Heat-killed Latilactobacillus sakei D279 Attenuates Lipopolysaccharide-Induced Intestinal Inflammation and Barrier Disruption

Intestinal barrier dysfunction and excessive inflammation contribute to the pathogenesis of various metabolic and gastrointestinal diseases. Lipopolysaccharide (LPS) induces systemic and intestinal inflammation, disrupts epithelial tight junctions, and impairs intestinal barrier integrity. Although heat-killed Latilactobacillus sakei D279 exhibits antiviral activity, its effects on intestinal barrier function remain unclear. In this study, we examined whether heat-killed D279 preserves intestinal barrier integrity and attenuates LPS-induced inflammatory responses in vivo (LPS-challenged mice), ex vivo (mouse peritoneal macrophages), and in vitro (IEC-6 intestinal epithelial cells). Cytokine and receptor gene expression in macrophages was measured to evaluate inflammatory responses. Furthermore, barrier function was assessed using transepithelial electrical resistance (TEER), and the expression of tight junction-related genes was assessed. D279 alleviated LPS-induced intestinal injury in LPS-challenged mice, as indicated by the attenuation of colon shortening and histopathological changes compared to those in the LPS control group. In peritoneal macrophages, D279 pretreatment suppressed LPS-induced expression of pro-inflammatory cytokines (TNF-α, IL-1β, and IL-12β), increased IL-10 expression, and reduced LPS-induced upregulation of MLCK expression. This postbiotic increased basal cell viability in a concentration-dependent manner in IEC-6 cells. Moreover, it enhanced epithelial barrier development (increased TEER) and upregulated tight junction gene expression. These findings demonstrate that heat-killed D279 primarily confers its benefits by attenuating LPS-induced cytokine responses, limiting the upregulation of MLCK expression, and partially preserving goblet cell abundance. This is consistent with its protective postbiotic role in intestinal homeostasis. Thus, this study introduces a candidate postbiotic for the promotion of intestinal resilience under systemic inflammatory stress.

Authors

Institutions

Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-11
DOI
https://doi.org/10.64898/2026.11.10.765754
Primary Topic
Probiotics and Fermented Foods
Type
preprint
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
NOV
preprint

Heat-killed Latilactobacillus sakei D279 Attenuates Lipopolysaccharide-Induced Intestinal Inflammation and Barrier Disruption

勝行 橋本, Takamasa Tsunoda, Nur Syafiqah Mohamad Ishak, Ryota Chihama
bioRxiv (Cold Spring Harbor Laboratory)
Probiotics and Fermented Foods
preprint

Heat-killed Latilactobacillus sakei D279 Attenuates Lipopolysaccharide-Induced Intestinal Inflammation and Barrier Disruption

勝行 橋本, Takamasa Tsunoda, Nur Syafiqah Mohamad Ishak, Ryota Chihama
preprint en

Abstract

Intestinal barrier dysfunction and excessive inflammation contribute to the pathogenesis of various metabolic and gastrointestinal diseases. Lipopolysaccharide (LPS) induces systemic and intestinal inflammation, disrupts epithelial tight junctions, and impairs intestinal barrier integrity. Although heat-killed Latilactobacillus sakei D279 exhibits antiviral activity, its effects on intestinal barrier function remain unclear. In this study, we examined whether heat-killed D279 preserves intestinal barrier integrity and attenuates LPS-induced inflammatory responses in vivo (LPS-challenged mice), ex vivo (mouse peritoneal macrophages), and in vitro (IEC-6 intestinal epithelial cells). Cytokine and receptor gene expression in macrophages was measured to evaluate inflammatory responses. Furthermore, barrier function was assessed using transepithelial electrical resistance (TEER), and the expression of tight junction-related genes was assessed. D279 alleviated LPS-induced intestinal injury in LPS-challenged mice, as indicated by the attenuation of colon shortening and histopathological changes compared to those in the LPS control group. In peritoneal macrophages, D279 pretreatment suppressed LPS-induced expression of pro-inflammatory cytokines (TNF-α, IL-1β, and IL-12β), increased IL-10 expression, and reduced LPS-induced upregulation of MLCK expression. This postbiotic increased basal cell viability in a concentration-dependent manner in IEC-6 cells. Moreover, it enhanced epithelial barrier development (increased TEER) and upregulated tight junction gene expression. These findings demonstrate that heat-killed D279 primarily confers its benefits by attenuating LPS-induced cytokine responses, limiting the upregulation of MLCK expression, and partially preserving goblet cell abundance. This is consistent with its protective postbiotic role in intestinal homeostasis. Thus, this study introduces a candidate postbiotic for the promotion of intestinal resilience under systemic inflammatory stress.

bioRxiv (Cold Spring Harbor Laboratory)
Mitsubishi Gas Chemical (Japan) (JP)
Probiotics and Fermented Foods
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon