1.Lactoferrin Stimulates Mouse Macrophage to Express BAFF via Smad3 Pathway.
Heynkeyung CHANG ; Bo Ra JIN ; Young Saeng JANG ; Woan Sub KIM ; Pyeung Hyeun KIM
Immune Network 2012;12(3):84-88
B cell-activating factor belonging to the TNF family (BAFF) is primarily expressed by macrophages and stimulates B cell proliferation, differentiation, survival, and Ig production. In this study, we explored the effect of lactoferrin (LF) on BAFF expression by murine macrophages. We determined the level of BAFF expression at the transcriptional and protein levels using RT-PCR and ELISA, respectively. LF markedly enhanced BAFF expression in mouse macrophages at both the transcriptional and protein levels. Overexpression of Smad3/4 further increased LF-induced BAFF transcription while DN-Smad3 abolished the LF-induced BAFF expression. These results demonstrate that LF can enhance BAFF expression through Smad3/4 pathway.
Animals
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Cell Proliferation
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Enzyme-Linked Immunosorbent Assay
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Humans
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Lactoferrin
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Macrophages
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Mice
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Transforming Growth Factor beta1
2.Lactoferrin Combined with Retinoic Acid Stimulates B1 Cells to Express IgA Isotype and Gut-homing Molecules.
Seong Ho KANG ; Bo Ra JIN ; Hyeon Jin KIM ; Goo Young SEO ; Young Saeng JANG ; Sun Jin KIM ; Sun Jin AN ; Seok Rae PARK ; Woan Sub KIM ; Pyeung Hyeun KIM
Immune Network 2015;15(1):37-43
It is well established that TGF-beta1 and retinoic acid (RA) cause IgA isotype switching in mice. We recently found that lactoferrin (LF) also has an activity of IgA isotype switching in spleen B cells. The present study explored the effect of LF on the Ig production by mouse peritoneal B cells. LF, like TGF-beta1, substantially increased IgA production in peritoneal B1 cells but little in peritoneal B2 cells. In contrast, LF increased IgG2b production in peritoneal B2 cells much more strongly than in peritoneal B1 cells. LF in combination with RA further enhanced the IgA production and, interestingly, this enhancement was restricted to IgA isotype and B1 cells. Similarly, the combination of the two molecules also led to expression of gut homing molecules alpha4beta7 and CCR9 on peritoneal B1 cells, but not on peritoneal B2 cells. Thus, these results indicate that LF and RA can contribute to gut IgA response through stimulating IgA isotype switching and expression of gut-homing molecules in peritoneal B1 cells.
Animals
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B-Lymphocytes
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Immunoglobulin A*
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Immunoglobulin Class Switching
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Immunoglobulin G
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Lactoferrin*
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Mice
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Spleen
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Transforming Growth Factor beta1
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Tretinoin*