Key result
Review summarizes the signaling mechanisms regulating brown and beige adipocyte thermogenic function.
Why the study?
The signaling mechanisms underlying brown adipocyte thermogenesis and their regulation by second messengers and non-coding RNAs require integrative understanding to inform obesity therapy strategies.
This review highlights the signaling cascades, including beta-adrenergic and natriuretic peptide pathways, and non-coding RNAs that regulate brown adipocyte thermogenesis.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for thermogenic targets in cardiometabolic disease; leaves open clinical translation and outcomes.
β-adrenergic receptors (βARs) are well established for conveying the signal from catecholamines to adipocytes. Acting through the second messenger cyclic adenosine monophosphate (cAMP) they stimulate lipolysis and also increase the activity of brown adipocytes and the 'browning' of adipocytes within white fat depots (so-called 'brite' or 'beige' adipocytes). Brown adipose tissue mitochondria are enriched with uncoupling protein 1 (UCP1), which is a regulated proton channel that allows the dissipation of chemical energy in the form of heat. The discovery of functional brown adipocytes in humans and inducible brown-like ('beige' or 'brite') adipocytes in rodents have suggested that recruitment and activation of these thermogenic adipocytes could be a promising strategy to increase energy expenditure for obesity therapy. More recently, the cardiac natriuretic peptides and their second messenger cyclic guanosine monophosphate (cGMP) have gained attention as a parallel signaling pathway in adipocytes, with some unique features. In this review, we begin with some important historical work that touches upon the regulation of brown adipocyte development and physiology. We then provide a synopsis of some recent advances in the signaling cascades from β-adrenergic agonists and natriuretic peptides to drive thermogenic gene expression in the adipocytes and how these two pathways converge at a number of unexpected points. Finally, moving from the physiologic hormonal signaling, we discuss yet another level of control downstream of these signals: the growing appreciation of the emerging roles of non-coding RNAs as important regulators of brown adipocyte formation and function. In this review, we discuss new developments in our understanding of the signaling mechanisms and factors including new secreted proteins and novel non-coding RNAs that control the function as well as the plasticity of the brown/beige adipose tissue as it responds to the energy needs and environmental conditions of the organism.
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Shi et al. (2017) conducted a review in Obesity / Brown adipocyte thermogenesis. This review summarizes the signaling mechanisms, including beta-adrenergic agonists, natriuretic peptides, and non-coding RNAs, that regulate brown and beige adipocyte thermogenic function.
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