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.

Autophagy
|April 7, 2020
PubMed

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.

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