Effects of testosterone either alone or with IGF-I on growth of cells derived from the proliferation zone of regenerating antlers in vitro

• Published in: Growth hormone & IGF research Vol. 11; no. 4; pp. 240 - 246
• Main Authors: Sadighi, M., Li, C., Littlejohn, R.P., Suttie, J.M.
• Format: Journal Article
• Language: English
• Published: Scotland Elsevier Ltd 01.08.2001
• Subjects: Animals; Antlers - cytology; Antlers - physiology; Binding Sites; Cartilage - cytology; Cell Division; Cells, Cultured; Deer; Dose-Response Relationship, Drug; Insulin-Like Growth Factor I - pharmacology; Male; Mesoderm - cytology; Regeneration; Testosterone - pharmacology; Time Factors; IGF-I; deer antler; testosterone; mitogenesis; in vitro
• ISSN: 1096-6374; 1532-2238
• DOI: 10.1054/ghir.2001.0232

Deer antlers are male secondary sexual characters and are the fastest growing mammalian tissue. As such, both androgens and growth factors play a major role in antler development. The timing of the antler cycle is controlled by the seasonal fluctuations of testosterone, and the actual growth of antlers is mainly stimulated by growth factors including insulin-like growth factor-1 (IGF-I). However, whether or not testosterone at low levels plays a growth-promoting role during antler formation is controversial. In the present study, we took an in vitro approach to investigate whether testosterone either alone or with IGF-I had mitogenic effects on mesenchymal or cartilaginous cells derived from the proliferation zone of regenerating antlers. In addition, a binding assay was carried out to determine whether the specific binding sites for testosterone were preserved after cell disaggregation. The results showed that testosterone either in physiological concentrations or at low levels did not exert direct mitogenic effects on antler cells derived from the proliferation zone in serum-free medium in vitro (P>0.05), even if the specific binding sites for testosterone in these cells were well preserved. Likewise, testosterone in a very wide range of concentrations not only failed to enhance (P>0.05), but at certain levels (0.1–5 nM) impaired the mitogenic effects of IGF-I on these antler cells in vitro (P<0.001). Therefore, these results support neither a conclusion that low level testosterone has growth-promoting effects on antler formation nor the hypothesis that testosterone effects may be achieved through sensitizing these antler cells to the mitogenic effects of IGF-I.