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CC16 Deficiency in the Context of Early-Life Mycoplasma pneumoniae Infection Results in Augmented Airway Responses in Adult Mice.
CC16 Deficiency in the Context of Early-Life Mycoplasma pneumoniae Infection Results in Augmented Airway Responses in Adult Mice.
- Source :
-
Infection and immunity [Infect Immun] 2022 Feb 17; Vol. 90 (2), pp. e0054821. Date of Electronic Publication: 2021 Nov 15. - Publication Year :
- 2022
-
Abstract
- Studies have shown that club cell secretory protein (CC16) plays important protective roles in the lungs, yet its complete biological functions are unclear. We devised a translational mouse model in order to investigate the impact of early life infections, in the context of CC16 deficiency, on lung function in adult mice. CC16 sufficient (WT) and deficient (CC16 <superscript>-/-</superscript> ) mice were infected with Mycoplasma pneumoniae (Mp) as weanlings and assessed as adults ( e arly l ife i nfection m odel; ELIM) and compared to adult mice infected for only 3 days ( a dult i nfection m odel; AIM). CC16 <superscript>-/-</superscript> Mp-infected mice had significantly increased airway hyperresponsiveness (AHR) in both models compared to WT mice. However, CC16 <superscript>-/-</superscript> mice infected in early life (ELIM) displayed significantly increased AHR compared to CC16 <superscript>-/-</superscript> mice infected in adulthood (AIM). In stark contrast, lung function in ELIM WT mice returned to levels similar to saline-treated controls. While WT mice cleared Mp infection in the ELIM, CC16 <superscript>-/-</superscript> mice remained colonized with Mp throughout the model, which likely contributed to increased airway remodeling and persistence of Muc5ac expression. When CC16 <superscript>-/-</superscript> mouse tracheal epithelial cells (MTECs) were infected with Mp, increased Mp colonization and collagen gene expression were also detected compared to WT cells, suggesting that CC16 plays a protective role during Mp infection, in part through epithelial-driven host defense mechanisms.
Details
- Language :
- English
- ISSN :
- 1098-5522
- Volume :
- 90
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Infection and immunity
- Publication Type :
- Academic Journal
- Accession number :
- 34780280
- Full Text :
- https://doi.org/10.1128/IAI.00548-21