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CRISPR-Cas9 knockdown of ESR1 in preoptic GABA-kisspeptin neurons suppresses the preovulatory surge and estrous cycles in female mice. | LitMetric

AI Article Synopsis

  • - Evidence indicates that GABA neurons in the preoptic area, which sense estradiol, play a crucial role in triggering the preovulatory surge for ovulation in female mice.
  • - Researchers used CRISPR-Cas9 to reduce estrogen receptor alpha (ESR1) in GABA neurons, discovering that deletion in these neurons led to decreased activity in gonadotropin-releasing hormone (GnRH) neurons during the surge.
  • - Analysis revealed that GABA neurons expressing kisspeptin are vital for the LH surge, as mice lacking kisspeptin activity showed continuous estrus and no surge activation, though they maintained pulsatile LH release.

Article Abstract

Evidence suggests that estradiol-sensing preoptic area GABA neurons are involved in the preovulatory surge mechanism necessary for ovulation. In vivo CRISPR-Cas9 editing was used to achieve a 60-70% knockdown in estrogen receptor alpha (ESR1) expression by GABA neurons located within the regions of the rostral periventricular area of the third ventricle (RP3V) and medial preoptic nuclei (MPN) in adult female mice. Mice exhibited variable reproductive phenotypes with the only significant finding being mice with bilateral ESR1 deletion in RP3V GABA neurons having reduced cFos expression in gonadotropin-releasing hormone (GnRH) neurons at the time of the surge. One sub-population of RP3V GABA neurons expresses kisspeptin. Re-grouping ESR1-edited mice on the basis of their RP3V kisspeptin expression revealed a highly consistent phenotype; mice with a near-complete loss of kisspeptin immunoreactivity displayed constant estrus and failed to exhibit surge activation but retained pulsatile luteinizing hormone (LH) secretion. These observations demonstrate that ESR1-expressing GABA-kisspeptin neurons in the RP3V are essential for the murine preovulatory LH surge mechanism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10735218PMC
http://dx.doi.org/10.7554/eLife.90959DOI Listing

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