1. Effect of hypoxia on the release of vascular endothelial growth factor and testosterone in mouse TM3 Leydig cells
- Author
-
Wen-Min Tseng, Guey-Shyang Hwang, Ching-Han Yu, Paulus S. Wang, and Shyi-Wu Wang
- Subjects
Male ,Vascular Endothelial Growth Factor A ,endocrine system ,medicine.medical_specialty ,Physiology ,Angiogenesis ,medicine.drug_class ,Endocrinology, Diabetes and Metabolism ,Radioimmunoassay ,Biology ,Chorionic Gonadotropin ,Immunoenzyme Techniques ,Mice ,chemistry.chemical_compound ,Vasculogenesis ,Mediator ,Physiology (medical) ,Internal medicine ,medicine ,Animals ,Testosterone ,Cell Proliferation ,Mitogen-Activated Protein Kinase 1 ,Mitogen-Activated Protein Kinase 3 ,Dose-Response Relationship, Drug ,Leydig cell ,Leydig Cells ,Hypoxia (medical) ,Androgen ,Cell Hypoxia ,Enzyme Activation ,Vascular endothelial growth factor ,medicine.anatomical_structure ,Endocrinology ,chemistry ,Liberation ,medicine.symptom - Abstract
Hypoxia has been shown to stimulate the expression of vascular endothelial growth factor (VEGF), which is a major mediator for angiogenesis and vasculogenesis. During hypoxia, VEGF promotes angiogenesis in the testis. However, the effect of VEGF on the steroidogenesis of testosterone and the cell proliferation in Leydig cells is unclear. To assess the effects and the action mechanisms of hypoxia, a mouse TM3 Leydig cell line was employed in the present study. The Leydig cells were incubated in an incubator chamber (95% N2-5% CO2) for 1–24 h. The cultured media were collected and assayed by testosterone RIA and VEGF enzyme immunoassay. 3-(4,50-Dimethylthiazol-2-yl)-2.5-diphenyltetrazolium bromide assay was used to detect the proliferation of Leydig cells. The present results showed that the proliferation of Leydig cells was enhanced significantly by hypoxia. The basal VEGF release was increased, and the response of VEGF production to human chorionic gonadotropin (hCG) was also enhanced in hypoxic condition. During hypoxia, administration of hCG or VEGF stimulated proliferation of Leydig cells, but the stimulatory effect was abolished by the administration of anti-VEGF antibody. Higher doses of VEGF stimulated testosterone release in a dose-dependent manner. Administration of anti-VEGF antibody abolished the stimulatory effect of VEGF on testosterone release. These data suggest that hypoxia stimulates cell proliferation and testosterone release in Leydig cells via an increase of VEGF production.
- Published
- 2007