Mitochondrially localized MPZL3 emerges as a signaling hub of mammalian physiology.
Tongyu C WikramanayakeCarina NicuJeremy ChéretTraci A CzyzykRalf PausPublished in: BioEssays : news and reviews in molecular, cellular and developmental biology (2021)
MPZL3 is a nuclear-encoded, mitochondrially localized, immunoglobulin-like V-type protein that functions as a key regulator of epithelial cell differentiation, lipid metabolism, ROS production, glycemic control, and energy expenditure. Recently, MPZL3 has surfaced as an important modulator of sebaceous gland function and of hair follicle cycling, an organ transformation process that is also governed by peripheral clock gene activity and PPARγ. Given the phenotype similarities and differences between Mpzl3 and Pparγ knockout mice, we propose that MPZL3 serves as a signaling hub that is regulated by core clock gene products and/or PPARγ to translate signals from these nuclear transcription factors to the mitochondria to modulate circadian and metabolic regulation. Conservation between murine and human MPZL3 suggests that human MPZL3 may have similarly complex functions in health and disease. We summarize current knowledge and discuss future directions to elucidate the full spectrum of MPZL3 functions in mammalian physiology.
Keyphrases
- glycemic control
- endothelial cells
- transcription factor
- healthcare
- insulin resistance
- type diabetes
- fatty acid
- genome wide
- public health
- cell death
- mental health
- dna damage
- reactive oxygen species
- metabolic syndrome
- network analysis
- gene expression
- pluripotent stem cells
- dna methylation
- amino acid
- weight loss
- dna binding
- protein protein