Altered mRNA levels of circulating peripheral blood mononuclear cells in adult and elderly men after the acute intake of milk or yogurt
Résumé
We have previously shown that the acute intake of dairy products, fermented can alter the
postprandial profiles of circulating metabolites. Interestingly, we noted that the postprandial
responses of the clusters of identified metabolites where different when considering the age of
the consumers, suggesting a major role of the ageing process on the metabolic response to
the dairy intake.
In order to investigate the mechanisms behind these changes, here we explored the mRNA
profiles of 44 targeted genes in the circulating peripheral blood mononuclear cells (PBMC) of
the FermentoMilk study participants, including adult (20-35yr, n=11) and elderly (65-80yr,
n=11) men. After a run-in period of three weeks, during which the consumption of dairy
products and other fermented products was excluded, the participants were asked to consume
600 ml of milk or yogurt. PBMC were collected before and after the run-in period, as well as
before (0h) and after (2h, 4h) the acute dairy intake. Following RNA extraction and
retrotranscription, the mRNA levels of 44 genes were simultaneously measured using TaqMan
Array Cards. The statistical analyses revealed that the most important alterations observed on
the studied genes came from the age factor, either during the restriction or the postprandial
period. Thus, 8 genes (mostly related to inflammation), namely CXCR2, Actn4, GPBAR1,
IFNG, MRPS33, SVPB, TLR4, TNFRSF1 were up-regulated in the elderly when compared to
the adult participants, irrespectively of the dairy product consumed or the period considered.
In addition to this, 16 genes showed postprandial changes, with at least one time point being
different from the basal value. Interestingly, some of the targets showed changes related to
specific interactions. When yogurt was consumed, several genes related to inflammation
(IFNG) apoptosis (SH3KBP1), lipid metabolism (NR1H2, NR1H3) and oxidative
phosphorylation (NDUFS4) were up-regulated only in the elderly participants.
We conclude that the ageing process has a predominant impact on the targeted mRNA levels
in circulating PBMC. In addition, some of the targets studied reacted to the short-term
(postprandial) stimulation, especially when yogurt was consumed by the elderly participants,
revealing age-related differences that can contribute to explain the population-specific
metabolic responses to dairy intake.