Osteoprotegerin is an effective countermeasure for spaceflight-induced bone loss in mice

被引:50
作者
Lloyd, Shane A. [1 ]
Morony, Sean E. [2 ]
Ferguson, Virginia L. [3 ,4 ]
Simske, Steven J. [3 ,5 ]
Stodieck, Louis S. [3 ]
Warmington, Kelly S. [2 ]
Livingston, Eric W. [6 ,7 ]
Lacey, David L. [2 ]
Kostenuik, Paul J. [2 ]
Bateman, Ted A. [3 ,6 ,7 ]
机构
[1] Penn State Univ, Coll Med, Dept Orthopaed & Rehabil, Hershey, PA 17033 USA
[2] Amgen Inc, Metab Disorders, Thousand Oaks, CA 91320 USA
[3] Univ Colorado, Dept Aerosp Engn & Sci, BioServe Space Technol, Boulder, CO 80309 USA
[4] Univ Colorado, Dept Mech Engn, Boulder, CO 80309 USA
[5] Hewlett Packard Labs, Ft Collins, CO 80528 USA
[6] Univ N Carolina, Dept Biomed Engn, Chapel Hill, NC 27599 USA
[7] Univ N Carolina, Dept Radiat Oncol, Chapel Hill, NC 27599 USA
关键词
Spaceflight; Osteoprotegerin; Mice; Bone loss; Countermeasure; LONG-DURATION SPACEFLIGHT; REGULATES OSTEOCLAST DIFFERENTIATION; ANTIRESORPTIVE DRUG; CALCIUM-METABOLISM; SPACE-FLIGHT; IN-VITRO; RESORPTION; LIGAND; BISPHOSPHONATES; RATS;
D O I
10.1016/j.bone.2015.08.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone loss associated with microgravity exposure poses a significant barrier to long-duration spaceflight. Osteoprotegerin-Fc (OPG-Fc) is a receptor activator of nuclear factor kappa-B ligand (RANKL) inhibitor that causes sustained inhibition of bone resorption after a single subcutaneous injection. We tested the ability of OPG-Fc to preserve bone mass during 12 days of spaceflight (SF). 64-day-old female C57BL/6J mice (n = 12/group) were injected subcutaneously with OPG-Fc (20 mg/kg) or an inert vehicle (VEH), 24 h prior to launch. Ground control (GC) mice (VEH or OPG-Fc) were maintained under environmental conditions that mimicked those in the space shuttle middeck. Age-matched baseline (BL) controls were sacrificed at launch. GC/VEH, but not SF/VEH mice, gained tibia BMD and trabecular volume fraction (BV/TV) during the mission (P < 0.05 vs. BL). SF/VEH mice had lower BV/TV vs. GC/VEH mice, while SF/OPG-Fc mice had greater BV/TV than SF/VEH or GC/VEH. SF reduced femur elastic and maximum strength in VEH mice, with OPG-Fc increasing elastic strength in SF mice. Serum TRAP5b was elevated in SF/VEH mice vs. GC/VEH mice. Conversely, SF/OPG-Fc mice had lower TRAP5b levels, suggesting that OPG-Fc preserved bone during spaceflight via inhibition of osteoclast-mediated bone resorption. Decreased bone formation also contributed to the observed osteopenia, based on the reduced femur periosteal bone formation rate and serum osteocalcin level. Overall, these observations suggest that the beneficial effects of OPG-Fc during SF are primarily due to dramatic and sustained suppression of bone resorption. In growing mice, this effect appears to compensate for the SF-related inhibition of bone formation, while preventing any SF-related increase in bone resorption. We have demonstrated that the young mouse is an appropriate new model for SF-induced osteopenia, and that a single pre-flight treatment with OPG-Fc can effectively prevent the deleterious effects of SF on mouse bone. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:562 / 572
页数:11
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