Reactive oxygen species and oxidative stress in osteoclastogenesis, skeletal aging and bone diseases

Verfasser / Beitragende:
[Danielle Callaway, Jean Jiang]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Bone and Mineral Metabolism, 33/4(2015-07-01), 359-370
Format:
Artikel (online)
ID: 605463360
LEADER caa a22 4500
001 605463360
003 CHVBK
005 20210128100253.0
007 cr unu---uuuuu
008 210128e20150701xx s 000 0 eng
024 7 0 |a 10.1007/s00774-015-0656-4  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00774-015-0656-4 
245 0 0 |a Reactive oxygen species and oxidative stress in osteoclastogenesis, skeletal aging and bone diseases  |h [Elektronische Daten]  |c [Danielle Callaway, Jean Jiang] 
520 3 |a Osteoclasts are cells derived from bone marrow macrophages and are important in regulating bone resorption during bone homeostasis. Understanding what drives osteoclast differentiation and activity is important when studying diseases characterized by heightened bone resorption relative to formation, such as osteoporosis. In the last decade, studies have indicated that reactive oxygen species (ROS), including superoxide and hydrogen peroxide, are crucial components that regulate the differentiation process of osteoclasts. However, there are still many unanswered questions that remain. This review will examine the mechanisms by which ROS can be produced in osteoclasts as well as how it may affect osteoclast differentiation and activity through its actions on osteoclastogenesis signaling pathways. In addition, the contribution of ROS to the aging-associated disease of osteoporosis will be addressed and how targeting ROS may lead to the development of novel therapeutic treatment options. 
540 |a The Japanese Society for Bone and Mineral Research and Springer Japan, 2015 
690 7 |a Osteoclast  |2 nationallicence 
690 7 |a Reactive oxygen species  |2 nationallicence 
690 7 |a Osteoclastogenesis  |2 nationallicence 
690 7 |a Oxidative stress  |2 nationallicence 
700 1 |a Callaway  |D Danielle  |u Department of Biochemistry, University of Texas Health Science Center, 7703 Floyd Curl Drive, 78229-3900, San Antonio, TX, USA  |4 aut 
700 1 |a Jiang  |D Jean  |u Department of Biochemistry, University of Texas Health Science Center, 7703 Floyd Curl Drive, 78229-3900, San Antonio, TX, USA  |4 aut 
773 0 |t Journal of Bone and Mineral Metabolism  |d Springer Japan  |g 33/4(2015-07-01), 359-370  |x 0914-8779  |q 33:4<359  |1 2015  |2 33  |o 774 
856 4 0 |u https://doi.org/10.1007/s00774-015-0656-4  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a review-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00774-015-0656-4  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Callaway  |D Danielle  |u Department of Biochemistry, University of Texas Health Science Center, 7703 Floyd Curl Drive, 78229-3900, San Antonio, TX, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Jiang  |D Jean  |u Department of Biochemistry, University of Texas Health Science Center, 7703 Floyd Curl Drive, 78229-3900, San Antonio, TX, USA  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Bone and Mineral Metabolism  |d Springer Japan  |g 33/4(2015-07-01), 359-370  |x 0914-8779  |q 33:4<359  |1 2015  |2 33  |o 774