Neuroprogesterone synthesis in hypothalamic astrocytes is associated with a pubertal increase in membrane ERα levels

Abstract

The development of estrogen positive feedback is a hallmark of female puberty. Both estrogen and progesterone signaling are required for the functioning of this neuroendocrine feedback loop but the physiological changes that underlie the emergence of positive feedback remain unknown. Only after puberty does estradiol (E2) facilitate progesterone synthesis in the rat female hypothalamus (neuroP), an event critical for positive feedback and the LH surge. We hypothesize that prior to puberty, these astrocytes have low levels of membrane estrogen receptor alpha (ER), which is needed for facilitation of neuroP synthesis. Thus, we hypothesized that prepubertal astrocytes are unable to respond to E2 with increased neuroP synthesis due a lack of membrane ER. To test this, hypothalamic tissues and enriched primary hypothalamic astrocyte cultures were acquired from pre-pubertal (postnatal week 3) and post- pubertal (week 8) female mice. E2-facilitated progesterone was measured in the hypothalamus pre- and post-puberty, and hypothalamic astrocyte responses were measured after treatment with E2. Prior to puberty, E2-facilitated progesterone synthesis did not occur in the hypothalamus, and mER expression was low in hypothalamic astrocytes, but E2-facilitated progesterone synthesis in the rostral hypothalamus and mER expression increased post- puberty. The increase in mER expression in hypothalamic astrocytes corresponded with an increase in caveolin-1 protein, PKA phosphorylation, and a more rapid [Ca2+]i flux in response to E2. Together, results from the present study indicate that E2-facilitated neuroP synthesis occurs in the rostral hypothalamus, develops during puberty, and corresponds to a post-pubertal increase in mER levels in hypothalamic astrocytes. SIGNIFICANCE STATEMENTEstradiol facilitation of hypothalamic neuroprogesterone synthesis is necessary for the positive feedback of the LH surge. The present study localized the increase of neuroprogesterone to the rostral hypothalamus, a region that mediates estrogen positive feedback. Across pubertal development, hypothalamic astrocytes increase levels of membrane ER and the cell signaling responses needed to facilitate neuroprogesterone synthesis that triggers the LH surge demonstrating a mechanism for pubertal maturation resulting in reproductive competence.