Nucleolar localization of influenza A NS1: striking differences between mammalian and avian cells

In mammalian cells, nucleolar localization of influenza A NS1 requires the presence of a C-terminal nucleolar localization signal. This nucleolar localization signal is present only in certain strains of influenza A viruses. Therefore, only certain NS1 accumulate in the nucleolus of mammalian cells. In contrast, we show that all NS1 tested in this study accumulated in the nucleolus of avian cells even in the absence of the above described C-terminal nucleolar localization signal. Thus, nucleolar localization of NS1 in avian cells appears to rely on a different nucleolar localization signal that is more conserved among influenza virus strains

McMaster-Toronto Arthritis Patient Preference Disability Questionnaire Sensitivity to Change in Low Back Pain: Influence of Shifts in Priorities

To assess the sensitivity to change of the McMaster Toronto Arthritis Patient Preference Disability Questionnaire (MACTAR) in chronic low back pain (CLBP) and shifts in patients' priorities of disabling activities over time.A prospective longitudinal survey of 100 patients (38 males) with CLBP in a tertiary care teaching hospital. Evaluation at baseline and 6 months by the MACTAR, Quebec Back Pain Disability Questionnaire (QUEBEC), Hospital Anxiety and Depression scale (HAD), Fear-Avoidance Beliefs Questionnaire (FABQ), Coping Strategies Questionnaire (CSQ), and pain and handicap visual analogue scales (VASs). Patients' perceived improvement or worsening of condition was assessed at 6 months. Effect size (ES) and Standardized response mean (SRM) and effect size (ES) were used to evaluate sensitivity to change of the MACTAR.The MACTAR SRM and ES values (SRM = 0.25; ES = 0.37) were among the highest for the instruments evaluated. For patients considering their condition as improved, the SRM was 0.66 and the ES 1. The 3 disability domains, classified by the International Classification of Functioning, Disability and Health (ICF), most often cited as priorities at baseline remained the most cited at follow-up: mobility (40.9% of patients); community, social and civic life (22.7%); and domestic life (22.4%). At 6 months, 48 patients shifted their priorities, for a decrease in MACTAR SRM and ES values for patients considering their condition improved and an increase in these values for those considering their condition deteriorated.Although the MACTAR has similar sensitivity to change as other outcome measures widely used in CLBP, shifts in patient priorities over time are common and influence scores and sensitivity to change

Original article Sirt1-deficient mice exhibit an altered cartilage phenotype

tObjective: We previously demonstrated that Sirt1 regulates apoptosis in cartilage in vitro. Here weattempt to examine in vivo cartilage homeostasis, using Sirt1 total body knockout (KO) mice.Method: Articular cartilage was harvested from hind paws of 1-week and 3-week-old mice carrying wildtype (WT) or null Sirt1 gene. Knees of Sirt1 haploinsufficient mice also were examined, at 6 months. Jointcartilage was processed for histologic examination or biochemical analyses of chondrocyte cultures.Results: We found that articular cartilage tissue sections from Sirt1 KO mice up to 3 weeks of age exhibitedlow levels of type 2 collagen, aggrecan, and glycosaminoglycan content. In contrast, protein levels of MMP-13 were elevated in the Sirt1 KO mice, leading to a potential increase of cartilage breakdown, alreadyshown in the heterozygous mice. Additional results showed elevated chondrocyte apoptosis in Sirt1 KOmice, as compared to WT controls. In addition to these observations, PTP1b (protein tyrosine phosphataseb) was elevated in the Sirt1 KO mice, in line with previous reports.Conclusion: The findings from this animal model demonstrated that Sirt1 KO mice presented an alteredcartilage phenotype, with an elevated apoptotic process and a potential degradative cartilage process

Original article Sirt1-deficient mice exhibit an altered cartilage phenotype

tObjective: We previously demonstrated that Sirt1 regulates apoptosis in cartilage in vitro. Here weattempt to examine in vivo cartilage homeostasis, using Sirt1 total body knockout (KO) mice.Method: Articular cartilage was harvested from hind paws of 1-week and 3-week-old mice carrying wildtype (WT) or null Sirt1 gene. Knees of Sirt1 haploinsufficient mice also were examined, at 6 months. Jointcartilage was processed for histologic examination or biochemical analyses of chondrocyte cultures.Results: We found that articular cartilage tissue sections from Sirt1 KO mice up to 3 weeks of age exhibitedlow levels of type 2 collagen, aggrecan, and glycosaminoglycan content. In contrast, protein levels of MMP-13 were elevated in the Sirt1 KO mice, leading to a potential increase of cartilage breakdown, alreadyshown in the heterozygous mice. Additional results showed elevated chondrocyte apoptosis in Sirt1 KOmice, as compared to WT controls. In addition to these observations, PTP1b (protein tyrosine phosphataseb) was elevated in the Sirt1 KO mice, in line with previous reports.Conclusion: The findings from this animal model demonstrated that Sirt1 KO mice presented an alteredcartilage phenotype, with an elevated apoptotic process and a potential degradative cartilage process

Urolithin A and B accelerate myocyte fusion into myotubes

peer reviewe

Évaluation de l’activité des urolithines A et B sur le muscle : modulation transcriptomique sur les myotubes primaires humains

peer reviewe

Découverte d’une statue celtique en ronde-bosse sur le sanctuaire de Couan/Cobannus (Saint-Aubin-des-Chaumes, Nièvre)

Le sanctuaire et la petite agglomération antique de Couan se situent à environ 7 km au sud-ouest du bourg de Vézelay (Yonne), sur la commune de Saint-Aubin-des-Chaumes (Nièvre). Ils se sont développés au pied occidental d’une butte résiduelle, à un point de passage assez important, point de franchissement de la voie dite « de la cuesta oxfordienne » qui permet la relation, depuis l’époque laténienne, entre le Bassin ligérien moyen et la vallée de la Meuse (VENAULT, NOUVEL dir., 2015). Ce comp..

L’analyse protéomique du sécrétome des ostéoblastes fournis de nouvelles indications sur les mécanismes de la sclérose sous-chondrale dans l’arthrose

peer reviewe