Department of Animal Sciences, The Ohio State University, Columbus, OH 43210, USA.
Cells. 2023 Feb 15;12(4):624. doi: 10.3390/cells12040624.
White adipose tissue serves as a metabolically dynamic organ that can synthesize and secrete biologically active compounds such as adipokines as well as a caloric reservoir for maintaining energy homeostasis. Adipokines are involved in diverse biological and physiological processes and there have been extensive attempts to characterize the effects of over two dozen adipokines. However, many of these adipokines are produced by not only adipose tissue, but also other tissues. Therefore, investigations into the effects of adipokines on physiological functions have been challenged. In this regard, we aimed to identify a new secreted protein that is encoded by genes specifically expressed in white adipose tissue through analysis of multi-tissue transcriptome and protein expression. As a result, we report a novel adipokine that is encoded by the adipose-specific gene, chordin-like 1 (), which is specifically expressed in white adipose tissue in mice; this expression pattern was conserved in the human orthologous gene. The expression of was enriched in fat cells and developmentally regulated in vitro and in vivo, and moreover, its retrovirus-mediated overexpression and recombinant protein treatment led to markedly increased adipogenesis. Further pathway enrichment analysis revealed enriched pathways related to lipogenesis and adipogenic signaling. Our findings support a pro-adipogenic role of CHRDL1 as a new adipokine and pave the way toward animal studies and future research on its clinical implications and development of anti-obesity therapy.
白色脂肪组织是一种代谢活跃的器官,可合成和分泌生物活性化合物,如脂肪因子,同时也是维持能量平衡的热量储存库。脂肪因子参与多种生物和生理过程,人们已经进行了广泛的尝试来描述超过二十多种脂肪因子的作用。然而,许多这些脂肪因子不仅由脂肪组织产生,而且还由其他组织产生。因此,研究脂肪因子对生理功能的影响受到了挑战。在这方面,我们旨在通过分析多组织转录组和蛋白质表达,鉴定一种仅在白色脂肪组织中特异性表达的基因编码的新型分泌蛋白。结果,我们报告了一种新型的脂肪因子,该脂肪因子由脂肪特异性基因 chordin-like 1 () 编码,在小鼠的白色脂肪组织中特异性表达;这种表达模式在人类同源基因中是保守的。在体外和体内, 的表达在脂肪细胞中富集,并受到发育调控,而且其逆转录病毒介导的过表达和重组蛋白处理导致脂肪生成明显增加。进一步的途径富集分析显示,与脂肪生成和脂肪生成信号相关的途径富集。我们的研究结果支持 CHRDL1 作为一种新型脂肪因子的促脂肪生成作用,并为动物研究以及对其临床意义和抗肥胖治疗发展的未来研究铺平了道路。