Occurrence of brown adipocytes in rat white adipose tissue: molecular and morphological characterization

褐色脂肪组织 脂肪组织 生物 白色脂肪组织 解偶联蛋白 内科学 内分泌学 PRDM16 免疫印迹 污渍 产热 脂肪组织巨噬细胞 脂肪细胞 产热素 生物化学 基因 医学
作者
Béatrice Cousin,Saverio Cinti,Manrico Morroni,S. Raimbault,Daniel Ricquier,Luc Pénicaud,Louis Casteilla
出处
期刊:Journal of Cell Science [The Company of Biologists]
卷期号:103 (4): 931-942 被引量:634
标识
DOI:10.1242/jcs.103.4.931
摘要

ABSTRACT Brown adipocytes are thermogenic cells which play an important role in energy balance. Their thermogenic activity is due to the presence of a mitochondrial uncoupling protein (UCP). Until recently, it was admitted that in rodents brown adipocytes were mainly located in classical brown adipose tissue (BAT). In the present study, we have investigated the presence of UCP protein or mRNA in white adipose tissue (WAT) of rats. Using polymerase chain reaction or Northern blot hybridization, UCP mRNA was detected in mesenteric, epidydimal, retroperitoneal, inguinal and particularly in periovarian adipose depots. The uncoupling protein was detected by Western blotting in mitochondria from periovarian adipose tissue. When rats were submitted to cold or to treatment with a -adrenoceptor agonist, UCP expression was increased in this tissue as in typical brown fat. Moreover, the expression was decreased in obese fa/fa rats compared to lean controls. Morphological studies showed that periovarian adipose tissue of rats kept at 24°C contained cells with numerous typical BAT mitochondria with or without multilocular lipid droplets. Immunocytochemistry confirmed that multilocular cells expressed mitochondrial UCP. Furthermore, the number of brown adipocytes and the density of mitochondrial cristae increased in parallel with exposure to cold. These results demonstrate that adipocytes expressing UCP are present in adipose deposits considered as white fat. They suggest the existence of a continuum in rodents between BAT and WAT, and a great plasticity between adipose tissue phenotypes. The physiological importance of brown adipocytes in WAT and the regulation of UCP expression remain open questions.
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