scholarly journals Transient active osmotic swelling of epithelium upon curvature induction

2020 ◽  
Author(s):  
Caterina Tomba ◽  
Valeriy Luchnikov ◽  
Luca Barberi ◽  
Carles Blanch-Mercader ◽  
Aurélien Roux

Generation of tissue curvature is essential to morphogenesis. However, how cells adapt to changing curvature is still unknown because tools to dynamically control curvature in vitro are lacking. Here we developed self-rolling substrates to study how flat epithelial cell monolayers adapt to a rapid, anisotropic change of curvature. We show that the primary response is an active and transient osmotic swelling of cells. This cell volume increase is not observed on inducible wrinkled substrates, where concave and convex regions alternate each other over short distances, identifying swelling as a collective response to changes of curvature with persistent sign over large distances. It is triggered by a drop in membrane tension and actin depolymerization, perceived by cells as a hypertonic shock. Osmotic swelling restores tension while actin reorganizes, probably to comply with curvature. Epithelia are thus unique materials that transiently, actively swell while adapting to large curvature induction.

2000 ◽  
Vol 12 (6) ◽  
pp. 237 ◽  
Author(s):  
L. Gillan ◽  
G. Evans ◽  
W. M. C. Maxwell

In order to investigate the interaction of fresh and frozen–thawed spermatozoa with oviduct epithelial cells, spermatozoa were co-incubated with ovine oviduct epithelial cell monolayers (OECM) derived from either complete oviducts, at any stage of the oestrous cycle (Experiments 1 and 2), or from different regions of the oviduct at different stages of the cycle (Experiment 3). Fresh and frozen—thawed spermatozoa displayed different patterns of binding to, and release from, the OECM. Frozen—thawed spermatozoa immediately bound to the complete oviduct OECM and were released after 2 h. A small proportion of fresh spermatozoa bound immediately, increasing to a maximum after 2 h, and were gradually released thereafter. When only the cells that were released from the OECM were observed by chlortetracycline staining in Experiment 2, it was found that the presence of an OECM increased the number of capacitated fresh spermatozoa while decreasing the number of capacitated frozen–thawed spermatozoa. Overall, the OECM advanced the membrane state of both types of spermatozoa from uncapacitated to acrosome-reacted. Fresh and frozen—thawed spermatozoa bound to OECM derived from the cells of the isthmus and the ampulla in similar proportions. However, more spermatozoa were capacitated when incubated with OECM derived from isthmic rather than ampullary cells. Higher proportions of fresh spermatozoa bound to, and were acrosome-reacted following incubation with OECM derived from post- rather than pre-ovulatory tracts. Such differences were not observed for frozen—thawed spermatozoa. The findings reported in this study show that fresh and frozen—thawed spermatozoa behave differently when in contact with oviduct cells in vitro. This may be a consequence of the more advanced membrane state of the frozen spermatozoa upon thawing.


Cytometry ◽  
2003 ◽  
Vol 53A (1) ◽  
pp. 1-8 ◽  
Author(s):  
Asifa S. Haider ◽  
Jerzy Grabarek ◽  
Ben Eng ◽  
Paulina Pedraza ◽  
Nicholas R. Ferreri ◽  
...  

2017 ◽  
Vol 7 (12) ◽  
pp. 1170-1177 ◽  
Author(s):  
Mahnaz Ramezanpour ◽  
Jae Murphy ◽  
Jason L.P. Smith ◽  
Sarah Vreugde ◽  
Alkis James Psaltis

1989 ◽  
Vol 31 (1) ◽  
pp. 197 ◽  
Author(s):  
L.L. Goodeaux ◽  
S.A. Voelkel ◽  
C.A. Anzalone ◽  
Y. Menezo ◽  
K.H. Graves

2005 ◽  
Vol 31 (12) ◽  
pp. 1701-1706 ◽  
Author(s):  
Gemma E. Hill ◽  
Steven Fenwick ◽  
Bridget J. Matthews ◽  
Robin A. Chivers ◽  
Jennifer Southgate

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