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Division of Endocrinology and Metabolism, Department of Medicine, Montefiore Hospital, and Medical Center, and the Albert Einstein College of Medicine 111 East 210th Street, Bronx, New York 10467
Abstract
A method combining enzymatic cellular dispersal, direct cell counting, differential cell counts at the electron microscope level and DNA determinations was devised and employed for determination of the cell numbers of each anterior pituitary cell type in euthyroid (E) and hypothyroid (Tx) rats. Pituitaries from Tx rats had increased cell number as demonstrated by a mean 33.7% increase in DNA content (µg DNA/pituitary). Total cells increased from (3.14 ± 0.36) x 106 in E rats to (3.98 ± 0.27) x 106 in Tx rats, P < 0.005. The cellular DNA content (pg/cell) in E rats, 10.84 ± 0.63 (SD), was indistinguishable statistically from that of Tx rats, 11.24 ± 0.52.
Cell distribution among various pituitary cell types was virtually identical when determined in pellets from dispersed cells and randomized solid tissue from the same groups of E and Tx rats. These data indicated that there was no selective cell loss during the cell dispersion procedure. Major changes in Tx rats compared to E rats were a marked increase in percentage of thyrotrophs, from 10.7 ± 1.75 (E) to 34.4 ± 1.0 (Tx), and a decrease in percentage of somatotrophs, from 55.3 ± 1.82 to 15.3 ± 0.97. The calculated cell distribution showed that the number of thyrotrophs increased from 0.34 ± 0.02 to 1.37 ± 0.05 millions per pituitary and somatotrophs decreased from 1.74 ± 0.11 to 0.61 ± 0.02 millions in hypothyroid rats. The method described herein thus provides a quantitative estimate of changes in pituitary cell populations in different hormonal states and should be useful in studies of the kinetics of pituitary cell replication and removal.
Footnotes
1 Supported by grants from the National Institutes of Health (1R01 CA 16463-03) and the American Cancer Society (BC-199).
2 Dr. Surks is the recipient of Research Career Development Award of the NIH (1K04 AM 19502-04). Reprint requests to: Martin I. Surks, M.D.
Received November 29, 1976.
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