Protein arginine methyltransferase 8 modulates mitochondrial bioenergetics and neuroinflammation after hypoxic stress

J Neurochem. 2021 Nov;159(4):742-761. doi: 10.1111/jnc.15462. Epub 2021 Aug 25.

Abstract

Protein arginine methyltransferases (PRMTs) are a family of enzymes involved in gene regulation and protein/histone modifications. PRMT8 is primarily expressed in the central nervous system, specifically within the cellular membrane and synaptic vesicles. Recently, PRMT8 has been described to play key roles in neuronal signaling such as a regulator of dendritic arborization, synaptic function and maturation, and neuronal differentiation and plasticity. Here, we examined the role of PRMT8 in response to hypoxia-induced stress in brain metabolism. Our results from liquid chromatography mass spectrometry, mitochondrial oxygen consumption rate, and protein analyses indicate that PRMT8(-/-) knockout mice presented with altered membrane phospholipid composition, decreased mitochondrial stress capacity, and increased neuroinflammatory markers, such as tumor necrosis factor alpha and ionized calcium binding adaptor molecule 1 (Iba1, a specific marker for microglia/macrophage activation) after hypoxic stress. Furthermore, adenovirus-based overexpression of PRMT8 reversed the changes in membrane phospholipid composition, mitochondrial stress capacity, and neuroinflammatory markers. Together, our findings establish PRMT8 as an important regulatory component of membrane phospholipid composition, short-term memory function, mitochondrial function, and neuroinflammation in response to hypoxic stress.

Keywords: hypoxic stress; mitochondrial function; neuroinflammation; phospholipids; protein arginine methyltransferase.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium-Binding Proteins / metabolism
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Cytokines / analysis
  • Cytokines / metabolism
  • Energy Metabolism / genetics*
  • Hypoxia / genetics*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microfilament Proteins / metabolism
  • Mitochondria / genetics*
  • Mitochondria / metabolism*
  • Neural Stem Cells
  • Neuroinflammatory Diseases / genetics*
  • Oxygen Consumption
  • Phospholipids / metabolism
  • Protein-Arginine N-Methyltransferases / genetics*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Aif1 protein, mouse
  • Calcium-Binding Proteins
  • Cytokines
  • Microfilament Proteins
  • Phospholipids
  • Tumor Necrosis Factor-alpha
  • PRMT8 protein, mouse
  • Protein-Arginine N-Methyltransferases