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Immunoregulatory effects on Caco-2 cells and mice of exopolysaccharides isolated from Lactobacillus acidophilus NCFM
On the basis of our previous results on potential immunoregulation of Lactobacillus acidophilus NCFM, the immunoregulatory effects of exopolysaccharides (EPS) isolated from L. acidophilus NCFM and their regulating mechanisms are further investigated in the current research. Stimulated by EPS prepara...
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Published in: | Food & function 2014-12, Vol.5 (12), p.3261-3268 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | On the basis of our previous results on potential immunoregulation of
Lactobacillus acidophilus
NCFM, the immunoregulatory effects of exopolysaccharides (EPS) isolated from
L. acidophilus
NCFM and their regulating mechanisms are further investigated in the current research. Stimulated by EPS preparations, four immune-related genes in the human colorectal adenocarcinoma cell line Caco-2 cells, namely, interleukin-1α (IL-1α), chemokine C-C motif 2 (CCL2), tumor necrosis factor α (TNF-α), and pentraxin 3 (PTX3), first showed an increase at 2-4 h, peaked at 4 h, and then decreased at 4-12 h. Similar trends were observed
in vivo
: four genes showed transient expression (highest on the 4th day) in the cecum and colon of mice. Meanwhile, the organ coefficient, clearance index and phagocytic index all significantly increased with time extension and dose increase of EPS stimulation. EPS triggered NF-κB and p38 mitogen-activated protein kinase (p38 MAPK) signaling pathways in Caco-2 cells, and the activated pathways initiated the genes expression. EPS compounds from
L. acidophilus
NCFM may play an important role in host immunoregulation and might be applied as a new type of immunoregulatory agent in functional foods.
This study proved the immunoregulatory effect of exopolysaccharides from
L. acidophilus
NCFM
in vitro
and
in vivo
, and preliminarily explored the mechanisms of immune related genes expression. |
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ISSN: | 2042-6496 2042-650X |
DOI: | 10.1039/c4fo00565a |