SHIP's C-terminus is essential for its hydrolysis of PIP3 and inhibition of mast cell degranulation

The SH2-containing inositol-5'-phosphatase, SHIP, restrains bone marrow-der ived mast cell(BMMC) degranulation, at least in part, by hydrolyzing phosph atidylinositol (PI)-3-kinase generated PI-3,4,5-P-3 (PIP3) to PI-3,4-P-2. T o determine which domains within SHIP influence its ability to hydrolyze PI PE, bone marrow from SHIP-/- mice was retrovirally infected with various SH IP constructs. Introduction of wild-type SHIP into SHIP-/- BMMCs reverted t he Steel factor (SF)-induced increases in PIP3, calcium entry, and degranul ation to those observed in SHIP+/+ BMMCs. A 5'-phosphatase dead SHIP, howev er, could not revert the SHIP-/- response, whereas a SHIP mutant in which t he 2 NPXY motifs were converted to NPXFs (2NPXF) could partially revert the SHIP-/- response. SF stimulation of BMMCs expressing the 2NPXF, which coul d not bind Shc, led to the same level of mitogen-activated protein kinase ( MAPK) phosphorylation as that seen in BMMCs expressing the other constructs . Surprisingly, C-terminally truncated forms of SHIP, lacking different amo unts of the proline rich C-terminus, could not revert the SHIP-/- response at all. These results suggest that the C-terminus plays a critical role in enabling SHIP to hydrolyze PIP3 and inhibit BMMC degranulation. (Blood. 200 1;97:1343-1351) (C) 2001 by The American Society of Hematology.