Chemotaxis of polymorphonuclear leukocytes in response to surface-bound complement-derived chemoattractants generated

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Polymorphonuclear leukocytes (PMNLs) migration is influenced by yeast particles. Complement activation on yeast surfaces generates chemoattractants, enhancing PMNL chemotaxis and indicating surface-bound attractants.

Area of Science:

  • Immunology
  • Cell Biology
  • Microbiology

Background:

  • Polymorphonuclear leukocytes (PMNLs) are crucial immune cells involved in inflammatory responses.
  • Chemoattractants play a vital role in directing leukocyte migration to sites of infection or injury.
  • The interaction between yeast particles and complement system components can influence immune cell behavior.

Purpose of the Study:

  • To investigate the role of complement activation on yeast particles in generating chemoattractants for PMNLs.
  • To determine if chemoattractants generated by yeast particles are surface-absorbed, influencing PMNL locomotion.
  • To visualize the deposition of complement factors on yeast particles during PMNL chemotaxis.

Main Methods:

  • PMNLs were induced to migrate on slides containing fixed yeast particles.
  • Locomotion was quantified by counting yeast particles associated with PMNLs.
  • Immunofluorescence techniques were employed to detect complement factor deposition.

Main Results:

  • Yeast particles varied in their ability to activate the complement system and generate chemoattractants.
  • Addition of complement source to activatable yeast particles induced PMNL chemotaxis, even without fluid-phase attractants.
  • Complement factor 5 (C5) was observed to coat yeast particles that activated the complement system.

Conclusions:

  • Chemoattractants generated by complement activation on yeast particles are surface-absorbed, directing PMNL migration.
  • The ability of yeast particles to activate the complement system directly correlates with their capacity to attract PMNLs.
  • Complement factor 5 deposition around yeast particles is a key indicator of complement system activation and subsequent PMNL chemotaxis.

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