The enormous phagocytic capacities, and can be divided into two 15900046 subtypes namely M1 and M2 [43]. M1-polarized macrophages could activate an inflammatory response via secreting granzyme, JNJ-7777120 web porforin and pro-inflammatory cytokines including IL-1b, IL-6 and TNF-a [44]. Therefore, they are beneficial during the early stage of infectionby eliminating pathogens, but may cause adverse effects through activating sustained inflammation response latter. M2-polarized macrophages secrete IL-10 and have high arginase activity to promote tissue restoration and reconstruction [40,45]. As such, polarization of macrophages is critical in the inflammatory reactivation outcomes [40,45]. Our immunohistochemistry results showed that the infiltrated inflammatory cells of Candida albicans vaginitis model rats were mainly M1 subtype macrophages (CD68 positive), after (CKPV)2 administration, these macrophages were mainly M2 positive (CD163 positive). Our results also showed that (CKPV)2 significantly inhibited macrophage phagocytosis and the production of pro-inflammatory cytokines(IL-1b,IL-6 and TNF-a). Meanwhile, (CKPV)2 enhanced IL-10 secretion and arginase activity in primary cultured macrophages, indicating a MedChemExpress JNJ-7706621 typical macrophageM1-to-M2 polarization. Melanocortin receptor 1 (MC1R), a G protein coupled receptor, can be activated by melanocortin peptides [46]. It widely participates in inflammatory and immune responses through activating downstream signals including adenylate cyclase (AC) [32,47,48]. Previous studies have confirmed that antiinflammatory effects of a-MSH were mainly depend on the MC1R [49,50]. Our results here suggested that (CKPV)2-induced cAMP production and anti-inflammatory and anti-fungal abilities were also dependent on MC1R, as MC1R RNAi knockdown almost blocked those effects.Conclusions(CKPV)2 showed an excellent anti-fungal and anti-inflammatory effect against Candida albicans vaginitis both in vivo and in vitro. (CKPV)2 inhibits macrophage infiltration in vaginal mucosa tissues and induces the macrophages M1 to M2 polarization.Supporting InformationAnti-acute inflammatory effects of (CKPV)2. (A) (CKPV)2 inhibits mouse ear edema induced by xylene. The inhibitory rate was determined from the discrimination between the two ears of each mouse. (B) (CKPV)2 inhibits rat paw edema induced by albumen. Volumes of paws were measured at 0.5, 1, 2, 4 and 6 h after 0.05 ml albumen (10 ) treatment. (C) (CKPV)2 inhibits rat foot itching induced by phosphate. The total amount of given histamine phosphate was the itching limens. Experiments in this figure were repeated three times and similar results were obtained. There was a significant difference between model and drug treatment groups. *p,0.01 (ANOVA). (EPS)Figure S1 Text S1 Protocol of acute inflammation models used in this study. (DOC)Author ContributionsConceived and designed the experiments: YY ZL CC. Performed the experiments: HJ YZ GL MT ZJ Xian-jing Li JD. Analyzed the data: YY MT GZ XD ZW LL YL Xian-jing Li LH. Contributed reagents/ materials/analysis tools: YY Xiao-yi Li CC. Wrote the paper: HJ YZ CC.
Bacteria adhere widely to surfaces of diverse composition in the environment. These biofilms cause problems in a number of activities, such as agriculture, industry, and healthcare [1]. In the dental field, oral biofilms are defined to consist of multiple bacterial species and to cause opportunistic infection, resulting in dental caries and periodontal disease [2,3]. Porphyromonas gingivalis, a.The enormous phagocytic capacities, and can be divided into two 15900046 subtypes namely M1 and M2 [43]. M1-polarized macrophages could activate an inflammatory response via secreting granzyme, porforin and pro-inflammatory cytokines including IL-1b, IL-6 and TNF-a [44]. Therefore, they are beneficial during the early stage of infectionby eliminating pathogens, but may cause adverse effects through activating sustained inflammation response latter. M2-polarized macrophages secrete IL-10 and have high arginase activity to promote tissue restoration and reconstruction [40,45]. As such, polarization of macrophages is critical in the inflammatory reactivation outcomes [40,45]. Our immunohistochemistry results showed that the infiltrated inflammatory cells of Candida albicans vaginitis model rats were mainly M1 subtype macrophages (CD68 positive), after (CKPV)2 administration, these macrophages were mainly M2 positive (CD163 positive). Our results also showed that (CKPV)2 significantly inhibited macrophage phagocytosis and the production of pro-inflammatory cytokines(IL-1b,IL-6 and TNF-a). Meanwhile, (CKPV)2 enhanced IL-10 secretion and arginase activity in primary cultured macrophages, indicating a typical macrophageM1-to-M2 polarization. Melanocortin receptor 1 (MC1R), a G protein coupled receptor, can be activated by melanocortin peptides [46]. It widely participates in inflammatory and immune responses through activating downstream signals including adenylate cyclase (AC) [32,47,48]. Previous studies have confirmed that antiinflammatory effects of a-MSH were mainly depend on the MC1R [49,50]. Our results here suggested that (CKPV)2-induced cAMP production and anti-inflammatory and anti-fungal abilities were also dependent on MC1R, as MC1R RNAi knockdown almost blocked those effects.Conclusions(CKPV)2 showed an excellent anti-fungal and anti-inflammatory effect against Candida albicans vaginitis both in vivo and in vitro. (CKPV)2 inhibits macrophage infiltration in vaginal mucosa tissues and induces the macrophages M1 to M2 polarization.Supporting InformationAnti-acute inflammatory effects of (CKPV)2. (A) (CKPV)2 inhibits mouse ear edema induced by xylene. The inhibitory rate was determined from the discrimination between the two ears of each mouse. (B) (CKPV)2 inhibits rat paw edema induced by albumen. Volumes of paws were measured at 0.5, 1, 2, 4 and 6 h after 0.05 ml albumen (10 ) treatment. (C) (CKPV)2 inhibits rat foot itching induced by phosphate. The total amount of given histamine phosphate was the itching limens. Experiments in this figure were repeated three times and similar results were obtained. There was a significant difference between model and drug treatment groups. *p,0.01 (ANOVA). (EPS)Figure S1 Text S1 Protocol of acute inflammation models used in this study. (DOC)Author ContributionsConceived and designed the experiments: YY ZL CC. Performed the experiments: HJ YZ GL MT ZJ Xian-jing Li JD. Analyzed the data: YY MT GZ XD ZW LL YL Xian-jing Li LH. Contributed reagents/ materials/analysis tools: YY Xiao-yi Li CC. Wrote the paper: HJ YZ CC.
Bacteria adhere widely to surfaces of diverse composition in the environment. These biofilms cause problems in a number of activities, such as agriculture, industry, and healthcare [1]. In the dental field, oral biofilms are defined to consist of multiple bacterial species and to cause opportunistic infection, resulting in dental caries and periodontal disease [2,3]. Porphyromonas gingivalis, a.
