Regulation by GH of insulin-like growth factor-I mRNA expression in rat epiphyseal growth plate as studied with in-situ hybridization

• DOI: 10.1677/joe.0.1250067
• Publication Date: 2008-12-11T23:11:20Z
• Authors: A. Nilsson; B. Carlsson; J. Isgaard; O. G. P. Isaksson; L. Rymo
• Keywords: Male; 0301 basic medicine; Molecular Probe Techniques; Cell Count; Rats, Inbred Strains; Rats; 03 medical and health sciences; Gene Expression Regulation; Somatomedins; Growth Hormone; Animals; Autoradiography; Growth Plate; RNA, Messenger; Insulin-Like Growth Factor I; Hypophysectomy

ABSTRACT Expression of insulin-like growth factor I (IGF-I) mRNA and its dependence on GH was studied in rat epiphyseal growth plate by in-situ hybridization. Methodological aspects of the technique were first evaluated on fixed sagittal cryosections from 28-day-old rat epiphyseal growth plates to ascertain specific hybridization. In-situ hybridization was compared on sections from 10- and 28-day-old rats and the GH-dependence was studied in 35-day-old hypophysectomized rats. Expression of IGF-I mRNA was apparent in chondrocytes of the proliferative, hypertrophic and early degenerative zones of the growth plate of 28-day-old rats. The epiphyseal growth plate from 10-day-old rats showed a weak hybridization signal compared with 28-day-old rats. In contrast, the mesenchymal cells of the periosteum of 10-day-old rats showed a rather strong hybridization signal. Hypophysectomy resulted in a reduction in hybridization signal and cell number of the growth plate compared with 35-day-old age-matched normal rats. GH-Replacement therapy (200 μg human GH s.c. every 4 h for 24 h) resulted in partially restored expression of IGF-I mRNA. The present study has shown that the IGF-I gene is expressed in the rat epiphyseal growth plate chondrocytes and that the expression is dependent on GH. The results support a paracrine/autocrine role of IGF-I for the expression of the stimulatory effect of GH on longitudinal bone growth. Journal of Endocrinology (1990) 125, 67–74