Pseudoalteromonas strains are potent immunomodulators owing to low-stimulatory LPS

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Standard

Pseudoalteromonas strains are potent immunomodulators owing to low-stimulatory LPS. / Maaetoft-Udsen, Kristina; Vynne, Nikolaj Grønnegaard; Heegaard, Peter M. H.; Gram, Lone; Frøkiær, Hanne.

I: Innate Immunity, Bind 19, Nr. 2, 2012, s. 160-173.

Publikation: Bidrag til tidsskriftTidsskriftartikelfagfællebedømt

Harvard

Maaetoft-Udsen, K, Vynne, NG, Heegaard, PMH, Gram, L & Frøkiær, H 2012, 'Pseudoalteromonas strains are potent immunomodulators owing to low-stimulatory LPS', Innate Immunity, bind 19, nr. 2, s. 160-173. https://doi.org/10.1177/1753425912455208

APA

Maaetoft-Udsen, K., Vynne, N. G., Heegaard, P. M. H., Gram, L., & Frøkiær, H. (2012). Pseudoalteromonas strains are potent immunomodulators owing to low-stimulatory LPS. Innate Immunity, 19(2), 160-173. https://doi.org/10.1177/1753425912455208

Vancouver

Maaetoft-Udsen K, Vynne NG, Heegaard PMH, Gram L, Frøkiær H. Pseudoalteromonas strains are potent immunomodulators owing to low-stimulatory LPS. Innate Immunity. 2012;19(2):160-173. https://doi.org/10.1177/1753425912455208

Author

Maaetoft-Udsen, Kristina ; Vynne, Nikolaj Grønnegaard ; Heegaard, Peter M. H. ; Gram, Lone ; Frøkiær, Hanne. / Pseudoalteromonas strains are potent immunomodulators owing to low-stimulatory LPS. I: Innate Immunity. 2012 ; Bind 19, Nr. 2. s. 160-173.

Bibtex

@article{b30cfa706b2340afbb3eac796feed257,
title = "Pseudoalteromonas strains are potent immunomodulators owing to low-stimulatory LPS",
abstract = "Many species of marine bacteria elicit a weak immune response. In this study, the aim was to assess the immunomodulatory properties of Gram-negative Pseudoalteromonas strains compared with other marine Gram-negative bacteria and to identify the molecular cause of the immunomodulation. Using murine bone-marrow derived dendritic cells (DCs), it was found that Pseudoalteromonas strains induced low cytokine production and modest up-regulation of surface markers CD40 and CD86 compared with other marine bacteria and Escherichia coli LPS. Two strains, Ps. luteoviolacea and Ps. ruthenica, were further investigated with respect to their immunomodulatory properties in DCs. Both inhibited IL-12 and increased IL-10 production induced by E. coli LPS. LPS isolated from the two Pseudoalteromonas strains had characteristic lipid A bands in SDS-PAGE. Stimulation of HEK293 TLR4/MD2 cells with the isolated LPS confirmed the involvement of LPS and TLR4 and established Pseudoalteromonas LPS as TLR4 antagonists. The isolated LPS was active in the endotoxin limulus amoebocyte lysate assay and capable of inducing increased endocytosis in DCs. This study highlights that antagonistic LPS from Pseudoalteromonas strains has potential as a new candidate of therapeutic agent capable of modulating immune responses.",
keywords = "Former LIFE faculty, Dendritic cells, immunomodulation, lipopolysaccharides, Pseudoalteromonas, Toll-like receptor 4 antagonists",
author = "Kristina Maaetoft-Udsen and Vynne, {Nikolaj Gr{\o}nnegaard} and Heegaard, {Peter M. H.} and Lone Gram and Hanne Fr{\o}ki{\ae}r",
year = "2012",
doi = "10.1177/1753425912455208",
language = "English",
volume = "19",
pages = "160--173",
journal = "Innate Immunity",
issn = "1940-3011",
publisher = "Landes Bioscience",
number = "2",

}

RIS

TY - JOUR

T1 - Pseudoalteromonas strains are potent immunomodulators owing to low-stimulatory LPS

AU - Maaetoft-Udsen, Kristina

AU - Vynne, Nikolaj Grønnegaard

AU - Heegaard, Peter M. H.

AU - Gram, Lone

AU - Frøkiær, Hanne

PY - 2012

Y1 - 2012

N2 - Many species of marine bacteria elicit a weak immune response. In this study, the aim was to assess the immunomodulatory properties of Gram-negative Pseudoalteromonas strains compared with other marine Gram-negative bacteria and to identify the molecular cause of the immunomodulation. Using murine bone-marrow derived dendritic cells (DCs), it was found that Pseudoalteromonas strains induced low cytokine production and modest up-regulation of surface markers CD40 and CD86 compared with other marine bacteria and Escherichia coli LPS. Two strains, Ps. luteoviolacea and Ps. ruthenica, were further investigated with respect to their immunomodulatory properties in DCs. Both inhibited IL-12 and increased IL-10 production induced by E. coli LPS. LPS isolated from the two Pseudoalteromonas strains had characteristic lipid A bands in SDS-PAGE. Stimulation of HEK293 TLR4/MD2 cells with the isolated LPS confirmed the involvement of LPS and TLR4 and established Pseudoalteromonas LPS as TLR4 antagonists. The isolated LPS was active in the endotoxin limulus amoebocyte lysate assay and capable of inducing increased endocytosis in DCs. This study highlights that antagonistic LPS from Pseudoalteromonas strains has potential as a new candidate of therapeutic agent capable of modulating immune responses.

AB - Many species of marine bacteria elicit a weak immune response. In this study, the aim was to assess the immunomodulatory properties of Gram-negative Pseudoalteromonas strains compared with other marine Gram-negative bacteria and to identify the molecular cause of the immunomodulation. Using murine bone-marrow derived dendritic cells (DCs), it was found that Pseudoalteromonas strains induced low cytokine production and modest up-regulation of surface markers CD40 and CD86 compared with other marine bacteria and Escherichia coli LPS. Two strains, Ps. luteoviolacea and Ps. ruthenica, were further investigated with respect to their immunomodulatory properties in DCs. Both inhibited IL-12 and increased IL-10 production induced by E. coli LPS. LPS isolated from the two Pseudoalteromonas strains had characteristic lipid A bands in SDS-PAGE. Stimulation of HEK293 TLR4/MD2 cells with the isolated LPS confirmed the involvement of LPS and TLR4 and established Pseudoalteromonas LPS as TLR4 antagonists. The isolated LPS was active in the endotoxin limulus amoebocyte lysate assay and capable of inducing increased endocytosis in DCs. This study highlights that antagonistic LPS from Pseudoalteromonas strains has potential as a new candidate of therapeutic agent capable of modulating immune responses.

KW - Former LIFE faculty

KW - Dendritic cells

KW - immunomodulation

KW - lipopolysaccharides

KW - Pseudoalteromonas

KW - Toll-like receptor 4 antagonists

U2 - 10.1177/1753425912455208

DO - 10.1177/1753425912455208

M3 - Journal article

C2 - 22890545

VL - 19

SP - 160

EP - 173

JO - Innate Immunity

JF - Innate Immunity

SN - 1940-3011

IS - 2

ER -

ID: 44559356