STUDIES ON REGULATION OF INSULIN-LIKE GROWTH-FACTOR BINDING-PROTEIN (IGFBP)-3 AND IGFBP-4 PRODUCTION IN HUMAN BONE-CELLS

被引:55
作者
MOHAN, S
STRONG, DD
LEMPERT, UG
TREMOLLIERES, F
WERGEDAL, JE
BAYLINK, DJ
机构
[1] LOMA LINDA UNIV,DEPT MED,LOMA LINDA,CA 92350
[2] LOMA LINDA UNIV,DEPT BIOCHEM,LOMA LINDA,CA 92350
[3] LOMA LINDA UNIV,DEPT MICROBIOL,LOMA LINDA,CA 92350
[4] LOMA LINDA UNIV,DEPT PHYSIOL,LOMA LINDA,CA 92350
来源
ACTA ENDOCRINOLOGICA | 1992年 / 127卷 / 06期
关键词
D O I
10.1530/acta.0.1270555
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Previous studies have shown that the actions of IGF-II in bone are determined not only by its concentration, but also by the concentration of IGFBP-4 as well as other IGFBPs. In this study, we sought to determine by Western ligand blotting the effects of growth hormone, IGF-I and IGF-II on the production of IGFBP-3 and IGFBP-4 in TE89 human osteosarcoma cells and in untransformed normal human bone cells derived from rib. Human growth hormone at 10 mug/l decreased the amount of IGFBP-4 but had no effect on the IGFBP-3 level in the conditioned medium of low density cultures of TE89 cells and human bone cells derived from rib. Human growth hormone had no effect on IGFBP-3 or IGFBP-4 levels in the conditioned medium of high density human bone cell cultures. IGF-I and IGF-II, which increased human bone cell proliferation, decreased the level of IGFBP-4 (30% of control at 100 mug/IIGF-I and IGF-II) but increased the level of IGFBP-3 (3-10 fold at 100 mug/l IGF-I and IGF-II) after 48 h of treatment in the conditioned medium of both low and high density TE89 cell cultures. Similar changes in IGFBP-3 and IGFBP-4 levels were also seen in the conditioned medium of human bone cells derived from rib after treatment with IGF-I and IGF-II. Studies to determine the underlying molecular mechanisms by which IGF-II decreased the amount of IGFBP-4 in the conditioned medium revealed that IGF-II decreased the IGFBP-4 mRNA abundance and increased the IGFBP-3 mRNA abundance in human bone cells. Based on the above findings, we conclude that the production of both IGFBP-3 and IGFBP-4 is regulated in bone cells and that local and systemic agents may modulate the responsiveness of bone cells to IGFs by regulated secretion of IGFBP-3 and IGFBP-4.
引用
收藏
页码:555 / 564
页数:10
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