Fig. 1.
Fig. 1. SHIP-1–mediated inositol 5′-phosphatase activity associates with shc and CD16 ζ chain after receptor engagement. / (A) Cell lysates from 3 × 107 unstimulated cultured NK cells were immunoprecipitated with anti-SHIP or control mAb; lysates from 10 × 107 unstimulated or anti-CD16–stimulated NK cells were immunoprecipitated with anti-ζ or anti-shc mAbs. Immunoprecipitates were assayed for 5′-inositol phosphatase activity toward 32P-PI3,4,5P3, and the reaction products were subjected to TLC followed by autoradiography. The positions of PI3,4P2 and PI3,4,5P3 are indicated on the right. (B) The 10 × 106 cell equivalent of the immunoprecipitated samples showed in panel A were analyzed by immunoblot with the indicated antibodies. The numbers to the left of the blots indicate molecular weight. (C) The percentage of substrate conversion (± SD) obtained by densitometric analysis of 4 different experiments is shown. The catalytic activity associated with SHIP-1 immunoprecipitates has been arbitrarily fixed at 100%. The percentage of conversion has been calculated on the basis of equivalent cell number within the single experiment.

SHIP-1–mediated inositol 5′-phosphatase activity associates with shc and CD16 ζ chain after receptor engagement.

(A) Cell lysates from 3 × 107 unstimulated cultured NK cells were immunoprecipitated with anti-SHIP or control mAb; lysates from 10 × 107 unstimulated or anti-CD16–stimulated NK cells were immunoprecipitated with anti-ζ or anti-shc mAbs. Immunoprecipitates were assayed for 5′-inositol phosphatase activity toward 32P-PI3,4,5P3, and the reaction products were subjected to TLC followed by autoradiography. The positions of PI3,4P2 and PI3,4,5P3 are indicated on the right. (B) The 10 × 106 cell equivalent of the immunoprecipitated samples showed in panel A were analyzed by immunoblot with the indicated antibodies. The numbers to the left of the blots indicate molecular weight. (C) The percentage of substrate conversion (± SD) obtained by densitometric analysis of 4 different experiments is shown. The catalytic activity associated with SHIP-1 immunoprecipitates has been arbitrarily fixed at 100%. The percentage of conversion has been calculated on the basis of equivalent cell number within the single experiment.

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