During the past few years, molecular cloning has established the exist
ence of a structurally diverse family of intracellular and transmembra
ne protein tyrosine phosphatases (PTPases). The importance of PTPases
in signaling is best understood in three model systems: the mammalian
transmembrane CD45 PTPase, the Drosophila Src homology (SH)2 domain co
ntaining corkscrew PTPase and its vertebrate homolog SH-PTP2, and the
mouse SH2-domain-containing hematopoietic cell PTPase. Whereas CD45, c
orkscrew and SH-PTP2 positively regulate tyrosine phosphorylation, the
hematopoietic cell PTPase negatively regulates or terminates signalin
g. Recent data indicate that several transmembrane PTPases mediate cel
l adhesion, suggesting that they effect adhesion-specific signaling ev
ents.