Dietary Postbiotics Reduce Cytotoxicity and Inflammation Induced by Crystalline Silica in an In Vitro RAW 264.7 Macrophage Model

Crystalline silica (cSiO<sub>2</sub>) particles are naturally existing environmental toxicants. Exposure to cSiO<sub>2</sub> could cause local or systemic inflammation and aggregate inflammation-associated diseases. Dietary postbiotics are reported to possess anti-inflammator...

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Main Authors: Xue Du, Jessica Rodriguez, Josephine Wee
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Foods
Subjects:
Online Access:https://www.mdpi.com/2304-8158/11/6/877
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author Xue Du
Jessica Rodriguez
Josephine Wee
author_facet Xue Du
Jessica Rodriguez
Josephine Wee
author_sort Xue Du
collection DOAJ
description Crystalline silica (cSiO<sub>2</sub>) particles are naturally existing environmental toxicants. Exposure to cSiO<sub>2</sub> could cause local or systemic inflammation and aggregate inflammation-associated diseases. Dietary postbiotics are reported to possess anti-inflammatory activities; however, their effects on cSiO<sub>2</sub>-triggered inflammation are unknown. Here, we investigate the impact of postbiotics from <i>Lacticaseibacillus rhamnosus</i> (LGG), <i>Limosilactobacillus reuteri</i> (L.reu), and <i>Bifidobacterium animalis</i> subsp. <i>lactis</i> Bb12 (BB12) on cSiO<sub>2</sub>-induced cytotoxicity and IL-1 cytokines in vitro using macrophages. The postbiotics used in this study were cell-free fractions of a probiotic growth medium collected at different time points. The in vitro model used was the wild-type murine macrophage RAW 264.7 cell line stably transfected with the inflammasome adapter protein, ASC. Our results indicate that all the postbiotics could reduce cSiO<sub>2</sub>-induced cytotoxicity in the wild-type and ASC macrophages and the effects were OD-dependent. Following priming with a lipopolysaccharide, cSiO<sub>2</sub> treatment resulted in robust inflammasome activation in ASC, as reflected by the IL-1β release. These responses were minimal or absent in the wild-type RAW cells. All the postbiotics decreased the release of IL-1β from ASC; however, only LGG and BB12 reduced the IL-1β secretion from wild-type cells. Only the L.reu postbiotics reduced the IL-1α release from ASC. We conclude that the postbiotics from LGG, BB12, and L.reu can protect macrophages against cSiO<sub>2</sub>-induced cytotoxicity and suppress IL-1β activation.
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spelling doaj.art-c7259b2066444525b7fd10e51537b6332023-11-24T01:11:19ZengMDPI AGFoods2304-81582022-03-0111687710.3390/foods11060877Dietary Postbiotics Reduce Cytotoxicity and Inflammation Induced by Crystalline Silica in an In Vitro RAW 264.7 Macrophage ModelXue Du0Jessica Rodriguez1Josephine Wee2Department of Food Science, The Pennsylvania State University, State College, PA 16802, USADepartment of Food Science, The Pennsylvania State University, State College, PA 16802, USADepartment of Food Science, The Pennsylvania State University, State College, PA 16802, USACrystalline silica (cSiO<sub>2</sub>) particles are naturally existing environmental toxicants. Exposure to cSiO<sub>2</sub> could cause local or systemic inflammation and aggregate inflammation-associated diseases. Dietary postbiotics are reported to possess anti-inflammatory activities; however, their effects on cSiO<sub>2</sub>-triggered inflammation are unknown. Here, we investigate the impact of postbiotics from <i>Lacticaseibacillus rhamnosus</i> (LGG), <i>Limosilactobacillus reuteri</i> (L.reu), and <i>Bifidobacterium animalis</i> subsp. <i>lactis</i> Bb12 (BB12) on cSiO<sub>2</sub>-induced cytotoxicity and IL-1 cytokines in vitro using macrophages. The postbiotics used in this study were cell-free fractions of a probiotic growth medium collected at different time points. The in vitro model used was the wild-type murine macrophage RAW 264.7 cell line stably transfected with the inflammasome adapter protein, ASC. Our results indicate that all the postbiotics could reduce cSiO<sub>2</sub>-induced cytotoxicity in the wild-type and ASC macrophages and the effects were OD-dependent. Following priming with a lipopolysaccharide, cSiO<sub>2</sub> treatment resulted in robust inflammasome activation in ASC, as reflected by the IL-1β release. These responses were minimal or absent in the wild-type RAW cells. All the postbiotics decreased the release of IL-1β from ASC; however, only LGG and BB12 reduced the IL-1β secretion from wild-type cells. Only the L.reu postbiotics reduced the IL-1α release from ASC. We conclude that the postbiotics from LGG, BB12, and L.reu can protect macrophages against cSiO<sub>2</sub>-induced cytotoxicity and suppress IL-1β activation.https://www.mdpi.com/2304-8158/11/6/877postbioticssilicamacrophageNLRP3 inflammasomecytotoxicityIL-1β
spellingShingle Xue Du
Jessica Rodriguez
Josephine Wee
Dietary Postbiotics Reduce Cytotoxicity and Inflammation Induced by Crystalline Silica in an In Vitro RAW 264.7 Macrophage Model
Foods
postbiotics
silica
macrophage
NLRP3 inflammasome
cytotoxicity
IL-1β
title Dietary Postbiotics Reduce Cytotoxicity and Inflammation Induced by Crystalline Silica in an In Vitro RAW 264.7 Macrophage Model
title_full Dietary Postbiotics Reduce Cytotoxicity and Inflammation Induced by Crystalline Silica in an In Vitro RAW 264.7 Macrophage Model
title_fullStr Dietary Postbiotics Reduce Cytotoxicity and Inflammation Induced by Crystalline Silica in an In Vitro RAW 264.7 Macrophage Model
title_full_unstemmed Dietary Postbiotics Reduce Cytotoxicity and Inflammation Induced by Crystalline Silica in an In Vitro RAW 264.7 Macrophage Model
title_short Dietary Postbiotics Reduce Cytotoxicity and Inflammation Induced by Crystalline Silica in an In Vitro RAW 264.7 Macrophage Model
title_sort dietary postbiotics reduce cytotoxicity and inflammation induced by crystalline silica in an in vitro raw 264 7 macrophage model
topic postbiotics
silica
macrophage
NLRP3 inflammasome
cytotoxicity
IL-1β
url https://www.mdpi.com/2304-8158/11/6/877
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AT jessicarodriguez dietarypostbioticsreducecytotoxicityandinflammationinducedbycrystallinesilicainaninvitroraw2647macrophagemodel
AT josephinewee dietarypostbioticsreducecytotoxicityandinflammationinducedbycrystallinesilicainaninvitroraw2647macrophagemodel