Increased classical endoplasmic reticulum stress is sufficient to reduce chondrocyte proliferation rate in the growth plate and decrease bone growth

Copyright: © 2015 Kung et al. Mutations in genes encoding cartilage oligomeric matrix protein and matrilin-3 cause a spectrum of chondrodysplasias called multiple epiphyseal dysplasia (MED) and pseudoachondroplasia (PSACH). The majority of these diseases feature classical endoplasmic reticulum (ER) stress and activation of the unfolded protein response (UPR) as a result of misfolding of the mutant protein. However, the importance and the pathological contribution of ER stress in the disease pathogenesis are unknown. The aim of this study was to investigate the generic role of ER stress and the UPR in the pathogenesis of these diseases. A transgenic mouse line (ColIITgcog) was generated using the collagen II promoter to drive expression of an ER stress-inducing protein (Tgcog) in chondrocytes. The skeletal and histological phenotypes of these ColIITgcog mice were characterised. The expression and intracellular retention of Tgcog induced ER stress and activated the UPR as characterised by increased BiP expression, phosphorylation of eIF2á and spliced Xbp1. ColIITgcog mice exhibited decreased long bone growth and decreased chondrocyte proliferation rate. However, there was no disruption of chondrocyte morphology or growth plate architecture and perturbations in apoptosis were not apparent. Our data demonstrate that the targeted induction of ER stress in chondrocytes was sufficient to reduce the rate of bone growth, a key clinical feature associated with MED and PSACH, in the absence of any growth plate dysplasia. This study establishes that classical ER stress is a pathogenic factor that contributes to the disease mechanism of MED and PSACH. However, not all the pathological features of MED and PSACH were recapitulated, suggesting that a combination of intra- and extra-cellular factors are likely to be responsible for the disease pathology as a whole

The unfolded protein response and its relevance to connective tissue diseases

The unfolded protein response (UPR) has evolved to counter the stresses that occur in the endoplasmic reticulum (ER) as a result of misfolded proteins. This sophisticated quality control system attempts to restore homeostasis through the action of a number of different pathways that are coordinated in the first instance by the ER stress-senor proteins IRE1, ATF6 and PERK. However, prolonged ER-stress-related UPR can have detrimental effects on cell function and, in the longer term, may induce apoptosis. Connective tissue cells such as fibroblasts, osteoblasts and chondrocytes synthesise and secrete large quantities of proteins and mutations in many of these gene products give rise to heritable disorders of connective tissues. Until recently, these mutant gene products were thought to exert their effect through the assembly of a defective extracellular matrix that ultimately disrupted tissue structure and function. However, it is now becoming clear that ER stress and UPR, because of the expression of a mutant gene product, is not only a feature of, but may be a key mediator in the initiation and progression of a whole range of different connective tissue diseases. This review focuses on ER stress and the UPR that characterises an increasing number of connective tissue diseases and highlights novel therapeutic opportunities that may arise

Site specificity in advertisement calls and responses to playbacks of local and foreign call variants in satin bowerbirds, Ptilonorhynchus violaceus

Avian vocalisations often show patterns of geographic variation. Previous work on the satin bowerbird has shown that although spatial variation in this species’ advertisement calls is strongly associated with habitat structure, some variation is apparent within habitat types. Seventeen populations located throughout the species’ distribution were used to examine whether spatial call variation could be influenced by other processes such as random drift or the presence of fine-scale vocal traditions; if this were the case, differing call variants would be expected at geographically discrete sampling sites both within and among habitat types. There were population-specific call variants at each of the sites sampled, with different variants apparent even within habitat types. At most sites, individuals gave only a single variant of advertisement call, and the call variant at one site, sampled after a 5-year interval, appears to have been relatively stable. Playback experiments were conducted at three populations to examine whether local call variants invoked a greater response than several non-local variants differing in their degree of similarity to the local variant. Birds responded strongly to local call variants but not to either of two foreign variants, one of which was similar to their local variant and one of which was very different. A pattern of geographic variation across populations, the fact that local and non-local variants evoke different responses and circumstantial evidence indicating that individuals can learn new calls all suggest that factors affecting song learning and the ability of males to establish and defend a bower site may have contributed to the establishment of geographically variable vocal cultures in this species