Neurovascular Unit Research Group, Korea Brain Research Institute, Daegu, Republic of Korea
Ri Yu
Neurovascular Unit Research Group, Korea Brain Research Institute, Daegu, Republic of Korea
Hyo-Shin Kwon
Neurovascular Unit Research Group, Korea Brain Research Institute, Daegu, Republic of Korea
Anji Song
Neurovascular Unit Research Group, Korea Brain Research Institute, Daegu, Republic of Korea
Mi-Hee Jun
Neurovascular Unit Research Group, Korea Brain Research Institute, Daegu, Republic of Korea
Jin-Young Jeong
Neurovascular Unit Research Group, Korea Brain Research Institute, Daegu, Republic of Korea; Department of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology, Daegu, Republic of Korea
Ji Hyun Lee
Neurovascular Unit Research Group, Korea Brain Research Institute, Daegu, Republic of Korea
Axon guidance molecules are critical for neuronal pathfinding because they regulate directionality and growth pace during nervous system development. However, the molecular mechanisms coordinating proper axonal extension and turning are poorly understood. Here, metastasis suppressor 1 (Mtss1), a membrane protrusion protein, ensured axonal extension while sensitizing axons to the Semaphorin 3E (Sema3E)-Plexin-D1 repulsive cue. Sema3E-Plexin-D1 signaling enhanced Mtss1 expression in projecting striatonigral neurons. Mtss1 localized to the neurite axonal side and regulated neurite outgrowth in cultured neurons. Mtss1 also aided Plexin-D1 trafficking to the growth cone, where it signaled a repulsive cue to Sema3E. Mtss1 ablation reduced neurite extension and growth cone collapse in cultured neurons. Mtss1-knockout mice exhibited fewer striatonigral projections and irregular axonal routes, and these defects were recapitulated in Plxnd1- or Sema3e-knockout mice. These findings demonstrate that repulsive axon guidance activates an exquisite autoregulatory program coordinating both axonal extension and steering during neuronal pathfinding.