Developmental exposure to 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin may alter LH release patterns by abolishing sex differences in GABA/glutamate cell number and modifying the transcriptome of the male anteroventral periventricular nucleus. (4th August 2016)

• Record Type: Journal Article
• Authors: Del Pino Sans, Javier; Clements, Kelsey J.; Suvorov, Alexander; Krishnan, Sudha; Adams, Hillary L.; Petersen, Sandra L.
• Is Part Of: Neuroscience. Volume 329(2016)
• Page Start: 239
• Page End: 253
• Publication Date: 2016-08-04
• Subjects: AhR arylhydrocarbon receptor -- AR androgen receptors -- AVPV anteroventral periventricular nucleus -- ER estrogen receptors -- GnRH gonadotropin releasing-hormone -- LH luteinizing hormone -- QPCR quantitative real-time polymerase chain reaction -- T testosterone -- TCDD 2, 3, 7, 8, -tetrachlorodibenzo-p-dioxin; defeminization -- AVPV -- Cugbp2 -- Mmp9 -- Sox11 -- LH; Neurochemistry -- Periodicals; Neurophysiology -- Periodicals; Neurology -- Periodicals; Neurochimie -- Périodiques; Neurophysiologie -- Périodiques; Neurochemistry; Neurophysiology; Electronic journals; Periodicals; Electronic journals; 612.8
• DOI: 10.1016/j.neuroscience.2016.04.051
• Languages: English
• ISSNs: 0306-4522

Abstract

Highlights: Neonatal TCDD exposure abolishes sex differences in AVPV GABA/Glutamate neuronal population. TCDD likely regulates genes important for neuron development, synaptic transmission and sterol biosynthesis. TCDD regulates gene sets that are also regulated by ER, AR, Srebp1 and 2, and E2f. Cugbp2, Prph, Nefh, Sox11 and Mmp9 are sex-specific genes found in this study to be regulated by TCDD. Abstract: Developmental exposure to arylhydrocarbon receptor (AhR) ligands abolishes sex differences in a wide range of neural structures and functions. A well-studied example is the anteroventral periventricular nucleus (AVPV), a structure that controls sex-specific luteinizing hormone (LH) release. In the male, testosterone (T) secreted by the developing testes defeminizes LH release mechanisms; conversely, perinatal AhR activation by 2, 3, 7, 8, -tetrachlorodibenzo- p -dioxin (TCDD) blocks defeminization. To better understand developmental mechanisms altered by TCDD exposure, we first verified that neonatal TCDD exposure in male rats prevented the loss of AVPV GABA/glutamate neurons that are critical for female-typical LH surge release. We then used whole genome arrays and quantitative real-time polymerase chain reaction (QPCR) to compare AVPV transcriptomes of males treated neonatally with TCDD or vehicle. Our bioinformatics analyses showed that TCDD enriched gene sets important for neuron development, synaptic transmission, ion homeostasis, and cholesterol biosynthesis. In addition, upstream regulatory analysis suggests that both estrogen receptors (ER) and androgen receptors (AR) regulate genes targeted by TCDD. Of the 23 mRNAs found to be changed by TCDD at least 2-fold ( p < 0.05), most participate in the functions identified in our bioinformatics analyses. Several, including matrix metallopeptidase 9 and SRY-box 11 ( Sox11 ), are known targets of E2 . CUG triplet repeat, RNA binding protein 2 ( cugbp2 ) is particularly interesting because it is sex-specific, oppositely regulated by estradiol (E2 ) and TCDD. Moreover, it regulates the post-transcriptional processing of molecules previously linked to sexual differentiation of the brain. These findings provide new insights into how TCDD may interfere with defeminization of LH release patterns.