Growth hormone (GH) is essential for normal longitudinal growth and metabolic homeostasis in children. While GH is itself an anabolic hormone, it is believed that most of its activity is mediated by the stimulation of insulin-like growth factors (IGF) or somatomedins. The complex hormonal regulation of GH secretion includes stimulatory (GH-releasing factor, GRF) and inhibitory (somatostatin) hypothalamic control as well as long loop feedback inhibition by the somatomedin peptides. The role of feedback inhibitor would be a unique action for the somatomedins whose major defined physiologic function is that of an anabolic growth factor. Moreover, the presence of insulin receptors on somatotrophic cells suggests that insulin may also play an important direct role in GH homeostasis. This grant will explore 2 major themes in the control of GH synthesis and release using continuous cell culture lines of rat somatotropinoma cells (GH3 cells) and primary cultures of pituitary cells derived from normal rats and from human somatotropinomas: 1) The regulation of GH synthesis by IGF and insulin will be examined by studying the hormonal regulation and ontogeny of IGF and insulin receptors. The ability of somatomedins and insulin to regulate GH secretion and mRNA synthesis will be examined using anti-receptor monoclonal antibodies and by measuring GH released into the medium and intracellular GH mRNA levels. 2) The regulation of IGF synthesis in the pituitary gland and brain will be studied using specific RIAs for the IGFs and RNA probes for each of the somatomedins. These studies will delineate a new feedback role for insulin-like growth factors and will greatly expand our understanding of how IGF, insulin and GRF can regulate pituitary function in normal individuals and in patients with diabetes, acromegaly and hypopituitarism.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK036054-03
Application #
3234373
Study Section
Endocrinology Study Section (END)
Project Start
1986-04-01
Project End
1990-03-31
Budget Start
1988-04-01
Budget End
1990-03-31
Support Year
3
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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Hoffman, Andrew R; Hu, Ji Fan (2006) Directing DNA methylation to inhibit gene expression. Cell Mol Neurobiol 26:425-38
Chen, Hui Ling; Li, Tao; Qiu, Xin Wen et al. (2006) Correction of aberrant imprinting of IGF2 in human tumors by nuclear transfer-induced epigenetic reprogramming. EMBO J 25:5329-38
Ling, Jian Qun; Li, Tao; Hu, Ji Fan et al. (2006) CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1. Science 312:269-72
Li, Tao; Vu, Thanh H; Ulaner, Gary A et al. (2005) IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch. Mol Hum Reprod 11:631-40
Vu, Thanh H; Li, Tao; Hoffman, Andrew R (2004) Promoter-restricted histone code, not the differentially methylated DNA regions or antisense transcripts, marks the imprinting status of IGF2R in human and mouse. Hum Mol Genet 13:2233-45
Vu, Thanh H; Chuyen, Nguyen V; Li, Tao et al. (2003) Loss of imprinting of IGF2 sense and antisense transcripts in Wilms' tumor. Cancer Res 63:1900-5

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