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Ureaplasma-driven neonatal neuroinflammation: novel insights from an ovine model

Please always quote using this URN: urn:nbn:de:bvb:20-opus-324285
  • Ureaplasma species (spp.) are considered commensals of the adult genitourinary tract, but have been associated with chorioamnionitis, preterm birth, and invasive infections in neonates, including meningitis. Data on mechanisms involved in Ureaplasma-driven neuroinflammation are scarce. The present study addressed brain inflammatory responses in preterm lambs exposed to Ureaplasma parvum (UP) in utero. 7 days after intra-amniotic injection of UP (n = 10) or saline (n = 11), lambs were surgically delivered at gestational day 128–129. ExpressionUreaplasma species (spp.) are considered commensals of the adult genitourinary tract, but have been associated with chorioamnionitis, preterm birth, and invasive infections in neonates, including meningitis. Data on mechanisms involved in Ureaplasma-driven neuroinflammation are scarce. The present study addressed brain inflammatory responses in preterm lambs exposed to Ureaplasma parvum (UP) in utero. 7 days after intra-amniotic injection of UP (n = 10) or saline (n = 11), lambs were surgically delivered at gestational day 128–129. Expression of inflammatory markers was assessed in different brain regions using qRT-PCR and in cerebrospinal fluid (CSF) by multiplex immunoassay. CSF was analyzed for UP presence using ureB-based real-time PCR, and MRI scans documented cerebral white matter area and cortical folding. Cerebral tissue levels of atypical chemokine receptor (ACKR) 3, caspases 1-like, 2, 7, and C–X–C chemokine receptor (CXCR) 4 mRNA, as well as CSF interleukin-8 protein concentrations were significantly increased in UP-exposed lambs. UP presence in CSF was confirmed in one animal. Cortical folding and white matter area did not differ among groups. The present study confirms a role of caspases and the transmembrane receptors ACKR3 and CXCR4 in Ureaplasma-driven neuroinflammation. Enhanced caspase 1-like, 2, and 7 expression may reflect cell death. Increased ACKR3 and CXCR4 expression has been associated with inflammatory central nervous system (CNS) diseases and impaired blood–brain barrier function. According to these data and previous in vitro findings from our group, we speculate that Ureaplasma-induced caspase and receptor responses affect CNS barrier properties and thus facilitate neuroinflammation.show moreshow less

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Metadaten
Author: Christine SilwedelORCiD, Matthias C. Hütten, Christian P. Speer, Christoph HärtelORCiD, Axel HaarmannORCiD, Birgit Henrich, Maud P. M. Tijssen, Abdullah Ahmed Alnakhli, Owen B. Spiller, Nicolas SchlegelORCiD, Silvia SeidenspinnerORCiD, Boris W. Kramer, Kirsten Glaser
URN:urn:nbn:de:bvb:20-opus-324285
Document Type:Journal article
Faculties:Medizinische Fakultät / Klinik und Poliklinik für Allgemein-, Viszeral-, Gefäß- und Kinderchirurgie (Chirurgische Klinik I)
Medizinische Fakultät / Kinderklinik und Poliklinik
Medizinische Fakultät / Neurologische Klinik und Poliklinik
Language:English
Parent Title (English):Cellular and Molecular Neurobiology
Year of Completion:2023
Volume:43
Issue:2
Pagenumber:785-795
Source:Cellular and Molecular Neurobiology (2023) 43:2, 785-795 DOI: 10.1007/s10571-022-01213-8
DOI:https://doi.org/10.1007/s10571-022-01213-8
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Tag:CNS integrity; Ureaplasma parvum; animal model; immaturity; neonatal meningitis; preterm birth
Release Date:2024/02/20
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International