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Recurrent infections drive persistent bladder dysfunction and pain via sensory nerve sprouting and mast cell activity

Title
Recurrent infections drive persistent bladder dysfunction and pain via sensory nerve sprouting and mast cell activity
Authors
HayesByron W.ChoiHae WoongRathoreAbhay P.S.BaoChunjingShiJianlingHuhYulKimMichael W.MencarelliAndreaBistPradeepNgChangmingNhoJoo HwanAramYoonHanaLimDonghoonHannanJohanna L.PurvesJ. ToddHughesFrancis M.Ru-RongJ.AbrahamSoman N.Lai Guan
Ewha Authors
윤하나
SCOPUS Author ID
윤하나scopus
Issue Date
2024
Journal Title
Science Immunology
ISSN
2470-9468JCR Link
Citation
Science Immunology vol. 9, no. 93
Publisher
American Association for the Advancement of Science
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
Urinary tract infections (UTIs) account for almost 25% of infections in women. Many are recurrent (rUTI), with patients frequently experiencing chronic pelvic pain and urinary frequency despite clearance of bacteriuria after antibiotics. To elucidate the basis for these bacteria-independent bladder symptoms, we examined the bladders of patients with rUTI. We noticed a notable increase in neuropeptide content in the lamina propria and indications of enhanced nociceptive activity. In mice subjected to rUTI, we observed sensory nerve sprouting that was associated with nerve growth factor (NGF) produced by recruited monocytes and tissue-resident mast cells. Treatment of rUTI mice with an NGF-neutralizing antibody prevented sprouting and alleviated pelvic sensitivity, whereas instillation of native NGF into naïve mice bladders mimicked nerve sprouting and pain behavior. Nerve activation, pain, and urinary frequency were each linked to the presence of proximal mast cells, because mast cell deficiency or treatment with antagonists against receptors of several direct or indirect mast cell products was each effective therapeutically. Thus, our findings suggest that NGF-driven sensory sprouting in the bladder coupled with chronic mast cell activation represents an underlying mechanism driving bacteria-independent pain and voiding defects experienced by patients with rUTI. © 2024 the authors, some rights reserved; exclusive licensee american association for the advancement of Science. no claim to original u.S. government Works.
DOI
10.1126/sciimmunol.adi5578
Appears in Collections:
의과대학 > 의학과 > Journal papers
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