Amphiregulin is a novel growth factor involved in normal bone development and in the cellular response to parathyroid hormone stimulation

被引:81
作者
Qin, L
Tamasi, J
Raggatt, L
Lit, X
Feyen, JHM
Lee, DC
DiCicco-Bloom, E
Partridge, NC
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Physiol & Biophys, Piscataway, NJ 08854 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, Piscataway, NJ 08854 USA
[3] Bristol Myers Squibb Co, Pharmaceut Res Inst, Pennington, NJ 08534 USA
[4] Univ N Carolina, Sch Med, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Sch Med, Ctr Comprehens Canc, Chapel Hill, NC 27599 USA
关键词
D O I
10.1074/jbc.M409807200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Parathyroid hormone (PTH) is the Major mediator of calcium homeostasis and bone remodeling and is now known to be an effective drug for osteoporosis treatment. Yet the mechanisms responsible for its functions in bone are largely unknown. Here we report that the expression of amphiregulin (AR), a member of the epidermal growth factor (EGF) family, is rapidly and highly up-regulated by PTH in several osteohlastic cell lines and bone tissues. Other osteotropic hormones (1alpha,25dihydroxyvitamin D-3 and prostaglandin E-2) also strongly stimulate AR expression. We found all EGF-like ligands and their receptors are expressed in osteoblasts, but AR is the only member that is highly regulated by PTH. Functional studies demonstrated that although AR is a potent growth factor for preosteoblasts, it completely inhibits further differentiation. AR also strongly and quickly stimulated Akt and ERK phosphorylation and c-fos and c-jun expression in an EGF receptor-dependent manner. Moreover, AR null mice displayed significantly less tibial trabecular bone than wild-type mice. Taken together, we have identified a novel growth factor that is PTH-regulated and appears to have an important role in bone metabolism.
引用
收藏
页码:3974 / 3981
页数:8
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