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Published on: November 27, 2014
The neuropeptides α-MSH and NPY modulate phagocytosis and phagolysosome activation in RAW 264.7 cells
1Department of Ophthalmology, Boston University School of Medicine, Boston, MA, USA.
Abstract:
Within the immunosuppressive ocular microenvironment, there are constitutively present the immunomodulating neuropeptides alpha-melanocyte stimulating hormone (α-MSH) and neuropeptide Y (NPY) that promote suppressor functionality in macrophages. In this study, we examined the possibility that α-MSH and NPY modulate phagocytic activity in macrophages. The macrophages treated with α-MSH and NPY were significantly suppressed in their capacity to phagocytize unopsonized Escherichia coli and Staphylococcus aureus bioparticles, but not antibody-opsonized bioparticles. The neuropeptides significantly suppressed phagolysosome activation, and the FcR-associated generation of reactive oxidative species as well. This suppression corresponds to neuropeptide modulation of macrophage functionality within the ocular microenvironment to suppress the activation of immunogenic inflammation.
Insights
Neuropeptides alpha-melanocyte stimulating hormone (α-MSH) and neuropeptide Y (NPY) suppress macrophage phagocytosis of unopsonized bacteria. This immune modulation in the eye prevents inflammatory responses.
Area of Science:
- Immunology
- Ophthalmology
- Neuroendocrinology
Background:
- The ocular microenvironment is immunosuppressive.
- Immunomodulating neuropeptides, alpha-melanocyte stimulating hormone (α-MSH) and neuropeptide Y (NPY), are present in the eye.
- These neuropeptides promote suppressor functionality in macrophages.
Purpose of the Study:
- To investigate the effect of α-MSH and NPY on macrophage phagocytic activity.
- To determine if these neuropeptides modulate the uptake of bacteria by macrophages.
Main Methods:
- Macrophages were treated with α-MSH and NPY.
- Phagocytosis assays were performed using unopsonized and antibody-opsonized Escherichia coli and Staphylococcus aureus bioparticles.
- Phagolysosome activation and FcR-associated reactive oxidative species generation were measured.
Main Results:
- α-MSH and NPY significantly suppressed the phagocytosis of unopsonized bacteria.
- Phagocytosis of antibody-opsonized bioparticles was not affected.
- Neuropeptide treatment suppressed phagolysosome activation and FcR-associated reactive oxidative species generation.
Conclusions:
- α-MSH and NPY modulate macrophage phagocytic activity in the ocular microenvironment.
- This suppression contributes to the regulation of immune responses within the eye.
- Neuropeptides play a role in preventing immunogenic inflammation in the eye.
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