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Aberrant cell migration contributes to defective airway epithelial repair in childhood wheeze
Thomas Iosifidis, Erika N. Sutanto, Alysia G. Buckley, Laura Coleman, Erin E. Gill, Amy H. Lee, Kak-Ming Ling, Jessica Hillas, Kevin Looi, Luke W. Garratt, Kelly M. Martinovich, Nicole C. Shaw, Samuel T. Montgomery, Elizabeth Kicic-Starcevich, Yuliya V. Karpievitch, Peter Le Souëf, Ingrid A. Laing, Shyan Vijayasekaran, Francis J. Lannigan, Paul J. Rigby, Robert E.W. Hancock, Darryl A. Knight, Stephen M. Stick, Anthony Kicic, Western Australian Epithelial Research Program (WAERP), Australian Respiratory Epithelium Consortium (AusREC)
Thomas Iosifidis, Erika N. Sutanto, Alysia G. Buckley, Laura Coleman, Erin E. Gill, Amy H. Lee, Kak-Ming Ling, Jessica Hillas, Kevin Looi, Luke W. Garratt, Kelly M. Martinovich, Nicole C. Shaw, Samuel T. Montgomery, Elizabeth Kicic-Starcevich, Yuliya V. Karpievitch, Peter Le Souëf, Ingrid A. Laing, Shyan Vijayasekaran, Francis J. Lannigan, Paul J. Rigby, Robert E.W. Hancock, Darryl A. Knight, Stephen M. Stick, Anthony Kicic, Western Australian Epithelial Research Program (WAERP), Australian Respiratory Epithelium Consortium (AusREC)
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Research Article Cell biology Pulmonology

Aberrant cell migration contributes to defective airway epithelial repair in childhood wheeze

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Abstract

Abnormal wound repair has been observed in the airway epithelium of patients with chronic respiratory diseases, including asthma. Therapies focusing on repairing vulnerable airways, particularly in early life, present a potentially novel treatment strategy. We report defective lower airway epithelial cell repair to strongly associate with common pre–school-aged and school-aged wheezing phenotypes, characterized by aberrant migration patterns and reduced integrin α5β1 expression. Next generation sequencing identified the PI3K/Akt pathway as the top upstream transcriptional regulator of integrin α5β1, where Akt activation enhanced repair and integrin α5β1 expression in primary cultures from children with wheeze. Conversely, inhibition of PI3K/Akt signaling in primary cultures from children without wheeze reduced α5β1 expression and attenuated repair. Importantly, the FDA-approved drug celecoxib — and its non–COX2-inhibiting analogue, dimethyl-celecoxib — stimulated the PI3K/Akt–integrin α5β1 axis and restored airway epithelial repair in cells from children with wheeze. When compared with published clinical data sets, the identified transcriptomic signature was also associated with viral-induced wheeze exacerbations highlighting the clinical potential of such therapy. Collectively, these results identify airway epithelial restitution via targeting the PI3K–integrin α5β1 axis as a potentially novel therapeutic avenue for childhood wheeze and asthma. We propose that the next step in the therapeutic development process should be a proof-of-concept clinical trial, since relevant animal models to test the crucial underlying premise are unavailable.

Authors

Thomas Iosifidis, Erika N. Sutanto, Alysia G. Buckley, Laura Coleman, Erin E. Gill, Amy H. Lee, Kak-Ming Ling, Jessica Hillas, Kevin Looi, Luke W. Garratt, Kelly M. Martinovich, Nicole C. Shaw, Samuel T. Montgomery, Elizabeth Kicic-Starcevich, Yuliya V. Karpievitch, Peter Le Souëf, Ingrid A. Laing, Shyan Vijayasekaran, Francis J. Lannigan, Paul J. Rigby, Robert E.W. Hancock, Darryl A. Knight, Stephen M. Stick, Anthony Kicic, Western Australian Epithelial Research Program (WAERP), Australian Respiratory Epithelium Consortium (AusREC)

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Figure 1

Defective cell migration of leading edge cells in pAEC of children with wheeze.

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Defective cell migration of leading edge cells in pAEC of children with ...
(A) Cultures from children without wheeze had the capacity to repair by 72 hours after wounding. (B) In contrast, cultures from children with wheeze failed to close the wound by 96 hours after wounding. (C) Leading edge pAEC of children without wheeze responded to the scratch wounding stimulus by migrating directionally, toward the center of the wound site. (D) Leading edge pAEC of children with wheeze showed a dysregulated response to wounding, where some cells migrated into the wound site in an uncoordinated manner and other cells did not migrate very far into the wound and even migrated backward into the leading edge. The green dot represents the mean center of mass of the endpoints of all tracked cells. (E and F) Leading edge pAEC from children without wheeze migrated far (E) and fast (F) into the wound site by 10 hours after wounding, although response to wounding was varied. However, leading edge cells of children with wheeze migrated shorter average distances (E) and at slower velocity (F) than their nonwheezing counterparts (P < 0.050). (G and H) Notably, leading edge cells of children without wheeze migrated directionally (G) and collectively into the center of the wound, as shown with high y axis forward migration index (yFMI) values (H). Conversely, leading edge pAEC of children with wheeze demonstrated migration trajectories with significantly less directionality (G) and yFMI (H), indicating a loss of coordination in their response to wounding. Cell migration trajectory data were generated from 296 and 228 leading edge cell tracks of children with wheeze (n = 14) and without wheeze (n = 9), respectively. All experiments were completed in 2 technical replicates. The data were represented as median ± IQR, *P < 0.050, Mann-Whitney U test.

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