Your browser doesn't support javascript.
loading
Histidine-rich glycoprotein and concanavalin A synergistically stimulate the phosphatidylinositol 3-kinase-independent signaling pathway in leukocytes leading to increased cell adhesion and changes in cell morphology.
Ohta, Takeshi; Ikemoto, Yoshitaka; Saeki, Koichi; Koide, Takehiko; Wakabayashi, Sadao.
Afiliação
  • Ohta T; Department of Life Science, Graduate School of Life Science, University of Hyogo, Harima Science Garden City, Hyogo, Japan.
Cell Immunol ; 259(1): 5-12, 2009.
Article em En | MEDLINE | ID: mdl-19535045
ABSTRACT
Histidine-rich glycoprotein (HRG) promoted the adhesion and morphological changes of human T-cell line MOLT-4 in a Con A-dependent manner. This morphological change-promoting activity was specific for HRG and the Arg23-Lys66 glycopeptide from human HRG. The carbohydrate chain at Asn45 was essential for this activity. The morphological changes of MOLT-4 cells caused by HRG and Con A (HRG/Con A) were not inhibited by phosphatidylinositol 3-kinase inhibitor, wortmannin or LY294002, while the changes by Con A alone were completely inhibited by these reagents, suggesting that HRG/Con A cooperate to activate leukocytes via a signaling pathway distinct from that by Con A alone. The morphological changes by Con A were associated with pseudopodia like structure. On the other hand, the morphological changes caused by HRG/Con A were associated not only with pseudopodia like structure but also with an increase of the F-actin-rich surface protrusions. Wortmannin inhibited only the formation of pseudopodia like structure.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Concanavalina A / Fosfatidilinositol 3-Quinases / Leucócitos Limite: Humans Idioma: En Revista: Cell Immunol Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Concanavalina A / Fosfatidilinositol 3-Quinases / Leucócitos Limite: Humans Idioma: En Revista: Cell Immunol Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Japão