Periostin deletion suppresses late-phase response in mouse experimental allergic conjunctivitis.


Journal

Allergology international : official journal of the Japanese Society of Allergology
ISSN: 1440-1592
Titre abrégé: Allergol Int
Pays: England
ID NLM: 9616296

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 25 08 2018
revised: 24 09 2018
accepted: 26 09 2018
pubmed: 14 11 2018
medline: 2 8 2019
entrez: 14 11 2018
Statut: ppublish

Résumé

To investigate the potential roles of periostin (POSTN), an extracellular matrix preferentially expressed in Th2-skewed conditions in the pathophysiology of allergic conjunctivitis. The roles of POSTN in ragweed-induced experimental allergic conjunctivitis (RW-EAC) were evaluated using both POSTN-knockout (KO) and congenic BALB/c wild-type mice. Histological analysis was carried out to enumerate eosinophils/basophils in the conjunctival tissue. Th2 cytokine expression was evaluated by quantitative polymerase chain reaction (Q-PCR), and microarray analysis was performed to elucidate genes differentially expressed in POSTN-KO and wild-type mice in the RW-EAC model. Upregulation of POSTN expression and eosinophil infiltration was observed in subconjunctival tissue of RW-EAC in the wild-type mice. The number of infiltrating eosinophils in the conjunctivae of RW-EAC was diminished in POSTN-KO mice compared to wild-type mice. Q-PCR analysis of conjunctival tissue showed induction of Th2 cytokine (Ccl5, Il4, Il5, Il13) expression in the RW-EAC and attenuated Ccl5, Il4, Il13 mRNA expression in the conjunctivae of the RW-EAC using POSTN-KO mice. Microarray analysis and immunohistochemical analysis showed diminished basophil marker (Mcpt8) expression and reduced numbers of infiltrating basophils in the conjunctivae of RW-EAC in POSTN-KO mice. POSTN expression in conjunctival tissue plays an indispensable role in the late-phase reaction of the RW-EAC model by facilitating eosinophil/basophil infiltration and augmenting Th2 cytokine expression.

Sections du résumé

BACKGROUND BACKGROUND
To investigate the potential roles of periostin (POSTN), an extracellular matrix preferentially expressed in Th2-skewed conditions in the pathophysiology of allergic conjunctivitis.
METHODS METHODS
The roles of POSTN in ragweed-induced experimental allergic conjunctivitis (RW-EAC) were evaluated using both POSTN-knockout (KO) and congenic BALB/c wild-type mice. Histological analysis was carried out to enumerate eosinophils/basophils in the conjunctival tissue. Th2 cytokine expression was evaluated by quantitative polymerase chain reaction (Q-PCR), and microarray analysis was performed to elucidate genes differentially expressed in POSTN-KO and wild-type mice in the RW-EAC model.
RESULTS RESULTS
Upregulation of POSTN expression and eosinophil infiltration was observed in subconjunctival tissue of RW-EAC in the wild-type mice. The number of infiltrating eosinophils in the conjunctivae of RW-EAC was diminished in POSTN-KO mice compared to wild-type mice. Q-PCR analysis of conjunctival tissue showed induction of Th2 cytokine (Ccl5, Il4, Il5, Il13) expression in the RW-EAC and attenuated Ccl5, Il4, Il13 mRNA expression in the conjunctivae of the RW-EAC using POSTN-KO mice. Microarray analysis and immunohistochemical analysis showed diminished basophil marker (Mcpt8) expression and reduced numbers of infiltrating basophils in the conjunctivae of RW-EAC in POSTN-KO mice.
CONCLUSIONS CONCLUSIONS
POSTN expression in conjunctival tissue plays an indispensable role in the late-phase reaction of the RW-EAC model by facilitating eosinophil/basophil infiltration and augmenting Th2 cytokine expression.

Identifiants

pubmed: 30420208
pii: S1323-8930(18)30144-8
doi: 10.1016/j.alit.2018.09.007
pii:
doi:

Substances chimiques

Allergens 0
Antigens, Plant 0
Cell Adhesion Molecules 0
Cytokines 0
Postn protein, mouse 0

Types de publication

Journal Article

Langues

eng

Pagination

233-239

Informations de copyright

Copyright © 2019 Japanese Society of Allergology. Production and hosting by Elsevier B.V. All rights reserved.

Auteurs

Yosuke Asada (Y)

Laboratory of Ocular Atopic Diseases, Department of Ophthalmology, Juntendo University School of Medicine, Tokyo, Japan.

Mikiko Okano (M)

Laboratory of Ocular Atopic Diseases, Department of Ophthalmology, Juntendo University School of Medicine, Tokyo, Japan; Department of Ophthalmology, Juntendo University Urayasu Hospital, Urayasu, Japan.

Waka Ishida (W)

Department of Ophthalmology, Kochi University School of Medicine, Nankoku, Japan.

Satoshi Iwamoto (S)

Laboratory of Ocular Atopic Diseases, Department of Ophthalmology, Juntendo University School of Medicine, Tokyo, Japan.

Ken Fukuda (K)

Department of Ophthalmology, Kochi University School of Medicine, Nankoku, Japan.

Toshiaki Hirakata (T)

Laboratory of Ocular Atopic Diseases, Department of Ophthalmology, Juntendo University School of Medicine, Tokyo, Japan.

Norihiro Tada (N)

Research Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo, Japan.

Atsuki Fukushima (A)

Department of Ophthalmology, Kochi University School of Medicine, Nankoku, Japan.

Nobuyuki Ebihara (N)

Laboratory of Ocular Atopic Diseases, Department of Ophthalmology, Juntendo University School of Medicine, Tokyo, Japan; Department of Ophthalmology, Juntendo University Urayasu Hospital, Urayasu, Japan.

Akira Kudo (A)

Department of Biological Information, Tokyo Institute of Technology, Yokohama, Japan.

Akira Matsuda (A)

Laboratory of Ocular Atopic Diseases, Department of Ophthalmology, Juntendo University School of Medicine, Tokyo, Japan. Electronic address: akimatsu@juntendo.ac.jp.

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Classifications MeSH