Mechanotransduction activates RhoA in the neighbors of apoptotic epithelial cells to engage apical extrusion
Date
2021
Authors
Duszyc, K.
Gomez, G.A.
Lagendijk, A.K.
Yau, M.K.
Nanavati, B.N.
Gliddon, B.L.
Hall, T.E.
Verma, S.
Hogan, B.M.
Pitson, S.M.
Editors
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Journal article
Citation
Current Biology, 2021; 31(6):1326-1336
Statement of Responsibility
Kinga Duszyc, Guillermo A. Gomez, Anne K. Lagendijk, Mei-Kwan Yau, Bageshri Naimish Nanavati, Briony L. Gliddon ... et al.
Conference Name
Abstract
Epithelia must eliminate apoptotic cells to preserve tissue barriers and prevent inflammation.1 Several different mechanisms exist for apoptotic clearance, including efferocytosis2,3 and apical extrusion.4,5 We found that extrusion was the first-line response to apoptosis in cultured monolayers and in zebrafish epidermis. During extrusion, the apoptotic cell elicited active lamellipodial protrusions and assembly of a contractile extrusion ring in its neighbors. Depleting E-cadherin compromised both the contractile ring and extrusion, implying that a cadherin-dependent pathway allows apoptotic cells to engage their neighbors for extrusion. We identify RhoA as the cadherin-dependent signal in the neighbor cells and show that it is activated in response to contractile tension from the apoptotic cell. This mechanical stimulus is conveyed by a myosin-VI-dependent mechanotransduction pathway that is necessary both for extrusion and to preserve the epithelial barrier when apoptosis was stimulated. Earlier studies suggested that release of sphingosine-1-phosphate (S1P) from apoptotic cells might define where RhoA was activated. However, we found that, although S1P is necessary for extrusion, its contribution does not require a localized source of S1P in the epithelium. We therefore propose a unified view of how RhoA is stimulated to engage neighbor cells for apoptotic extrusion. Here, tension-sensitive mechanotransduction is the proximate mechanism that activates RhoA specifically in the immediate neighbors of apoptotic cells, but this also must be primed by S1P in the tissue environment. Together, these elements provide a coincidence detection system that confers robustness on the extrusion response.
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© 2021 Elsevier Inc.
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http://purl.org/au-research/grants/nhmrc/1123816
http://purl.org/au-research/grants/nhmrc/1164462
http://purl.org/au-research/grants/nhmrc/1136592
http://purl.org/au-research/grants/nhmrc/1155221
http://purl.org/au-research/grants/nhmrc/1156693
http://purl.org/au-research/grants/nhmrc/1117017
http://purl.org/au-research/grants/nhmrc/1150083
http://purl.org/au-research/grants/nhmrc/1140064
http://purl.org/au-research/grants/arc/CE140100036
http://purl.org/au-research/grants/arc/CE140100011
http://purl.org/au-research/grants/arc/DP180103244
http://purl.org/au-research/grants/arc/DP19010287
http://purl.org/au-research/grants/nhmrc/1164462
http://purl.org/au-research/grants/nhmrc/1136592
http://purl.org/au-research/grants/nhmrc/1155221
http://purl.org/au-research/grants/nhmrc/1156693
http://purl.org/au-research/grants/nhmrc/1117017
http://purl.org/au-research/grants/nhmrc/1150083
http://purl.org/au-research/grants/nhmrc/1140064
http://purl.org/au-research/grants/arc/CE140100036
http://purl.org/au-research/grants/arc/CE140100011
http://purl.org/au-research/grants/arc/DP180103244
http://purl.org/au-research/grants/arc/DP19010287