Neurons are polarized cells, the activity of which relies on the morphologi
cal and functional differences between their axonal and somatodendritic dom
ains. One mechanism for establishing and maintaining neuronal polarity is v
ia the selective targeting of proteins to these domains. The endocytic path
way plays a major role in the generation and maintenance of cellular polari
ty by selectively sorting and recycling endocytosed plasma membrane protein
s. In this study we first show that endogenous syntaxin 13 localizes to tub
ulovesicular organelles that are present in the somatodendritic and axonal
domains of neurons. These organelles contain and actively recycle transferr
in receptor and are sensitive to brefeldin A, suggesting that they are anal
ogous to the tubulovesicular recycling endosomes in nonneuronal cells. We n
ext use a syntaxin 13-GFP fusion protein transiently expressed in hippocamp
al neurons, together with time-lapse microscopy, to study the dynamics of t
he endosomal system in neurons. The analysis revealed the presence of two d
istinct classes of syntaxin 13-labeled endosomes: round-oval stationary org
anelles and highly mobile tubulovesicular structures. The dynamic populatio
n of tubulovesicular endosomes travels in both directions along microtubule
s in dendrites and axons. The mobile organelles appear to fuse with and bud
from the stationary endosomes, possibly as a means of delivering and picki
ng up their cargo.