4.5 Article

Differential Effects of the G-Protein-Coupled Estrogen Receptor (GPER) on Rat Embryonic (E18) Hippocampal and Cortical Neurons

期刊

ENEURO
卷 9, 期 4, 页码 -

出版社

SOC NEUROSCIENCE
DOI: 10.1523/ENEURO.0475-21.2022

关键词

electrophysiology; estrogen; G-protein-coupled estrogen receptor (GPER/GPR30); hippocampus; neurodevelopment; transcriptome

资金

  1. National Science Foundation [1916563]
  2. Saint Louis University Start-up Fund
  3. Saint Louis University OVPR Spark Microgrant Fund
  4. Sigma Xi [G2017031593406127]
  5. Saint Louis University
  6. Division Of Integrative Organismal Systems
  7. Direct For Biological Sciences [1916563] Funding Source: National Science Foundation

向作者/读者索取更多资源

Estrogen plays important roles in nervous system development and function. The activation of GPER has differential effects on rat hippocampal and cortical neurons, with a stronger response observed in hippocampal neurons. The GPER-mediated increase in Ca2+ in hippocampal neurons involves both the release of intracellular Ca2+ stores and the entry of extracellular Ca2+ through Ca2+ channels.
Estrogen plays fundamental roles in nervous system development and function. Traditional studies examining the effect of estrogen in the brain have focused on the nuclear estrogen receptors (ERs), ER alpha and ER beta. Studies related to the extranuclear, membrane-bound G-protein-coupled ER (GPER/GPR30) have revealed a neuroprotective role for GPER in mature neurons. In this study, we investigated the differential effects of GPER activation in primary rat embryonic day 18 (E18) hippocampal and cortical neurons. Microscopy imaging, multielectrode array (MEA), and Ca2+ imaging experiments revealed that GPER activation with selective agonist, G-1, and nonselective agonist, 17 beta -estradiol (E2), increased neural growth, neural firing activity, and intracellular Ca2+ more profoundly in hippocampal neurons than in cortical neurons. The GPER-mediated Ca2+ rise in hippocampal neurons involves internal Ca2+ store release via activation of phospholipase C (PLC) and extracellular entry via Ca2+ channels. Immunocytochemistry results revealed no observable difference in GPER expression/localization in neurons, yet real-time qPCR (RT-qPCR) and Western blotting showed a higher GPER expression in the cortex than hippocampus, implying that GPER expression level may not fully account for its robust physiological effects in hippocampal neurons. We used RNA sequencing data to identify distinctly enriched pathways and significantly expressed genes in response to G-1 or E2 in cultured rat E18 hippocampal and cortical neurons. In summary, the identification of differential effects of GPER activation on hippocampal and cortical neurons in the brain and the determination of key genes and molecular pathways are instrumental toward an understanding of estrogen's action in early neuronal development.

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