, the number and size of osteoclastic resorption pits, the amount of bone resorbed, as well as the amount of matrix AGEs released in the medium by resorption. In addition, the in situ concentration of matrix AGEs at each resorption pit was also estimated based on its AGEs autofluorescent intensity. The results indicated that (1) osteoclastic resorption activities were significantly correlated with the donor age, showing larger but shallower resorption pits on the elderly bone substrates than on the younger ones; (2) osteoclast resorption activities were not significantly dependent on the in situ AGEs concentration in bone matrix, and (3) a correlation was observed between osteoclast activities and the concentration of AGEs released by the resorption. These results suggest that osteoclasts tend to migrate away from initial anchoring sites on elderly bone substrate during resorption compared to younger bone substrates. However, such behavior is not directly related to the in situ concentration of AGEs in bone matrix at the resorption sites. 
540 |a Springer Science+Business Media New York, 2015 
690 7 |a Bone  |2 nationallicence 
690 7 |a Osteoclast  |2 nationallicence 
690 7 |a Advanced glycation end products (AGEs)  |2 nationallicence 
690 7 |a Bone resorption  |2 nationallicence 
700 1 |a Yang  |D Xiao  |u School of Biological Sciences and Medical Engineering, Beihang University, Beijing, China  |4 aut 
700 1 |a Gandhi  |D Chintan  |u Departments of Biomedical Engineering, The University of Texas at San Antonio (UTSA), One UTSA Circle, 78249, San Antonio, TX, USA  |4 aut 
700 1 |a Rahman  |D MD  |u Department of Medicine, University of Texas Health Science Center at San Antonio (UTHSCSA), San Antonio, USA  |4 aut 
700 1 |a Appleford  |D Mark  |u Departments of Biomedical Engineering, The University of Texas at San Antonio (UTSA), One UTSA Circle, 78249, San Antonio, TX, USA  |4 aut 
700 1 |a Sun  |D Lian-Wen  |u School of Biological Sciences and Medical Engineering, Beihang University, Beijing, China  |4 aut 
700 1 |a Wang  |D Xiaodu  |u Departments of Biomedical Engineering, The University of Texas at San Antonio (UTSA), One UTSA Circle, 78249, San Antonio, TX, USA  |4 aut 
773 0 |t Calcified Tissue International  |d Springer US; http://www.springer-ny.com  |g 97/6(2015-12-01), 592-601  |x 0171-967X  |q 97:6<592  |1 2015  |2 97  |o 223 
856 4 0 |u https://doi.org/10.1007/s00223-015-0042-1  |q text/html  |z Onlinezugriff via DOI 
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900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
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950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00223-015-0042-1  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Yang  |D Xiao  |u School of Biological Sciences and Medical Engineering, Beihang University, Beijing, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Gandhi  |D Chintan  |u Departments of Biomedical Engineering, The University of Texas at San Antonio (UTSA), One UTSA Circle, 78249, San Antonio, TX, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Rahman  |D MD  |u Department of Medicine, University of Texas Health Science Center at San Antonio (UTHSCSA), San Antonio, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Appleford  |D Mark  |u Departments of Biomedical Engineering, The University of Texas at San Antonio (UTSA), One UTSA Circle, 78249, San Antonio, TX, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Sun  |D Lian-Wen  |u School of Biological Sciences and Medical Engineering, Beihang University, Beijing, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Wang  |D Xiaodu  |u Departments of Biomedical Engineering, The University of Texas at San Antonio (UTSA), One UTSA Circle, 78249, San Antonio, TX, USA  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Calcified Tissue International  |d Springer US; http://www.springer-ny.com  |g 97/6(2015-12-01), 592-601  |x 0171-967X  |q 97:6<592  |1 2015  |2 97  |o 223