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Corrigendum Free access | 10.1172/JCI82138

CGRP induction in cystic fibrosis airways alters the submucosal gland progenitor cell niche in mice

Weiliang Xie, John T. Fisher, Thomas J. Lynch, Meihui Luo, Turan I.A. Evans, Traci L. Neff, Weihong Zhou, Yulong Zhang, Yi Ou, Nigel W. Bunnett, Andrew F. Russo, Michael J. Goodheart, Kalpaj R. Parekh, Xiaoming Liu, and John F. Engelhardt

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Published May 1, 2015 - More info

Published in Volume 125, Issue 5 on May 1, 2015
J Clin Invest. 2015;125(5):2179–2179. https://doi.org/10.1172/JCI82138.
Copyright © 2015, American Society for Clinical Investigation
Published May 1, 2015 - Version history
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Related article:

CGRP induction in cystic fibrosis airways alters the submucosal gland progenitor cell niche in mice
Weiliang Xie, … , Xiaoming Liu, John F. Engelhardt
Weiliang Xie, … , Xiaoming Liu, John F. Engelhardt
Research Article Article has an altmetric score of 3

CGRP induction in cystic fibrosis airways alters the submucosal gland progenitor cell niche in mice

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Abstract

In cystic fibrosis (CF), a lack of functional CF transmembrane conductance regulator (CFTR) chloride channels causes defective secretion by submucosal glands (SMGs), leading to persistent bacterial infection that damages airways and necessitates tissue repair. SMGs are also important niches for slow-cycling progenitor cells (SCPCs) in the proximal airways, which may be involved in disease-related airway repair. Here, we report that calcitonin gene–related peptide (CGRP) activates CFTR-dependent SMG secretions and that this signaling pathway is hyperactivated in CF human, pig, ferret, and mouse SMGs. Since CGRP-expressing neuroendocrine cells reside in bronchiolar SCPC niches, we hypothesized that the glandular SCPC niche may be dysfunctional in CF. Consistent with this hypothesis, CFTR-deficient mice failed to maintain glandular SCPCs following airway injury. In wild-type mice, CGRP levels increased following airway injury and functioned as an injury-induced mitogen that stimulated SMG progenitor cell proliferation in vivo and altered the proliferative potential of airway progenitors in vitro. Components of the receptor for CGRP (RAMP1 and CLR) were expressed in a very small subset of SCPCs, suggesting that CGRP indirectly stimulates SCPC proliferation in a non-cell-autonomous manner. These findings demonstrate that CGRP-dependent pathways for CFTR activation are abnormally upregulated in CF SMGs and that this sustained mitogenic signal alters properties of the SMG progenitor cell niche in CF airways. This discovery may have important implications for injury/repair mechanisms in the CF airway.

Authors

Weiliang Xie, John T. Fisher, Thomas J. Lynch, Meihui Luo, Turan I.A. Evans, Traci L. Neff, Weihong Zhou, Yulong Zhang, Yi Ou, Nigel W. Bunnett, Andrew F. Russo, Michael J. Goodheart, Kalpaj R. Parekh, Xiaoming Liu, John F. Engelhardt

×

Original citation: J Clin Invest. 2011;121(8):3144–3158. doi:10.1172/JCI41857.

Citation for this corrigendum: J Clin Invest. 2015;125(5):2179. doi:10.1172/JCI82138.

During the preparation of this manuscript, the labels for the data lines in Figure 5, C and D, were inadvertently switched. The correct figure parts are below.

The authors regret the error.

Footnotes

See the related article beginning on page 3144.

Version history
  • Version 1 (May 1, 2015): No description

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