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Shear stress induces noncanonical autophagy in intestinal epithelial monolayers

Flow of fluids through the gut, such as milk from a neonatal diet, generates a shear stress on the unilaminar epithelium lining the lumen. We report that exposure to physiological levels of fluid shear stress leads to the formation of large vacuoles, containing extracellular contents within polarizi...

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Autores principales: Kim, Sun Wook, Ehrman, Jonathan, Ahn, Mok-Ryeon, Kondo, Jumpei, Lopez, Andrea A. Mancheno, Oh, Yun Sik, Kim, Xander H., Crawley, Scott W., Goldenring, James R., Tyska, Matthew J., Rericha, Erin C., Lau, Ken S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662261/
https://www.ncbi.nlm.nih.gov/pubmed/28855375
http://dx.doi.org/10.1091/mbc.E17-01-0021
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author Kim, Sun Wook
Ehrman, Jonathan
Ahn, Mok-Ryeon
Kondo, Jumpei
Lopez, Andrea A. Mancheno
Oh, Yun Sik
Kim, Xander H.
Crawley, Scott W.
Goldenring, James R.
Tyska, Matthew J.
Rericha, Erin C.
Lau, Ken S.
author_facet Kim, Sun Wook
Ehrman, Jonathan
Ahn, Mok-Ryeon
Kondo, Jumpei
Lopez, Andrea A. Mancheno
Oh, Yun Sik
Kim, Xander H.
Crawley, Scott W.
Goldenring, James R.
Tyska, Matthew J.
Rericha, Erin C.
Lau, Ken S.
author_sort Kim, Sun Wook
collection PubMed
description Flow of fluids through the gut, such as milk from a neonatal diet, generates a shear stress on the unilaminar epithelium lining the lumen. We report that exposure to physiological levels of fluid shear stress leads to the formation of large vacuoles, containing extracellular contents within polarizing intestinal epithelial cell monolayers. These observations lead to two questions: how can cells lacking primary cilia transduce shear stress, and what molecular pathways support the formation of vacuoles that can exceed 80% of the cell volume? We find that shear forces are sensed by actin-rich microvilli that eventually generate the apical brush border, providing evidence that these structures possess mechanosensing ability. Importantly, we identified the molecular pathway that regulates large vacuole formation downstream from mechanostimulation to involve central components of the autophagy pathway, including ATG5 and LC3, but not Beclin. Together our results establish a novel link between the actin-rich microvilli, the macroscopic transport of fluids across cells, and the noncanonical autophagy pathway in organized epithelial monolayers.
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spelling pubmed-56622612018-01-16 Shear stress induces noncanonical autophagy in intestinal epithelial monolayers Kim, Sun Wook Ehrman, Jonathan Ahn, Mok-Ryeon Kondo, Jumpei Lopez, Andrea A. Mancheno Oh, Yun Sik Kim, Xander H. Crawley, Scott W. Goldenring, James R. Tyska, Matthew J. Rericha, Erin C. Lau, Ken S. Mol Biol Cell Articles Flow of fluids through the gut, such as milk from a neonatal diet, generates a shear stress on the unilaminar epithelium lining the lumen. We report that exposure to physiological levels of fluid shear stress leads to the formation of large vacuoles, containing extracellular contents within polarizing intestinal epithelial cell monolayers. These observations lead to two questions: how can cells lacking primary cilia transduce shear stress, and what molecular pathways support the formation of vacuoles that can exceed 80% of the cell volume? We find that shear forces are sensed by actin-rich microvilli that eventually generate the apical brush border, providing evidence that these structures possess mechanosensing ability. Importantly, we identified the molecular pathway that regulates large vacuole formation downstream from mechanostimulation to involve central components of the autophagy pathway, including ATG5 and LC3, but not Beclin. Together our results establish a novel link between the actin-rich microvilli, the macroscopic transport of fluids across cells, and the noncanonical autophagy pathway in organized epithelial monolayers. The American Society for Cell Biology 2017-11-01 /pmc/articles/PMC5662261/ /pubmed/28855375 http://dx.doi.org/10.1091/mbc.E17-01-0021 Text en © 2017 Kim et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Kim, Sun Wook
Ehrman, Jonathan
Ahn, Mok-Ryeon
Kondo, Jumpei
Lopez, Andrea A. Mancheno
Oh, Yun Sik
Kim, Xander H.
Crawley, Scott W.
Goldenring, James R.
Tyska, Matthew J.
Rericha, Erin C.
Lau, Ken S.
Shear stress induces noncanonical autophagy in intestinal epithelial monolayers
title Shear stress induces noncanonical autophagy in intestinal epithelial monolayers
title_full Shear stress induces noncanonical autophagy in intestinal epithelial monolayers
title_fullStr Shear stress induces noncanonical autophagy in intestinal epithelial monolayers
title_full_unstemmed Shear stress induces noncanonical autophagy in intestinal epithelial monolayers
title_short Shear stress induces noncanonical autophagy in intestinal epithelial monolayers
title_sort shear stress induces noncanonical autophagy in intestinal epithelial monolayers
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662261/
https://www.ncbi.nlm.nih.gov/pubmed/28855375
http://dx.doi.org/10.1091/mbc.E17-01-0021
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