College of Veterinary Medicine, Yangzhou University/Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonosis, Yangzhou, 225009, Jiangsu, People's Republic of China.
Biocytogen JiangSu Co., Ltd., Nantong, 226000, Jiangsu, People's Republic of China.
Sci Rep. 2023 Aug 12;13(1):13153. doi: 10.1038/s41598-023-40350-y.
This study aimed to investigate the effects of different levels of autophagy induced by transient serum starvation on the metabolism, lipid metabolism, and differentiation of porcine skeletal muscle satellite cells (SMSCs) to preliminary elucidate the role and function of autophagy in the regulatory network of skeletal muscle development. Different levels of autophagy were induced by controlling the serum concentration in the culture system for 24 h. Apoptosis, membrane potential, reactive oxygen species (ROS), ATP, and myogenic and lipogenic differentiation markers were monitored to determine if autophagy affected the metabolism and differentiation of SMSCs. Autophagy was induced in SMSCs via serum starvation (5%, 15%), as evidenced by decreased p62 and mTOR phosphorylation levels and increased LC3B lipidation and AMPK phosphorylation levels. Transmission electron microscopy revealed the presence of autophagosomes, and the rates of morphologically abnormal nuclei and mitochondria gradually increased with the decrease in serum concentration, the number of autophagic lysosomes also increased, indicating that 5% serum starvation induced severe autophagy, while 15% serum starvation induced mild autophagy. Compared with the control group and 15% serum-starved SMSCs, SMSCs undergoing 5% serum starvation had the highest intracellular ATP and ROS levels, the highest percentage of apoptotic cells, and the lowest membrane potential. The 15% serum-starved SMSCs had the highest membrane potential, but the percentage of apoptotic cells did not change significantly compared with the control group. The levels of the myogenic markers MyoD1 and MHC were significantly higher in 15% serum-starved SMSCs than in serum-sufficient SMSCs and the lowest in the 5% serum-starved SMSCs. The lipid contents (measured by Oil Red O staining and quantification of triglycerides) and lipogenic markers Peroxisome Proliferators-activated Receptors γ and Lipoprotein Lipase were also significantly higher in SMSCs undergoing 15% serum starvation than in the control group, and the lowest in the 5% serum-starved SMSCs. Different levels of starvation stress induce different levels of autophagy. Mild autophagy induced by moderate serum starvation promotes the metabolism and differentiation of SMSCs, while severe autophagy renders SMSCs more apoptotic, abnormal metabolism and suppresses SMSC differentiation into adipocytes or myocytes, and reduces lipid metabolisms. Our study suggests that autophagy plays a role in skeletal muscle development and may help design strategies for improving meat production traits in domestic pigs.
本研究旨在探讨短暂血清饥饿诱导的不同水平自噬对猪骨骼肌卫星细胞(SMSCs)代谢、脂质代谢和分化的影响,初步阐明自噬在骨骼肌发育调控网络中的作用和功能。通过控制培养系统中的血清浓度 24 小时来诱导不同水平的自噬。监测细胞凋亡、膜电位、活性氧(ROS)、ATP 以及成肌和成脂分化标志物,以确定自噬是否影响 SMSC 的代谢和分化。通过血清饥饿(5%、15%)诱导 SMSC 中的自噬,表现为 p62 和 mTOR 磷酸化水平降低,LC3B 脂质化和 AMPK 磷酸化水平升高。透射电子显微镜显示自噬体的存在,并且随着血清浓度的降低,形态异常核和线粒体的比例逐渐增加,自噬溶酶体的数量也增加,表明 5%血清饥饿诱导严重的自噬,而 15%血清饥饿诱导轻度自噬。与对照组和 15%血清饥饿的 SMSC 相比,5%血清饥饿的 SMSC 具有最高的细胞内 ATP 和 ROS 水平、最高的凋亡细胞比例和最低的膜电位。15%血清饥饿的 SMSC 具有最高的膜电位,但与对照组相比,凋亡细胞的比例没有明显变化。15%血清饥饿的 SMSC 中的成肌标志物 MyoD1 和 MHC 水平明显高于血清充足的 SMSC,而 5%血清饥饿的 SMSC 中的水平最低。脂质含量(通过油红 O 染色和甘油三酯定量测量)和脂生成标志物过氧化物酶体增殖物激活受体 γ 和脂蛋白脂肪酶在 15%血清饥饿的 SMSC 中也明显高于对照组,而在 5%血清饥饿的 SMSC 中最低。不同水平的饥饿应激诱导不同水平的自噬。适度血清饥饿诱导的轻度自噬促进 SMSC 的代谢和分化,而严重的自噬使 SMSC 更易凋亡、代谢异常,并抑制 SMSC 分化为成肌细胞或成脂细胞,降低脂质代谢。我们的研究表明自噬在骨骼肌发育中起作用,并可能有助于设计提高家猪肉质生产特性的策略。