Frontiers in Mitochondrial Aerobic Respiration

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Mitochondria".

Deadline for manuscript submissions: closed (15 February 2022) | Viewed by 618

Special Issue Editor


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Guest Editor
Dip.to di Farmacia (DIFAR), Scuola di Scienze Mediche e Farmaceutiche, Università degli Studi di Genova, V.le Benedetto XV, 3, 16132 Genoa, Italy
Interests: bioenergetics; neurosciences; metabolism; photoreceptor
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Special Issue Information

Dear Colleagues,

Most of the cell ATP is produced by the mitochondrial oxidative phosphorylation (OxPhos). Mitochondria have long been identified as responsible for most of cell energy production. Furthermore, these organelles play key roles in intercellular communication, cell proliferation, and apoptosis. Mitochondria are also the main intracellular sources of reactive oxygen species (ROS) as a by-product of oxidative phosphorylation under physiological conditions. It appears that ,apart from the absolute number of mitochondria present in a cell, their morphology is important: mitochondria are dynamic, being present not only as individual (fissioned) organelles, but also as an extensive network resulting from their fusion. Elongated mitochondria display a higher OxPhos. In fact, the highly variable mitochondrial morphology and number likely reflect the metabolic needs of the cell. The mitochondrial respiration rates can differ up to a 100-fold between tissues, depending on an efficient control of the machinery for both mitochondrial biogenesis and mitophagy. Recent evidence points to the existence of a connection of the mitochondrial reticulum to the Endoplasmic reticulum. Mitochondria are also implicated in cancer cells metabolic reprogramming. Cancer cells can rewire their metabolism, and, in addition to the Warburg effect (aerobic glycolysis) and glutaminolysis, fatty acid oxidation is a newly recognised hallmark of metastasizing cancer cells. Moreover, in the past years an ectopic OxPhos activity, has been described in membranes other than mitochondrial. The electron transport chain, and F1Fo‐ATP synthase are active in the rod outer segment disks, myelin sheath, and plasma membranes of hepatocytes, cancer and endothelial cells, as well as exosomes and microvesicles. The complex of data allow to explore other exciting aspects of the mitochondrial functioning, taking hints at a potentially discovery that can bring science exploration towards new ideas.

Prof. Dr. Isabella Panfoli
Guest Editor

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Keywords

  • ATP
  • cancer cells
  • endoplasmic reticulum
  • F1Fo-ATP synthase
  • metabolic reprogramming
  • mitochondria
  • mitofusins
  • mitophagy
  • Oxidative Phosphorylation
  • reactive oxygen species

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