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Cited by 352

The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.

The adipose organ at a glance

Open access
Cinti, Saverio·2012·Disease Models & Mechanisms

Abstract

The main parenchymal cells of the adipose organ are adipocytes. White adipocytes store energy, whereas brown adipocytes dissipate energy for thermogenesis. These two cell types with opposing functions can both originate from endothelial cells, and co-exist in the multiple fat depots of the adipose organ – a feature that I propose is crucial for this organ’s plasticity. This poster review provides an overview of the adipose organ, describing its anatomy, cytology, physiological function and histopathology in obesity. It also highlights the remarkable plasticity of the adipose organ, explaining theories of adipocyte transdifferentiation during chronic cold exposure, physical exercise or lactation, as well as in obesity. White-to-brown adipocyte transdifferentiation is of particular medical relevance, because animal data indicate that higher amounts of brown adipose tissue are positively associated with resistance to obesity and its co-morbidities, and that ‘browning’ of the adipose organ curbs these disorders.

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Metadata

Authors
Cinti, S.
Venue
Disease Models & Mechanisms
Published
2012-09-01
Volume
5
Issue
5
Pages
588-594
ISSN
  • 1754-8403 (ISSN-L)
  • 1754-8411
OpenAlex
W2098207861
Cited by
352
References
30
FWCI
17.17
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: The adipose organ at a glance. https://app.cochat.ai/papers/10.1242/dmm.009662
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Cinti, S. (2012). The adipose organ at a glance. Disease Models & Mechanisms. https://doi.org/10.1242/dmm.009662

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.