Collaborative Research: Hyaluronan, NRF2 and Protracted Female Fertility in Long-lived Naked Mole-Rats

Project: Research project

Project Details

Description

The main focus of this proposal is to discover the physiological mechanisms that underlie the remarkably long reproductive lifespan of female naked mole-rats, which are exceptional for their lack of age-associated declines in fertility and fecundity into their third decade of life. Naked mole-rats are renowned for being the longest-lived rodent species (>30 years) and for their extraordinary cancer resistance. These characteristics have been attributed to an enhanced cytoprotective signaling pathway (nuclear factor erythroid 2-related factor, NRF2) and an exceptionally high molecular weight (HMW) form of hyaluronan (hyaluronic acid, HA), which is a key component of the extracellular matrix (ECM). Two complementary model systems, naked mole-rats themselves and a transgenic mouse line that expresses the synthase for naked mole-rat HMW-HA (nmrHas2) will be used to determine if nmrHMW-HA attenuates the adverse effects of aging on ovarian structure and function via direct means and/or through enhanced signaling of the NRF2 cytoprotective pathway. Aim 1 will interrogate ovaries from nmrHas2 mice to determine if aging-associated inflammation, fibrosis, tissue stiffness, and reduced fertility are attenuated by nmrHMW-HA. Aim 2 will interrogate naked mole-rat ovaries for HA content and localization to specific cell types, and to determine the degree of similarity between them and nmrHas2 mouse ovaries. Aim 3 will interrogate ovaries from nmrHas2 mice and naked mole-rats for NRF2 signaling to test the hypothesis that nmrHMW-HA expression enhances this cytoprotective pathway. And because Nrf2-null mice demonstrated increased sensitivity to the ovarian toxicant 4-vinylcyclohexane diepoxide (VCD), nmrHas2 mice will be evaluated for reduced sensitivity to VCD, which would manifest as a larger ovarian reserve of follicles and better fertility.
StatusActive
Effective start/end date8/15/207/31/21

Funding

  • Cornell University (PRESPEND)
  • National Science Foundation (PRESPEND)

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