Bone marrow-derived and resident liver macrophages display unique transcriptomic signatures but similar biological

Lynette Beattie1, Amy Sawtell2, Jason Mann2

  • 1Centre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK; QIMR Berghofer Medical Research Institute, 300 Herston Rd, Herston, Queensland 4006, Australia.

Abstract

Insights

Resident liver macrophages, Kupffer cells (KCs), have distinct origins. While bone marrow-derived KCs resemble yolk sac KCs, subtle functional differences exist, impacting liver injury and infectious disease models.

Area of Science:

  • Immunology
  • Cell Biology
  • Hepatology

Background:

  • Kupffer cells (KCs) are resident liver macrophages crucial for pathogen clearance.
  • KCs originate from yolk sac precursors and are distinct from monocyte-derived macrophages.
  • The functional similarity between yolk sac-derived and bone marrow-derived KCs after injury is not fully understood.

Purpose of the Study:

  • To investigate the functional and molecular differences between yolk sac-derived and bone marrow-derived Kupffer cells.
  • To determine the extent to which bone marrow-derived macrophages functionally replace resident KCs after liver injury.

Main Methods:

  • Intravital microscopy, morphometric analysis, and gene expression profiling were used to study KC populations.
  • An ion homeostasis gene signature was developed to differentiate KC subtypes.
  • Functional assays assessed lipoprotein uptake, bacterial phagocytosis, and response to LPS.

Main Results:

  • Bone marrow-derived KCs resemble yolk sac KCs but are not identical.
  • Yolk sac KCs showed higher acetylated LDL uptake, while bone marrow-derived KCs were more effective at phagocytosing bacteria.
  • Both KC populations exhibited similar responses to LPS, effete red blood cell phagocytosis, and Leishmania donovani infection control.

Conclusions:

  • Bone marrow-derived KCs differentiate locally and largely resemble yolk sac-derived KCs but retain some functional distinctions.
  • These findings have implications for understanding infectious diseases, liver injury, and bone marrow transplantation outcomes.
  • A novel gene signature aids in distinguishing KC subpopulations based on their origin.