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E. Henry Keutman Laboratories, Endocrine-Metabolism Unit, Department of Medicine [M. L. N., D. A. Y.], and Department of Radiation Biology and Biophysics [D. A. Y.], University of Rochester School of Medicine and Dentistry, Rochester, New York 14642
Exposure of rat thymus cells to glucocorticoids leads to a decreased ability of nuclei to survive the lysis of whole cells by hypotonic shock. In this study, a similar glucocorticoid-induced increase in "nuclear fragility" was found in both corticoid-sensitive and -resistant lines of P1798 mouse lymphosarcoma cells. In corticoid-sensitive cells a small increase in nuclear fragility is seen after a 2-hr exposure to cortisol (10-6 M); by 3 hr it is 20 to 40% above control values. This effect appears to be a specific glucocorticoid response. Both cortisol and dexamethasone at 10-7 M produce an effect, 10-6 M testosterone is inactive, and cortexolone, which binds to glucocorticoid receptors, reduces the effect. Cycloheximide, at concentrations that inhibit protein synthesis, also blocks this effect. While the corticoid-resistant line also demonstrates an effect of similar magnitude, it requires a much longer exposure to the hormone (6 hr). Distinct differences in the "hardiness" of the two cell lines (nuclei of the corticoid-resistant line are less fragile) measurable in the absence of hormones appears to account for the differential susceptibility to steroids. On this basis a new theory of resistance is advanced where the emergence of resistance is related to structural differences in the cells.
1 This research was supported by NIH Grant AM-16177, the Monroe County Cancer and Leukemia Association, and USPHS Grant CA-05381 from the National Cancer Institute.
2 NIH Postdoctoral Fellow Grant CA-05381.
3 To whom requests for reprints should be addressed.
Received 8/31/77. Accepted 7/26/78.
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