| Literature DB >> 35296864 |
Margo P Emont1,2, Christopher Jacobs1,2, Adam L Essene1, Deepti Pant1, Danielle Tenen1,2, Georgia Colleluori3, Angelica Di Vincenzo3, Anja M Jørgensen4, Hesam Dashti2, Adam Stefek2, Elizabeth McGonagle2, Sophie Strobel2, Samantha Laber2, Saaket Agrawal2,5, Gregory P Westcott1, Amrita Kar1,2, Molly L Veregge1, Anton Gulko1, Harini Srinivasan1,2, Zachary Kramer1, Eleanna De Filippis6, Erin Merkel1, Jennifer Ducie7, Christopher G Boyd8, William Gourash9, Anita Courcoulas9, Samuel J Lin10, Bernard T Lee10, Donald Morris10, Adam Tobias10, Amit V Khera2,5,10, Melina Claussnitzer2,11, Tune H Pers4, Antonio Giordano3, Orr Ashenberg12, Aviv Regev12,13,14, Linus T Tsai1,2,15, Evan D Rosen16,17,18.
Abstract
White adipose tissue, once regarded as morphologically and functionally bland, is now recognized to be dynamic, plastic and heterogenous, and is involved in a wide array of biological processes including energy homeostasis, glucose and lipid handling, blood pressure control and host defence1. High-fat feeding and other metabolic stressors cause marked changes in adipose morphology, physiology and cellular composition1, and alterations in adiposity are associated with insulin resistance, dyslipidemia and type 2 diabetes2. Here we provide detailed cellular atlases of human and mouse subcutaneous and visceral white fat at single-cell resolution across a range of body weight. We identify subpopulations of adipocytes, adipose stem and progenitor cells, vascular and immune cells and demonstrate commonalities and differences across species and dietary conditions. We link specific cell types to increased risk of metabolic disease and provide an initial blueprint for a comprehensive set of interactions between individual cell types in the adipose niche in leanness and obesity. These data comprise an extensive resource for the exploration of genes, traits and cell types in the function of white adipose tissue across species, depots and nutritional conditions.Entities:
Mesh:
Year: 2022 PMID: 35296864 PMCID: PMC9504827 DOI: 10.1038/s41586-022-04518-2
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 69.504