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Thyroid hormones increase insulin‐like growth factor I content in the medium of rat bone tissue
Author(s) -
Lakatos Peter,
Caplice Matthew D.,
Khanna Vikram,
Stern Paula H.
Publication year - 1993
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1002/jbmr.5650081210
Subject(s) - endocrinology , medicine , hormone , bone resorption , trypan blue , thyroid , resorption , incubation , in vitro , multinucleate , in vivo , growth factor , chemistry , cell culture , bone cell , biology , receptor , biochemistry , microbiology and biotechnology , genetics
The mechanism of action of thyroid hormones on bone is still not clear. At low concentrations, they stimulate bone formation; at high concentrations, they elicit bone resorption in vitro and in vivo. In the present study we investigated the effect of T 3 and T 4 as well as their active and inactive analogs (TRIAC, SKF L‐94901, rT 3 , and DIT) on the IGF‐I and TNF‐α content in the medium of UMR‐106 rat osteoblastic cells and fetal rat limb bones. In the dose‐response studies, a biphasic increase in medium IGF‐I was observed in both cells and limb bones, with peak stimulatory concentrations of 10 −8 M for T 3 and 10 −7 M for T 4 in both systems. At higher concentrations, at which thyroid hormones elicit bone resorption, the stimulatory effect diminished and finally was no longer detectable. The active analogs TRIAC and SKF L‐94901 also enhanced IGF‐I release in UMR‐106 cells. The inactive compounds rT 3 and DIT failed to increase IGF‐I in these cultures. The protein content of the cell culture wells exposed to high concentrations of thyroid hormones was similar to those containing low concentrations, indicating that the decrease in IGF‐I content at high doses was not due to toxic effects. This was also confirmed by trypan blue exclusion. Time course studies with UMR‐106 cells revealed a significant increase in medium IGF‐I after 2 days of incubation. No significant further increase was observed after this up to 5 days of culture. In contrast, the medium of limb bone cultures showed a linear increase in IGF‐I content up to 7 days of culture. No TNF‐α production was observed in either UMR‐106 cells or fetal limb bones. Also, no increase in medium TNF‐α levels was seen in response to thyroid hormones. Based on our results, we conclude that IGF‐I may be responsible for some of the anabolic effects of thyroid hormones in bone tissue, but TNF‐α, at least in the models we used, does not play a role in the mediation of thyroid hormone action.