Cloning and characterization of the highly expressed ETEA gene from blood cells of atopic dermatitis patients

16Citations
Citations of this article
12Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Analysis of patients with atopic dermatitis (AD) for differential expression of genes, as compared to normal individuals, will be useful for understanding the molecular pathogenesis of AD. We found that the expression of the gene ETEA in human peripheral blood CD3-positive cells from patients with atopic dermatitis was significantly higher than in normal individuals. Eosinophils from AD patients expressed ETEA at a significantly higher level than the healthy controls. The overall sequence of the 445 aa deduced polypeptide from the cloned ETEA cDNA showed homology to human Fas-associated factor 1 (FAF1), which is involved in Fas-mediated apoptosis. However, the interaction of ETEA with the Fas death domain was weaker than that of FAF1, as studied in yeast two-hybrid experiments. The ETEA-EGFP fusion protein was expressed in cytoplasm. During the course of activation-induced cell death of primary T cells, transcription levels of ETEA and FAF1 were upregulated with similar kinetics. The enhanced expression of ETEA may play a role in the regulating the resistance to apoptosis that is observed in T cells and eosinophils of AD patients. © 2002 Elsevier Science (USA). All rights reserved.

Cite

CITATION STYLE

APA

Imai, Y., Nakada, A., Hashida, R., Sugita, Y., Tanaka, T., Tsujimoto, G., … Oshida, T. (2002). Cloning and characterization of the highly expressed ETEA gene from blood cells of atopic dermatitis patients. Biochemical and Biophysical Research Communications, 297(5), 1282–1290. https://doi.org/10.1016/S0006-291X(02)02380-X

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free