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J. Biol. Chem., Vol. 262, Issue 3, 1010-1015, Jan, 1987
G Guillemette, T Balla, AJ Baukal, A Spat and KJ Catt
Many cells (including angiotensin II target cells) respond to external
stimuli with accelerated hydrolysis of phosphatidylinositol 4,5-
bisphosphate, generating 1,2-diacylglycerol and inositol 1,4,5-
trisphosphate, a rapidly diffusible and potent Ca2+-mobilizing factor.
Following its production at the plasma membrane level, inositol 1,4,5-
trisphosphate is believed to interact with specific sites in the
endoplasmic reticulum and triggers the release of stored Ca2+. Specific
receptor sites for inositol 1,4,5-trisphosphate were recently identified in
the bovine adrenal cortex (Baukal, A. J., Guillemette, G., Rubin, R., Spat,
A., and Catt, K. J. (1985) Biochem. Biophys. Res. Commun. 133, 532-538) and
have been further characterized in the adrenal cortex and other target
tissues. The inositol 1,4,5- trisphosphate-binding sites are saturable and
present in low concentration (104 +/- 48 fmol/mg protein) and exhibit high
affinity for inositol 1,4,5-trisphosphate (Kd 1.7 +/- 0.6 nM). Their ligand
specificity is illustrated by their low affinity for inositol 1,4-
bisphosphate (Kd approximately 10(-7) M), inositol 1-phosphate and phytic
acid (Kd approximately 10(-4) M), fructose 1,6-bisphosphate and
2,3-bisphosphoglycerate (Kd approximately 10(-3) M), with no detectable
affinity for inositol 1-phosphate and myo-inositol. These binding sites are
distinct from the degradative enzyme, inositol trisphosphate phosphatase,
which has a much lower affinity for inositol trisphosphate (Km = 17
microM). Furthermore, submicromolar concentrations of inositol
1,4,5-trisphosphate evoked a rapid release of Ca2+ from nonmitochondrial
ATP-dependent storage sites in the adrenal cortex. Specific and saturable
binding sites for inositol 1,4,5-trisphosphate were also observed in the
anterior pituitary (Kd = 0.87 +/- 0.31 nM, Bmax = 14.8 +/- 9.0 fmol/mg
protein) and in the liver (Kd = 1.66 +/- 0.7 nM, Bmax = 147 +/- 24 fmol/mg
protein). These data suggest that the binding sites described in this study
are specific receptors through which inositol 1,4,5-trisphosphate mobilizes
Ca2+ in target tissues for angiotensin II and other calcium-dependent
hormones.
Intracellular receptors for inositol 1,4,5-trisphosphate in angiotensin II target tissues
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