The Centre of Inflammation and Metabolism and Centre for Physical Activity Research Rigshospitalet, University Hospital of Copenhagen, 2100, Denmark; Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Danish PhD School of Molecular Metabolism, Odense, Denmark.
Novo Nordisk Research Center Oxford, Denmark.
Mol Metab. 2019 Jun;24:30-43. doi: 10.1016/j.molmet.2019.03.005. Epub 2019 Mar 15.
Increasing the amounts of functionally competent brown adipose tissue (BAT) in adult humans has the potential to restore dysfunctional metabolism and counteract obesity. In this study, we aimed to characterize the human perirenal fat depot, and we hypothesized that there would be regional, within-depot differences in the adipose signature depending on local sympathetic activity.
We characterized fat specimens from four different perirenal regions of adult kidney donors, through a combination of qPCR mapping, immunohistochemical staining, RNA-sequencing, and pre-adipocyte isolation. Candidate gene signatures, separated by adipocyte morphology, were recapitulated in a murine model of unilocular brown fat induced by thermoneutrality and high fat diet.
We identified widespread amounts of dormant brown adipose tissue throughout the perirenal depot, which was contrasted by multilocular BAT, primarily found near the adrenal gland. Dormant BAT was characterized by a unilocular morphology and a distinct gene expression profile, which partly overlapped with that of subcutaneous white adipose tissue (WAT). Brown fat precursor cells, which differentiated into functional brown adipocytes were present in the entire perirenal fat depot, regardless of state. We identified SPARC as a candidate adipokine contributing to a dormant BAT state, and CLSTN3 as a novel marker for multilocular BAT.
We propose that perirenal adipose tissue in adult humans consists mainly of dormant BAT and provide a data set for future research on factors which can reactivate dormant BAT into active BAT, a potential strategy for combatting obesity and metabolic disease.
增加成年人体内功能健全的棕色脂肪组织(BAT)的数量,有可能恢复功能失调的代谢并对抗肥胖。在这项研究中,我们旨在描述人类肾周脂肪组织,并假设根据局部交感神经活动,脂肪特征在不同的区域和脂肪组织内会存在差异。
我们通过 qPCR 图谱、免疫组织化学染色、RNA 测序和前体脂肪细胞分离,对成人肾脏供体的四个不同肾周区域的脂肪标本进行了特征描述。通过热中性和高脂肪饮食诱导的单房棕色脂肪的小鼠模型,对根据脂肪细胞形态分离的候选基因特征进行了重现。
我们发现,在整个肾周脂肪组织中存在广泛的休眠棕色脂肪组织,与之形成对比的是主要位于肾上腺附近的多房 BAT。休眠 BAT 的特征是具有单房形态和独特的基因表达谱,部分与皮下白色脂肪组织(WAT)重叠。存在于整个肾周脂肪组织中的棕色脂肪前体细胞分化为功能性棕色脂肪细胞,无论其状态如何。我们确定了 SPARC 作为一种候选脂肪因子,有助于休眠 BAT 状态,并确定了 CLSTN3 作为多房 BAT 的新标志物。
我们提出,成年人体内的肾周脂肪组织主要由休眠 BAT 组成,并为未来研究能将休眠 BAT 重新激活为活跃 BAT 的因素提供了数据集,这是对抗肥胖和代谢性疾病的潜在策略。