Regulation of protein function through tyrosine phosphorylation is cri
tical to many developmental processes involving cell-cell communicatio
n. A number of protein tyrosine phosphatases (PTPs) have been identifi
ed in the early postnatal and mature central nervous system (CNS), but
the PTPs expressed during its development have not been well characte
rized. Using a polymerase chain reaction with degenerate primers, we a
nalyzed PTPs expressed in fetal (E18) rat brain and Muller glia cultur
es from embryonic chick retina, two systems in which cell-to-cell cont
acts are numerous. Fetal rat brain expressed four known receptor-like
PTPs (PTP delta, LAR, LAR-PTP2, LRP (PTP alpha)) and the non-receptor
phosphatase PTP1B. Muller glia exhibited a distinct but overlapping pa
ttern of expression: four known receptor PTPs (PTP alpha, PTP gamma, P
TP delta, PTP zeta) and PTP1B. In addition, two novel PTPs, termed MG-
PTP1 and 2 (Muller glia PTP 1 and 2) were identified in Muller glia cD
NA. MG-PTP1 was related to, but distinct from PTP delta, while MG-PTP2
was related to, but distinct from the cytosolic T-cell phosphatase. T
hese results demonstrate that a distinct but overlapping set of PTPs i
s expressed in the developing brain and retinal Muller glia, including
two novel PTPs that may participate in neural cell communication.