| First Author | Ten Klooster JP | Year | 2018 |
| Journal | Arch Biochem Biophys | Volume | 644 |
| Pages | 81-92 | PubMed ID | 29526533 |
| Mgi Jnum | J:261116 | Mgi Id | MGI:6153643 |
| Doi | 10.1016/j.abb.2018.03.003 | Citation | Ten Klooster JP, et al. (2018) Type 2 diabetes-related proteins derived from an in vitro model of inflamed fat tissue. Arch Biochem Biophys 644:81-92 |
| abstractText | Currently, there is a worldwide increase of patients with type 2 diabetes (T2D). During the progression of healthy obese to T2D status, there is an influx of immune cells, in particular macrophages, into visceral adipose tissue, accompanied by an increase of inflammatory cytokines, such as, IL6, TNFalpha and Hp. To get a better insight in the underlying mechanisms, we performed a quantitative LCMS analysis on a modified in vitro assay, combining 3T3L1 adipocytes and activated RAW264.7 macrophages, thus mimicking inflamed adipose tissue. Clinically known proteins, e.g. IL6, TNFalpha, AdipoQ, complement factor C3, B and D were identified, thus confirming the assay. In addition, we found 54 new proteins that can potentially be used for research into the mechanism of T2D. Comparison of our results to a study on human visceral fat of obese non-diabetic and obese diabetic subjects, indicated that AUH, NAGK, pCYT2, NNMT, STK39 and CSNK2A2 might indeed be linked to insulin resistance in humans. Moreover, the expression of some of these genes was also altered in human blood samples at early or later stages of insulin desensitization. Overall, we conclude that the direct contact co-culture of 3T3L1 adipocytes with activated macrophages could be a mechanistically relevant and partially translational model of inflamed visceral adipose tissue. |
