| Literature DB >> 26406372 |
Wenwen Zeng1, Roksana M Pirzgalska2, Mafalda M A Pereira2, Nadiya Kubasova2, Andreia Barateiro3, Elsa Seixas2, Yi-Hsueh Lu4, Albina Kozlova4, Henning Voss5, Gabriel G Martins6, Jeffrey M Friedman1, Ana I Domingos7.
Abstract
Leptin is a hormone produced by the adipose tissue that acts in the brain, stimulating white fat breakdown. We find that the lipolytic effect of leptin is mediated through the action of sympathetic nerve fibers that innervate the adipose tissue. Using intravital two-photon microscopy, we observe that sympathetic nerve fibers establish neuro-adipose junctions, directly "enveloping" adipocytes. Local optogenetic stimulation of sympathetic inputs induces a local lipolytic response and depletion of white adipose mass. Conversely, genetic ablation of sympathetic inputs onto fat pads blocks leptin-stimulated phosphorylation of hormone-sensitive lipase and consequent lipolysis, as do knockouts of dopamine β-hydroxylase, an enzyme required for catecholamine synthesis. Thus, neuro-adipose junctions are necessary and sufficient for the induction of lipolysis in white adipose tissue and are an efferent effector of leptin action. Direct activation of sympathetic inputs to adipose tissues may represent an alternative approach to induce fat loss, circumventing central leptin resistance. PAPERCLIP.Entities:
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Year: 2015 PMID: 26406372 DOI: 10.1016/j.cell.2015.08.055
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582