60% of women will suffer from a urinary tract infection (UTI) at some point in their lives and a third of women with an acute UTI will suffer recurrent UTIs. This disease is especially problematic for post- menopausal women where over 50% will have recurrent infections that cannot be cured with antibiotics. This increased susceptibility is likely due to reduced estrogen levels that accompany aging. However, the mechanisms behind this increased susceptibility are unknown, and this lack of knowledge impedes our ability to develop new strategies for the treatment and prevention of UTIs, especially in post-menopausal women. Here, we focus on the cytokine, interleukin-6 (IL-6), which is rapidly upregulated during UTIs in humans, and multiple studies have shown that postmenopausal women have elevated serum levels of IL-6. Recent studies indicate that IL-6 signaling not only modulates innate immune responses but also is essential for timely wound healing and tissue regeneration. In preliminary studies, we demonstrate that loss of IL-6 impairs the host response to UPEC and that aged female mice exhibit high levels of IL-6, increased recruitment of macrophages, and impaired tissue repair. Our objective here is to determine how balance is achieved between 1) activating the innate immune system (macrophages) to destroy the pathogen (predominantly uropathogenic E. coli [UPEC]) and 2) repairing the bladder epithelium. We will test the central hypothesis that IL-6 is a key regulator of the balance between host defense and epithelial homeostasis.
In Aim 1, we will dissect the function of IL-6 signaling in modulating the immune and epithelial response to a UTI and how loss of function of this protein impairs host defense response.
In Aim 2, we will determine the mechanisms whereby aging influences UTI outcome in mice and women. Importantly, we will leverage our mechanistic insights to determine whether selective estrogen receptor agonists or anti-IL6 therapies will be effective treatments. We anticipate that our work will provide new insights into the molecular interplay between estrogen and bladder host defense during a UTI. In addition, the experiments will provide a foundation upon which to determine whether estrogen and anti-IL-6 therapies will be effective interventions in post-menopausal women suffering from chronic, recurrent UTIs and will help to develop preventive interventions and treatments that are optimized for menopausal women.

Public Health Relevance

Recurrent urinary tract infections afflict millions of post-menopausal women in the US each year, imposing a tremendous personal and financial burden on society. Our goal here is to understand how the sex hormone estrogen regulates the course of UTIs and bladder recovery after the infection. This work will lead to development of therapeutic interventions for this recalcitrant disease in aging menopausal populations.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
1R01AG052494-01
Application #
9078434
Study Section
Special Emphasis Panel (ZRG1-DKUS-G (90)S)
Program Officer
Fuldner, Rebecca A
Project Start
2016-09-30
Project End
2021-05-31
Budget Start
2016-09-30
Budget End
2017-05-31
Support Year
1
Fiscal Year
2016
Total Cost
$312,625
Indirect Cost
$107,625
Name
Washington University
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Ligon, Marianne M; Mysorekar, Indira U (2018) Trans-mission control in the urinary tract: Local cytokine regulation of monocyte proliferation to combat infection. J Leukoc Biol 103:5-7
Wang, Caihong; Ross, Whitney Trotter; Mysorekar, Indira U (2017) Urothelial generation and regeneration in development, injury, and cancer. Dev Dyn 246:336-343
Ma, Emily; Vetter, Joel; Bliss, Laura et al. (2016) A multiplexed analysis approach identifies new association of inflammatory proteins in patients with overactive bladder. Am J Physiol Renal Physiol 311:F28-34
Bauckman, Kyle A; Mysorekar, Indira U (2016) Ferritinophagy drives uropathogenic Escherichia coli persistence in bladder epithelial cells. Autophagy 12:850-63