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Published Erratum
. 2022 Oct 1;323(4):R483.
doi: 10.1152/ajpregu.00270.2017_cor.

Corrigendum for Alexander et al., volume 314, 2018, p. R834-R847

No authors listed
Published Erratum

Corrigendum for Alexander et al., volume 314, 2018, p. R834-R847

No authors listed. Am J Physiol Regul Integr Comp Physiol. .
No abstract available

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Figures

Figure 3.
Figure 3.
Mice that inhaled EV for an hour daily had inflammatory changes only at the protein level. A: lung parenchyma was stained with hematoxylin and eosin (H&E) and Masson’s trichrome stains. One lung slice per mouse, including large, medium, and small airways, was evaluated by a blinded pathologist, and no pulmonary inflammation, emphysema, or fibrosis was found in EV mice relative to air controls (n = 6/group). B: the airways of mice, as measured through bronchoalveolar lavage (BAL), had alterations in the inflammatory cytokine profile. BAL was pooled within EV and air control groups (n = 6 within groups) and was evaluated by 111-cytokine antibody array (Proteome Profiler Mouse XL Array; R&D Systems) and graphed as a ratio of EV/air. BAL from EV mice had decreased levels of LIX (murine version of IL-8; 519-fold lower or ∼0.2% of air levels) and VCAM-1 (99-fold lower or 1% of air levels). EV BAL had increased levels of DPPIV (1.7-fold or 58% higher than air levels).
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