2016
DOI: 10.1186/s12890-016-0317-y
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Overexpression of programmed cell death 5 in a mouse model of ovalbumin-induced allergic asthma

Abstract: BackgroundProgrammed cell death 5 (PDCD5) was first identified as an apoptosis-promoting protein and involved in some autoimmune diseases and inflammatory processes. Our previous study demonstrated greater expression of serum PDCD5 in asthmatic patients than controls. This study aimed to further explore the significance of PDCD5 in mice with induced allergic asthma.MethodsWe divided 16 female mice into 2 groups: control (n = 8) and allergen (ovalbumin, OVA)-challenged mice (n = 8). The modified ovalbumin inhal… Show more

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Cited by 10 publications
(9 citation statements)
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“…Previous research has indicated that AKT1 is related to pathway mechanisms in children with severe asthma [ 33 ]; IL6 polymorphisms are related to the effects of smoking on the risk of adult asthma [ 34 ]; VEGFA rs833069 SNPs are associated with asthma [ 35 ]; VEGFA is associated with the response to inhaled corticosteroids in children with asthma [ 36 ]; smoking aggravates airway inflammation by activating the c -Jun amino terminal kinase pathway in asthma [ 37 ]; EGFR activation-induced decreases in claudin 1 promote MUC5AC expression and exacerbated asthma in mice [ 38 ]; the EGRF-dependent signaling pathway is associated with diseases, such as asthma [ 39 ]; neutrophils release CXCL8, NE, and MMP-9 in response to viral surrogates with R848-induced CXCL8 release being specifically enhanced in neutrophils in asthma [ 40 ]. CASP3 may play a role in allergic asthma [ 41 ]; the PTGS2 gene is associated with diisocyanate-induced asthma [ 42 ]. The relationships between these key targets and CVA, some of which have been well studied, could be further studied, and possible mechanisms that have not been previously studied could be explored.…”
Section: Discussionmentioning
confidence: 99%
“…Previous research has indicated that AKT1 is related to pathway mechanisms in children with severe asthma [ 33 ]; IL6 polymorphisms are related to the effects of smoking on the risk of adult asthma [ 34 ]; VEGFA rs833069 SNPs are associated with asthma [ 35 ]; VEGFA is associated with the response to inhaled corticosteroids in children with asthma [ 36 ]; smoking aggravates airway inflammation by activating the c -Jun amino terminal kinase pathway in asthma [ 37 ]; EGFR activation-induced decreases in claudin 1 promote MUC5AC expression and exacerbated asthma in mice [ 38 ]; the EGRF-dependent signaling pathway is associated with diseases, such as asthma [ 39 ]; neutrophils release CXCL8, NE, and MMP-9 in response to viral surrogates with R848-induced CXCL8 release being specifically enhanced in neutrophils in asthma [ 40 ]. CASP3 may play a role in allergic asthma [ 41 ]; the PTGS2 gene is associated with diisocyanate-induced asthma [ 42 ]. The relationships between these key targets and CVA, some of which have been well studied, could be further studied, and possible mechanisms that have not been previously studied could be explored.…”
Section: Discussionmentioning
confidence: 99%
“…Caspase 3 is a terminal effector molecule of the apoptosis signal transduction pathway. Numerous studies have demonstrated that H-PDCD5 promotes its cleavage and activation, leading to the occurrence of apoptosis (59, 60). H-PDCD5 causes cell apoptosis by regulating the expression of BCL-2 family members (61).…”
Section: Discussionmentioning
confidence: 99%
“…The modified OVA inhalation method was used to generate the allergic asthma mouse model as described in [14]. In brief, OVA sensitization involved an intraperitoneal injection of 20 μ g OVA absorbed with 2.25 mg aluminum hydroxide gel on days 1 and 14.…”
Section: Methodsmentioning
confidence: 99%
“…Fixed lung tissues were embedded in paraffin, and sections were stained with hematoxylin and eosin (H&E) for inflammatory cell infiltration and proliferation of smooth muscle, Masson's trichrome for airway fibrosis and collagen deposition, and periodic acid-Schiff (PAS) for goblet cells. An expert respiratory pathologist blinded to treatment groups graded the extent of inflammation in the lungs according to a semiquantitative scoring system [14].…”
Section: Methodsmentioning
confidence: 99%
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