According to Dr. Enríquez, "This adjustment can be likened to refitting your boiler to burn natural gas or butane." The proportion of different food fuels available to cells can be affected by diet, exercise, or a period of fasting, and cells need to be able to adapt to these changes. In some specific situations, for example during the activation of immune cells to defend the body against infection, cells change their activity even if the fuel source is unaltered, and this can be accompanied by changes in the preferential use of glucose instead of fatty acids or vice versa. In all these cases, mitochondria need to adapt their 'fuel burners', technically known as the electron transport chain (ETC). "The ETC was known to adapt, but the signals that promote this change and the molecules responsible for it were not known."
The
Cell Metabolism article describes the signals and molecules that regulate this adaptation. Combustion of nutrient fuels in mitochondria requires oxygen, and the process produces, in addition to energy, water (H2O) and carbon dioxide (CO2). But when the ETC switches from burning sugars to fatty acids, it is at first not adjusted to burning the new fuel, and additional oxygen derivatives are produced called reactive oxygen species (ROS), among them hydrogen peroxide (H2O2). Production of H2O2 activates a molecular sensor called Fgr (Fgr-tyrosine kinase), which raises the alarm that the ETC is not adjusted to burn the fatty acids arriving in the mitochondria. It does this by modifying one of the components of the ETC, adding a phosphate group that makes it more active. This triggers a change in the organization of the ETC so that burns fatty acids more efficiently. The modification, called phosphorylation, is reversible, and the CNIC team believes that another, as-yet-unidentified molecule must trigger the reverse modification (dephosphorylation) when the mitochondrion's fuel burners need to switch back to burning glucose. The study published in
Cell Metabolism demonstrates the importance of this mechanism in the adaptation of cells to fasting and a limited oxygen supply (ischemia), and in the activation of cells of the immune system.
Source: Eurekalert
