Distinct lactate metabolism between hepatocytes and myotubes revealed by live cell imaging with genetically encoded indicators

• Published in: Biochemical and biophysical research communications Vol. 694; p. 149416
• Main Authors: Horikoshi, Mina, Harada, Kazuki, Tsuno, Saki, Kitaguchi, Tetsuya, Hirai, Masami Yokota, Matsumoto, Mitsuharu, Terada, Shin, Tsuboi, Takashi
• Format: Journal Article
• Language: English
• Published: United States 29.01.2024
• Subjects: Adenosine Triphosphate - metabolism; Glucose - metabolism; Hepatocytes - metabolism; Lactic Acid; Muscle Fibers, Skeletal - metabolism; Pyruvates; Hepatocytes; Lactate metabolism; L6 cells; Cori cycle; Live cell imaging
• ISSN: 0006-291X; 1090-2104; 1090-2104
• DOI: 10.1016/j.bbrc.2023.149416

The process of glycolysis breaks down glycogen stored in muscles, producing lactate through pyruvate to generate energy. Excess lactate is then released into the bloodstream. When lactate reaches the liver, it is converted to glucose, which muscles utilize as a substrate to generate ATP. Although the biochemical study of lactate metabolism in hepatocytes and skeletal muscle cells has been extensive, the spatial and temporal dynamics of this metabolism in live cells are still unknown. We observed the dynamics of metabolism-related molecules in primary cultured hepatocytes and a skeletal muscle cell line upon lactate overload. Our observations revealed an increase in cytoplasmic pyruvate concentration in hepatocytes, which led to glucose release. Skeletal muscle cells exhibited elevated levels of lactate and pyruvate levels in both the cytoplasm and mitochondrial matrix. However, mitochondrial ATP levels remained unaffected, indicating that the increased lactate can be converted to pyruvate but is unlikely to be utilized for ATP production. The findings suggest that excess lactate in skeletal muscle cells is taken up into mitochondria with little contribution to ATP production. Meanwhile, lactate released into the bloodstream can be converted to glucose in hepatocytes for subsequent utilization in skeletal muscle cells.