Morphological Changes of 3T3 Cells under Simulated Microgravity

Author:

Tran Minh Thi1,Ho Chi Nguyen Quynh23,Hoang Son Nghia23,Doan Chung Chinh23,Nguyen Minh Thai2,Van Huy Duc2ORCID,Ly Cang Ngoc2,Le Cuong Phan Minh2,Hoang Huy Nghia Quang23,Nguyen Han Thai Minh24ORCID,Truong Han Thi5,To Quan Minh6,Nguyen Tram Thi Thuy27,Le Long Thanh23ORCID

Affiliation:

1. Faculty of Applied Technology, School of Technology, Van Lang University, Ho Chi Minh City 70000, Vietnam

2. Animal Biotechnology Department, Institute of Tropical Biology, Vietnam Academy of Science and Technology, Ho Chi Minh City 70000, Vietnam

3. Biotechnology Department, Graduate University of Science and Technology, Vietnam Academy of Science and Technology, Ha Noi City 100000, Vietnam

4. Biotechnology Innovation Center, University of New Hampshire, Manchester, NH 03101, USA

5. Department of Biophysics, Sungkyunkwan University, Suwon 16419, Republic of Korea

6. Faculty of Biology and Biotechnology, University of Science, Ho Chi Minh City 70000, Vietnam

7. Faculty of General Biomedical, University of Physical Education and Sport, Ho Chi Minh City 70000, Vietnam

Abstract

Background: Cells are sensitive to changes in gravity, especially the cytoskeletal structures that determine cell morphology. The aim of this study was to assess the effects of simulated microgravity (SMG) on 3T3 cell morphology, as demonstrated by a characterization of the morphology of cells and nuclei, alterations of microfilaments and microtubules, and changes in cycle progression. Methods: 3T3 cells underwent induced SMG for 72 h with Gravite®, while the control group was under 1G. Fluorescent staining was applied to estimate the morphology of cells and nuclei and the cytoskeleton distribution of 3T3 cells. Cell cycle progression was assessed by using the cell cycle app of the Cytell microscope, and Western blot was conducted to determine the expression of the major structural proteins and main cell cycle regulators. Results: The results show that SMG led to decreased nuclear intensity, nuclear area, and nuclear shape and increased cell diameter in 3T3 cells. The 3T3 cells in the SMG group appeared to have a flat form and diminished microvillus formation, while cells in the control group displayed an apical shape and abundant microvilli. The 3T3 cells under SMG exhibited microtubule distribution surrounding the nucleus, compared to the perinuclear accumulation in control cells. Irregular forms of the contractile ring and polar spindle were observed in 3T3 cells under SMG. The changes in cytoskeleton structure were caused by alterations in the expression of major cytoskeletal proteins, including β-actin and α-tubulin 3. Moreover, SMG induced 3T3 cells into the arrest phase by reducing main cell cycle related genes, which also affected the formation of cytoskeleton structures such as microfilaments and microtubules. Conclusions: These results reveal that SMG generated morphological changes in 3T3 cells by remodeling the cytoskeleton structure and downregulating major structural proteins and cell cycle regulators.

Funder

Vietnam Academy of Science and Technology

Publisher

MDPI AG

Reference45 articles.

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