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Deciliation is associated with dramatic remodeling of epithelial cell junctions and surface domains
Journal article   Open access   Peer reviewed

Deciliation is associated with dramatic remodeling of epithelial cell junctions and surface domains

Christian E Overgaard, Kaitlin M Sanzone, Krystle S Spiczka, David R Sheff, Alexander Sandra and Charles Yeaman
Molecular biology of the cell, Vol.20(1), pp.102-113
01/2009
DOI: 10.1091/mbc.E08-07-0741
PMCID: PMC2613083
PMID: 19005211
url
https://doi.org/10.1091/mbc.E08-07-0741View
Published (Version of record) Open Access

Abstract

Stress-induced shedding of motile cilia (autotomy) has been documented in diverse organisms and likely represents a conserved cellular reaction. However, little is known about whether primary cilia are shed from mammalian epithelial cells and what impact deciliation has on polarized cellular organization. We show that several chemically distinct agents trigger autotomy in epithelial cells. Surprisingly, deciliation is associated with a significant, but reversible increase in transepithelial resistance. This reflects substantial reductions in tight junction proteins associated with "leaky" nephron segments (e.g., claudin-2). At the same time, apical trafficking of gp80/clusterin and gp114/CEACAM becomes randomized, basal-lateral delivery of Na,K-ATPase is reduced, and expression of the nonciliary apical protein gp135/podocalyxin is greatly decreased. However, ciliogenesis-impaired MDCK cells do not undergo continual junction remodeling, and mature cilia are not required for autotomy-associated remodeling events. Deciliation and epithelial remodeling may be mechanistically linked processes, because RNAi-mediated reduction of Exocyst subunit Sec6 inhibits ciliary shedding and specifically blocks deciliation-associated down-regulation of claudin-2 and gp135. We propose that ciliary autotomy represents a signaling pathway that impacts the organization and function of polarized epithelial cells.
Tight Junctions - metabolism Cell Line Cell Polarity Epithelial Cells - metabolism Membrane Glycoproteins - metabolism Calcium - metabolism Sialoglycoproteins - metabolism Cell Adhesion Molecules - metabolism Cilia - metabolism Antigens, CD - metabolism Clusterin - metabolism Animals Dogs Signal Transduction - physiology Biological Transport - physiology Epithelial Cells - cytology

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