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重新审视褐色脂肪细胞的细胞起源。

Cellular Origins of Beige Fat Cells Revisited.

机构信息

Touchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.

Department of Molecular and Cellular Endocrinology, Diabetes and Metabolism Research Institute, Beckman Research Institute of City of Hope, Duarte, CA.

出版信息

Diabetes. 2019 Oct;68(10):1874-1885. doi: 10.2337/db19-0308.

Abstract

Activated beige adipocytes have therapeutic potential due to their ability to improve glucose and lipid homeostasis. To date, the origin of beige adipocytes remains enigmatic. Whether beige cells arise through de novo differentiation from resident precursors or through reprogramming of mature white adipocytes has been a topic of intense discussion. Here, we offer our perspective on the natural origin of beige adipocytes in mice. In particular, we revisit recent lineage-tracing studies that shed light on this issue and offer new insight into how environmental housing temperatures early in life influence the mode of beige adipocyte biogenesis upon cold exposure later in life. We suggest a unified model in which beige adipocytes (UCP1 multilocular cells) in rodents initially arise predominantly from progenitors (i.e., de novo beige adipogenesis) upon the first exposure to cold temperatures and then interconvert between "dormant beige" and "active beige" phenotypes (i.e., beige cell activation) upon subsequent changes in environmental temperature. Importantly, we highlight experimental considerations needed to visualize de novo adipogenesis versus beige cell activation in mice. A precise understanding of the cellular origins of beige adipocytes emanating in response to physiological and pharmacological stimuli may better inform therapeutic strategies to recruit beige adipocytes in vivo.

摘要

激活的米色脂肪细胞具有治疗潜力,因为它们能够改善葡萄糖和脂质的稳态平衡。迄今为止,米色脂肪细胞的起源仍然是个谜。米色细胞是通过从头从驻留前体细胞分化而来,还是通过成熟白色脂肪细胞的重编程而来,一直是激烈讨论的话题。在这里,我们提供了我们对小鼠米色脂肪细胞的自然起源的看法。特别是,我们重新审视了最近的谱系追踪研究,这些研究阐明了这个问题,并为环境温度如何影响生命早期冷暴露后米色脂肪细胞生成的模式提供了新的见解。我们提出了一个统一的模型,其中啮齿动物的米色脂肪细胞(UCP1 多泡细胞)最初主要在第一次暴露于低温时,通过前体细胞(即从头米色脂肪生成)产生,然后在环境温度的后续变化下,在“休眠米色”和“活跃米色”表型之间相互转换(即米色细胞激活)。重要的是,我们强调了在小鼠中可视化从头脂肪生成与米色细胞激活所需要的实验考虑因素。对生理和药理学刺激下产生的米色脂肪细胞的细胞起源的精确理解,可能会更好地为体内招募米色脂肪细胞的治疗策略提供信息。

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