Receptor protein tyrosine phosphatases (RPTPs) are implicated as regulators
of axon growth and guidance. Genetic deletions in the fly have shown that
type III RPTPs are important in axon pathfinding, but nothing is known abou
t their function on a cellular level. Previous experiments in our lab have
identified a type III RPTP, CRYP-2/cPTPRO, specifically expressed during th
e period of axon outgrowth in the chick brain; cPTPRO is expressed in the a
xons and growth cones of retinal and tectal projection neurons. We construc
ted a fusion protein containing the extracellular domain of cPTPRO fused to
the Fc portion of mouse immunoglobulin G-1, and used it to perform in vitr
o functional assays. We found that the extracellular domain of cPTPRO is an
antiadhesive, neurite inhibitory molecule for retinal neurons. In addition
, cPTPRO had potent growth cone collapsing activity in vitro, and locally a
pplied gradients of cPTPRO repelled growing retinal axons. This chemorepuls
ive effect could be regulated by the level of cGMP in the growth cone. Immu
nohistochemical examination of the retina indicated that cPTPRO has at leas
t one heterophilic binding partner in the retina. Taken together, our resul
ts indicate that cPTPRO may act as a guidance cue for retinal ganglion cell
s during vertebrate development.