Related Experiment Video
Updated: Dec 25, 2025

Visualizing Mitophagy with Fluorescent Dyes for Mitochondria and Lysosome
Published on: November 30, 2022
The AMPK-MFN2 axis regulates MAM dynamics and autophagy induced by energy stresses
Yongquan Hu1,2, Hao Chen1,3, Luying Zhang1,2
1Guangzhou Municipal and Guangdong Provincial Key Laboratory of Protein Modification and Degradation, Affiliated Cancer Hospital & Institute of Guangzhou Medical University, School of Basic Medical Sciences, Guangzhou Medical University, 511436, Guangzhou, China.
Abstract:
Energy deprivation activates the cellular energy sensor AMP-activated protein kinase (AMPK), which in turn induces macroautophagy/autophagy. The mitochondrial-associated ER membrane (MAM) plays a key role in mitochondrial division and autophagy, and the mitochondrial fusion protein MFN2 (mitofusin 2) tethers the MAM, but the mechanism by which AMPK and MFN2 regulate autophagy in response to energy stress remains unclear. Here, we found that energy stress not only triggers mitochondrial fission and autophagy, but more importantly increases the number of MAMs, a process that requires AMPK. Interestingly, under energy stress, considerable amounts of AMPK translocate from cytosol to the MAM and the mitochondrion as mitochondrial fission occurs. Unexpectedly, AMPK interacts directly with MFN2. The autophagic ability of mouse embryonic fibroblasts (MEFs) lacking MFN2 (mfn2) is significantly attenuated in response to energy stress as compared to wild-type MEFs (WT MEFs), while re-expression of MFN2 in mfn2 cells rescues the autophagy defects of these cells. The abundance of MAMs is also greatly reduced in MFN2-deficient cells. Functional experiments show that the oxygen consumption rate and the glycolytic function of cells lacking MFN2 but not MFN1 are obviously attenuated, and MFN2 is important for cell survival under energy stress. In conclusion, our study establishes the molecular link between the energy sensor AMPK and the MAM tether MFN2, and reveals the important role of AMPK and MFN2 in energy stress-induced autophagy and MAM dynamics.Abbreviations: ACTB, actin beta; AMPK, AMP-activated protein kinase; BECN1, beclin 1; CANX, calnexin; ER, endoplasmic reticulum; HRP, horseradish peroxidase; EM, electron microscopy; FL, full-length; KD, kinase dead, KO, knockout; MAb, monoclonal antibody; MAMs, mitochondria-associated membranes; MAP1LC3/LC3B, microtubule associated protein 1 light chain 3; MFN2, mitofusin 2; OPA1, OPA1 mitochondrial dynamin like GTPase; PAb, polyclonal antibody; PtdIns3K, class III phosphatidylinositol 3-kinase; PtdIns3P, phosphatidylinositol 3-phosphate; SD, standard deviation; TEM, transmission electron microscopy; TOMM20, translocase of outer mitochondrial membrane 20; ULK1, unc-51 like autophagy activating kinase 1; MEF, mouse embryonic fibroblast; WT, wildtype.
Insights
Energy deprivation activates AMP-activated protein kinase (AMPK), which enhances autophagy. This study reveals AMPK directly interacts with mitofusin 2 (MFN2), crucial for mitochondrial-associated membranes (MAMs) and cell survival during energy stress.
Area of Science:
- Cellular Biology
- Molecular Biology
- Metabolism
Background:
- Energy deprivation activates AMP-activated protein kinase (AMPK), a key cellular energy sensor.
- AMPK activation induces macroautophagy/autophagy, a cellular degradation process.
- Mitochondrial-associated ER membranes (MAMs) are critical for mitochondrial dynamics and autophagy, with mitofusin 2 (MFN2) tethering MAMs.
Purpose of the Study:
- To elucidate the mechanism by which AMPK and MFN2 regulate autophagy in response to energy stress.
- To investigate the role of AMPK and MFN2 in MAM dynamics and cellular adaptation to energy deprivation.
Main Methods:
- Utilized mouse embryonic fibroblasts (MEFs) with and without MFN2 (wild-type vs. mfn2 knockout).
- Assessed autophagy levels, MAM abundance, and AMPK translocation under energy stress conditions.
- Performed co-immunoprecipitation to detect AMPK-MFN2 interaction and measured cellular metabolic functions (oxygen consumption, glycolysis).
Main Results:
- Energy stress increases MAMs, requiring AMPK, and induces AMPK translocation to MAMs and mitochondria.
- AMPK directly interacts with MFN2.
- MFN2-deficient MEFs exhibit significantly attenuated autophagy and reduced MAMs under energy stress, impairing cell survival; MFN2 is essential for metabolic function and survival.
Conclusions:
- This study establishes a direct molecular link between the energy sensor AMPK and the MAM tether MFN2.
- AMPK and MFN2 play crucial roles in regulating autophagy and MAM dynamics during energy stress.
- MFN2 is vital for cellular adaptation and survival under conditions of energy deprivation.
More Related Videos
Related Concept Videos
PI3K/mTOR/AKT Signaling Pathway
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
MAPK Signaling Cascades
Autophagy
An autophagic pathway consists of a series of signaling events activated in response to diverse stress and physiological conditions such as food deprivation,...
Mitochondrial Membranes
Translocation of Proteins into the Mitochondria
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...

