We have directly imaged the dynamic behavior of a variety of morphologicall
y different peroxisomal structures in HepG2 and COS-7 cells transfected wit
h a construct encoding GFP bearing the C-terminal peroxisomal targeting sig
nal 1. Real time imaging revealed that moving peroxisomes interacted with e
ach other and were engaged in transient contacts, and at higher magnificati
on, tubular peroxisomes appeared to form a peroxisomal reticulum, Local rem
odeling of these structures could be observed involving the formation and d
etachment of tubular processes that interconnected adjacent organelles. Inh
ibition of cytoplasmic dynein based motility by overexpression of the dynac
tin subunit, dynamitin (p50), inhibited the movement of peroxisomes in vivo
and interfered with the reestablishment of a uniform distribution of perox
isomes after recovery from nocodazole treatment. Isolated peroxisomes moved
in vitro along microtubules in the presence of a microtubule motor fractio
n. Our data reveal that peroxisomal behavior in vivo is significantly more
dynamic and interactive than previously thought and suggest a role for the
dynein/dynactin motor in peroxisome motility.