2019
DOI: 10.1080/08923973.2019.1569046
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Silica nanoparticles as an enhancer in the IL-1β-induced inflammation cycle of A549 cells

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Cited by 22 publications
(13 citation statements)
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“…The RHS-induced IL-1β, IL-6, IL-15, and TNF-α cytokine and COX-2a expression in zebrafish suggests that RHS could enhance immunity against bacterial infection. Studies have reported that exposure to silica nanoparticles induced cytokine (IL-1β, IL-6, and TNF-α) expression in cell lines, mice, and zebrafish, also supporting the results of the present study, although the subjects of these studies focus on the toxicity of silica nanoparticles [45][46][47]. Lysozyme is an indispensable enzyme that functions as a humoral component of the innate immune defense system in resisting pathogen infections by hydrolyzing the peptidoglycan of bacterial cell walls.…”
Section: Discussionsupporting
confidence: 89%
“…The RHS-induced IL-1β, IL-6, IL-15, and TNF-α cytokine and COX-2a expression in zebrafish suggests that RHS could enhance immunity against bacterial infection. Studies have reported that exposure to silica nanoparticles induced cytokine (IL-1β, IL-6, and TNF-α) expression in cell lines, mice, and zebrafish, also supporting the results of the present study, although the subjects of these studies focus on the toxicity of silica nanoparticles [45][46][47]. Lysozyme is an indispensable enzyme that functions as a humoral component of the innate immune defense system in resisting pathogen infections by hydrolyzing the peptidoglycan of bacterial cell walls.…”
Section: Discussionsupporting
confidence: 89%
“…In contrast, both cell systems revealed an increased IL-8 expression, in contrast to the observation of Wand and colleagues, who observed a cell-system-specific IL-8 response [ 26 ]. All of these genes are cellular markers for a pro-inflammatory response [ 52 , 53 , 54 ]; therefore, the up-regulation of these genes indicates an inflammatory potential of CuO NP. However, the dose-dependent down-regulation of CCL22 and IL-1b does not match this scenario.…”
Section: Discussionmentioning
confidence: 99%
“…The results of other studies are compatible with the results of the present study, associating the increase in the toxic effects with an increase in the concentration of A-SiO 2 (Ahamed, 2013; Lee et al, 2013) and iron oxide nanoparticles (Helmig et al, 2018; Khan et al, 2012). Wu et al (2019) stated that A-SiO 2 nanoparticles induce the cytokine compounds such as interleukin-6 and promote the A 549 cells’ inflammatory response and cytotoxicity. Some authors in respect to iron nanoparticle exposure stated that iron overload in cells could initiate Fenton’s reaction and production of ROS, followed by a change in the MMP and cellular damage (Kai et al, 2011).…”
Section: Discussionmentioning
confidence: 99%