Values were obtained using qBase software. Each assay was performed in

Values were obtained using qBase software. Each assay was performed in duplicate.PVM inoculationPVM strain J3666 (generously supplied by A. Easton, University of Warwick, Coventry, UK) was first passed in 10-week-old BALB/c mice and then grown once onto BS-C-1 cells to produce the stock solution. The stock solution was then diluted to 1025 in MEM, divided into aliquots, and stored at280uC to serve as inoculum. Randomly selected aliquots yielded highly reproducible titers on BS-C-1 cells, amounting to <56105 PFU/mL. The inoculation procedure consisted of slowly instilling 50 mL of the viral suspension into the nostrils of the anesthetized mouse maintained in a vertical position (35 mg/kg pentobarbital sodium intraperitoneally). Mice were inoculated under brief anaesthesia (ketamine, Pfizer, 50 mg/kg, and xylazine, Bayer, 10 mg/kg, i.p.) by intranasal instillation of 50 ml of a viral suspension containing 1000 PFU and 1 BSA in PBS [10]. At selected time intervals (8, 9, 10 and 12 day post-infection), groups of minimum 6 mice were sacrificed with sodium thiopental (5 mg/animal, i.p.) and exsanguination. Broncho-alveolar lavage fluids (BALFs) were obtained by flushing the lungs with sterileProtective Role of P2Y2 against Pneumonia VirusHistological analysis of inflamed lungs of P2Y2+/+ and P2Y22/2 miceLeft lungs were insufflated with 700 ml of 4 paraformaldehyde, and embedded in 26001275 paraffin. Sections (7 mm) were stained with haematoxylin and eosin and assessed by light microscopy. Histological analysis has been performed according to the score related to PVM infection defined by Anh et al [10]. Lung slides have been examined independently and blindly by two individuals.cell counting was similar in P2Y2+/+ and P2Y22/2 mice (Fig. 2A). ATP level was then quantified in the BALF of P2Y2+/+ and P2Y22/2 mice using ATP detection assay system ATPlite at day 8, day 9 and day 10 post-infection (Fig. 2B). A lower ATP content was detected in P2Y22/2 compared to P2Y2+/+ infected lungs atStatistical analysisFor all experiments, data are presented as mean 6 S.E.M. and the statistical significance between samples was calculated using the Student’s t test or one-way analysis of variance, using the Prism 5 software (GraphPad). The normal distribution of the data was checked using Kolmogorov mirnov, D’Agostino earson, and Shapiro ilk tests. Kaplan-Meier survival curves were compared using the Log-rank (Mantel-Cox) Test and the Gehan-BreslowWilcoxon Test.Results Survival and order Anlotinib weight loss of P2Y2+/+ and P2Y22/2 mice after lung infection with Pneumonia Virus of Mice (PVM)To assess the role of P2Y2R in the lung, 8-week-old P2Y2 wildtype (WT) and P2Y22/2 mice were infected with 1000 plaqueforming units (PFUs) of PVM and were monitored daily for survival (Fig. 1A) and weight loss (Fig. 1B). Mice recovered quickly from the anaesthesia and appeared to be normal over the first 6 days. P2Y2+/+ and P2Y22/2 mice began to lose weight on the same day (at day 7, Fig. 1B). Thereafter, the weight curves were roughly the same until day 11, when P2Y2+/+ mice stabilized their weight before recovering, whereas most of the P2Y22/2 mice continued to lose weight 1 day more and then stabilized before death (Fig. 1A and 1B). Survival of P2Y22/2 mice was thus significantly decreased compared to P2Y2+/+ mice (12.8 (N = 51) vs. 54.6 (N = 41) respectively; ***; p,0.001) (Fig. 1A). Furthermore, from day 7 post-infection, infected P2Y22/2 mice exhibited a more severe Homotaurine site pattern of illness signs.Values were obtained using qBase software. Each assay was performed in duplicate.PVM inoculationPVM strain J3666 (generously supplied by A. Easton, University of Warwick, Coventry, UK) was first passed in 10-week-old BALB/c mice and then grown once onto BS-C-1 cells to produce the stock solution. The stock solution was then diluted to 1025 in MEM, divided into aliquots, and stored at280uC to serve as inoculum. Randomly selected aliquots yielded highly reproducible titers on BS-C-1 cells, amounting to <56105 PFU/mL. The inoculation procedure consisted of slowly instilling 50 mL of the viral suspension into the nostrils of the anesthetized mouse maintained in a vertical position (35 mg/kg pentobarbital sodium intraperitoneally). Mice were inoculated under brief anaesthesia (ketamine, Pfizer, 50 mg/kg, and xylazine, Bayer, 10 mg/kg, i.p.) by intranasal instillation of 50 ml of a viral suspension containing 1000 PFU and 1 BSA in PBS [10]. At selected time intervals (8, 9, 10 and 12 day post-infection), groups of minimum 6 mice were sacrificed with sodium thiopental (5 mg/animal, i.p.) and exsanguination. Broncho-alveolar lavage fluids (BALFs) were obtained by flushing the lungs with sterileProtective Role of P2Y2 against Pneumonia VirusHistological analysis of inflamed lungs of P2Y2+/+ and P2Y22/2 miceLeft lungs were insufflated with 700 ml of 4 paraformaldehyde, and embedded in 26001275 paraffin. Sections (7 mm) were stained with haematoxylin and eosin and assessed by light microscopy. Histological analysis has been performed according to the score related to PVM infection defined by Anh et al [10]. Lung slides have been examined independently and blindly by two individuals.cell counting was similar in P2Y2+/+ and P2Y22/2 mice (Fig. 2A). ATP level was then quantified in the BALF of P2Y2+/+ and P2Y22/2 mice using ATP detection assay system ATPlite at day 8, day 9 and day 10 post-infection (Fig. 2B). A lower ATP content was detected in P2Y22/2 compared to P2Y2+/+ infected lungs atStatistical analysisFor all experiments, data are presented as mean 6 S.E.M. and the statistical significance between samples was calculated using the Student’s t test or one-way analysis of variance, using the Prism 5 software (GraphPad). The normal distribution of the data was checked using Kolmogorov mirnov, D’Agostino earson, and Shapiro ilk tests. Kaplan-Meier survival curves were compared using the Log-rank (Mantel-Cox) Test and the Gehan-BreslowWilcoxon Test.Results Survival and weight loss of P2Y2+/+ and P2Y22/2 mice after lung infection with Pneumonia Virus of Mice (PVM)To assess the role of P2Y2R in the lung, 8-week-old P2Y2 wildtype (WT) and P2Y22/2 mice were infected with 1000 plaqueforming units (PFUs) of PVM and were monitored daily for survival (Fig. 1A) and weight loss (Fig. 1B). Mice recovered quickly from the anaesthesia and appeared to be normal over the first 6 days. P2Y2+/+ and P2Y22/2 mice began to lose weight on the same day (at day 7, Fig. 1B). Thereafter, the weight curves were roughly the same until day 11, when P2Y2+/+ mice stabilized their weight before recovering, whereas most of the P2Y22/2 mice continued to lose weight 1 day more and then stabilized before death (Fig. 1A and 1B). Survival of P2Y22/2 mice was thus significantly decreased compared to P2Y2+/+ mice (12.8 (N = 51) vs. 54.6 (N = 41) respectively; ***; p,0.001) (Fig. 1A). Furthermore, from day 7 post-infection, infected P2Y22/2 mice exhibited a more severe pattern of illness signs.