Zebrafish models for glucocorticoid-induced osteoporosis

被引:4
作者
Lin, Wen-Ying [1 ]
Dharini, Kameshwara Kumar [2 ]
Peng, Cheng-Huan [1 ,2 ,3 ]
Lin, Chung-Yen [4 ]
Yeh, Kuang-Ting [1 ,3 ]
Lee, Wen-Chih [5 ]
Lin, Ming-Der [2 ,6 ]
机构
[1] Buddhist Tzu Chi Med Fdn, Hualien Tzu Chi Hosp, Dept Orthoped, Hualien, Taiwan
[2] Tzu Chi Univ, Inst Med Sci, Hualien, Taiwan
[3] Tzu Chi Univ, Sch Med, Hualien, Taiwan
[4] Acad Sinica, Inst Informat Sci, Taipei, Taiwan
[5] Tzu Chi Univ, Res Ctr Global SDGs Challenges, Off Res & Dev, 701 Zhongyang Rd,Sect 3, Hualien, Taiwan
[6] Tzu Chi Univ, Dept Mol Biol & Human Genet, 701 Zhongyang Rd,Sect 3, Hualien, Taiwan
来源
TZU CHI MEDICAL JOURNAL | 2022年 / 34卷 / 04期
关键词
Glucocorticoid-induced osteoporosis; Osteoporosis; Zebrafish; DEXAMETHASONE-INDUCED OSTEOPOROSIS; BONE-FORMATION; IN-VIVO; OSTEOBLASTS; SCALE; OSTEOGENESIS; PREDNISOLONE; PHENOTYPE; ACID; FIN;
D O I
10.4103/tcmj.tcmj_80_22
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucocorticoid-induced osteoporosis (GIOP) is the most common form of secondary osteoporosis due to excessive or long-term glucocorticoid administration, disturbing the homeostasis between bone formation and bone resorption. The bone biology of zebrafish shares a high degree of similarities with mammals. In terms of molecular level, genes and signaling pathways related to skeletogenesis are also highly correlated between zebrafish and humans. Therefore, zebrafish have been utilized to develop multiple GIOP models. Taking advantage of the transparency of zebrafish larvae, their skeletal development and bone mineralization can be readily visualized through in vivo staining without invasive experimental handlings. Moreover, the feasibility of using scales or fin rays to study bone remodeling makes adult zebrafish an ideal model for GIOP research. Here, we reviewed current zebrafish models for GIOP research, focused on the tools and methods established for examining bone homeostasis. As an in vivo, convenient, and robust model, zebrafish have an advantage in performing high-throughput drug screening and could be used to investigate the action mechanisms of therapeutic drugs.
引用
收藏
页码:373 / 380
页数:8
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