Leukemia inhibitory factor as an intrapituitary mediator of ACTH secretion

Citation
J. Schwartz et al., Leukemia inhibitory factor as an intrapituitary mediator of ACTH secretion, NEUROENDOCR, 69(1), 1999, pp. 34-43
Citations number
32
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROENDOCRINOLOGY
ISSN journal
00283835 → ACNP
Volume
69
Issue
1
Year of publication
1999
Pages
34 - 43
Database
ISI
SICI code
0028-3835(199901)69:1<34:LIFAAI>2.0.ZU;2-I
Abstract
In the normal anterior pituitary, intercellular interactions are important for the expression of hormones including adrenocorticotropin (ACTH). Leukem ia inhibitory factor (LIF) is secreted by anterior pituitary cells and stim ulates both basal and corticotropin-releasing hormone (CRH)stimulated ACTH secretion in AtT20 cells. To determine the effects of LIF on normal pituita ry cells, we measured the effects of LIF and an immunoneutralizing antiseru m against LIF on ACTH secretion by cultured sheep anterior pituitary cells. In intact populations of anterior pituitary cells, LIF (10 nM) stimulated ACTH secretion (from 0.30 +/- 0.06 to 0.77 +/- 0.01 ng/well per 3 h) and an tiserum to LIF (by itself) had no effect (0.29 +/- 0.05 ng/well per 3 h). I n marked contrast, following pharmacological elimination of CRH-target cell s, a condition known to disinhibit ACTH secretion, basal ACTH secretion was elevated (0.74 +/- 0.13 ng/well per 3 h); LIF produced no further stimulat ion (0.73 +/- 0.22 ng/well per 3 h) but immunoneutralization of LIF signifi cantly reduced secretion to 0.50 +/- 0.10 ng/well per 3 h. Medium, conditio ned by exposure to CRH-target-depleted cultures of anterior pituitary cells , increased net ACTH secretion (from 0.29 +/- 0.03 to 6.54 +/- 0.71 ng/well per 3 h), when added as a challenge to naive, cultured anterior pituitary cells. Inclusion of antiserum to LIF significantly attenuated (5.29 +/- 0.6 2 ng/ well per 3 h) this response. The presence in and secretion of LIF by normal individual pituitary cells was detected using immunocytochemical met hods. Seven to 8% of all cells stained positively for LIF, with 66 +/- 11% of those secreting detectable amounts of LIF under unstimulated conditions. LIF colocalized with TSH and LH in pituitary cells. Taken together, these data suggest that LIF can stimulate ACTH secretion by normal anterior pitui tary cells, and potentially plays a role as an intrapituitary stimulator of ACTH secretion under certain conditions.