Hsieh Paishiun N, Fan Liyan, Sweet David R, Jain Mukesh K
Case Cardiovascular Research Institute, Case Western Reserve University, Cleveland, Ohio.
Department of Pathology, Case Western Reserve University, Cleveland, Ohio.
Endocr Rev. 2019 Feb 1;40(1):137-152. doi: 10.1210/er.2018-00151.
Nutrient handling by higher organisms is a complex process that is regulated at the transcriptional level. Studies over the past 15 years have highlighted the critical importance of a family of transcriptional regulators termed the Krüppel-like factors (KLFs) in metabolism. Within an organ, distinct KLFs direct networks of metabolic gene targets to achieve specialized functions. This regulation is often orchestrated in concert with recruitment of tissue-specific transcriptional regulators, particularly members of the nuclear receptor family. Upon nutrient entry into the intestine, gut, and liver, KLFs control a range of functions from bile synthesis to intestinal stem cell maintenance to effect nutrient acquisition. Subsequently, coordinated KLF activity across multiple organs distributes nutrients to sites of storage or liberates them for use in response to changes in nutrient status. Finally, in energy-consuming organs like cardiac and skeletal muscle, KLFs tune local metabolic programs to precisely match substrate uptake, flux, and use, particularly via mitochondrial function, with energetic demand; this is achieved in part via circulating mediators, including glucocorticoids and insulin. Here, we summarize current understanding of KLFs in regulation of nutrient absorption, interorgan circulation, and tissue-specific use.
高等生物对营养物质的处理是一个在转录水平受到调控的复杂过程。过去15年的研究突出了一类名为Krüppel样因子(KLFs)的转录调节因子家族在代谢中的关键重要性。在一个器官内,不同的KLFs指导代谢基因靶标网络以实现特定功能。这种调节通常与组织特异性转录调节因子的招募协同进行,尤其是核受体家族的成员。营养物质进入肠道、消化道和肝脏后,KLFs控制从胆汁合成到肠道干细胞维持等一系列功能,以实现营养物质的获取。随后,多个器官中协调的KLF活性将营养物质分配到储存部位,或根据营养状态的变化释放它们以供使用。最后,在心脏和骨骼肌等耗能器官中,KLFs调节局部代谢程序,以精确匹配底物摄取、通量和利用,特别是通过线粒体功能,与能量需求相匹配;这部分是通过包括糖皮质激素和胰岛素在内的循环介质实现的。在这里,我们总结了目前对KLFs在营养吸收、器官间循环和组织特异性利用调节方面的理解。