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Journal Article

Lactoferrin and its digestive peptides induce interferon-α production and activate plasmacytoid dendritic cells ex vivo

Shutaro Kubo; Momoko Miyakawa; Asuka Tada; Hirotsugu Oda; Hideki Motobayashi; Sadahiro Iwabuchi; Shinobu Tamura; Miyuki Tanaka; Shinichi Hashimoto
BioMetals · Vol. 36, Issue 3 · pp. 563-573 · 2023

Abstract

Plasmacytoid dendritic cells (pDCs) recognise viral single-stranded RNA (ssRNA) or CpG DNA via Toll-like receptor (TLR)-7 and TLR9, and produce interferon (IFN)-α. Activated pDCs upregulate human leukocyte antigen (HLA)-DR and CD86 expression levels. Ingestion of bovine lactoferrin (LF) activates pDCs, but little is known about its effects. In this study, the effects of LF and its pepsin hydrolysate (LFH) on the production of IFN-α from peripheral blood mononuclear cells (PBMCs) and pDCs were examined. PBMCs were prepared from peripheral blood of healthy adults and incubated with LF, LFH, or lactoferricin (LFcin) in the absence or presence of ssRNA derived from human immunodeficiency virus. The concentration of IFN-α in the supernatant and the expression levels of IFN-α, HLA-DR, and CD86 in pDCs were quantified by enzyme-linked immunosorbent assay and flow cytometry. In the absence of ssRNA, the concentration of IFN-α was negligible and LF had no effect on it. In the presence of ssRNA, IFN-α was detected at a certain level, and LF and LFH significantly increased its concentration. The increase caused by LFH and LFcin were comparable. In addition, LF significantly upregulated the expression levels of IFN-α, HLA-DR, and CD86 in pDCs. LF and its digestive peptides induced IFN-α production and activated pDCs in the presence of ssRNA, suggesting that LF modulates the immune system by promoting pDC activation upon viral recognition.

Bibliographic Information

JournalBioMetals
PublisherSpringer
Publication Date2023-06-01
Publication Year2023
Volume36
Issue3
Pages563-573
Document TypeJournal Article
Print ISSN0966-0844
eISSN1572-8773
DOI10.1007/s10534-022-00436-y

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NARA Access Coverage1988-01-01~Current
Journal Homepagehttps://www.springer.com/journal/10534
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