Table 1.
Roles of signaling pathways involved in regulating mitochondrial function in mitochondrial dysfunction
Signaling pathways | Roles in mitochondrial dysfunction | References |
---|---|---|
FoxOs | Activate UPS and ALP; upregulate Mul1, influence mitochondrial dynamics (increased mitochondrial fission, accelerated mitochondrial fusion protein degradation), and induce excessive autophagy | [83, 102] |
AMPK/SIRT1/PGC-1α | Promote mitochondrial biosynthesis; involve in the regulation of energy metabolism-related genes; reduce oxidative stress | [103, 105, 106] |
IGF-1/PI3K/Akt/mTOR | Promote complex I-driven mitochondrial respiration and supercomplex assembly; regulate the balance between mitochondrial fusion and fission; inhibit oxidative stress and autophagy | [111–114] |
JAK/STAT3 | Induce mitochondrial respiration; promote mitochondrial apoptosis and autophagy; increase the expression of mitochondria-related proteins (PGC-1α, OPA1, MFN2, cytochrome C) | [14, 117–119] |
TGF-β/Smad2/3 | Disrupt redox signaling and result in the accumulation of ROS; inhibit mitochondrial biogenesis; downregulate the abundance of PGC-1α, AMPK-α2, TFAM, and mitochondrial enzymes | [121–124] |
IKK/NF-κB | Inhibit differentiation and promotes mitochondrial biogenesis; increase the expression of autophagy-related Beclin1; disrupt mitochondrial respiratory function/morphology, induce ROS production, and increase the expression of key mitochondrial genes (SDHA, ANT-1, UCP3, and MFN2) | [125, 126, 128] |