Models to elucidate the regulation of adrenal cell death

Citation
Rv. Carsia et al., Models to elucidate the regulation of adrenal cell death, ENDOCRINE R, 24(3-4), 1998, pp. 899-908
Citations number
21
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
ENDOCRINE RESEARCH
ISSN journal
07435800 → ACNP
Volume
24
Issue
3-4
Year of publication
1998
Pages
899 - 908
Database
ISI
SICI code
0743-5800(1998)24:3-4<899:MTETRO>2.0.ZU;2-O
Abstract
Hypophysectomy-induced apoptosis in the rat adrenal gland is slow (not appa rent until 12-24 h) and in-situ, 3'-end labeling (ISEL) of DNA strand break s is restricted to a subpopulation of zona reticularis cells. In addition, it is completely blocked by ACTH. By contrast, apoptosis in the intact rat adrenal gland, cultured in the absence of trophic support, is extensive and rapid. Culture-triggered apoptosis las determined by oligonucleosome forma tion) is attenuated by ACTH and is largely restricted to the zonae fascicul ata and reticularis even at 3 h las determined by ISEL and DAPI cytochemist ry). Thus, this organ culture system may help elucidate factors that can ac utely regulate adrenocortical cell survival. Quartered glands have a nearly 2-fold increase in oligonucleosome formation compared to intact glands at 3 h and are resistant to the antiapoptotic action of ACTH. In contrast, ACT H-induced corticosterone secretion is not attenuated. Angiotensin II (Ang I I) enhances culture-triggered apoptosis, and its apoptotic action is attenu ated by ACTH. These observations suggest that 1) acute hormonal modulation of apoptosis may require some level of gross adrenal structural integrity, and 2) ACTH and Ang II act in an antagonistic fashion to regulate adrenocor tical apoptosis. The apoptotic effect of Ang II may be mediated via the typ e 2 receptor.