ABHD12 is a lysophosphatidylserine lipase responsible for regulation of immune and neurological processes, and shown to act on the endocannabinoid arachidonoylglycerol as a monoacylglycerol lipase. Endocannabinoids are associated with a range of physiological processes. ABHD12 acts on 2-AG, and accounts for approximately 9% of 2-AG hydrolysis in the brain. Along with MAGL and ABHD6, ABHD12 is responsible for 99% of 2-AG hydrolysis in the brain, and has also been shown to act on the 1-AG isomer. Based on the extracellular face of the ABHD12 active site and its ability to act on multiple isomeric substrates, ABHD12 has been suggested to act as a guard to the extracellular 2-AG-CB2R signalling pathway in microglia, and peripheral 2-AG signalling, however this has not been confirmed. ABHD12 transcription is abundant in the brain, specifically microglia, but has also been identified in peripheral cell types like macrophages and osteoclasts. Murine models have shown ABHD12 plays a role in regulation of lysophosphatidylserine pathways in the brain.
Mutations in ABHD12 are associated with the rare neurodegenerative disorder PHARC, as well as retinitis pigmentosa. Null mutations have been shown to lead to development of PHARC, while other mutations can result in a range of phenotypes, from non-syndromic retinal degeneration to PHARC. Currently, PHARC has been identified in at least 27 individuals, with 15 identified loss of function variants of ABHD12, comprising four nonsense, four missense, four frameshift and one splicingmutation. ABHD12 missense mutations have been identified in individuals with retinitis pigmentosa, and a growing range of phenotypes associated with ABHD12 mutations from PHARC to non-syndromic retinal degeneration are being discovered. In vitro, enzymatic activity of ABHD12 can be eliminated by site mutation the residues Serine-246, Aspartate-333, or Histidine-372, which form a catalytic triad in the hydrolase domain.
The α/β hydrolase domain including lipase motif and catalytic triad is conserved between murine and human ABHD12. Based on the observation of ABHD12 mutation in PHARC affected subjects, PHARC cell lines have been considered as human models of ABHD12 knockout. Mouse knockout models demonstrate cerebellarmicrogliosis, motor and auditory impairment, alongside elevated neuroinflammation with progression associated with age. These characteristics are considered PHARC-like phenotypes as a murine model for human PHARC, however the mouse knockout model doesn’t demonstrate ocular or myelination defects, or early onset typical of PHARC. The ABHD -/- murine model shows increased long-chain lysoPS accumulation in the brain suggesting lysoPS signalling contributes to PHARC-like pathology. A zebrafishknockdown model has been developed which demonstrates defects including microphthalmia, lack of lens clarity, and disrupted retina architecture.
Interactions
Elevated lysoPS accumulation in ABHD12 knockout mice suggests lysoPS as an in vivosubstrate of ABHD12. Elevated lysoPS production in ABHD12 null cells from PHARC subjects can be reversed using an inhibitor of ABHD16A. In vitro studies demonstrate enzymatic hydrolysis of monoacylglycerol long lipid chains by ABHD12. ABHD12 can use both 1-AG and 2-AG as substrates at comparable enzymatic rates. ABHD12 has been shown to be associated with AMPA type glutamate receptors in the brains of rats.