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软骨细胞中Spry1的过表达导致FGFR泛素化减弱和ERK持续激活,从而引起软骨发育异常。

Overexpression of Spry1 in chondrocytes causes attenuated FGFR ubiquitination and sustained ERK activation resulting in chondrodysplasia.

作者信息

Yang Xuehui, Harkins Lauren K, Zubanova Olga, Harrington Anne, Kovalenko Dmitry, Nadeau Robert J, Chen Pei-Yu, Toher Jessica L, Lindner Volkhard, Liaw Lucy, Friesel Robert

机构信息

Center for Molecular Medicine, Maine Medical Center Research Institute, 81 Research Drive, Scarborough, Maine 04074, USA.

出版信息

Dev Biol. 2008 Sep 1;321(1):64-76. doi: 10.1016/j.ydbio.2008.05.555. Epub 2008 Jun 9.

Abstract

The FGF signaling pathway plays essential roles in endochondral ossification by regulating osteoblast proliferation and differentiation, chondrocyte proliferation, hypertrophy, and apoptosis. FGF signaling is controlled by the complementary action of both positive and negative regulators of the signal transduction pathway. The Spry proteins are crucial regulators of receptor tyrosine kinase-mediated MAPK signaling activity. Sprys are expressed in close proximity to FGF signaling centers and regulate FGFR-ERK-mediated organogenesis. During endochondral ossification, Spry genes are expressed in prehypertrophic and hypertrophic chondrocytes. Using a conditional transgenic approach in chondrocytes in vivo, the forced expression of Spry1 resulted in neonatal lethality with accompanying skeletal abnormalities resembling thanatophoric dysplasia II, including increased apoptosis and decreased chondrocyte proliferation in the presumptive reserve and proliferating zones. In vitro chondrocyte cultures recapitulated the inhibitory effect of Spry1 on chondrocyte proliferation. In addition, overexpression of Spry1 resulted in sustained ERK activation and increased expression of p21 and STAT1. Immunoprecipitation experiments revealed that Spry1 expression in chondrocyte cultures resulted in decreased FGFR2 ubiquitination and increased FGFR2 stability. These results suggest that constitutive expression of Spry1 in chondrocytes results in attenuated FGFR2 degradation, sustained ERK activation, and up-regulation of p21Cip and STAT1 causing dysregulated chondrocyte proliferation and terminal differentiation.

摘要

FGF信号通路通过调节成骨细胞的增殖和分化、软骨细胞的增殖、肥大及凋亡,在软骨内成骨过程中发挥着重要作用。FGF信号由信号转导通路的正、负调节因子的互补作用所控制。Spry蛋白是受体酪氨酸激酶介导的MAPK信号活性的关键调节因子。Spry蛋白在靠近FGF信号中心的位置表达,并调节FGFR-ERK介导的器官发生。在软骨内成骨过程中,Spry基因在肥大前和肥大软骨细胞中表达。利用体内软骨细胞条件性转基因方法,Spry1的强制表达导致新生小鼠死亡,并伴有类似致死性发育异常II型的骨骼异常,包括假定储备区和增殖区细胞凋亡增加以及软骨细胞增殖减少。体外软骨细胞培养重现了Spry1对软骨细胞增殖的抑制作用。此外,Spry1的过表达导致ERK持续激活以及p21和STAT1表达增加。免疫沉淀实验表明,软骨细胞培养物中Spry1的表达导致FGFR2泛素化减少和FGFR2稳定性增加。这些结果表明,软骨细胞中Spry1的组成性表达导致FGFR2降解减弱、ERK持续激活以及p21Cip和STAT1上调,从而导致软骨细胞增殖失调和终末分化异常。

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