Increased expression of triggering receptor expressed on myeloid cells-1 in the population with obesity and insulin resistance.
case_control · Level III
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- Record sourced from PubMed, PMID 28111922.
- Also identified by DOI 10.1002/oby.21714 and PMC identifier 5323323.
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Abstract
Triggering receptor expressed on myeloid cells (TREM)-1 has recently been recognized as one of the potent amplifiers of acute and chronic inflammation. However, the exact role of TREM-1 in regard to insulin insensitivity is unknown. mRNA transcripts and protein expression of TREM-1, TREM-2, and TREM-1/TREM-2 ratio were examined in the tissue biopsies (liver, omentum, and subcutaneous fat) and blood samples (neutrophils and monocytes) of subjects with obesity and diabetes (SO<sup>+</sup> D<sup>+</sup> ; n = 15), subjects with obesity but not diabetes (SO<sup>+</sup> D<sup>-</sup> ; n = 7), and subjects without obesity (BMI < 30) and diabetes (SO<sup>-</sup> D<sup>-</sup> ; n = 5). The immunofluorescence and RT-PCR revealed significant increase in TREM-1, decrease in TREM-2, and increase in the TREM1/TREM2 ratio in SO<sup>+</sup> D<sup>+</sup> group compared with other groups. Overall, increased liver TREM-1 expression and soluble-TREM-1 were found in SO<sup>+</sup> D<sup>+</sup> group compared with SO<sup>+</sup> D<sup>-</sup> group (100% vs. 57.14%, r = 0.582; P = 0.023). TREM-1 was significantly increased in all subjects with obesity and those with HOMA-IR index of >2. TREM-1 was found to be significantly higher in tissues biopsies and blood of subjects with obesity. Greater expression and activity of TREM-1 suggest a possible role in the underlying pathophysiology of obesity and associated comorbidities.
Medical subject headings
- Insulin Resistance
- Membrane Glycoproteins
- Myeloid Cells
- Obesity
- Receptors, Immunologic