We have demonstrated that human fat cells must be grown in 3D cultures to respond to pro-resolving lipids. Traditionally, human fat cells are differentiated from the stromal vascular fraction of homogenized tissue, but we have shown that such cells do not respond to stimuli in a manner befitting mature adipocytes, and thus they have limited applicability when evaluating drug responses. This finding goes beyond the state of the art.
In addition, we have investigated the role of adipose extracellular matrix composition, not only in metabolically healthy vs unhealthy patients, but also in lean controls. It is notoriously difficult to obtain omental adipose tissue from lean and healthy controls, as they rarely undergo the type of surgery where it is possible to access visceral fat. Through a unique collaboration, we have been able to assemble such a control group, and this demonstrates that adipose tissue fibrosis surprisingly is reduced in obese patients, as determined through several complementary experimental approaches. It was somewhat challenging to publish this data, as it challenges the current paradigm, but we succeeded and I believe that it makes an important contribution to the scientific community, and enhances our understanding of the complex changes that the adipose tissue undergoes during the expansion associated with development of severe adiposity.
We now continue to pursue our research goals, as outlined above, where we hope and believe that our research will continue to expand the state of the art of the scientific field.