The Rel subunit of NF - kappaB - like transcription factors is a positive and negative regulator of macrophage gene expression: distinct roles for Rel in different
macrophage populations.
Steve Gerondakis and colleagues establish that Rel (from the c - rel gene) in mice is a positive or negative regulator of transcription in macrophages and that Rel has distinct roles in different
macrophage populations.
To test whether adipose tissue F4 / 80 + cells shared a common bone marrow origin with other tissue
macrophage populations, we transplanted bone marrow from C57BL / 6J mice expressing the CD45.1 leukocyte marker into 6 - week - old lethally irradiated C57BL / 6J mice expressing the CD45.2 leukocyte marker.
Separately, the high levels of a type of T cell called Th17 cells secrete gobs of interleukin - 17 (IL - 17), expanding
macrophage populations.
Trapnell and Suzuki were prompted to test the novel macrophage transplantation therapy by studies showing that resident
macrophage populations (such as those residing in the lung) can self - maintain without the cells having to regenerate directly from the bone marrow.
«I think the key is the immune system needs to be balanced,» says Dhandapani, noting the seesaw effect on
the macrophage population that happens following injury.
Not exact matches
We also discovered that when we depleted neutrophils, nerve debris clearance was significantly halted in both normal mice and mice lacking a major
population of
macrophages.»
In this study, the researchers found that a specific
population of immune cells called
macrophages have the ability to secrete or produce a protective or healing factor known as Interleukin - 10 (IL - 10), which can interact with receptors on intestinal epithelial cells to promote wound healing.
Different clonal memory cell
populations had different B cell or
macrophage helper compositions that matched effector cell
populations generated much earlier in the response.
Among the three isolated cell
populations, the relative gene expression of
macrophage markers was highest among the F4 / 80 + cells.
The adipocyte - enriched
population (gray bars) expressed small amounts of the
macrophage markers (a), consistent with residual
macrophage contamination seen by immunofluorescent staining of live cells (b).
Expression analysis of
macrophage and nonmacrophage cell
populations isolated from adipose tissue showed that adipose tissue
macrophages are the primary sources of TNF - α and other proinflammatory molecules in adipose tissue.
Of the three adipose tissue cell
populations, the F4 / 80 + adipose tissue
macrophages were the predominant source of TNF - α expression.
Nos2 was expressed by both
macrophages and F4 / 80 — SVCs, and Il6 was detectably expressed by all three
populations in adipose tissue.
To determine whether adipose tissue
macrophages express any molecules implicated in obesity - associated complications, we isolated three cell
populations from the parametrial adipose tissue of three obese B6.V Lepob / ob mice: (a) an adipocyte - enriched
population, (b) a stromal vascular
macrophage F4 / 80 +
population, and (c) an F4 / 80 — stromal vascular
population.
Intriguingly, these cells, which resemble perivascular
macrophages or so - called «Mato Cells» in mammals, appear to emerge by transdifferentiation from endothelium of the optic choroidal vascular plexus, and as such would represent the first described perivascular cell
population in the brain derived from vascular endothelium.
This confirmed that the gene regulatory switch is highly specific to one cell type, monocytes and that tumor cell invasion in the absence of this
population had nothing to do with deregulated
macrophage activity.