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How do red blood cells know when to die?

Clemente Fernandez Arias1,2, Cristina Fernandez Arias3

  • 1Departamento de Matemática Aplicada, Universidad Complutense de Madrid, Spain.

Royal Society Open Science
|May 10, 2017
PubMed
Summary

Red blood cell (RBC) destruction is governed by phosphatidylserine (PS) and CD47. This study presents a model where these molecules dictate RBC lifespan, explaining variations in oxygen availability.

Keywords:
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Area of Science:

  • Hematology
  • Cell Biology
  • Systems Biology

Background:

  • Human red blood cells (RBCs) have a finite lifespan, typically around 120 days.
  • RBC clearance is mediated by macrophages in the spleen and liver.
  • The interaction between phosphatidylserine (PS) and CD47 on RBCs regulates macrophage phagocytosis.

Purpose of the Study:

  • To introduce a conceptual model explaining RBC lifespan based on molecular dynamics.
  • To propose that PS and CD47 constitute a molecular algorithm determining RBC phagocytosis timing.
  • To unify diverse empirical observations on RBC lifespan within a theoretical framework.

Main Methods:

  • Development of a theoretical model based on the antagonistic effects of PS and CD47.
  • Analysis of how oxygen availability influences the execution of the proposed molecular algorithm.
  • Comparison of model predictions with existing literature data on RBC lifespan variations.

Main Results:

  • The model successfully explains RBC lifespan as a consequence of PS and CD47 dynamics.
  • Variations in RBC lifespan observed under different oxygen conditions are predictable outcomes of the model.
  • The molecular algorithm involving PS and CD47 provides a unified explanation for empirical findings.

Conclusions:

  • The proposed molecular algorithm offers a novel framework for understanding RBC aging and clearance.
  • RBC lifespan is a critical component of maintaining RBC homeostasis.
  • This model provides insights into RBC biology and potential therapeutic targets.