Amphiregulin attenuates bleomycin-induced pneumopathy in mice

1 Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu University, Fukuoka; and ; 2 Division of Respiratory Diseases, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan Submitted 26 November 2008 ; accepted in final form 12 Novembe...

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Published inAmerican journal of physiology. Lung cellular and molecular physiology Vol. 298; no. 2; pp. L131 - L138
Main Authors Fukumoto, Jutaro, Harada, Chika, Kawaguchi, Tomonobu, Suetsugu, Saiko, Maeyama, Takashige, Inoshima, Ichiro, Hamada, Naoki, Kuwano, Kazuyoshi, Nakanishi, Yoichi
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Published United States American Physiological Society 01.02.2010
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Abstract 1 Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu University, Fukuoka; and ; 2 Division of Respiratory Diseases, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan Submitted 26 November 2008 ; accepted in final form 12 November 2009 Amphiregulin, an EGF receptor (EGFR) ligand, is essential for epithelial development in various organs. A recent report suggested that amphiregulin acts as a protective factor in a liver injury model. Little is known about the roles of amphiregulin in lung injury and pulmonary fibrosis. The purpose of the present study was to investigate the role of amphiregulin in an experimental model of bleomycin-induced pneumopathy in mice. C57BL/6 mice were administered a bleomycin hydrochloride solution intratracheally. Recombinant human amphiregulin was injected intraperitoneally at 6, 8, 10, and 12 days after the bleomycin instillation. The grades of inflammation and fibrosis were assessed histologically and biochemically, and the numbers of apoptotic cells were counted after TdT-mediated dUTP nick end labeling (TUNEL) staining in the lung tissues. We also examined downstream survival signals of EGFR, namely phosphorylated Akt and phosphorylated Erk, in lung tissues by Western blotting analysis and immunohistochemistry. Expression of intrinsic amphiregulin was increased in murine lung tissues after bleomycin instillation. Administration of recombinant amphiregulin improved the survival rate and suppressed the degrees of inflammation and fibrosis and the number of TUNEL-positive cells in lung tissues. Amphiregulin treatment enhanced the activation of Akt and Erk in lung epithelial cells. Amphiregulin may play a protective role in bleomycin-induced pneumopathy in mice, probably through the activation of survival signals. Administration of amphiregulin may be a novel therapeutic strategy against lung injury and fibrosis. epidermal growth factor; lung injury; apoptosis Address for reprint requests and other correspondence: J. Fukumoto, Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu Univ., 3-1-1, Maidashi, Higashiku, Fukuoka 812-8582, Japan (e-mail: fukumoto{at}kokyu.med.kyushu-u.ac.jp ).
AbstractList 1 Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu University, Fukuoka; and ; 2 Division of Respiratory Diseases, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan Submitted 26 November 2008 ; accepted in final form 12 November 2009 Amphiregulin, an EGF receptor (EGFR) ligand, is essential for epithelial development in various organs. A recent report suggested that amphiregulin acts as a protective factor in a liver injury model. Little is known about the roles of amphiregulin in lung injury and pulmonary fibrosis. The purpose of the present study was to investigate the role of amphiregulin in an experimental model of bleomycin-induced pneumopathy in mice. C57BL/6 mice were administered a bleomycin hydrochloride solution intratracheally. Recombinant human amphiregulin was injected intraperitoneally at 6, 8, 10, and 12 days after the bleomycin instillation. The grades of inflammation and fibrosis were assessed histologically and biochemically, and the numbers of apoptotic cells were counted after TdT-mediated dUTP nick end labeling (TUNEL) staining in the lung tissues. We also examined downstream survival signals of EGFR, namely phosphorylated Akt and phosphorylated Erk, in lung tissues by Western blotting analysis and immunohistochemistry. Expression of intrinsic amphiregulin was increased in murine lung tissues after bleomycin instillation. Administration of recombinant amphiregulin improved the survival rate and suppressed the degrees of inflammation and fibrosis and the number of TUNEL-positive cells in lung tissues. Amphiregulin treatment enhanced the activation of Akt and Erk in lung epithelial cells. Amphiregulin may play a protective role in bleomycin-induced pneumopathy in mice, probably through the activation of survival signals. Administration of amphiregulin may be a novel therapeutic strategy against lung injury and fibrosis. epidermal growth factor; lung injury; apoptosis Address for reprint requests and other correspondence: J. Fukumoto, Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu Univ., 3-1-1, Maidashi, Higashiku, Fukuoka 812-8582, Japan (e-mail: fukumoto{at}kokyu.med.kyushu-u.ac.jp ).
