The Impact of Spaceflight and Simulated Microgravity on Cell Adhesion

Int J Mol Sci. 2020 Apr 25;21(9):3031. doi: 10.3390/ijms21093031.

Abstract

Microgravity induces a number of significant physiological changes in the cardiovascular, nervous, immune systems, as well as the bone tissue of astronauts. Changes in cell adhesion properties are one aspect affected during long-term spaceflights in mammalian cells. Cellular adhesion behaviors can be divided into cell-cell and cell-matrix adhesion. These behaviors trigger cell-cell recognition, conjugation, migration, cytoskeletal rearrangement, and signal transduction. Cellular adhesion molecule (CAM) is a general term for macromolecules that mediate the contact and binding between cells or between cells and the extracellular matrix (ECM). In this review, we summarize the four major classes of adhesion molecules that regulate cell adhesion, including integrins, immunoglobulin superfamily (Ig-SF), cadherins, and selectin. Moreover, we discuss the effects of spaceflight and simulated microgravity on the adhesion of endothelial cells, immune cells, tumor cells, stem cells, osteoblasts, muscle cells, and other types of cells. Further studies on the effects of microgravity on cell adhesion and the corresponding physiological behaviors may help increase the safety and improve the health of astronauts in space.

Keywords: adhesion molecules; cell adhesion; cytoskeleton; simulated microgravity; spaceflight.

Publication types

  • Review

MeSH terms

  • Animals
  • Astronauts
  • Cell Adhesion Molecules / classification
  • Cell Adhesion Molecules / physiology
  • Cell Adhesion*
  • Cytoskeleton / ultrastructure
  • Endothelial Cells / cytology
  • Extracellular Matrix / metabolism
  • Humans
  • Immune System / cytology
  • Mice
  • Muscle Cells / cytology
  • Neoplasm Proteins / metabolism
  • Neoplastic Stem Cells / cytology
  • Organ Specificity
  • Osteoblasts / cytology
  • Rats
  • Space Flight*
  • Stem Cells / cytology
  • Weightlessness Simulation*

Substances

  • Cell Adhesion Molecules
  • Neoplasm Proteins