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Publication : Biphasic regulation of chondrocytes by Rela through induction of anti-apoptotic and catabolic target genes.

First Author  Kobayashi H Year  2016
Journal  Nat Commun Volume  7
Pages  13336 PubMed ID  27830706
Mgi Jnum  J:242716 Mgi Id  MGI:5906092
Doi  10.1038/ncomms13336 Citation  Kobayashi H, et al. (2016) Biphasic regulation of chondrocytes by Rela through induction of anti-apoptotic and catabolic target genes. Nat Commun 7:13336
abstractText  In vitro studies have shown that Rela/p65, a key subunit mediating NF-kappaB signalling, is involved in chondrogenic differentiation, cell survival and catabolic enzyme production. Here, we analyse in vivo functions of Rela in embryonic limbs and adult articular cartilage, and find that Rela protects chondrocytes from apoptosis through induction of anti-apoptotic genes including Pik3r1. During skeletal development, homozygous knockout of Rela leads to impaired growth through enhanced chondrocyte apoptosis, whereas heterozygous knockout of Rela does not alter growth. In articular cartilage, homozygous knockout of Rela at 7 weeks leads to marked acceleration of osteoarthritis through enhanced chondrocyte apoptosis, whereas heterozygous knockout of Rela results in suppression of osteoarthritis development through inhibition of catabolic gene expression. Haploinsufficiency or a low dose of an IKK inhibitor suppresses catabolic gene expression, but does not alter anti-apoptotic gene expression. The biphasic regulation of chondrocytes by Rela contributes to understanding the pathophysiology of osteoarthritis.
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