The GARP complex prevents sterol accumulation at the trans-Golgi network during dendrite remodeling

O'Brien et al. show that both the GARP and EARP complexes regulate dendrite development. Sterol accumulates specifically in GARP(KO) neurons at the trans-Golgi. Targeting Osbp rescues sterol accumulation, Golgi morphology, and adult dendrite growth, implicating sterol transport in dendrite development. Membrane trafficking is essential for sculpting neuronal morphology. The GARP and EARP complexes are conserved tethers that regulate vesicle trafficking in the secretory and endolysosomal pathways, respectively. Both complexes contain the Vps51, Vps52, and Vps53 proteins, and a complex-specific protein: Vps54 in GARP and Vps50 in EARP. In Drosophila, we find that both complexes are required for dendrite morphogenesis during developmental remodeling of multidendritic class IV da (c4da) neurons. Having found that sterol accumulates at the trans-Golgi network (TGN) in Vps54(KO/KO) neurons, we investigated genes that regulate sterols and related lipids at the TGN. Overexpression of oxysterol binding protein (Osbp) or knockdown of the PI4K four wheel drive (fwd) exacerbates the Vps54(KO/KO) phenotype, whereas eliminating one allele of Osbp rescues it, suggesting that excess sterol accumulation at the TGN is, in part, responsible for inhibiting dendrite regrowth. These findings distinguish the GARP and EARP complexes in neurodevelopment and implicate vesicle trafficking and lipid transfer pathways in dendrite morphogenesis.

Automated summary

The study by O'Brien et al. demonstrates that both the GARP and EARP complexes play a role in dendrite development and highlights the importance of sterol transport in this process.