Calcium-regulated intramembrane proteolysis of the RAGE receptor

Autor: Arnaud Galichet, Claus W. Heizmann, Mirjam Weibel
Přispěvatelé: University of Zurich, Heizmann, C W
Jazyk: angličtina
Rok vydání: 2008
Předmět:
medicine.medical_specialty
Cytoplasm
1303 Biochemistry
endocrine system diseases
ADAM10
Receptor for Advanced Glycation End Products
Biophysics
Regulator
Context (language use)
610 Medicine & health
Biochemistry
Regulated Intramembrane Proteolysis
Antibodies
RAGE (receptor)
Cell Line
1307 Cell Biology
ADAM10 Protein
Internal medicine
medicine
1312 Molecular Biology
Humans
Dimethyl Sulfoxide
cardiovascular diseases
Receptors
Immunologic

Receptor
Molecular Biology
Cell Nucleus
Chemistry
Ionomycin
Alternative splicing
Cell Membrane
nutritional and metabolic diseases
Membrane Proteins
Cell Biology
Cell biology
Protein Structure
Tertiary

ADAM Proteins
Endocrinology
10036 Medical Clinic
cardiovascular system
Tetradecanoylphorbol Acetate
Calcium
Amyloid Precursor Protein Secretases
human activities
1304 Biophysics
Popis: The receptor for advanced glycation endproducts (RAGE) interacts with several ligands and is involved in various human diseases. RAGE_v1 or sRAGE, a RAGE splice variant, is secreted and contributes to the removal of RAGE ligands. Because RAGE blockade by specific antibodies directed against RAGE extracellular domains and the use of sRAGE have been proven to be beneficial in the context of pathological settings, both RAGE and sRAGE are considered as therapeutic target. Here, we show that sRAGE is also produced through regulated intramembrane proteolysis of the RAGE receptor, which is catalyzed by ADAM10 and the gamma-secretase and that calcium is an essential regulator of RAGE processing. Furthermore, RAGE intracellular domain localizes both in the cytoplasm and the nucleus and induces apoptosis when expressed in cells. These findings reveal new aspects of RAGE regulation and signaling and also provide a new interaction between RAGE and human pathologies.
Databáze: OpenAIRE