Mitochondrial NAD+-mediated mitophagy alleviates type I interferon response to the cytosolic mitochondrial DNA

Tian Lan1, Dantong Shang1, Lan Lin1

  • 1Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, China.

Autophagy
|November 13, 2025
PubMed

Insights

Mitochondrial NAD+ depletion impairs mitophagy and promotes inflammation by releasing mtDNA, highlighting NAD+ as a therapeutic target for sterile inflammation.

Area of Science:

  • Cellular Biology
  • Immunology
  • Metabolism

Background:

  • Mitochondrial nicotinamide adenine dinucleotide (NAD+) is crucial for energy metabolism.
  • Its roles in mitophagy and innate immunity are not well understood.
  • Dysfunctional mitophagy and inflammation are linked to various diseases.

Purpose of the Study:

  • To investigate the role of mitochondrial NAD+ in mitophagy and innate immunity.
  • To elucidate the mechanisms by which mitochondrial NAD+ affects these processes.
  • To identify potential therapeutic targets for sterile inflammation.

Main Methods:

  • Genetic manipulation of cell lines, including knockout (KO) models.
  • Assessment of mitophagy using techniques like MAP1LC3B/LC3B recruitment.
  • Analysis of mitochondrial DNA (mtDNA) release and type I interferon response.
  • Measurement of NAD+ levels using sensors like SoNar.

Main Results:

  • Mitochondrial NAD+ depletion, caused by SLC25A51 deficiency, impairs BNIP3-mediated mitophagy.
  • Loss of mitochondrial NAD+ inhibits SIRT3-mediated FOXO3 deacetylation, downregulating BNIP3.
  • Depleted mitochondrial NAD+ promotes mtDNA release and exacerbates type I interferon response via CGAS-STING1 signaling.

Conclusions:

  • Mitochondrial NAD+ depletion disrupts mitophagy and triggers inflammation.
  • A mechanistic link exists between mitochondrial NAD+, mitophagy, and mtDNA-induced inflammation.
  • Mitochondrial NAD+ is a potential therapeutic target for sterile inflammation caused by free mtDNA.

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