Camerino Claudia, Conte Elena, Carratù Maria Rosaria, Fonzino Adriano, Lograno Marcello Diego, Tricarico Domenico
Department of Biomedical Sciences and Human Oncology (Section of Pharmacology), School of Medicine, University of Bari Aldo Moro, Bari, Italy.
Department of Pharmacy-Pharmaceutical Sciences, University of Bari Aldo Moro, Bari, Italy.
Front Physiol. 2019 Nov 27;10:1437. doi: 10.3389/fphys.2019.01437. eCollection 2019.
Oxytocin (Oxt), osteocalcin (Ost), and NGF/BDNF have a role in bone homeostasis, reproduction, and cognition. Oxt/Ost is required for muscle repair. We investigated gene response of muscle and the inter-organ communication following cold stress (CS). The mRNA quantity of , , , , , , , , , , and genes in bone, brain, soleus (SOL), and (TA) muscles from adult mice following CS were investigated. The myosin heavy-chain , , , and gene expression were investigated. Mice were maintained at = 23°C or 4°C for 6 h and 5-days (5d). CS mice did not show signs of muscle degeneration. An upregulation of and genes by 2 and 1.5 folds, respectively, in TA after 6 h CS and by 4 and 22 folds in SOL muscle after 6 h and 5d CS, respectively, was observed; while after 6 h CS was downregulated in either muscle. was unaffected, while after 5d CS was upregulated in TA. was downregulated in SOL by 0.9-folds at 5d. Following 5d CS, and genes were upregulated, respectively, by 1 and 1.5 folds in SOL. A downregulation of , respectively, by 0.96 and 0.88-folds after 6 h and 5d CS in SOL and was also downregulated by 0.88-fold after 5d CS in TA. and were not affected. Changes in the expression levels of genes in TA and SOL muscles, bone, and brain following CS were regulated by IL6 and Oxt. CS potentiates the slow-twitch phenotype of SOL which is in line with the metabolic need of this muscle, and the potentiation of the slow-twitch phenotype in TA. Oxt and IL6 coordinate a phenotype-dependent tonic effect of slow-twitch muscle and Oxt regulates the inter-organ interaction between brain and SOL muscle. Muscle tropism is maintained by NGF signaling following CS.
催产素(Oxt)、骨钙素(Ost)以及神经生长因子/脑源性神经营养因子(NGF/BDNF)在骨稳态、生殖和认知方面发挥作用。肌肉修复需要Oxt/Ost。我们研究了冷应激(CS)后肌肉的基因反应以及器官间的通讯。对成年小鼠在CS后,其骨骼、大脑、比目鱼肌(SOL)和趾长伸肌(TA)中 、 、 、 、 、 、 、 、 、 和 基因的mRNA量进行了研究。对肌球蛋白重链 、 、 和 基因表达进行了研究。将小鼠分别维持在23°C或4°C环境下6小时和5天(5d)。CS小鼠未表现出肌肉退化的迹象。观察到在CS 6小时后,TA中 和 基因分别上调2倍和1.5倍,在CS 6小时和5天后,SOL肌肉中分别上调4倍和22倍;而在CS 6小时后,两种肌肉中的 均下调。 未受影响,而在CS 5天后,TA中的 上调。在CS 5天后,SOL中的 下调0.9倍。在CS 5天后,SOL中 和 基因分别上调1倍和1.5倍。在CS 6小时和5天后,SOL中的 分别下调0.96倍和0.88倍,在CS 5天后,TA中的 也下调0.88倍。 和 未受影响。CS后TA和SOL肌肉、骨骼及大脑中基因表达水平的变化受白细胞介素6(IL6)和Oxt调控。CS增强了SOL的慢肌表型,这与该肌肉的代谢需求一致,同时也增强了TA的慢肌表型。Oxt和IL6协调慢肌的表型依赖性紧张性效应,且Oxt调节大脑与SOL肌肉之间的器官间相互作用。CS后,肌肉嗜性由NGF信号维持。