EventsCells, Cells and Nothing but Cells: Discoveries, Challenges and Directions
Published
This submission belongs to the session CELLS_S7. Cell Motility and Adhesion of the event Cells, Cells and Nothing but Cells: Discoveries, Challenges and Directions
Published date
07 Feb, 2023
Academic Editor
author-avatarAlexander E. Kalyuzhny
Citation
Marika Berardini, Luisa Gesualdi, Francesca Ferranti, Maria Addolorata Mariggiò, Caterina Morabito, Simone Guarnieri, Giulia Ricci, Angela Catizone, Microgravity exposure alterations of cellular junctions proteins in TCam-2 cells: localization and interaction, in Proceedings of Cells, Cells and Nothing but Cells: Discoveries, Challenges and Directions, 6 March–8 March 2023, MDPI: Basel, Switzerland
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Microgravity exposure alterations of cellular junctions proteins in TCam-2 cells: localization and interaction

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1. Dept of Anatomy, Histology, Forensic-Medicine and Orthopedics, Section of Histology and Embryology, “Sapienza” University of Rome, Rome, Italy
2. Human Spaceflight and Scientific Research Unit, Italian Space Agency, Rome, Italy
3. Dept of Neuroscience, Imaging and Clinical Sciences-CAST, “G. d’Annunzio” University of Chieti-Pescara, Chieti, Italy
4. Dept of Experimental Medicine, Università degli Studi della Campania “Luigi Vanvitelli”, Naples, Italy
Abstract

One of the most important hazards of space environment is microgravity, which causes alteration in the physiology of different systems, including the reproductive one. It is widely accepted that cytoskeleton is the microgravity-sensitive apparatus of the cells, and that cytoskeletal modifications are responsible of microgravity-triggered cell alterations. We established a 3D free floating culture system from TCam2 cell, a human seminoma cell line, and then exposed the obtained TCam2 spheroids for 24h at unitary gravity (UG) or under simulated microgravity condition (SM), by using the Random Position Machine (RPM). We tested cytoskeletal and junctional features of these samples by western blot and confocal microscopy analysis to elucidate the impact of microgravity on adherent and occluding junctions of TCam2 spheroids. The junctional ultrastructure was studied by Transmission electron microscopy (TEM).
TEM analysis revealed the presence of occluding junctions both in UG or SM samples. Even if western blot revealed no quantitative difference of actin and occludin proteins both in UG and SM exposed samples, fluorescence colocalization analysis showed a significative increase of colocalization area of occludin and actin proteins in the superficial layer of TCam2 spheroids grown in RPM conditions. This result let us speculate that tight junction functionality is different id UG and SM exposed spheroids.
As far as adherent junctions is concerned, TEM analysis revealed adherent junctions both in UG or SM samples. Moreover, we observed by western blot a trend in increase of vimentin expression in SM exposed spheroids. Confocal microscopy analyses confirm this significant increase..
All together these data suggest that simulated microgravity conditions in TCam2 spheroids alters tight junction assembly, while the increase in intermediate filaments structures can in part be associated with an enrichment in adherent junctions. Functional investigation are needed to deeper clarify this hypothesis.

Keywords
Microgravity
Cytoskeleton
TCam2 cell
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