Amphiregulin, an EGF receptor (EGFR) ligand, is essential for epithelial development in various organs. A recent report suggested that amphiregulin acts as a protective factor in a liver injury model. Little is known about the roles of amphiregulin in lung injury and pulmonary fibrosis. The purpose of the present study was to investigate the role of amphiregulin in an experimental model of bleomycin-induced pneumopathy in mice. C57BL/6 mice were administered a bleomycin hydrochloride solution intratracheally. Recombinant human amphiregulin was injected intraperitoneally at 6, 8, 10, and 12 days after the bleomycin instillation. The grades of inflammation and fibrosis were assessed histologically and biochemically, and the numbers of apoptotic cells were counted after TdT-mediated dUTP nick end labeling (TUNEL) staining in the lung tissues. We also examined downstream survival signals of EGFR, namely phosphorylated Akt and phosphorylated Erk, in lung tissues by Western blotting analysis and immunohistochemistry. Expression of intrinsic amphiregulin was increased in murine lung tissues after bleomycin instillation. Administration of recombinant amphiregulin improved the survival rate and suppressed the degrees of inflammation and fibrosis and the number of TUNEL-positive cells in lung tissues. Amphiregulin treatment enhanced the activation of Akt and Erk in lung epithelial cells. Amphiregulin may play a protective role in bleomycin-induced pneumopathy in mice, probably through the activation of survival signals. Administration of amphiregulin may be a novel therapeutic strategy against lung injury and fibrosis.
Amphiregulin, an EGF receptor (EGFR) ligand, is essential for epithelial development in various organs. A recent report suggested that amphiregulin acts as a protective factor in a liver injury model. Little is known about the roles of amphiregulin in lung injury and pulmonary fibrosis. The purpose of the present study was to investigate the role of amphiregulin in an experimental model of bleomycin-induced pneumopathy in mice. C57BL/6 mice were administered a bleomycin hydrochloride solution intratracheally. Recombinant human amphiregulin was injected intraperitoneally at 6, 8, 10, and 12 days after the bleomycin instillation. The grades of inflammation and fibrosis were assessed histologically and biochemically, and the numbers of apoptotic cells were counted after TdT-mediated dUTP nick end labeling (TUNEL) staining in the lung tissues. We also examined downstream survival signals of EGFR, namely phosphorylated Akt and phosphorylated Erk, in lung tissues by Western blotting analysis and immunohistochemistry. Expression of intrinsic amphiregulin was increased in murine lung tissues after bleomycin instillation. Administration of recombinant amphiregulin improved the survival rate and suppressed the degrees of inflammation and fibrosis and the number of TUNEL-positive cells in lung tissues. Amphiregulin treatment enhanced the activation of Akt and Erk in lung epithelial cells. Amphiregulin may play a protective role in bleomycin-induced pneumopathy in mice, probably through the activation of survival signals. Administration of amphiregulin may be a novel therapeutic strategy against lung injury and fibrosis. [PUBLICATION ABSTRACT]
Author Harada, Chika
Kawaguchi, Tomonobu
Maeyama, Takashige
Kuwano, Kazuyoshi
Suetsugu, Saiko
Fukumoto, Jutaro
Inoshima, Ichiro
Hamada, Naoki
Nakanishi, Yoichi
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Cites_doi 10.1164/ajrccm.156.6.9611057
10.1165/ajrcmb.22.5.3851
10.1136/jcp.54.2.132
10.1165/ajrcmb.24.5.4333
10.1126/science.2466334
10.1093/oxfordjournals.jbchem.a021283
10.1056/NEJMra003200
10.1172/JCI117152
10.1152/physiolgenomics.00110.2005
10.1164/rccm.200509-1534OC
10.1002/jlb.57.5.782
10.1172/JCI5628
10.1016/j.jaci.2004.11.037
10.1164/ajrccm.165.2.ats01
10.1074/jbc.273.27.17258
10.1164/ajrccm.154.2.8756825
10.1089/10430340260355356
10.1165/ajrcmb.11.5.7524566
10.1164/ajrccm.162.6.9908097
10.1242/dev.122.6.1759
10.1073/pnas.85.17.6528
