A Review of Notch Processing With New Insights Into Ligand-Independent Notch Signaling in T-Cells

The Notch receptor is an evolutionarily highly conserved transmembrane protein essential to a wide spectrum of cellular systems, and its deregulation has been linked to a vast number of developmental disorders and malignancies. Regulated Notch function is critical for the generation of T-cells, in w...

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Main Authors: Martin Peter Steinbuck, Susan Winandy
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-06-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2018.01230/full
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spelling doaj-56271fbc69cb4c95a9cd56bc94ce9ef82020-11-24T23:15:33ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-06-01910.3389/fimmu.2018.01230369403A Review of Notch Processing With New Insights Into Ligand-Independent Notch Signaling in T-CellsMartin Peter SteinbuckSusan WinandyThe Notch receptor is an evolutionarily highly conserved transmembrane protein essential to a wide spectrum of cellular systems, and its deregulation has been linked to a vast number of developmental disorders and malignancies. Regulated Notch function is critical for the generation of T-cells, in which abnormal Notch signaling results in leukemia. Notch activation through trans-activation of the receptor by one of its ligands expressed on adjacent cells has been well defined. In this canonical ligand-dependent pathway, Notch receptor undergoes conformational changes upon ligand engagement, stimulated by a pulling-force on the extracellular fragment of Notch that results from endocytosis of the receptor-bound ligand into the ligand-expressing cell. These conformational changes in the receptor allow for two consecutive proteolytic cleavage events to occur, which release the intracellular region of the receptor into the cytoplasm. It can then travel to the nucleus, where it induces gene transcription. However, there is accumulating evidence that other pathways may induce Notch signaling. A ligand-independent mechanism of Notch activation has been described in which receptor processing is initiated via cell-internal signals. These signals result in the internalization of Notch into endosomal compartments, where chemical changes existing in this microenvironment result in the conformational modifications required for receptor processing. This review will present mechanisms underlying both canonical ligand-dependent and non-canonical ligand-independent Notch activation pathways and discuss the latter in the context of Notch signaling in T-cells.https://www.frontiersin.org/article/10.3389/fimmu.2018.01230/fullNotchT-cellendocytosisligand-independentT-cell receptorprotein kinase C
collection DOAJ
language English
format Article
sources DOAJ
author Martin Peter Steinbuck
Susan Winandy
spellingShingle Martin Peter Steinbuck
Susan Winandy
A Review of Notch Processing With New Insights Into Ligand-Independent Notch Signaling in T-Cells
Frontiers in Immunology
Notch
T-cell
endocytosis
ligand-independent
T-cell receptor
protein kinase C
author_facet Martin Peter Steinbuck
Susan Winandy
author_sort Martin Peter Steinbuck
title A Review of Notch Processing With New Insights Into Ligand-Independent Notch Signaling in T-Cells
title_short A Review of Notch Processing With New Insights Into Ligand-Independent Notch Signaling in T-Cells
title_full A Review of Notch Processing With New Insights Into Ligand-Independent Notch Signaling in T-Cells
title_fullStr A Review of Notch Processing With New Insights Into Ligand-Independent Notch Signaling in T-Cells
title_full_unstemmed A Review of Notch Processing With New Insights Into Ligand-Independent Notch Signaling in T-Cells
title_sort review of notch processing with new insights into ligand-independent notch signaling in t-cells
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2018-06-01
description The Notch receptor is an evolutionarily highly conserved transmembrane protein essential to a wide spectrum of cellular systems, and its deregulation has been linked to a vast number of developmental disorders and malignancies. Regulated Notch function is critical for the generation of T-cells, in which abnormal Notch signaling results in leukemia. Notch activation through trans-activation of the receptor by one of its ligands expressed on adjacent cells has been well defined. In this canonical ligand-dependent pathway, Notch receptor undergoes conformational changes upon ligand engagement, stimulated by a pulling-force on the extracellular fragment of Notch that results from endocytosis of the receptor-bound ligand into the ligand-expressing cell. These conformational changes in the receptor allow for two consecutive proteolytic cleavage events to occur, which release the intracellular region of the receptor into the cytoplasm. It can then travel to the nucleus, where it induces gene transcription. However, there is accumulating evidence that other pathways may induce Notch signaling. A ligand-independent mechanism of Notch activation has been described in which receptor processing is initiated via cell-internal signals. These signals result in the internalization of Notch into endosomal compartments, where chemical changes existing in this microenvironment result in the conformational modifications required for receptor processing. This review will present mechanisms underlying both canonical ligand-dependent and non-canonical ligand-independent Notch activation pathways and discuss the latter in the context of Notch signaling in T-cells.
topic Notch
T-cell
endocytosis
ligand-independent
T-cell receptor
protein kinase C
url https://www.frontiersin.org/article/10.3389/fimmu.2018.01230/full
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