Ubiquitination-deubiquitination balance dictates ligand-stimulated PTHR sorting.
Ubiquitination-deubiquitination balance dictates ligand-stimulated PTHR sorting.
复制标题
DOI:
10.1002/jbmr.494
复制
发表时间:
2011-12
影响因子:
6.2
通讯作者:
Friedman, Peter A.
中科院分区:
文献类型:
--
作者:
Alonso, Veronica;Magyar, Clara E.;Wang, Bin;Bisello, Alessandro;Friedman, Peter A.
Parathyroid hormone receptors (PTHR) are promptly internalized upon stimulation by activating [PTH(1–84), PTH(1–34)] and non-activating [PTH(7–84), PTH(7–34)] ligands. Here, we characterized the mechanism regulating the sorting of internalized receptors between recycling and degradative pathways. PTHR recycles faster after challenge with PTH(1–34) than with PTH(7–34). PTHR recycling is complete by 2 hr after PTH(1–34) stimulation but incomplete at this time in cells treated with PTH(7–34). The slower and incomplete recycling induced by PTH(7–34) is due to proteasomal degradation. Both PTH(1–34) and PTH(7–34) induced PTHR polyubiquitination. Ubiquitination by PTH(1–34) was transient, whereas receptor ubiquitination following PTH(7–34) was sustained. PTH(1–34), but not PTH(7–34), induced expression of the PTHR-specific deubiquitinating enzyme USP2. Overexpression of USP2 prevented PTH(7–34)-induced PTHR degradation. We conclude that PTH(1–34) promotes coupled PTHR ubiquitination and deubiquitination, whereas PTH(7–34) activates only ubiquitination, thereby leading to PTHR downregulation. These findings may explain PTH resistance in diseases associated with elevated PTH(7–84) levels.
登录
查看更多内容
影响因子:
--
作者:
Cook, LB;Zhu, CC;Hinkle, PM
通讯作者:
Hinkle, PM
影响因子:
3.1
作者:
Edwards, RM;Contino, LC;Brooks, DP
通讯作者:
Brooks, DP
影响因子:
4.8
作者:
de Melker, AA;van der Horst, G;Borst, J
通讯作者:
Borst, J
影响因子:
4.8
作者:
Bhowmick, N;Narayan, P;Puett, D
通讯作者:
Puett, D
影响因子:
4.8
作者:
ABOUSAMRA, AB;GOLDSMITH, PK;SEGRE, GV
通讯作者:
SEGRE, GV