G-protein stimulatory subunit alpha and Gq/11α G-proteins are both required to maintain quiescent stem-like chondrocytes

被引:39
作者
Chagin, Andrei S. [1 ,2 ,3 ]
Vuppalapati, Karuna K. [1 ]
Kobayashi, Tatsuya [2 ,3 ]
Guo, Jun [2 ,3 ]
Hirai, Takao [2 ,3 ]
Chen, Min [4 ]
Offermanns, Stefan [5 ]
Weinstein, Lee S. [4 ]
Kronenberg, Henry M. [2 ,3 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, S-17177 Stockholm, Sweden
[2] Massachusetts Gen Hosp, Endocrine Unit, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Boston, MA 02114 USA
[4] Natl Inst Diabet Digest & Kidney Dis, Metab Dis Branch, NIH, Bethesda, MD 20892 USA
[5] Max Planck Inst Heart & Lung Res, Dept Pharmacol, D-61231 Bad Nauheim, Germany
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
GROWTH-PLATE; PARATHYROID-HORMONE; KINASE-A; RECEPTOR; DIFFERENTIATION; HYPERTROPHY; ACTIVATION; CHONDROGENESIS; PROLIFERATION; EXPRESSION;
D O I
10.1038/ncomms4673
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
Round chondrocytes in the resting zone of the growth plate provide precursors for columnar chondrocytes and have stem-like properties. Here we demonstrate that these stem-like chondrocytes undergo apoptosis in the absence of the receptor (PPR) for parathyroid hormone-related protein. We examine the possible roles of heterotrimeric G-proteins activated by the PPR. Inactivation of the G-protein stimulatory alpha-subunit (G(s)alpha) leads to accelerated differentiation of columnar chondrocytes, as seen in the PPR knockout, but a remnant of growth cartilage remains, in contrast to disappearance of the growth cartilage in the PPR knockout. Stem-like chondrocytes lose their quiescence and proliferate upon Gsa ablation. Inactivation of Gsa in mice with a mutant PPR that cannot activate G proteins, Gq and G11, leads to a PPR knockout-like phenotype. Thus, G(s)alpha is the major mediator of the anti-differentiation action of the PPR, while activation of both Gsa and Gq/11 alpha is required for quiescence of stem-like chondrocytes.
引用
收藏
页数:14
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