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PMID: 3463968 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Mechanosensitivity of cultured ciliated cells from the mammalian respiratory tract: implications for the regulation of mucociliary transport.

Sanderson MJ, Dirksen ER

Abstract

Mechanical stimulation of the cell surface or cilia of cultured ciliated epithelial cells derived from the rabbit tracheal mucosa resulted in a transitory ciliary beat frequency increase of 20% or more. This response was composed of a lag, rise, and recovery phase. The duration of the response, but not the maximal frequency, was increased by stronger stimulation. The ability of these ciliated cells to respond to stimulation depended on culture age; generally, cultures younger than 4 days were insensitive. The frequency response was transmitted to adjacent and more distal cells in all directions. The lag phase but not the rise time of the adjacent cell response was extended. These ciliary responses were lost when extracellular Ca2+ was removed. Replacement of Ca2+ resulted in a restoration of mechanosensitivity. In 1 mM verapamil and Ca2+ the frequency response was also lost. These results suggest that the frequency response is dependent on Ca2+ influx (although its intracellular action is unknown) and imply that mucociliary clearance is a localized self-regulating process.

MeSH Terms
Animals Calcium/physiology Cell Communication Cell Survival Cilia/drug effects,physiology Culture Techniques Epithelium/physiology Microscopy, Electron, Scanning Mucus/physiology Rabbits Stress, Mechanical Trachea/physiology Verapamil/pharmacology
Chemicals
Verapamil Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sanderson M J
Dirksen E R
References (13)
13 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1986-10-00
Pages
7302-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC386704
Subset
IM
Grants
NICHD NIH HHS · HD-11792 · United States
NHLBI NIH HHS · HL-23428 · United States
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