Sanchez Gurmaches Lab
Adipose Tissue Distribution and Function

Understanding how metabolic and signaling pathways impact adipose tissue distribution and function

Decades of clinical data show that the key factor that explains the negative roles of excessive adipose tissue in whole body homeostasis is not the total amount of adipose tissue, but rather its distribution. However, how fat distribution is mechanistically determined is not clear. We recently found that differences in the activation of the PI3K/Akt signaling pathway between adipocyte lineages dramatically affects adipose tissue distribution and function. This opens a new and exciting model in the field in which natural differences in signaling and/or metabolism between adipocytes lineages may be one of the key factors regulating adipose tissue distribution.

We are pursuing efforts to understand the biology of distinct sub-pool of progenitor cells and the main signaling and transcriptional pathways that differentially regulate them to mechanistically understand fat distribution.

Figure 1.

Cover image of Cell Metabolism. Understanding the origins of adipose tissue may explain fat depot heterogeneity and variations in body fat patterning. We revealed that subsets of white adipocytes arise from the Myf5 lineage, thought to give rise only to brown fat and skeletal muscle, and that deleting PTEN in the Myf5 lineage redistributes body fat. The cover image illustrates the relative contribution of Myf5-positive (orange) and Myf5-negative (blue) adipocyte precursor cells to brown and white fat depots, with a modified hematoxylin and eosin-stained white fat section image as background.