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Human milk affects TLR4 activation and LPS-induced inflammatory cytokine expression in Caco-2 intestinal epithelial cells.
- Source :
-
Scientific reports [Sci Rep] 2024 Jun 11; Vol. 14 (1), pp. 13448. Date of Electronic Publication: 2024 Jun 11. - Publication Year :
- 2024
-
Abstract
- Human milk (HM) components affect immune cell toll-like receptor 4 (TLR4) signaling. However, studies examining the immunomodulatory impacts of HM on TLR4 signaling in intestinal epithelial cells (IECs) are limited. This study utilized both a TLR4 reporter cell line and a Caco-2 IEC model to examine the effects of HM on lipopolysaccharide (LPS)-induced TLR4 activation and cytokine responses, respectively. Additionally, we performed fast protein liquid chromatography and mass spectrometry to identify a HM component that contributes to the effect of HM on LPS/TLR4 signaling. HM enhances LPS-induced TLR4 signaling as well as LPS-induced IEC gene expression of pro-inflammatory cytokines and negative regulators of NF-κB. Human serum albumin (HSA) present in HM contributes to these effects. HSA within HM synergizes with LPS to induce IEC gene expression of pro-inflammatory cytokines and negative regulators of NF-κB. Altogether, this study provides mechanistic evidence behind the immunomodulatory function of HM on IECs, which may contribute to an enhanced immune response in breast-fed neonates.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Caco-2 Cells
Epithelial Cells metabolism
Epithelial Cells drug effects
Intestinal Mucosa metabolism
Intestinal Mucosa drug effects
Gene Expression Regulation drug effects
Toll-Like Receptor 4 metabolism
Toll-Like Receptor 4 genetics
Milk, Human metabolism
Milk, Human chemistry
Lipopolysaccharides pharmacology
Cytokines metabolism
Signal Transduction drug effects
NF-kappa B metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 14
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 38862662
- Full Text :
- https://doi.org/10.1038/s41598-024-64000-z