دورية أكاديمية

Novel CD47-dependent intercellular adhesion modulates cell migration.

التفاصيل البيبلوغرافية
العنوان: Novel CD47-dependent intercellular adhesion modulates cell migration.
المؤلفون: Rebres RA; Program in Microbial Pathogenesis and Host Defense, University of California, San Francisco, California, USA., Kajihara K, Brown EJ
المصدر: Journal of cellular physiology [J Cell Physiol] 2005 Nov; Vol. 205 (2), pp. 182-93.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural
اللغة: English
بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 0050222 Publication Model: Print Cited Medium: Print ISSN: 0021-9541 (Print) Linking ISSN: 00219541 NLM ISO Abbreviation: J Cell Physiol Subsets: MEDLINE
أسماء مطبوعة: Publication: New York, NY : Wiley-Liss
Original Publication: Philadelphia, Wistar Institute of Anatomy and Biology.
مواضيع طبية MeSH: CD47 Antigen/*physiology , Cell Movement/*physiology , Fibroblasts/*drug effects , Heterotrimeric GTP-Binding Proteins/*metabolism , rac GTP-Binding Proteins/*metabolism, Animals ; Bacterial Proteins/pharmacology ; Bacterial Toxins/pharmacology ; CD47 Antigen/metabolism ; Cell Adhesion/drug effects ; Cell Aggregation/immunology ; Cell Membrane/metabolism ; Cell Movement/drug effects ; Cells, Cultured ; Chemokine CXCL12 ; Chemokines, CXC/genetics ; Chemokines, CXC/metabolism ; Chemotaxis/drug effects ; Fibroblasts/metabolism ; Humans ; Jurkat Cells ; Lymphocytes/metabolism ; Lymphocytes/physiology ; Mice ; Pertussis Toxin/pharmacology ; Recombinant Proteins/metabolism ; Thrombospondins/metabolism ; Tumor Cells, Cultured
مستخلص: CD47 is a ubiquitously expressed plasma membrane protein, also known as Integrin Associated Protein, that modulates cell adhesion both through alteration of the avidity of integrin binding and through interaction with its own ligands, the extracellular matrix protein thrombospondin (TSP) and the plasma membrane response regulator SIRPalpha1. We now show that CD47 expression on fibroblasts can induce intercellular adhesion resulting in cell aggregation in the absence of active integrins, SIRPalpha1 binding, and detectable TSP. CD47-expressing cells preferentially bind to other CD47-expressing cells, and intercellular adhesion requires stimulation by serum or a CD47-binding peptide from TSP. Cell-cell adhesion is inhibited by pertussis toxin and C. difficile toxin B, and both adherent and aggregating CD47-expressing fibroblasts have more rac in the GTP bound state than CD47-deficient cells. Spontaneous migration of Jurkat lymphocytes through a fibroblast monolayer is decreased by fibroblast expression of CD47, consistent with an increased barrier function of the CD47 expressing cells. The lymphocyte chemoattractant SDF-1alpha stimulates migration of Jurkat cells through this monolayer only if both the lymphocytes and fibroblasts express CD47, and the inhibition of migration by a CD47-interacting peptide from TSP similarly requires CD47 expression on both cell types. Thus, signaling dependent on both heterotrimeric and rho family GTPases can induce CD47 to participate in cell-cell interactions independent of known ligands that enhance intercellular adhesion and modulate cell migration.
(Copyright 2005 Wiley-Liss, Inc.)
معلومات مُعتمدة: AI53194 United States AI NIAID NIH HHS; GM38330 United States GM NIGMS NIH HHS
المشرفين على المادة: 0 (Bacterial Proteins)
0 (Bacterial Toxins)
0 (CD47 Antigen)
0 (CXCL12 protein, human)
0 (Chemokine CXCL12)
0 (Chemokines, CXC)
0 (Cxcl12 protein, mouse)
0 (Recombinant Proteins)
0 (Thrombospondins)
0 (toxB protein, Clostridium difficile)
EC 2.4.2.31 (Pertussis Toxin)
EC 3.6.5.1 (Heterotrimeric GTP-Binding Proteins)
EC 3.6.5.2 (rac GTP-Binding Proteins)
تواريخ الأحداث: Date Created: 20050510 Date Completed: 20051222 Latest Revision: 20171116
رمز التحديث: 20240628
DOI: 10.1002/jcp.20379
PMID: 15880429
قاعدة البيانات: MEDLINE