Effects of cyclic strain on the morphology and phagocytosis of macrophages

H Miyazaki1, K Hayashi

  • 1Division of Mechanical Science, Department of Systems and Human Science, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka, Japan. oboe@me.es.osaka-u.ac.jp

Insights

Cyclic strain alters macrophage morphology and significantly suppresses their phagocytosis of latex particles. This study reveals mechanical forces impact immune cell function, affecting cellular shape and particle uptake over time.

Area of Science:

  • Cellular Biology
  • Immunology
  • Biomechanics

Background:

  • Macrophages are crucial immune cells involved in phagocytosis.
  • Mechanical forces, such as cyclic strain, can influence cell behavior and function.
  • Understanding these mechanical effects is vital for tissue engineering and understanding inflammatory responses.

Purpose of the Study:

  • To investigate the effects of cyclic strain on macrophage morphology and phagocytic activity.
  • To quantify changes in macrophage shape index and latex particle uptake under mechanical stress.

Main Methods:

  • Peritoneal macrophages from C57BL/6J mice were cultured on silicone sheets.
  • Cells were subjected to cyclic strain (5% amplitude, 1 Hz) or maintained without strain for 24 and 48 hours.
  • Morphology was assessed using light and scanning electron microscopy, and shape index (SI) was calculated.
  • Phagocytosis was measured by the uptake of 1.5 µm latex particles.

Main Results:

  • Cyclic strain significantly affected macrophage morphology and phagocytosis, but not differentiation.
  • The shape index (SI) of macrophages decreased over time in the strained group compared to the non-strained group.
  • Phagocytosis of latex particles was suppressed by cyclic strain, with a significant difference observed after 24 hours.

Conclusions:

  • Cyclic strain negatively impacts macrophage phagocytic function.
  • Mechanical forces play a significant role in modulating macrophage immune responses.
  • These findings have implications for biomaterial design and understanding mechanobiology in immune contexts.