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Müller, G. ; Müller, T.D.

(Patho)Physiology of glycosylphosphatidylinositol-anchored proteins I: localization at plasma membranes and extracellular compartments.

Biomolecules 13:41 (2023)
Verlagsversion DOI PMC
Open Access Gold
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Glycosylphosphatidylinositol (GPI)-anchored proteins (APs) are anchored at the outer leaflet of plasma membranes (PMs) of all eukaryotic organisms studied so far by covalent linkage to a highly conserved glycolipid rather than a transmembrane domain. Since their first description, experimental data have been accumulating for the capability of GPI-APs to be released from PMs into the surrounding milieu. It became evident that this release results in distinct arrangements of GPI-APs which are compatible with the aqueous milieu upon loss of their GPI anchor by (proteolytic or lipolytic) cleavage or in the course of shielding of the full-length GPI anchor by incorporation into extracellular vesicles, lipoprotein-like particles and (lyso)phospholipid- and cholesterol-harboring micelle-like complexes or by association with GPI-binding proteins or/and other full-length GPI-APs. In mammalian organisms, the (patho)physiological roles of the released GPI-APs in the extracellular environment, such as blood and tissue cells, depend on the molecular mechanisms of their release as well as the cell types and tissues involved, and are controlled by their removal from circulation. This is accomplished by endocytic uptake by liver cells and/or degradation by GPI-specific phospholipase D in order to bypass potential unwanted effects of the released GPI-APs or their transfer from the releasing donor to acceptor cells (which will be reviewed in a forthcoming manuscript).
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter (g)pi-specific Phospholipase D (gpld1) ; Adipose Cells ; Extracellular Vesicles ; Glycosylphosphatidylinositol (gpi)-anchored Proteins (gpi-aps) ; Metabolic Diseases ; Protein Release ; Sulfonylurea Drugs; Phosphatidylinositol-specific Phospholipase; Intestinal Alkaline-phosphatase; Decay-accelerating Factor; Angiotensin-converting Enzyme; Variant Surface Glycoprotein; Human-erythrocyte Acetylcholinesterase; Inhibitor Protectin Cd59; Fibroblast-growth-factor; Rat Adipocytes Depends; Colon-cancer-cells
Sprache englisch
Veröffentlichungsjahr 2023
HGF-Berichtsjahr 2023
ISSN (print) / ISBN 2218-273X
e-ISSN 2218-273X
Zeitschrift Biomolecules
Quellenangaben Band: 13, Heft: 5, Seiten: , Artikelnummer: 41 Supplement: ,
Verlag MDPI
Verlagsort Basel
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Diabetes and Obesity (IDO)
POF Topic(s) 90000 - German Center for Diabetes Research
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-501900-221
Förderungen
European Research Council ERC-CoG Trusted
German Center for Diabetes Research (DZD e.V.)
German Research Foundation (DFG)
DOI 10.3390/biom13050855
WOS ID 000995593900001
Scopus ID 85160380452
PubMed ID 37238725
Erfassungsdatum 2023-10-06
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