Back to Search Start Over

Involvement of testicular growth factors in fetal Leydig cell aggregation after exposure to phthalate in utero.

Authors :
Han Lin
Ren-Shan Ge
Guo-Rong Chen
Guo-Xin Hu
Lei Dong
Qing-Quan Lian
Hardy, Dianne O.
Sottas, Chantal M.
Xiao-Kun Li
Hardy, Matthew P.
Source :
Proceedings of the National Academy of Sciences of the United States of America; 5/20/2008, Vol. 105 Issue 20, p7218-7222, 5p, 3 Charts, 3 Graphs
Publication Year :
2008

Abstract

Exposures to di-(2-ethylhexyl) phthalate (DEHP) have been shown to be associated with decreased adult testosterone (T) levels and increased Leydig cell numbers. As yet, little is known about DEHP effects in utero on fetal Leydig cells (FLC). The present study investigated effects of DEHP on FLC function. Pregnant Long-Evans female rats received vehicle (corn oil) or DEHP at 10, 100, or 750 mg/kg by oral gavage from gestational day (GD)2-20. At GD21, T production, FLC numbers and distribution, and testicular gene expression were examined. The percentage of FLC clusters containing 6-30 cells increased in all treatment groups, with 29 ± 2% in control vs. 37 ± 3, 35 ± 3, and 56 ± 4% in rats receiving 10, 100, and 750 mg/kg DEHP, respectively. In contrast, FLC numbers were 33% and 39% lower than control after exposures to 100 and 750 mg/kg DEHP, respectively. At these doses, mRNA levels of leukemia inhibitory factor (LIF) increased. LIF was found to -induce cell aggregation in FLCs in vitro, consistent with the hypothesis that DEHP induced FLC aggregation. Testicular T levels were doubled by the 10 mg/kg dose and halved at 750 mg/kg. The mRNA levels of IGF-1 and c-Kit ligand (KITL) were induced by 10mg/kg DEHP. These results, taken together, indicate that fetal exposures to DEHP have effects on FIC number, distribution, and most importantly, steroidogenic capacity and suggest that abnormal expressions of IGF1, KITL, and LIF genes may contribute to the reproductive toxicity of phthalates. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
105
Issue :
20
Database :
Complementary Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
32491791
Full Text :
https://doi.org/10.1073/pnas.0709260105