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Departments of 1 Pediatrics, 2 Basic Nursing, and 4 Gynecology, Fukui Medical University, Fukui 910-1193; and 3 Institute for Virus Research, Kyoto University, Kyoto 606-8507, Japan
We report here an
examination of the effect of thioredoxin (TRX) on the secretion of
growth hormone (GH) from rat anterior pituitary cells in vitro.
Treatment of rat pituitary cells with growth hormone-releasing factor
(GRF), but not GH, led to a significant increase in intracellular TRX
protein levels. GRF, recombinant human TRX (rhTRX), and a combination
thereof were all shown to induce immediate GH secretion from pituitary
cells, as evidenced by perifusion experiments. RhTRX, but not other
reducing agents such as
-mercaptoethanol and
N-acetyl-L-cysteine, augmented GRF-stimulated and -unstimulated GH secretion from rat pituitary cells in a
dose-dependent manner. RhTRX did not significantly affect the GH mRNA
expression of pituitary cells stimulated in the presence or absence of
GRF. In addition, rhTRX-augmented GH secretion was not significantly affected by the presence of cycloheximide. Collectively, these findings
suggest that TRX is induced by stimulation with GRF and plays a
regulatory role in GH secretion from rat anterior pituitary cells by
enhancing the secretion of stored GH, rather than by the synthesis of GH.
redox; growth hormone-releasing factor; disulfide bonds
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