Asia Pacific Center for Theoretical Physics, Pohang, Gyeongbuk, 37673, Korea.
Laboratory of Biological Modeling, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, 20892, United States of America.
Sci Rep. 2017 May 9;7(1):1602. doi: 10.1038/s41598-017-01806-0.
Counter-regulatory elements maintain dynamic equilibrium ubiquitously in living systems. The most prominent example, which is critical to mammalian survival, is that of pancreatic α and β cells producing glucagon and insulin for glucose homeostasis. These cells are not found in a single gland but are dispersed in multiple micro-organs known as the islets of Langerhans. Within an islet, these two reciprocal cell types interact with each other and with an additional cell type: the δ cell. By testing all possible motifs governing the interactions of these three cell types, we found that a unique set of positive/negative intra-islet interactions between different islet cell types functions not only to reduce the superficially wasteful zero-sum action of glucagon and insulin but also to enhance/suppress the synchronization of hormone secretions between islets under high/normal glucose conditions. This anti-symmetric interaction motif confers effective controllability for network (de)synchronization.
在生命系统中,拮抗调节元件普遍维持着动态平衡。其中最显著的例子,对于哺乳动物的生存至关重要,那就是胰腺的α和β细胞分别产生胰高血糖素和胰岛素以维持血糖平衡。这些细胞不是分布在单一的腺体中,而是分散在多个被称为胰岛的微器官中。在胰岛内,这两种相互作用的细胞类型与另一种细胞类型——δ细胞相互作用。通过测试控制这三种细胞类型相互作用的所有可能的基序,我们发现一组独特的正/负胰岛内不同细胞类型之间的相互作用不仅有助于减少胰高血糖素和胰岛素表面上浪费的零和作用,而且有助于在高/正常葡萄糖条件下增强/抑制胰岛间激素分泌的同步性。这种非对称相互作用模式赋予了网络(去)同步的有效可控性。