TY - JOUR
T1 - Cytokine and free radical production by porcine microglia
AU - Hu, Shuxian
AU - Chao, Chun C.
AU - Khanna, Kristin V.
AU - Gekker, Genya
AU - Peterson, Phillip K.
AU - Molitor, Thomas W
N1 - Funding Information:
This study was supported in part by USPHS Grants DA-04381, DA-09924, DA-08496, AI-35110, and T32-DA-07239.
PY - 1996
Y1 - 1996
N2 - Swine have been used increasingly as an animal model for a variety of immunologic purposes. Because the functional activities of porcine microglia, the resident macrophages of the brain, have not been elucidated, highly enriched porcine microglial cell cultures were developed in the present study to assess cytokine and free radical production by these cells compared to microglia of human and murine origin. Porcine microglial cells were found to behave similarly to both human and murine cells in releasing tumor necrosis factor-α and interleukin-1 and in generating superoxide anion. In contrast to murine cells, porcine microglial cells, like human cells, failed to generate NO in response to cytokine stimulation. These findings suggest that swine will serve as an excellent model for investigations of central nervous system diseases in which microglia are involved in host defense or neuronal injury.
AB - Swine have been used increasingly as an animal model for a variety of immunologic purposes. Because the functional activities of porcine microglia, the resident macrophages of the brain, have not been elucidated, highly enriched porcine microglial cell cultures were developed in the present study to assess cytokine and free radical production by these cells compared to microglia of human and murine origin. Porcine microglial cells were found to behave similarly to both human and murine cells in releasing tumor necrosis factor-α and interleukin-1 and in generating superoxide anion. In contrast to murine cells, porcine microglial cells, like human cells, failed to generate NO in response to cytokine stimulation. These findings suggest that swine will serve as an excellent model for investigations of central nervous system diseases in which microglia are involved in host defense or neuronal injury.
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U2 - 10.1006/clin.1996.0015
DO - 10.1006/clin.1996.0015
M3 - Article
C2 - 8599892
AN - SCOPUS:0029981976
SN - 0090-1229
VL - 78
SP - 93
EP - 96
JO - Clinical Immunology and Immunopathology
JF - Clinical Immunology and Immunopathology
IS - 1
ER -