Recombinant Human Parathyroid Hormone Related Protein 1-34 and 1-84 and Their Roles in Osteoporosis Treatment

被引:13
|
作者
Wang, Hua [1 ,2 ]
Liu, Jingning [1 ,3 ]
Yin, Ying [1 ,2 ]
Wu, Jun [1 ]
Wang, Zilu [2 ]
Miao, Dengshun [1 ]
Sun, Wen [1 ]
机构
[1] Nanjing Med Univ, Dept Anat Histol & Embryol, Res Ctr Bone & Stem Cells, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Stomatol Coll, Inst Dent Res, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 2, Dept Geriatr, Nanjing, Jiangsu, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 02期
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
PLACENTAL CALCIUM-TRANSPORT; SHORT-TERM TREATMENT; PTH-RELATED PROTEIN; EXTRACELLULAR CALCIUM; BONE-FORMATION; PEPTIDE PTHRP; VITAMIN-D; SKELETAL DEVELOPMENT; RAT OSTEOCLASTS; IN-VITRO;
D O I
10.1371/journal.pone.0088237
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Osteoporosis is a common disorder characterized by compromised bone strength that predisposes patients to increased fracture risk. Parathyroid hormone related protein (PTHrP) is one of the candidates for clinical osteoporosis treatment. In this study, GST Gene Fusion System was used to express recombinant human PTHrP (hPTHrP) 1-34 and 1-84. To determine whether the recombinant hPTHrP1-34 and 1-84 can enhance renal calcium reabsorption and promote bone formation, we examined effects of recombinant hPTHrP1-34 and 1-84 on osteogenic lineage commitment in a primary bone marrow cell culture system and on osteoporosis treatment. Results revealed that both of recombinant hPTHrP1-34 and 1-84 increased colony formation and osteogenic cell differentiation and mineralization in vitro; however, the effect of recombinant hPTHrP1-84 is a little stronger than that of hPTHrP1-34. Next, ovariectomy was used to construct osteoporosis animal model (OVX) to test activities of these two recombinants in vivo. HPTHrP1-84 administration elevated serum calcium by up-regulating the expression of renal calcium transporters, which resulted in stimulation of osteoblastic bone formation. These factors contributed to augmented bone mass in hPTHrP1-84 treated OVX mice but did not affect bone resorption. There was no obvious bone mass alteration in hPTHrP1-34 treated OVX mice, which may be, at least partly, associated with shorter half-life of hPTHrP1-34 compared to hPTHrP1-84 in vivo. This study implies that recombinant hPTHrP1-84 is more effective than hPTHrP1-34 to enhance renal calcium reabsorption and to stimulate bone formation in vivo.
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页数:12
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