A comparative study of the turnover of multiciliated cells in the mouse trachea, oviduct, and brain

Background In mammals, multiciliated cells (MCCs) line the lumen of the trachea, oviduct, and brain ventricles, where they drive fluid flow across the epithelium. Each MCC population experiences vastly different local environments that may dictate differences in their lifetime and turnover rates. Ho...

Full description

Saved in:
Bibliographic Details
Published in:Developmental dynamics Vol. 249; no. 7; pp. 898 - 905
Main Authors: Roberson, Elle C., Tran, Ngan K., Konjikusic, Mia J., Fitch, Rebecca D., Gray, Ryan S., Wallingford, John B.
Format: Journal Article
Language:English
Published: Hoboken, USA John Wiley & Sons, Inc 01-07-2020
Wiley Subscription Services, Inc
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Background In mammals, multiciliated cells (MCCs) line the lumen of the trachea, oviduct, and brain ventricles, where they drive fluid flow across the epithelium. Each MCC population experiences vastly different local environments that may dictate differences in their lifetime and turnover rates. However, with the exception of MCCs in the trachea, the turnover rates of these multiciliated epithelial populations at extended time scales are not well described. Results Here, using genetic lineage‐labeling techniques we provide a direct comparison of turnover rates of MCCs in these three different tissues. Conclusion We find that oviduct turnover is similar to that in the airway (~6 months), while multiciliated ependymal cells turnover more slowly.
Bibliography:Funding information
Eunice Kennedy Shriver National Institute of Child Health and Human Development, Grant/Award Numbers: F32HD095618, HD085901; National Heart, Lung, and Blood Institute, Grant/Award Number: HL117164; NIAMS; Provost Graduate Excellence Fellowship through the Institute of Cell and Molecular Biology at the University of Texas at Austin; TIDES Summer Fellowship Program from the University of Texas at Austin
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
These authors contributed equally
ISSN:1058-8388
1097-0177
DOI:10.1002/dvdy.165