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Isolation of Murine Peritoneal Macrophages to Carry Out Gene Expression Analysis Upon Toll-like Receptors Stimulation
Published on: April 29, 2015
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.
Background & Aims:
Kupffer cells (KCs), the resident tissue macrophages of the liver, play a crucial role in the clearance of pathogens and other particulate materials that reach the systemic circulation. Recent studies have identified KCs as a yolk sac-derived resident macrophage population that is replenished independently of monocytes in the steady state. Although it is now established that following local tissue injury, bone marrow derived monocytes may infiltrate the tissue and differentiate into macrophages, the extent to which newly differentiated macrophages functionally resemble the KCs they have replaced has not been extensively studied.
Methods:
We studied the two populations of KCs using intravital microscopy, morphometric analysis and gene expression profiling. An ion homeostasis gene signature, including genes associated with scavenger receptor function and extracellular matrix deposition, allowed discrimination between these two KC sub-types.
Results:
Bone marrow derived "KCs" accumulating as a result of genotoxic injury, resemble but are not identical to their yolk sac counterparts. Reflecting the differential expression of scavenger receptors, yolk sac-derived KCs were more effective at accumulating acetylated low density lipoprotein, whereas surprisingly, they were poorer than bone marrow-derived KCs when assessed for uptake of a range of bacterial pathogens. The two KC populations were almost indistinguishable in regard to i) response to lipopolysaccharide challenge, ii) phagocytosis of effete red blood cells and iii) their ability to contain infection and direct granuloma formation against Leishmania donovani, a KC-tropic intracellular parasite.
Conclusions:
Bone marrow-derived KCs differentiate locally to resemble yolk sac-derived KC in most but not all respects, with implications for models of infectious diseases, liver injury and bone marrow transplantation. In addition, the gene signature we describe adds to the tools available for distinguishing KC subpopulations based on their ontology.
Lay Summary:
Liver macrophages play a major role in the control of infections in the liver and in the pathology associated with chronic liver diseases. It was recently shown that liver macrophages can have two different origins, however, the extent to which these populations are functionally distinct remains to be fully addressed. Our study demonstrates that whilst liver macrophages share many features in common, regardless of their origin, some subtle differences in function exist.
Data Repository:
Gene expression data are available from the European Bioinformatics Institute ArrayExpress data repository (accession number E-MTAB-4954).
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.
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