TSLP Expression: Cellular Sources, Triggers, and Regulatory Mechanisms

Thymic stromal lymphopoietin (TSLP) is an IL-7-like cytokine initially identified in the culture supernatant of a thymic stromal cell line. Highly expressed in the epidermis in skin lesions of atopic dermatitis patients, TSLP was subsequently found to be a critical factor linking responses at interf...

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Main Author: Toshiro Takai
Format: Article
Language:English
Published: Elsevier 2012-01-01
Series:Allergology International
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S132389301530188X
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spelling doaj-b771f49c7d8049008b38f76cb1c029502020-11-25T00:44:58ZengElsevierAllergology International1323-89302012-01-0161131710.2332/allergolint.11-RAI-0395TSLP Expression: Cellular Sources, Triggers, and Regulatory MechanismsToshiro Takai0Atopy (Allergy) Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan.Thymic stromal lymphopoietin (TSLP) is an IL-7-like cytokine initially identified in the culture supernatant of a thymic stromal cell line. Highly expressed in the epidermis in skin lesions of atopic dermatitis patients, TSLP was subsequently found to be a critical factor linking responses at interfaces between the body and environment (skin, airway, gut, ocular tissues, and so on) to Th2 responses. Recent studies have revealed that various cell types other than epithelial cells and epidermal keratinocytes (such as mast cells, airway smooth muscle cells, fibroblasts, dendritic cells, trophoblasts, and cancer or cancer-associated cells) also express TSLP. Environmental factors such as Toll-like receptor ligands, a Nod2 ligand, viruses, microbes, allergen sources, helminths, diesel exhaust, cigarette smoke, and chemicals trigger TSLP production. Proinflammatory cytokines, Th2-related cytokines, and IgE also induce or enhance TSLP production, indicating cycles of amplification. Skin barrier injury, increased epidermal endogenous protease activity, and less epidermal Notch signaling, all of which have been reported in atopic dermatitis, and keratinocyte-specific loss of retinoid X receptors and treatment of skin with agonists for vitamin D receptor in mice induce TSLP production, Th2 response, or atopic dermatitis-like inflammation. The transcription factors NF-κB and AP-1, nuclear receptors, single nucleotide polymorphisms, microRNAs, and the peptidyl-proryl isomerase Pin1 regulate TSLP mRNA expression transcriptionally or posttranscriptionally. This review focuses on events upstream of TSLP production, which is critical in allergic diseases and important in other TSLP-related disorders i.e. production sites, cellular sources, environmental and endogenous triggers and regulatory factors, and regulatory mechanisms of gene expression.http://www.sciencedirect.com/science/article/pii/S132389301530188Xcellular sourcesendogenous triggers and regulatorsenvironmental triggersregulation of gene expressionthymic stromal lymphopoietin
collection DOAJ
language English
format Article
sources DOAJ
author Toshiro Takai
spellingShingle Toshiro Takai
TSLP Expression: Cellular Sources, Triggers, and Regulatory Mechanisms
Allergology International
cellular sources
endogenous triggers and regulators
environmental triggers
regulation of gene expression
thymic stromal lymphopoietin
author_facet Toshiro Takai
author_sort Toshiro Takai
title TSLP Expression: Cellular Sources, Triggers, and Regulatory Mechanisms
title_short TSLP Expression: Cellular Sources, Triggers, and Regulatory Mechanisms
title_full TSLP Expression: Cellular Sources, Triggers, and Regulatory Mechanisms
title_fullStr TSLP Expression: Cellular Sources, Triggers, and Regulatory Mechanisms
title_full_unstemmed TSLP Expression: Cellular Sources, Triggers, and Regulatory Mechanisms
title_sort tslp expression: cellular sources, triggers, and regulatory mechanisms
publisher Elsevier
series Allergology International
issn 1323-8930
publishDate 2012-01-01
description Thymic stromal lymphopoietin (TSLP) is an IL-7-like cytokine initially identified in the culture supernatant of a thymic stromal cell line. Highly expressed in the epidermis in skin lesions of atopic dermatitis patients, TSLP was subsequently found to be a critical factor linking responses at interfaces between the body and environment (skin, airway, gut, ocular tissues, and so on) to Th2 responses. Recent studies have revealed that various cell types other than epithelial cells and epidermal keratinocytes (such as mast cells, airway smooth muscle cells, fibroblasts, dendritic cells, trophoblasts, and cancer or cancer-associated cells) also express TSLP. Environmental factors such as Toll-like receptor ligands, a Nod2 ligand, viruses, microbes, allergen sources, helminths, diesel exhaust, cigarette smoke, and chemicals trigger TSLP production. Proinflammatory cytokines, Th2-related cytokines, and IgE also induce or enhance TSLP production, indicating cycles of amplification. Skin barrier injury, increased epidermal endogenous protease activity, and less epidermal Notch signaling, all of which have been reported in atopic dermatitis, and keratinocyte-specific loss of retinoid X receptors and treatment of skin with agonists for vitamin D receptor in mice induce TSLP production, Th2 response, or atopic dermatitis-like inflammation. The transcription factors NF-κB and AP-1, nuclear receptors, single nucleotide polymorphisms, microRNAs, and the peptidyl-proryl isomerase Pin1 regulate TSLP mRNA expression transcriptionally or posttranscriptionally. This review focuses on events upstream of TSLP production, which is critical in allergic diseases and important in other TSLP-related disorders i.e. production sites, cellular sources, environmental and endogenous triggers and regulatory factors, and regulatory mechanisms of gene expression.
topic cellular sources
endogenous triggers and regulators
environmental triggers
regulation of gene expression
thymic stromal lymphopoietin
url http://www.sciencedirect.com/science/article/pii/S132389301530188X
work_keys_str_mv AT toshirotakai tslpexpressioncellularsourcestriggersandregulatorymechanisms
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