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Moderate Prenatal Ethanol Exposure Stimulates CXCL12/CXCR4 Chemokine System in Radial Glia Progenitor Cells in Hypothalamic Neuroepithelium and Peptide Neurons in Lateral Hypothalamus of the Embryo and Postnatal Offspring.
- Source :
-
Alcoholism, clinical and experimental research [Alcohol Clin Exp Res] 2020 Apr; Vol. 44 (4), pp. 866-879. Date of Electronic Publication: 2020 Feb 26. - Publication Year :
- 2020
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Abstract
- Background: Prenatal exposure to ethanol (EtOH) has lasting effects on neuropeptide and neuroimmune systems in the brain alongside detrimental alcohol-related behaviors. At low-to-moderate doses, prenatal EtOH stimulates neurogenesis in lateral hypothalamus (LH) and increases neurons that express the orexigenic peptides hypocretin/orexin (Hcrt/OX) and melanin-concentrating hormone (MCH), and the proinflammatory chemokine CCL2, which through its receptor CCR2 stimulates cell differentiation and movement. Our recent studies demonstrated that CCL2 and CCR2 colocalize with MCH neurons and are involved in EtOH's stimulatory effect on their development but show no relation to Hcrt/OX. Here, we investigated another chemokine, CXCL12, and its receptor, CXCR4, which promote neurogenesis and neuroprogenitor cell proliferation, to determine if they also exhibit peptide specificity in their response to EtOH exposure.<br />Methods: Pregnant rats were intraorally administered a moderate dose of EtOH (2 g/kg/d) from embryonic day 10 (E10) to E15. Their embryos and postnatal offspring were examined using real-time quantitative PCR and immunofluorescence histochemistry, to determine if EtOH affects CXCL12 and CXCR4 and the colocalization of CXCR4 with Hcrt/OX and MCH neurons in the LH and with radial glia neuroprogenitor cells in the hypothalamic neuroepithelium (NEP).<br />Results: Prenatal EtOH strongly stimulated CXCL12 and CXCR4 in LH neurons of embryos and postnatal offspring. This stimulation was significantly stronger in Hcrt/OX than MCH neurons in LH and also occurred in radial glia neuroprogenitor cells dense in the NEP. These effects were sexually dimorphic, consistently stronger in females than males.<br />Conclusions: While showing prenatal EtOH exposure to have a sexually dimorphic, stimulatory effect on CXCL12 and CXCR4 in LH similar to CCL2 and its receptor, these results reveal their distinct relationship to the peptide neurons, with the former closely related to Hcrt/OX and the latter to MCH, and they link EtOH's actions in LH to a stimulatory effect on neuroprogenitor cells in the NEP.<br /> (© 2020 by the Research Society on Alcoholism.)
- Subjects :
- Animals
Animals, Newborn
Cell Proliferation drug effects
Chemokine CXCL12 metabolism
Embryo, Mammalian
Ependymoglial Cells metabolism
Hypothalamic Area, Lateral cytology
Hypothalamic Area, Lateral metabolism
Hypothalamic Hormones metabolism
Hypothalamus cytology
Hypothalamus drug effects
Hypothalamus metabolism
Immunohistochemistry
Melanins metabolism
Neural Stem Cells metabolism
Neurogenesis drug effects
Neurons metabolism
Orexins metabolism
Pituitary Hormones metabolism
Rats
Real-Time Polymerase Chain Reaction
Receptors, CXCR4 metabolism
Central Nervous System Depressants pharmacology
Chemokine CXCL12 drug effects
Ependymoglial Cells drug effects
Ethanol pharmacology
Hypothalamic Area, Lateral drug effects
Neural Stem Cells drug effects
Neurons drug effects
Receptors, CXCR4 drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1530-0277
- Volume :
- 44
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Alcoholism, clinical and experimental research
- Publication Type :
- Academic Journal
- Accession number :
- 32020622
- Full Text :
- https://doi.org/10.1111/acer.14296