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Updated: May 28, 2026

Isolation of Murine Peritoneal Macrophages to Carry Out Gene Expression Analysis Upon Toll-like Receptors Stimulation
Published on: April 29, 2015
Mesothelial cells can detach from the mesentery and differentiate into macrophage-like cells
Sándor Katz1, Petra Balogh, Anna L Kiss
1Department of Human Morphology and Developmental Biology, Semmelweis University, Budapest, Hungary.
Abstract:
Peritoneal cell suspension is composed of heterogeneous cell population. Macrophages are the most numerous cells among them. They can originate from different sources and can be resident, exudate and elicited. When we used Freund's adjuvant to elicit peritoneal macrophages, cells having large amount of caveolae on their plasma membrane appeared in the peritoneal wash. The number of these caveolae-rich cells increased by the time of the Freund's adjuvant treatment. Although their morphology was different form from the common macrophages, they were labelled with pan-macrophage antibodies. As the origin of these cells is unknown in this work, we tried to find out where they can originate from. Our interest turned towards the mesothelial cells. We found that the adjuvant treatment resulted in significant morphological changes in these cells and stimulate them to leave the surface of the mesentery. By the time of the adjuvant treatment, the macrophage markers expression increased in the mesothelial cells and more cells were found to detach from the mesentery. These results strongly suggest that under special stimuli mesothelial cells can leave the mesentery and differentiate into phagocytotic (macrophage-like) cells. These data raises the idea that mesothelial cells might not entirely differentiated and represent a multipotential cell lineage. To study whether this is the case we used anti-nestin antibody, which is a specific marker for multifunctional, multi-lineage progenitor cells. Mesothelial cells showed strong labelling with this antibody indicating that these cells really represent a 'young', not entirely differentiated cell population.
Insights
Mesothelial cells, stimulated by Freund's adjuvant, transform into macrophage-like cells. This suggests mesothelial cells are multipotential progenitor cells, not fully differentiated.
Area of Science:
- Cell Biology
- Immunology
- Histology
Background:
- Peritoneal cell suspensions contain diverse cell types, with macrophages being the most abundant.
- Elicited peritoneal macrophages, particularly those induced by Freund's adjuvant, exhibit distinct morphological features, including abundant caveolae.
- The origin of these caveolae-rich cells in peritoneal washes following adjuvant treatment remained unclear.
Purpose of the Study:
- To investigate the origin of caveolae-rich cells observed in peritoneal washes after Freund's adjuvant administration.
- To determine if mesothelial cells can differentiate into macrophage-like cells under specific stimuli.
- To explore the potential multipotency of mesothelial cells.
Main Methods:
- Induction of peritoneal macrophages using Freund's adjuvant in a mouse model.
- Morphological analysis of peritoneal cells and mesothelial cells using microscopy.
- Immunohistochemical staining with pan-macrophage antibodies and anti-nestin antibody.
- Observation of mesothelial cell detachment from the mesentery.
Main Results:
- Freund's adjuvant treatment led to an increase in caveolae-rich cells in peritoneal washes.
- Mesothelial cells showed significant morphological changes, increased detachment from the mesentery, and upregulated macrophage marker expression post-adjuvant treatment.
- Mesothelial cells exhibited strong positive staining for nestin, a marker for progenitor cells, indicating a less differentiated state.
Conclusions:
- Mesothelial cells can differentiate into phagocytic (macrophage-like) cells upon stimulation with Freund's adjuvant.
- These findings suggest that mesothelial cells possess multipotential progenitor characteristics.
- Mesothelial cells represent a potentially 'young', undifferentiated cell population capable of lineage plasticity.
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