4.7 Article

Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity

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SCIENTIFIC REPORTS
卷 8, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-018-26065-5

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  1. National Institutes of Health [S06GM008016-320107, S06GM008016-380111, 1RC4MD005964-0]
  2. National Center for Research Resources (NCRR), a component of National Institutes of Health (NIH) [2M01RR010284]
  3. Intramural Research Program of the Center for Research in Genomics and Global Health
  4. National Human Genome Research Institute
  5. National Institute of Diabetes and Digestive and Kidney Diseases
  6. Center for Information Technology
  7. Office of the Director at the National Institutes of Health [Z01HG200362]

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Obese individuals without expected metabolic co-morbidities are referred to as metabolically healthy obese (MHO). The molecular mechanisms underlying this phenotype remain elusive. MicroRNAs may be involved in the MHO phenotype. To test this hypothesis, we screened 179 serum miRNAs in 20 AfricanAmerican women (10 MHOs and 10 metabolically abnormal obese individuals - MAO). We identified 8 differentially expressed miRNAs (DEMs) with validation in an independent sample of 64 MHO and 34 MAO. Of the eight DEMs in the screening phase (p = 0.05), miR-374a-5p remained significant (p = 0.04) with directional consistency in the validation sample. Ingenuity Pathway analysis revealed that miR-374a-5p putatively targeted 37 mRNAs (e.g. chemokines and transcription factors) which are members of canonical pathways involved in inflammation (IL-17A signaling) and lipid metabolism. Analysis restricted to adipocytes, the main source of circulating miRNAs in obesity, identified 3 mRNAs (CCL2, STEAP2, EN1) as the main target of miR-374a-5p. Evaluation of the 3 mRNAs in an independent sample showed that CCL2 was significantly downregulated (p = 0.0005). In summary, MiR-374a-5p is upregulated in MHO compared to MAO individuals and appears to show association with downregulation of pro-inflammatory markers that are linked to insulin resistance. Given the correlative nature of our findings, functional studies are needed.

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