1. LGR signaling mediates muscle-adipose tissue crosstalk and protects against diet-induced insulin resistance.
- Author
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Kubrak, Olga, Jørgensen, Anne F., Koyama, Takashi, Lassen, Mette, Nagy, Stanislav, Hald, Jacob, Mazzoni, Gianluca, Madsen, Dennis, Hansen, Jacob B., Larsen, Martin Røssel, Texada, Michael J., Hansen, Jakob L., Halberg, Kenneth V., and Rewitz, Kim
- Subjects
INSULIN resistance ,BONE morphogenetic proteins ,INSULIN sensitivity ,G protein coupled receptors ,ADIPOSE tissues ,TYPE 2 diabetes - Abstract
Obesity impairs tissue insulin sensitivity and signaling, promoting type-2 diabetes. Although improving insulin signaling is key to reversing diabetes, the multi-organ mechanisms regulating this process are poorly defined. Here, we screen the secretome and receptome in Drosophila to identify the hormonal crosstalk affecting diet-induced insulin resistance and obesity. We discover a complex interplay between muscle, neuronal, and adipose tissues, mediated by Bone Morphogenetic Protein (BMP) signaling and the hormone Bursicon, that enhances insulin signaling and sugar tolerance. Muscle-derived BMP signaling, induced by sugar, governs neuronal Bursicon signaling. Bursicon, through its receptor Rickets, a Leucine-rich-repeat-containing G-protein coupled receptor (LGR), improves insulin secretion and insulin sensitivity in adipose tissue, mitigating hyperglycemia. In mouse adipocytes, loss of the Rickets ortholog LGR4 blunts insulin responses, showing an essential role of LGR4 in adipocyte insulin sensitivity. Our findings reveal a muscle-neuronal-fat-tissue axis driving metabolic adaptation to high-sugar conditions, identifying LGR4 as a critical mediator in this regulatory network. Obesity induces insulin resistance and impairs insulin signaling, causing diabetes. Here, the authors show that BMP and LGR signaling mediate communication between muscle, neuronal, and adipose tissues to enhance insulin signaling, identifying LGR as key in protecting against insulin resistance. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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