TY - JOUR
T1 - Supplementation with lactobacillus plantarum wcfs1 prevents decline of mucus barrier in colon of accelerated aging Ercc1-/Δ7 mice
AU - van Beek, Adriaan A.
AU - Sovran, Bruno
AU - Hugenholtz, Floor
AU - Meijer, Ben
AU - Hoogerland, Joanne A.
AU - Mihailova, Violeta
AU - van der Ploeg, Corine
AU - Belzer, Clara
AU - Boekschoten, Mark V.
AU - Hoeijmakers, Jan H.J.
AU - Vermeij, Wilbert P.
AU - de Vos, Paul
AU - Wells, Jerry M.
AU - Leenen, Pieter J.M.
AU - Nicoletti, Claudio
AU - Hendriks, Rudi W.
AU - Savelkoul, Huub F.J.
N1 - Publisher Copyright:
© 2016 van Beek, Sovran, Hugenholtz, Meijer, Hoogerland, Mihailova, van der Ploeg, Belzer, Boekschoten, Hoeijmakers, Vermeij, de Vos, Wells, Leenen, Nicoletti, Hendriks and Savelkoul.
PY - 2016/10/7
Y1 - 2016/10/7
N2 - Although it is clear that probiotics improve intestinal barrier function, little is known about the effects of probiotics on the aging intestine. We investigated effects of 10-week bacterial supplementation of Lactobacillus plantarum WCFS1, Lactobacillus casei BL23, or Bifidobacterium breve DSM20213 on gut barrier and immunity in 16-week-old accelerated aging Ercc1-/Δ7 mice, which have a median lifespan of ~20 weeks, and their wild-type littermates. The colonic barrier in Ercc1-/Δ7 mice was characterized by a thin (< 10 μm) mucus layer. L. plantarum prevented this decline in mucus integrity in Ercc1-/Δ7 mice, whereas B. breve exacerbated it. Bacterial supplementations affected the expression of immune-related genes, including Toll-like receptor 4. Regulatory T cell frequencies were increased in the mesenteric lymph nodes of L. plantarum- and L. casei-treated Ercc1-/Δ7 mice. L. plantarum- and L. casei-treated Ercc1-/Δ7 mice showed increased specific antibody production in a T cell-dependent immune response in vivo. By contrast, the effects of bacterial supplementation on wild-type control mice were negligible. Thus, supplementation with L. plantarum - but not with L. casei and B. breve - prevented the decline in the mucus barrier in Ercc1-/Δ7 mice. Our data indicate that age is an important factor influencing beneficial or detrimental effects of candidate probiotics. These findings also highlight the need for caution in translating beneficial effects of probiotics observed in young animals or humans to the elderly.
AB - Although it is clear that probiotics improve intestinal barrier function, little is known about the effects of probiotics on the aging intestine. We investigated effects of 10-week bacterial supplementation of Lactobacillus plantarum WCFS1, Lactobacillus casei BL23, or Bifidobacterium breve DSM20213 on gut barrier and immunity in 16-week-old accelerated aging Ercc1-/Δ7 mice, which have a median lifespan of ~20 weeks, and their wild-type littermates. The colonic barrier in Ercc1-/Δ7 mice was characterized by a thin (< 10 μm) mucus layer. L. plantarum prevented this decline in mucus integrity in Ercc1-/Δ7 mice, whereas B. breve exacerbated it. Bacterial supplementations affected the expression of immune-related genes, including Toll-like receptor 4. Regulatory T cell frequencies were increased in the mesenteric lymph nodes of L. plantarum- and L. casei-treated Ercc1-/Δ7 mice. L. plantarum- and L. casei-treated Ercc1-/Δ7 mice showed increased specific antibody production in a T cell-dependent immune response in vivo. By contrast, the effects of bacterial supplementation on wild-type control mice were negligible. Thus, supplementation with L. plantarum - but not with L. casei and B. breve - prevented the decline in the mucus barrier in Ercc1-/Δ7 mice. Our data indicate that age is an important factor influencing beneficial or detrimental effects of candidate probiotics. These findings also highlight the need for caution in translating beneficial effects of probiotics observed in young animals or humans to the elderly.
KW - Aging
KW - Immunity
KW - Intestinal barrier
KW - Microbiota
KW - Mucus
KW - Probiotics
UR - https://www.mendeley.com/catalogue/a066b904-a382-3e39-8656-d251f868efa3/
U2 - 10.3389/fimmu.2016.00408
DO - 10.3389/fimmu.2016.00408
M3 - Article
C2 - 27774093
SN - 1664-3224
VL - 7
SP - 408
JO - Frontiers in immunology
JF - Frontiers in immunology
IS - OCT
M1 - 408
ER -