Main Page
About
Faculty
Dean
Organizational Structure
Academic Accreditations
"Strategic Plan "Ebtesama-Smile
Administration
Vice Deanships
Academic Affairs
Female Section
Graduate Studies and Research
University Dental Hospital
Development
Departments
Diagnostic Oral Sciences
Periodontology
Oral Biology
Oral & Maxillofacial Prosthodontics
Oral & Maxillofacial Surgery
Endodontics
Restorative Dentistry
Orthodontics
Pediatric Dentistry
Dental Public Health
Goals and Objectives
Education
Bachelor
Interns Program
Postgraduate Studies
Research
University Dental Hospital
Community Services
House of Expertise
Files
Contact Us
Directory of Faculty Staff
عربي
English
About
Admission
Academic
Research and Innovations
University Life
E-Services
Search
Faculty of Dentistry
Document Details
Document Type
:
Article In Journal
Document Title
:
Role for Moesin in Lipopolysaccharide-Stimulated Signal Transduction
Role for Moesin in Lipopolysaccharide-Stimulated Signal Transduction
Document Language
:
English
Abstract
:
Moesin is a 78-kDa protein with diverse functions in linking the cytoskeleton to the membrane while controlling cell shape, adhesion, locomotion, and signaling. The aim of this study was to characterize the expression and localization of moesin in mononuclear phagocytes by using confocal microscopy, flow cytom· etry, immunoprecipitation, and Western blotting and to analyze the function of moesin as a lipopolysaccharide receptor, utilizing an antisense oligonucleotide approach to knock down the moesin gene. Results revealed that moesin is expressed on the surface of monocytes/macrophages and surface expression is increased after lipopolysaccharide stimulation. The total protein mass of moesin is increased in monocytes after lipopolysaccharide stimulation. Immunoprecipitation showed that moesin coprecipitates with TLR4, a well-known lipopolysaccharide receptor, suggesting an early role of moesin in the formation of the initiation complex for lipopolysaccharide signaling. Two antisense and two control sense oligonucleotides were synthesized and introduced every 4 h for 48 h in adherent macrophage-like cells. Cells were then stimulated with lipopolysaccharide for 4 h, and the supernatants were assayed for tumor necrosis factor alpha (TNF-a) production. Cell Iysates were assayed for moesin expression by Western blotting immediately after the 48-h treatment period and also after 116 h of recovery to assess the return of moesin expression and function. Moesin gene expression was completely suppressed after 48 h of incubation with antisense oligonucleotides. The antisense elimination of moesin gene expression led to a significant reduction of lipopolysaccharide-induced TNF-a secretion. Restoration of moesin gene expression led to restoration of TNF-a production. These data suggest an important role for moesin in lipopolysaccharide-induced TNF-a production, highlighting its importance in lipopolysaccharide- mediated signal transduction.
ISSN
:
0
Journal Name
:
american society for microbiology
Volume
:
72
Issue Number
:
4
Publishing Year
:
2004 AH
2004 AD
Article Type
:
Article
Added Date
:
Thursday, December 6, 2007
Researchers
Researcher Name (Arabic)
Researcher Name (English)
Researcher Type
Dr Grade
Email
خالد زواوي
zwawi, Khalid
Investigator
Doctorate
kzawawi@kau.edu.sa
Files
File Name
Type
Description
Role for Moesin in Lipopolysaccharide-Stimulated Signal Transduction.pdf
pdf
Back To Researches Page