Kit W-sh Mutation Prevents Cancellous Bone Loss during Calcium Deprivation
Autor: | Suchit Poolthong, Jaijam Suwanwela, Roland Baron, Sutada Lotinun |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Chemistry Endocrinology Diabetes and Metabolism Osteoporosis chemistry.chemical_element Osteoblast Calcium medicine.disease Bone remodeling Osteopenia 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Endocrinology medicine.anatomical_structure Osteoclast 030220 oncology & carcinogenesis Internal medicine medicine Orthopedics and Sports Medicine Cortical bone Cancellous bone |
Zdroj: | Calcified Tissue International. 102:93-104 |
ISSN: | 1432-0827 0171-967X |
DOI: | 10.1007/s00223-017-0334-8 |
Popis: | Calcium is essential for normal bone growth and development. Inadequate calcium intake increases the risk of osteoporosis and fractures. Kit ligand/c-Kit signaling plays an important role in regulating bone homeostasis. Mice with c-Kit mutations are osteopenic. The present study aimed to investigate whether impairment of or reduction in c-Kit signaling affects bone turnover during calcium deprivation. Three-week-old male WBB6F1/J-Kit W /Kit W-v /J (W/W v ) mice with c-Kit point mutation, Kit W-sh /HNihrJaeBsmJ (W sh /W sh ) mice with an inversion mutation in the regulatory elements upstream of the c-Kit promoter region, and their wild-type controls (WT) were fed either a normal (0.6% calcium) or a low calcium diet (0.02% calcium) for 3 weeks. μCT analysis indicated that both mutants fed normal calcium diet had significantly decreased cortical thickness and cancellous bone volume compared to WT. The low calcium diet resulted in a comparable reduction in cortical bone volume and cortical thickness in the W/W v and W sh /W sh mice, and their corresponding controls. As expected, the low calcium diet induced cancellous bone loss in the W/W v mice. In contrast, W sh /W sh cancellous bone did not respond to this diet. This c-Kit mutation prevented cancellous bone loss by antagonizing the low calcium diet-induced increase in osteoblast and osteoclast numbers in the W sh /W sh mice. Gene expression profiling showed that calcium deficiency increased Osx, Ocn, Alp, type I collagen, c-Fms, M-CSF, and RANKL/OPG mRNA expression in controls; however, the W sh mutation suppressed these effects. Our findings indicate that although calcium restriction increased bone turnover, leading to osteopenia, the decreased c-Kit expression levels in the W sh /W sh mice prevented the low calcium diet-induced increase in cancellous bone turnover and bone loss but not the cortical bone loss. |
Databáze: | OpenAIRE |
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