Chronicles of Cell Death Foretold: Specificities in the Mechanism of Disposal

Standard

Chronicles of Cell Death Foretold: Specificities in the Mechanism of Disposal. / Hughes, Lindsey D; Bosurgi, Lidia; Ghosh, Sourav; Rothlin, Carla V.

in: FRONT IMMUNOL, Jahrgang 8, 2017, S. 1743.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ReviewForschung

Harvard

APA

Vancouver

Bibtex

@article{f499fe36f5b044e0afbb584dba633651,
title = "Chronicles of Cell Death Foretold: Specificities in the Mechanism of Disposal",
abstract = "Massive turnover of cells occurs through apoptosis during the constant remodeling of our tissues at homeostasis, from the shedding of cells at exposed barrier surfaces to the elimination of autoreactive lymphocytes. However, a surge of apoptotic cells also accompanies tissue damage, infection, and inflammation. A salient feature of apoptosis in either scenario is the exposure of phosphatidylserine (PtdSer) on the outer leaflet of the plasma membrane. In response to this cue, a range of phagocytes are charged with the sizeable task of engulfing apoptotic bodies and disposing of the billions of cells that perish each day. The presence of apoptotic cells in the remarkably distinct immunological settings described above, therefore, raises the question of how phagocytes are able to coordinate appropriate responses to apoptotic cells-from their silent removal to the production of growth factors or tissue repair molecules-following such a ubiquitous signal as PtdSer exposure. Here, we consider several emergent properties of phagocytes and apoptotic cell clearance that may facilitate specification among this suite of potential responses.",
keywords = "Journal Article, Review",
author = "Hughes, {Lindsey D} and Lidia Bosurgi and Sourav Ghosh and Rothlin, {Carla V}",
year = "2017",
doi = "10.3389/fimmu.2017.01743",
language = "English",
volume = "8",
pages = "1743",
journal = "FRONT IMMUNOL",
issn = "1664-3224",
publisher = "Lausanne : Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Chronicles of Cell Death Foretold: Specificities in the Mechanism of Disposal

AU - Hughes, Lindsey D

AU - Bosurgi, Lidia

AU - Ghosh, Sourav

AU - Rothlin, Carla V

PY - 2017

Y1 - 2017

N2 - Massive turnover of cells occurs through apoptosis during the constant remodeling of our tissues at homeostasis, from the shedding of cells at exposed barrier surfaces to the elimination of autoreactive lymphocytes. However, a surge of apoptotic cells also accompanies tissue damage, infection, and inflammation. A salient feature of apoptosis in either scenario is the exposure of phosphatidylserine (PtdSer) on the outer leaflet of the plasma membrane. In response to this cue, a range of phagocytes are charged with the sizeable task of engulfing apoptotic bodies and disposing of the billions of cells that perish each day. The presence of apoptotic cells in the remarkably distinct immunological settings described above, therefore, raises the question of how phagocytes are able to coordinate appropriate responses to apoptotic cells-from their silent removal to the production of growth factors or tissue repair molecules-following such a ubiquitous signal as PtdSer exposure. Here, we consider several emergent properties of phagocytes and apoptotic cell clearance that may facilitate specification among this suite of potential responses.

AB - Massive turnover of cells occurs through apoptosis during the constant remodeling of our tissues at homeostasis, from the shedding of cells at exposed barrier surfaces to the elimination of autoreactive lymphocytes. However, a surge of apoptotic cells also accompanies tissue damage, infection, and inflammation. A salient feature of apoptosis in either scenario is the exposure of phosphatidylserine (PtdSer) on the outer leaflet of the plasma membrane. In response to this cue, a range of phagocytes are charged with the sizeable task of engulfing apoptotic bodies and disposing of the billions of cells that perish each day. The presence of apoptotic cells in the remarkably distinct immunological settings described above, therefore, raises the question of how phagocytes are able to coordinate appropriate responses to apoptotic cells-from their silent removal to the production of growth factors or tissue repair molecules-following such a ubiquitous signal as PtdSer exposure. Here, we consider several emergent properties of phagocytes and apoptotic cell clearance that may facilitate specification among this suite of potential responses.

KW - Journal Article

KW - Review

U2 - 10.3389/fimmu.2017.01743

DO - 10.3389/fimmu.2017.01743

M3 - SCORING: Review article

C2 - 29312294

VL - 8

SP - 1743

JO - FRONT IMMUNOL

JF - FRONT IMMUNOL

SN - 1664-3224

ER -