Contribution of Macrophage Efferocytosis to Liver Homeostasis and Disease

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Contribution of Macrophage Efferocytosis to Liver Homeostasis and Disease. / Horst, Andrea Kristina; Tiegs, Gisa; Diehl, Linda.

in: FRONT IMMUNOL, Jahrgang 10, 2019, S. 2670.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ReviewForschung

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@article{cf4c0eea4eae470fadd274cb0ab56d41,
title = "Contribution of Macrophage Efferocytosis to Liver Homeostasis and Disease",
abstract = "The clearance of apoptotic cells is pivotal for both maintaining tissue homeostasis and returning to homeostasis after tissue injury as part of the regenerative resolution response. The liver is known for its capacity to remove aged and damaged cells from the circulation and can serve as a graveyard for effector T cells. In particular Kupffer cells are active phagocytic cells, but during hepatic inflammatory responses incoming neutrophils and monocytes may contribute to pro-inflammatory damage. To stimulate resolution of such inflammation, myeloid cell function can change, via sensing of environmental changes in the inflammatory milieu. Also, the removal of apoptotic cells via efferocytosis and the signaling pathways that are activated in macrophages/phagocytes upon their engulfment of apoptotic cells are important for a return to tissue homeostasis. Here, we will discuss, how efferocytosis mechanisms in hepatic macrophages/phagocytes may regulate tissue homeostasis and be involved in tissue regeneration in liver disease.",
author = "Horst, {Andrea Kristina} and Gisa Tiegs and Linda Diehl",
note = "Copyright {\textcopyright} 2019 Horst, Tiegs and Diehl.",
year = "2019",
doi = "10.3389/fimmu.2019.02670",
language = "English",
volume = "10",
pages = "2670",
journal = "FRONT IMMUNOL",
issn = "1664-3224",
publisher = "Lausanne : Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Contribution of Macrophage Efferocytosis to Liver Homeostasis and Disease

AU - Horst, Andrea Kristina

AU - Tiegs, Gisa

AU - Diehl, Linda

N1 - Copyright © 2019 Horst, Tiegs and Diehl.

PY - 2019

Y1 - 2019

N2 - The clearance of apoptotic cells is pivotal for both maintaining tissue homeostasis and returning to homeostasis after tissue injury as part of the regenerative resolution response. The liver is known for its capacity to remove aged and damaged cells from the circulation and can serve as a graveyard for effector T cells. In particular Kupffer cells are active phagocytic cells, but during hepatic inflammatory responses incoming neutrophils and monocytes may contribute to pro-inflammatory damage. To stimulate resolution of such inflammation, myeloid cell function can change, via sensing of environmental changes in the inflammatory milieu. Also, the removal of apoptotic cells via efferocytosis and the signaling pathways that are activated in macrophages/phagocytes upon their engulfment of apoptotic cells are important for a return to tissue homeostasis. Here, we will discuss, how efferocytosis mechanisms in hepatic macrophages/phagocytes may regulate tissue homeostasis and be involved in tissue regeneration in liver disease.

AB - The clearance of apoptotic cells is pivotal for both maintaining tissue homeostasis and returning to homeostasis after tissue injury as part of the regenerative resolution response. The liver is known for its capacity to remove aged and damaged cells from the circulation and can serve as a graveyard for effector T cells. In particular Kupffer cells are active phagocytic cells, but during hepatic inflammatory responses incoming neutrophils and monocytes may contribute to pro-inflammatory damage. To stimulate resolution of such inflammation, myeloid cell function can change, via sensing of environmental changes in the inflammatory milieu. Also, the removal of apoptotic cells via efferocytosis and the signaling pathways that are activated in macrophages/phagocytes upon their engulfment of apoptotic cells are important for a return to tissue homeostasis. Here, we will discuss, how efferocytosis mechanisms in hepatic macrophages/phagocytes may regulate tissue homeostasis and be involved in tissue regeneration in liver disease.

U2 - 10.3389/fimmu.2019.02670

DO - 10.3389/fimmu.2019.02670

M3 - SCORING: Review article

C2 - 31798592

VL - 10

SP - 2670

JO - FRONT IMMUNOL

JF - FRONT IMMUNOL

SN - 1664-3224

ER -