Heat shock proteins are no DAMPs, rather 'DAMPERs'. (Q53680750)

17 May 2018

title

Heat shock proteins are no DAMPs, rather 'DAMPERs'. (English)

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17 May 2018

author

Femke Broere

series ordinal

1

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17 May 2018

Ruurd van der Zee

series ordinal

2

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17 May 2018

Willem van Eden

series ordinal

3

object named as

Willem van Eden

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17 May 2018

25 July 2011

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17 May 2018

Nature Reviews Immunology

published in

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17 May 2018

volume

11

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17 May 2018

issue

8

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17 May 2018

page(s)

565; author reply 565

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17 May 2018

Sterile inflammation: sensing and reacting to damage

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In vivo treatment of mice with heat shock protein, gp 96, improves survival of skin grafts with minor and major antigenic disparity.

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The stress protein gp96 is not an activator of resting rat bone marrow-derived dendritic cells, but is a costimulator and activator of CD3+ T cells.

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The HSP60 immune system network

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Endotoxin contamination in recombinant human heat shock protein 70 (Hsp70) preparation is responsible for the induction of tumor necrosis factor alpha release by murine macrophages

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Enteric flora and lymphocyte-derived cytokines determine expression of heat shock proteins in mouse colonic epithelial cells

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Regional differences in colonic mucosa-associated microbiota determine the physiological expression of host heat shock proteins

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Recognition of commensal microflora by toll-like receptors is required for intestinal homeostasis

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Membrane-associated Hsp72 from tumor-derived exosomes mediates STAT3-dependent immunosuppressive function of mouse and human myeloid-derived suppressor cells

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21785457

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRI2873-C1

1 reference

17 May 2018

PubMed ID

21785457

1 reference

17 May 2018