Stumpf W E, Sar M, Zuber T J, Soini E, Tuohimaa P
Departments of Anatomy and Pharmacology (W.E.S.; M.S.; T.J.Z.), University of North Carolina, Chapel Hill, North Carolina 27514, Research Department, Wallac Oy (E.S.), Turku, Finland, and Department of Biomedical Sciences (P.T.), University of Tampere, Tampere 52, Finland.
J Histochem Cytochem. 1981 Jan;29(1A_suppl):201-206. doi: 10.1177/29.1A_SUPPL.7288156.
A procedure for the quantitative assessment of nuclear receptors for steroid hormones-and other substances-in individual cells is presented. Thaw-mount autoradiography, a procedure developed earlier in our laboratory, is utilized. The silver grain yield (specific activity) is 16.6 disintegrations per silver grain as determined for tritium in guinea pig uterine tissues. An integrated formula is presented and applied for 3H-estradioI, 3H-diethyl-stilbestrol, and 3H-aldosterone in sampled tissues. A comparison with data derived from the literature that are based on the homogenization of whole uteri and biochemical analysis shows comparable values with the autoradiographic data if the latter are pooled. The pooled data indicate 12-14,000 molecules of 3H-estradiol per uterine nucleus, while subpopulations of target cells vary between 5,000 and 28,000 per nucleus.