10.1074/jbc.M413344200
10.1016/S0002-9440(10)65115-2
10.1165/ajrcmb.16.1.8998084
10.1172/JCI117086
10.4049/jimmunol.175.2.1224
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References B20
Yi ES (B30) 1996; 149
B22
Deterding RR (B6) 1997; 109
B24
B25
B26
B27
B28
B29
Chandler DB (B5) 1983; 112
B10
B11
B12
B13
B14
B15
B16
B17
B18
B19
B1
B2
B3
B4
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Suzuki H (B23) 2003; 63
Schuger L (B21) 1996; 122
References_xml – ident: B29
  doi: 10.1164/ajrccm.156.6.9611057
– ident: B18
  doi: 10.1165/ajrcmb.22.5.3851
– volume: 63
  start-page: 5054
  year: 2003
  ident: B23
  publication-title: Cancer Res
  contributor:
    fullname: Suzuki H
– ident: B2
  doi: 10.1136/jcp.54.2.132
– volume: 149
  start-page: 1963
  year: 1996
  ident: B30
  publication-title: Am J Pathol
  contributor:
    fullname: Yi ES
– ident: B19
  doi: 10.1165/ajrcmb.24.5.4333
– ident: B25
  doi: 10.1126/science.2466334
– volume: 109
  start-page: 254
  year: 1997
  ident: B6
  publication-title: Proc Assoc Am Physicians
  contributor:
    fullname: Deterding RR
– ident: B17
  doi: 10.1093/oxfordjournals.jbchem.a021283
– ident: B9
  doi: 10.1056/NEJMra003200
– volume: 112
  start-page: 170
  year: 1983
  ident: B5
  publication-title: Am J Pathol
  contributor:
    fullname: Chandler DB
– ident: B13
  doi: 10.1172/JCI117152
– ident: B8
  doi: 10.1152/physiolgenomics.00110.2005
– ident: B12
  doi: 10.1164/rccm.200509-1534OC
– ident: B22
  doi: 10.1002/jlb.57.5.782
– ident: B14
  doi: 10.1172/JCI5628
– ident: B28
  doi: 10.1016/j.jaci.2004.11.037
– ident: B1
  doi: 10.1164/ajrccm.165.2.ats01
– ident: B4
  doi: 10.1074/jbc.273.27.17258
– ident: B15
  doi: 10.1164/ajrccm.154.2.8756825
– ident: B26
  doi: 10.1089/10430340260355356
– ident: B16
  doi: 10.1165/ajrcmb.11.5.7524566
– ident: B7
  doi: 10.1164/ajrccm.162.6.9908097
– volume: 122
  start-page: 1759
  year: 1996
  ident: B21
  publication-title: Development
  doi: 10.1242/dev.122.6.1759
  contributor:
    fullname: Schuger L
– ident: B24
  doi: 10.1073/pnas.85.17.6528
– ident: B3
  doi: 10.1074/jbc.M413344200
– ident: B20
  doi: 10.1016/S0002-9440(10)65115-2
– ident: B10
  doi: 10.1165/ajrcmb.16.1.8998084
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  doi: 10.1172/JCI117086
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  doi: 10.4049/jimmunol.175.2.1224
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Snippet 1 Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu University, Fukuoka; and ; 2 Division of Respiratory Diseases,...
Amphiregulin, an EGF receptor (EGFR) ligand, is essential for epithelial development in various organs. A recent report suggested that amphiregulin acts as a...
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SubjectTerms Amphiregulin
Animals
Antibiotics, Antineoplastic - adverse effects
Antibiotics, Antineoplastic - therapeutic use
Bleomycin - adverse effects
Bleomycin - therapeutic use
Cell growth
Cells
Collagen - metabolism
Cystic fibrosis
EGF Family of Proteins
Extracellular Signal-Regulated MAP Kinases - metabolism
Female
Glycoproteins - administration & dosage
Glycoproteins - genetics
Glycoproteins - metabolism
Humans
Immunohistochemistry
Intercellular Signaling Peptides and Proteins - administration & dosage
Intercellular Signaling Peptides and Proteins - genetics
Intercellular Signaling Peptides and Proteins - metabolism
Liver diseases
Lung - cytology
Lung - drug effects
Lung - metabolism
Lung - pathology
Lung Diseases - chemically induced
Lung Diseases - pathology
Mice
Mice, Inbred C57BL
Molecules
Proliferating Cell Nuclear Antigen - metabolism
Proto-Oncogene Proteins c-akt - metabolism
Pulmonary Fibrosis - chemically induced
Pulmonary Fibrosis - pathology
Recombinant Proteins - administration & dosage
Recombinant Proteins - genetics
Recombinant Proteins - metabolism
Rodents
Signal Transduction - physiology
Survival analysis
Survival Rate
Title Amphiregulin attenuates bleomycin-induced pneumopathy in mice
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