New perspectives reveal browning improves thermogenesis in adipose tissues, suggesting links to breast cancer.
White and brown adipose tissues are organized to form a true organ. White store energy that is provided to the organism in the intervals between meals and brown burns lipids to produce heat. When the cold exposure is chronic, white convert into brown (browning) to help thermogenesis and when the energy balance is chronically positive, brown convert into white (whitening) to help store energy. The plastic property of the adipose organ also allows a reversible formation of milk-producing alveolar cells in the mammary fat during pregnancy and lactation (pinking, because the organ is pink during pregnancy). This last striking property of the adipose organ is challenged by other Authors, but our data based on morphology (including electron microscopy), immunohistochemistry, lineage tracing, explants and in vitro data described here support this phenomenon. Our experiments, including Microarrays data comparing cleared fat pad with normal glands in pregnant mice, allowed us to detect four molecular players in the pinking phenomenon: ELF5 (E74 like ETS transcription factor), osteopontin, GATA3 (GATA binding protein 3) and Mir200c. Another molecular player could be the PTHrP (Parathyroid hormone-related protein). Mice lacking each of these molecules have impaired alveologenesis during pregnancy. Finally, several data seem to suggest a strong functional relationship between the onco suppressor gene BRCA1 (Breast cancer gene 1) and the reversible adipo-epithelial transdifferentiation phenomenon opening new avenues for future studies in the connection between pinking and breast cancer.
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Saverio Cinti (2025) studied this question.
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