White, brown and pink adipocytes: the extraordinary plasticity of the adipose organ
- PMID: 24468979
- DOI: 10.1530/EJE-13-0945
White, brown and pink adipocytes: the extraordinary plasticity of the adipose organ
Abstract
In mammals, adipocytes are lipid-laden cells making up the parenchyma of the multi-depot adipose organ. White adipocytes store lipids for release as free fatty acids during fasting periods; brown adipocytes burn glucose and lipids to maintain thermal homeostasis. A third type of adipocyte, the pink adipocyte, has recently been characterised in mouse subcutaneous fat depots during pregnancy and lactation. Pink adipocytes are mammary gland alveolar epithelial cells whose role is to produce and secrete milk. Emerging evidence suggests that they derive from the transdifferentiation of subcutaneous white adipocytes. The functional response of the adipose organ to a range of metabolic and environmental challenges highlights its extraordinary plasticity. Cold exposure induces an increase in the 'brown' component of the organ to meet the increased thermal demand; in states of positive energy balance, the 'white' component expands to store excess nutrients; finally, the 'pink' component develops in subcutaneous depots during pregnancy to ensure litter feeding. At the cell level, plasticity is provided not only by stem cell proliferation and differentiation but also, distinctively, by direct transdifferentiation of fully differentiated adipocytes by the stimuli that induce genetic expression reprogramming and through it a change in phenotype and, consequently function. A greater understanding of adipocyte transdifferentiation mechanisms would have the potential to shed light on their biology as well as inspire novel therapeutic strategies against metabolic syndrome (browning) and breast cancer (pinking).
Similar articles
-
UCP1 protein: The molecular hub of adipose organ plasticity.Biochimie. 2017 Mar;134:71-76. doi: 10.1016/j.biochi.2016.09.008. Epub 2016 Sep 10. Biochimie. 2017. PMID: 27622583 Review.
-
White, brown, beige/brite: different adipose cells for different functions?Endocrinology. 2013 Sep;154(9):2992-3000. doi: 10.1210/en.2013-1403. Epub 2013 Jun 19. Endocrinology. 2013. PMID: 23782940 Review.
-
Reversible physiological transdifferentiation in the adipose organ.Proc Nutr Soc. 2009 Nov;68(4):340-9. doi: 10.1017/S0029665109990140. Epub 2009 Aug 24. Proc Nutr Soc. 2009. PMID: 19698198
-
Brown adipocytes can display a mammary basal myoepithelial cell phenotype in vivo.Mol Metab. 2017 Oct;6(10):1198-1211. doi: 10.1016/j.molmet.2017.07.015. Epub 2017 Aug 5. Mol Metab. 2017. PMID: 29031720 Free PMC article.
-
Pink adipose tissue: A paradigm of adipose tissue plasticity.Ann Endocrinol (Paris). 2024 Jun;85(3):248-251. doi: 10.1016/j.ando.2024.05.004. Epub 2024 Jun 12. Ann Endocrinol (Paris). 2024. PMID: 38871512 Review.
Cited by
-
Adipokines in the Crosstalk between Adipose Tissues and Other Organs: Implications in Cardiometabolic Diseases.Biomedicines. 2024 Sep 19;12(9):2129. doi: 10.3390/biomedicines12092129. Biomedicines. 2024. PMID: 39335642 Free PMC article. Review.
-
Adipose Tissue Plasticity in Response to Pathophysiological Cues: A Connecting Link between Obesity and Its Associated Comorbidities.Int J Mol Sci. 2022 May 14;23(10):5511. doi: 10.3390/ijms23105511. Int J Mol Sci. 2022. PMID: 35628322 Free PMC article. Review.
-
Interaction between the amount of dietary protein and the environmental temperature on the expression of browning markers in adipose tissue of rats.Genes Nutr. 2019 Jun 4;14:19. doi: 10.1186/s12263-019-0642-x. eCollection 2019. Genes Nutr. 2019. PMID: 31178938 Free PMC article.
-
The Dual Role of the Pervasive "Fattish" Tissue Remodeling With Age.Front Endocrinol (Lausanne). 2019 Feb 26;10:114. doi: 10.3389/fendo.2019.00114. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 30863366 Free PMC article. Review.
-
Central nervous system regulation of brown adipose tissue.Compr Physiol. 2014 Oct;4(4):1677-713. doi: 10.1002/cphy.c140013. Compr Physiol. 2014. PMID: 25428857 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources