Phosphoproteomic analysis of AML14.3D10 cell line as a model system of eosinophilia = Eosinophilia 모델로서의 AML14.3D10 세포주의 인산화단백질체 연구

Cited 0 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorSoo In Ryu-
dc.contributor.authorWon Kon-Kim-
dc.contributor.authorHyun Ju Cho-
dc.contributor.authorPhil Young Lee-
dc.contributor.authorH Jung-
dc.contributor.authorTae-Sung Yoon-
dc.contributor.authorJeong Hee Moon-
dc.contributor.authorSunghyun Kang-
dc.contributor.authorHaryoung Poo-
dc.contributor.authorKwang-Hee Bae-
dc.contributor.authorSang Chul Lee-
dc.date.accessioned2017-04-19T09:08:01Z-
dc.date.available2017-04-19T09:08:01Z-
dc.date.issued2007-
dc.identifier.issn1225-8687-
dc.identifier.uri10.5483/BMBRep.2007.40.5.765ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8077-
dc.description.abstractEosinophils act as effectors in the inflammatory reactions of allergic diseases including atopic dermatitis. Atopic dermatitis patients and others with allergic disorders suffer from eosinophilia, an accumulation of eosinophils due to increased survival or decreased apoptosis of eosinophils. In this study, a differential phosphoproteome analysis of AML14.3D10 eosinophil cell line after treatment with IL-5 or dexamethasone was conducted in an effort to identify the phosphoproteins involved in the proliferation or apoptosis of eosinophils. Proteins were separated by 2-DE and alterations in phosphoproteins were then detected by Pro-Q Diamond staining. The significant quantitative changes were shown in nineteen phosphoproteins including retinoblastoma binding protein 7, MTHSP75, and lymphocyte cytosolic protein 1. In addition, seven phosphoproteins including galactokinase I, and proapolipoprotein, were appeared after treatment with IL-5 or dexamethasone. Especially, the phospho-APOE protein was down-regulated in IL-5 treated AML14.3D10, while the more heavily phosphorylated APOE form was induced after dexamethasone treatment. These phosphoproteome data for the AML14.3D10 cell line may provide clues to understand the mechanism of eosinophilia as well as allergic disorders including atopic dermatitis.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titlePhosphoproteomic analysis of AML14.3D10 cell line as a model system of eosinophilia = Eosinophilia 모델로서의 AML14.3D10 세포주의 인산화단백질체 연구-
dc.title.alternativePhosphoproteomic analysis of AML14.3D10 cell line as a model system of eosinophilia-
dc.typeArticle-
dc.citation.titleBMB Reports-
dc.citation.number5-
dc.citation.endPage772-
dc.citation.startPage765-
dc.citation.volume40-
dc.contributor.affiliatedAuthorWon Kon-Kim-
dc.contributor.affiliatedAuthorHyun Ju Cho-
dc.contributor.affiliatedAuthorPhil Young Lee-
dc.contributor.affiliatedAuthorTae-Sung Yoon-
dc.contributor.affiliatedAuthorJeong Hee Moon-
dc.contributor.affiliatedAuthorSunghyun Kang-
dc.contributor.affiliatedAuthorHaryoung Poo-
dc.contributor.affiliatedAuthorKwang-Hee Bae-
dc.contributor.affiliatedAuthorSang Chul Lee-
dc.contributor.alternativeName유수인-
dc.contributor.alternativeName김원곤-
dc.contributor.alternativeName조현주-
dc.contributor.alternativeName이필영-
dc.contributor.alternativeName정혜윤-
dc.contributor.alternativeName윤태성-
dc.contributor.alternativeName문정희-
dc.contributor.alternativeName강성현-
dc.contributor.alternativeName부하령-
dc.contributor.alternativeName배광희-
dc.contributor.alternativeName이상철-
dc.identifier.bibliographicCitationBMB Reports, vol. 40, no. 5, pp. 765-772-
dc.identifier.doi10.5483/BMBRep.2007.40.5.765-
dc.subject.keywordAML14.3D10-
dc.subject.keywordatopic dermatitis-
dc.subject.keywordeosinophilia-
dc.subject.keywordphosphoproteome-
dc.subject.localAML14.3D10-
dc.subject.localAtopic Dermatitis-
dc.subject.localAtopic dermatitis-
dc.subject.localatopic dermatitis-
dc.subject.localatopic dermatitis (AD)-
dc.subject.localAtopic dermatitis (AD)-
dc.subject.localEosinophilia-
dc.subject.localeosinophilia-
dc.subject.localPhosphoproteome-
dc.subject.localphosphoproteome-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
Critical Diseases Diagnostics Convergence Research Center > 1. Journal Articles
Division of Bio Technology Innovation > Core Research Facility & Analysis Center > 1. Journal Articles
Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.