Abstract
Regulation of the rapid compensatory growth seen in the remaining adrenal gland of rats following unilateral adrenalectomy is poorly understood. The role of adrenocorticotropic hormone (ACTH) is obscure1,2 as immunoneutralization of circulating ACTH does not affect the observed compensatory growth or hyperplasia1. This finding, together with the fact that mechanical manipulation of one adrenal without extirpation is followed by growth only in the contralateral gland3, has led to the concept of neural regulation of compensatory adrenal growth via a loop from one adrenal through the hypothalamus and back to the contralateral gland which is independent of ACTH secretion3. We recently showed that peptides from the N terminal of ACTH precursor proopiocortin (POC), not containing the γ-melanocyte-stimulating hormone (γ-MSH) sequence, can stimulate adrenal mitogenesis and proposed that normal long-term adrenal growth and proliferation involves post-secretional proteolytic cleavage of pro-γ-MSH [or N-POC(1–74)] to generate the mitogenic factor N-POC(1–48/49) and a C-terminal fragment N-POC(50–74), or rat γ3-MSH4. We have now investigated this hypothesis further in rats by selectively quenching different regions of circulating POC peptides with specific antisera and observing the effect on the increases in weight, RNA and DNA normally seen in the remaining gland following unilateral adrenalectomy1–3. Our results, reported here, suggest that neurally mediated proteolytic cleavage of the circulating inactive mitogenic precursor pro-γ-MSH at the adrenal gland is the major mechanism of control of compensatory growth.
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References
Long, J. A. & Ramachandran, J. J. Endocr. 102, 371–378 (1978).
Dallman, M. F., Engeland, W. C., Holzwarth, M. A. & Scholtz, P. M. Endocrinology 107, 1397–1404 (1980).
Dallman, M. F., Engeland, W. C. & Shinsako, J. Am. J. Physiol. 231, 408–414 (1976).
Estivariz, F., Iturriza, F., McLean, C., Hope, J. & Lowry, P. J. Nature 297, 419–422 (1982).
Al-Dujaili, E. A. S., Williams, B. C., Edwards, C. R. W., Salacinski, P. & Lowry, P. J. Biochem. J. 204, 301–305 (1982).
Al-Dujaili, E. A. S., Hope, J., Estivariz, F., Lowry, P. J. & Edwards, C. R. W. Nature 291, 156–159 (1981).
Pedersen, R. C., Brownie, A. C. & Ling, N. Science 208, 1044–1045 (1980).
Eipper, B. A. & Mains, R. E. J. submolec. Struct. 8, 249–262 (1978).
Hope, J. & Lowry, P. J. Frontiers Horm. Res. 8, 44–61 (1981).
Hope, J., Ratter, S. J., Estivariz, F., McLoughlin, L. & Lowry, P. J. Clin Endocr. 15, 221–227 (1981).
Estivariz, F., Gillies, G. & Lowry, P. J. Pharmac. Ther. 13, 61–67 (1981).
Eipper, B. A. & Mains, R. E. Endocr. Rev. 1, 1–27 (1980).
Jackson, S. & Lowry, P. J. J. Endocr. 86, 205–219 (1980).
Mains, R. E. & Eipper, B. A. J. biol. Chem. 251, 7885–7894 (1979).
Crine, P., Seidah, N. G., Routhier, R., Gossard, F. & Chretien, M. Eur. J. Biochem. 110, 387–396 (1980).
Mains, R. E. & Eipper, B. A. Ann. N. Y. Acad. Sci. 343, 94–110 (1980).
Penny, R. J. & Thody, A. J. Neuroendocrinology 25, 193–203 (1978).
Tilders, F. J. H. & Smelik, P. G. Neuroendocrinology 25, 275–290 (1978).
Engeland, W. C. & Dallman, M. F. Endocrinology 99, 1659–1662 (1976).
Greer, M. A., Allen, C. F., Panton, P. & Allen, P. G. Endocrinology 96, 718–724 (1975).
Scott, A. P. & Lowry, P. J. Biochem. J. 139, 593–602 (1974).
McLean, C., Hope, J., Salacinski, P., Estivariz, F. & Lowry, P. J. Biosci. Rep. 1, 843–849 (1981).
Drouin, J. & Goodman, H. M. Nature 288, 610–618 (1980).
Estivariz, F., Hope, J., McLean, C & Lowry, P. J. Biochem. J. 191, 125–132 (1980).
Schneider, W. C. Biol. Chem. 161, 293–303 (1945).
Mejbaum, W. Physiol. Chem. 258, 117–120 (1939).
Giles, K. W. & Myers, A. Nature 206, 93 (1965).
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Lowry, P., Silas, L., McLean, C. et al. Pro-γ-melanocyte-stimulating hormone cleavage in adrenal gland undergoing compensatory growth. Nature 306, 70–73 (1983). https://doi.org/10.1038/306070a0
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DOI: https://doi.org/10.1038/306070a0
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