Department of Animal Physiology, Biochemistry and Biostructure, Poznań University of Life Sciences, Poznań, Poland.
Department of Hepatology and Gastroenterology, Charité-University Medicine Berlin, Germany.
FEBS Lett. 2024 Aug;598(16):1996-2010. doi: 10.1002/1873-3468.14934. Epub 2024 May 25.
Neuronostatin suppresses the differentiation of white preadipocytes. However, the role of neuronostatin in brown adipose tissue remains elusive. Therefore, we investigated the impact of neuronostatin on the proliferation and differentiation of isolated rat brown preadipocytes. We report that neuronostatin and its receptor (GPR107) are synthesized in brown preadipocytes and brown adipose tissue. Furthermore, neuronostatin promotes the replication of brown preadipocytes via the AKT pathway. Notably, neuronostatin suppresses the expression of markers associated with brown adipogenesis (PGC-1α, PPARγ, PRDM16, and UCP1) and reduces cellular mitochondria content. Moreover, neuronostatin impedes the differentiation of preadipocytes by activating the JNK signaling pathway. These effects were not mimicked by somatostatin. Our results suggest that neuronostatin is involved in regulating brown adipogenesis.
神经降压素抑制白色前体脂肪细胞的分化。然而,神经降压素在棕色脂肪组织中的作用仍不清楚。因此,我们研究了神经降压素对分离的大鼠棕色前体脂肪细胞增殖和分化的影响。我们报告说,神经降压素及其受体(GPR107)在棕色前体脂肪细胞和棕色脂肪组织中合成。此外,神经降压素通过 AKT 途径促进棕色前体脂肪细胞的复制。值得注意的是,神经降压素抑制与棕色脂肪生成相关的标志物的表达(PGC-1α、PPARγ、PRDM16 和 UCP1),并减少细胞线粒体含量。此外,神经降压素通过激活 JNK 信号通路来阻止前体脂肪细胞的分化。生长抑素不能模拟这些作用。我们的结果表明,神经降压素参与调节棕色脂肪生成。