Osteocalcin attenuates oligodendrocyte differentiation and myelination via GPR37 signaling in the mouse brain

The bone-derived hormone osteocalcin (OCN) is crucial for brain development and neural cognitive functions, yet the exact roles of OCN in central nervous system (CNS) remain elusive. Here, we find that genetic deletion of OCN facilitates oligodendrocyte (OL) differentiation and hypermyelination in the CNS. Although dispensable for the proliferation of oligodendrocyte precursor cells (OPCs), OCN is critical for the myelination of OLs, which affects myelin production and remyelination after demyelinating injury. Genome-wide RNA sequencing analyses reveal that OCN regulates a number of G protein-coupled receptors and myelination-associated transcription factors, of which Myrf might be a key downstream effector in OLs. GPR37 is identified as a previously unknown receptor for OCN, thus regulating OL differentiation and CNS myelination. Overall, these findings suggest that OCN orchestrates the transition between OPCs and myelinating OLs via GPR37 signaling, and hence, the OCN/GPR37 pathway regulates myelin homeostasis in the CNS.

Automated summary

The bone-derived hormone osteocalcin plays a crucial role in regulating oligodendrocyte differentiation and myelination in the central nervous system. Through the OCN/GPR37 pathway, it orchestrates the transition between oligodendrocyte precursor cells and myelinating oligodendrocytes, ultimately maintaining myelin homeostasis.