Article ID Journal Published Year Pages File Type
3064267 Journal of Neuroimmunology 2013 8 Pages PDF
Abstract

•The neuropeptides α-MSH and NPY suppress phagocytosis of unopsonized bioparticles.•The neuropeptides α-MSH and NPY do not suppress FcR-mediated phagocytosis.•α-MSH and NPY suppress phagolysosome activation of FcR-mediated phagosomes.•α-MSH and NPY suppress FcR-mediated generation of reactive oxygen species.

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.

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