TY - JOUR
T1 - Physiological roles of mitochondrial reactive oxygen species
AU - Sena, Laura A.
AU - Chandel, Navdeep S.
N1 - Funding Information:
This work was supported by NIH grants F30ES019815 (L.A.S.), T32-HL76139 (L.A.S.), 5P01HL071643 (N.S.C.), and RO1CA123067 (N.S.C.). We apologize to those investigators whose important work we did not discuss for the sake of conciseness.
PY - 2012/10/26
Y1 - 2012/10/26
N2 - Historically, mitochondrial reactive oxygen species (mROS) were thought to exclusively cause cellular damage and lack a physiological function. Accumulation of ROS and oxidative damage have been linked to multiple pathologies, including neurodegenerative diseases, diabetes, cancer, and premature aging. Thus, mROS were originally envisioned as a necessary evil of oxidative metabolism, a product of an imperfect system. Yet few biological systems possess such flagrant imperfections, thanks to the persistent optimization of evolution, and it appears that oxidative metabolism is no different. More and more evidence suggests that mROS are critical for healthy cell function. In this Review, we discuss this evidence following some background on the generation and regulation of mROS.
AB - Historically, mitochondrial reactive oxygen species (mROS) were thought to exclusively cause cellular damage and lack a physiological function. Accumulation of ROS and oxidative damage have been linked to multiple pathologies, including neurodegenerative diseases, diabetes, cancer, and premature aging. Thus, mROS were originally envisioned as a necessary evil of oxidative metabolism, a product of an imperfect system. Yet few biological systems possess such flagrant imperfections, thanks to the persistent optimization of evolution, and it appears that oxidative metabolism is no different. More and more evidence suggests that mROS are critical for healthy cell function. In this Review, we discuss this evidence following some background on the generation and regulation of mROS.
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U2 - 10.1016/j.molcel.2012.09.025
DO - 10.1016/j.molcel.2012.09.025
M3 - Review article
C2 - 23102266
AN - SCOPUS:84868007565
SN - 1097-2765
VL - 48
SP - 158
EP - 167
JO - Molecular cell
JF - Molecular cell
IS - 2
ER -