EphA4-ADAM10 Interplay Patterns the Cochlear Sensory Epithelium through Local Disruption of Adherens Junctions
Summary: The cochlear sensory epithelium contains a functionally important triangular fluid-filled space between adjacent pillar cells referred to as the tunnel of Corti. However, the molecular mechanisms leading to local cell-cell separation during development remain elusive. Here we show that EphA...
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doaj-20e0ac31ca164c319ce20a4c12f6ec422020-11-24T22:00:42ZengElsevieriScience2589-00422019-01-0111246257EphA4-ADAM10 Interplay Patterns the Cochlear Sensory Epithelium through Local Disruption of Adherens JunctionsJean Defourny0Christiane Peuckert1Klas Kullander2Brigitte Malgrange3GIGA-Neurosciences, Unit of Cell and Tissue Biology, University of Liège, C.H.U. B36, 4000 Liège, Belgium; GIGA-Neurosciences, Developmental Neurobiology Unit, University of Liège, C.H.U. B36, 4000 Liège, BelgiumDepartment of Neuroscience, Uppsala University, Box 593, Uppsala 75124, SwedenDepartment of Neuroscience, Uppsala University, Box 593, Uppsala 75124, SwedenGIGA-Neurosciences, Developmental Neurobiology Unit, University of Liège, C.H.U. B36, 4000 Liège, Belgium; Corresponding authorSummary: The cochlear sensory epithelium contains a functionally important triangular fluid-filled space between adjacent pillar cells referred to as the tunnel of Corti. However, the molecular mechanisms leading to local cell-cell separation during development remain elusive. Here we show that EphA4 associates with ADAM10 to promote the destruction of E-cadherin-based adhesions between adjacent pillar cells. These cells fail to separate from each other, and E-cadherin abnormally persists at the pillar cell junction in EphA4 forward-signaling-deficient mice, as well as in the presence of ADAM10 inhibitor. Using immunolabeling and an in situ proximity ligation assay, we found that EphA4 forms a complex with E-cadherin and its sheddase ADAM10, which could be activated by ephrin-B2 across the pillar cell junction to trigger the cleavage of E-cadherin. Altogether, our findings provide a new molecular insight into the regulation of adherens junctions, which might be extended to a variety of physiological or pathological processes. : Physiology; Cell Biology; Developmental Biology Subject Areas: Physiology, Cell Biology, Developmental Biologyhttp://www.sciencedirect.com/science/article/pii/S2589004218302475 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jean Defourny Christiane Peuckert Klas Kullander Brigitte Malgrange |
spellingShingle |
Jean Defourny Christiane Peuckert Klas Kullander Brigitte Malgrange EphA4-ADAM10 Interplay Patterns the Cochlear Sensory Epithelium through Local Disruption of Adherens Junctions iScience |
author_facet |
Jean Defourny Christiane Peuckert Klas Kullander Brigitte Malgrange |
author_sort |
Jean Defourny |
title |
EphA4-ADAM10 Interplay Patterns the Cochlear Sensory Epithelium through Local Disruption of Adherens Junctions |
title_short |
EphA4-ADAM10 Interplay Patterns the Cochlear Sensory Epithelium through Local Disruption of Adherens Junctions |
title_full |
EphA4-ADAM10 Interplay Patterns the Cochlear Sensory Epithelium through Local Disruption of Adherens Junctions |
title_fullStr |
EphA4-ADAM10 Interplay Patterns the Cochlear Sensory Epithelium through Local Disruption of Adherens Junctions |
title_full_unstemmed |
EphA4-ADAM10 Interplay Patterns the Cochlear Sensory Epithelium through Local Disruption of Adherens Junctions |
title_sort |
epha4-adam10 interplay patterns the cochlear sensory epithelium through local disruption of adherens junctions |
publisher |
Elsevier |
series |
iScience |
issn |
2589-0042 |
publishDate |
2019-01-01 |
description |
Summary: The cochlear sensory epithelium contains a functionally important triangular fluid-filled space between adjacent pillar cells referred to as the tunnel of Corti. However, the molecular mechanisms leading to local cell-cell separation during development remain elusive. Here we show that EphA4 associates with ADAM10 to promote the destruction of E-cadherin-based adhesions between adjacent pillar cells. These cells fail to separate from each other, and E-cadherin abnormally persists at the pillar cell junction in EphA4 forward-signaling-deficient mice, as well as in the presence of ADAM10 inhibitor. Using immunolabeling and an in situ proximity ligation assay, we found that EphA4 forms a complex with E-cadherin and its sheddase ADAM10, which could be activated by ephrin-B2 across the pillar cell junction to trigger the cleavage of E-cadherin. Altogether, our findings provide a new molecular insight into the regulation of adherens junctions, which might be extended to a variety of physiological or pathological processes. : Physiology; Cell Biology; Developmental Biology Subject Areas: Physiology, Cell Biology, Developmental Biology |
url |
http://www.sciencedirect.com/science/article/pii/S2589004218302475 |
work_keys_str_mv |
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