Corrigendum: Lactate Metabolism and Satellite Cell Fate (Front. Physiol., (2020), 11, (610983), 10.3389/fphys.2020.610983)

Minas Nalbandian*, Zsolt Radak, Masaki Takeda

*Corresponding author for this work

Research output: Contribution to journalComment/debatepeer-review

Abstract

In the original article, there was an error. We state that LDHA isoform converts lactate to pyruvate and that LDHB converts pyruvate into lactate. The current evidence suggests that LDHA and LDHB both can favor the lactate to pyruvate conversion in any direction. A correction has been made to “LACTATE AS A KEY METABOLITE IN THE CONTROL OF CELL SIGNALING,” Paragraph 1: “Lactate is a metabolite produced from pyruvate by lactate dehydrogenase (LDH), with the LDH isoform A (LDHA) facilitating the pyruvate-to-lactate conversion in cells with high glycolytic rates, and the LDH isoform B (LDHB) facilitating the lactateto- pyruvate conversion in highly oxidative cells. When the cytoplasmic lactate concentration is elevated, lactate can be co-transported with one H+ ion outside the cell by facilitated diffusion via monocarboxylate transporters (MCTs; Halestrap and Wilson, 2012; Kitaoka et al., 2012; Halestrap, 2013; Perez-Escuredo et al., 2016). MCT1 and MCT4 are MCT isoforms expressed in skeletal muscle (Bonen, 2001). MCT1, which has a relatively low Km (3.5–10mM; Halestrap, 2012), is the predominant isoform in oxidative skeletal muscle fibers and considered responsible for lactate uptake (Mccullagh et al., 1997; Juel and Halestrap, 1999; Pilegaard et al., 1999; Halestrap, 2012; Chatel et al., 2017). On the other hand, MCT4, which has a much higher Km (22–28mM; Halestrap, 2012), is the isoform predominantly expressed in glycolytic skeletal muscle fibers and considered responsible for lactate release (Dimmer et al., 2000; Fox et al., 2000; Bisetto et al., 2019). Extracellular lactate can travel through the blood stream to many cells, serving as an important energy source for several tissues and organs such as the brain (van Hall et al., 2009; Mosienko et al., 2015), liver, and skeletal muscle (Hui et al., 2017; Brooks, 2020). Given lactate’s ability to travel between cells, tissues, and organs, recently it was proposed to be a signaling molecule (Nalbandian and Takeda, 2016; Brooks, 2020).” The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Original languageEnglish
Article number817264
JournalFrontiers in Physiology
Volume12
DOIs
Publication statusPublished - 2022 Feb 15
Externally publishedYes

Keywords

  • lactate
  • metabolism
  • muscle regeneration
  • muscle stem cell
  • skeletal muscle

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)

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