4.7 Article

TLR2 and TLR4 Surface and Gene Expression in White Blood Cells after Fasting and Oral Glucose, Lipid and Protein Challenges: Influence of Obesity and Sex Hormones

期刊

BIOMOLECULES
卷 10, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/biom10010111

关键词

sex hormones; leukocytes; macronutrient loads; obesity; polycystic ovary syndrome; toll-like receptors; postprandial response

资金

  1. Instituto de Salud Carlos III (Plan Estatal de I+D+i 2013-2016) [PI11/00357, PI15/01686, PIE16/00050]
  2. European Development Regional Fund A way to achieve Europe (ERDF)
  3. Diabetes Trans-national Research Advancement for Investigators (DIATRAIN) mobility program
  4. FP7 Marie Curie Actions-People-2010-COFUND program of the European Commission [267248]

向作者/读者索取更多资源

We studied if macronutrients of the diet have different effects on leukocyte activation, and if these effects are influenced by sex hormones or obesity. We analyzed leukocyte cell surface and gene expression of toll-like receptors 2 and 4 (TLR2 and TLR4) during fasting and after macronutrient loads in women with polycystic ovary syndrome and female and male controls. Fasting TLR2 surface expression in neutrophils was higher in men than in women. Obese subjects presented higher TLR2 gene expression than nonobese individuals, particularly in men. In contrast, surface TLR4 expression was lower in men and in obese individuals. Postprandial cell-surface expression decreased similarly after all macronutrient loads. Neutrophil TLR2 decreased only in obese subjects whereas TLR4 showed a greater decrease in nonobese individuals. However, TLR2 gene expression increased after glucose ingestion and decreased during the lipid load, while TLR4 was induced in response to lipids and mostly to glucose. Postprandial TLR gene expression was not influenced by group of subjects or obesity. Both cell-surface and gene postprandial expression inversely correlated with their fasting levels. These responses suggest a transient compensatory response aiming to prevent postprandial inflammation. However, obesity and sex hormones showed opposite influences on surface expression of TLR2 and TLR4, but not on their gene expression, pointing to regulatory posttranscriptional mechanisms.

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