Kao T L, Meyer W J
Department of Human Biological Chemistry & Genetics, University of Texas Medical Branch, Galveston 77555-0429.
Life Sci. 1992;51(13):1033-9. doi: 10.1016/0024-3205(92)90502-g.
The regulation of irGH secretion by the immune system was examined using lymphoid cell lines, H9 and IM9. Using a highly sensitive immunoassay, irGH secretion by H9 was negatively regulated by dexamethasone, whereas many other regulators of hGH secretion, including hormones, monoamines, and second messenger, had no measurable effect on irGH secretion. Treatment of H9 cells with dexamethasone for 48 hours could cause as high as 70% reduction in irGH secretion without affecting either cell numbers or viability. Using IM9, neither growth hormone releasing hormone nor thyrotropin releasing hormone had significant effect on either irGH steady-state level transcripts or irGH secretion. These findings suggest that irGH secretion by lymphocytes was regulated in a different manner from that by pituitary cells.
利用淋巴样细胞系H9和IM9研究了免疫系统对irGH分泌的调节。采用高灵敏度免疫测定法,地塞米松对H9分泌irGH具有负调节作用,而许多其他生长激素(hGH)分泌调节因子,包括激素、单胺和第二信使,对irGH分泌均无显著影响。用地塞米松处理H9细胞48小时可使irGH分泌减少高达70%,而不影响细胞数量或活力。对于IM9,生长激素释放激素和促甲状腺激素释放激素对irGH稳态水平转录本或irGH分泌均无显著影响。这些发现表明,淋巴细胞分泌irGH的调节方式与垂体细胞不同。