Validation of an automated counting procedure for phthalate-induced testicular multinucleated germ cells. (15th June 2018)

• Record Type: Journal Article
• Authors: Spade, Daniel J.; Bai, Cathy Yue; Lambright, Christy; Conley, Justin M.; Boekelheide, Kim; Gray, L. Earl
• Is Part Of: Toxicology letters. Volume 290(2018)
• Page Start: 55
• Page End: 61
• Publication Date: 2018-06-15
• Subjects: Phthalate esters -- Quantitative pathology -- Multinucleated germ cells; Toxicology -- Periodicals; 363.179
• DOI: 10.1016/j.toxlet.2018.03.018
• Languages: English
• ISSNs: 0378-4274

Abstract

Highlights: Developed an ImageJ procedure to count multinucleated germ cells (MNGs). Four medium-chain ortho-phthalates induced MNGs in fetal rat testis. For each compound, induction of MNGs was concordant with testosterone reduction. Abstract: In utero exposure to certain phthalate esters results in testicular toxicity, characterized at the tissue level by induction of multinucleated germ cells (MNGs) in rat, mouse, and human fetal testis. Phthalate exposures also result in a decrease in testicular testosterone in rats. The anti-androgenic effects of phthalates have been more thoroughly quantified than testicular pathology due to the significant time requirement associated with manual counting of MNGs on histological sections. An automated counting method was developed in ImageJ to quantify MNGs in digital images of hematoxylin-stained rat fetal testis tissue sections. Timed pregnant Sprague Dawley rats were exposed by daily oral gavage from gestation day 17 to 21 with one of eight phthalate test compounds or corn oil vehicle. Both the manual counting method and the automated image analysis method identified di- n -butyl phthalate, butyl benzyl phthalate, dipentyl phthalate, and di-(2-ethylhexyl) phthalate as positive for induction of MNGs. Dimethyl phthalate, diethyl phthalate, the brominated phthalate di-(2-ethylhexyl) tetrabromophthalate, and dioctyl terephthalate were negative. The correlation between automated and manual scoring metrics was high (r = 0.923). Results of MNG analysis were consistent with these compounds' anti-androgenic activities, which were confirmed in an ex vivo testosterone production assay. In conclusion, we have developed a reliable image analysis method that can be used to facilitate dose-response studies for the reproducible induction of MNGs by in utero phthalate exposure.