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Literature DB >> 24117007

Normal prion protein is expressed on exosomes isolated from human plasma.

Adam J Ritchie¹, Damian M Crawford, David J P Ferguson, John Burthem, David J Roberts.

Abstract

Entities: Chemical

Keywords: Prion; exosome; plasma; transfusion; variant Creutzfeldt-Jakob disease

Mesh：

Substances：

Year: 2013 PMID： 24117007 DOI： 10.1111/bjh.12543

Source DB: PubMed Journal: Br J Haematol ISSN： 0007-1048 Impact factor: 6.998

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Cited

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14 in total

1. First demonstration of transmissible spongiform encephalopathy-associated prion protein (PrPTSE) in extracellular vesicles from plasma of mice infected with mouse-adapted variant Creutzfeldt-Jakob disease by in vitro amplification.

Authors: Paula Saá; Oksana Yakovleva; Jorge de Castro; Irina Vasilyeva; Silvia H De Paoli; Jan Simak; Larisa Cervenakova
Journal: J Biol Chem Date: 2014-08-25 Impact factor: 5.157

Review 2. Cellular mechanisms responsible for cell-to-cell spreading of prions.

Authors: Didier Vilette; Josquin Courte; Jean Michel Peyrin; Laurent Coudert; Laurent Schaeffer; Olivier Andréoletti; Pascal Leblanc
Journal: Cell Mol Life Sci Date: 2018-05-14 Impact factor: 9.261

Review 3. Anchorless risk or released benefit? An updated view on the ADAM10-mediated shedding of the prion protein.

Authors: Behnam Mohammadi; Feizhi Song; Andreu Matamoros-Angles; Mohsin Shafiq; Markus Damme; Berta Puig; Markus Glatzel; Hermann Clemens Altmeppen
Journal: Cell Tissue Res Date: 2022-01-27 Impact factor: 5.249

4. A Soluble PrP^C Derivative and Membrane-Anchored PrP^C in Extracellular Vesicles Attenuate Innate Immunity by Engaging the NMDA-R/LRP1 Receptor Complex.

Authors: Elisabetta Mantuano; Pardis Azmoon; Michael A Banki; Christina J Sigurdson; Wendy M Campana; Steven L Gonias
Journal: J Immunol Date: 2021-11-22 Impact factor: 5.422

Normal prion protein is expressed on exosomes isolated from human plasma.

1. First demonstration of transmissible spongiform encephalopathy-associated prion protein (PrPTSE) in extracellular vesicles from plasma of mice infected with mouse-adapted variant Creutzfeldt-Jakob disease by in vitro amplification.

Review 2. Cellular mechanisms responsible for cell-to-cell spreading of prions.

Review 3. Anchorless risk or released benefit? An updated view on the ADAM10-mediated shedding of the prion protein.

4. A Soluble PrP^C Derivative and Membrane-Anchored PrP^C in Extracellular Vesicles Attenuate Innate Immunity by Engaging the NMDA-R/LRP1 Receptor Complex.

Review 5. Salivary biomarkers in cancer detection.

Review 6. Exosome analysis: a promising biomarker system with special attention to saliva.

7. Plasma soluble prion protein, a potential biomarker for sport-related concussions: a pilot study.

8. Salivary exosomal PSMA7: a promising biomarker of inflammatory bowel disease.

9. The Biological Function of the Prion Protein: A Cell Surface Scaffold of Signaling Modules.

Review 10. Salivary Exosomes: Emerging Roles in Systemic Disease.

Normal prion protein is expressed on exosomes isolated from human plasma.

1. First demonstration of transmissible spongiform encephalopathy-associated prion protein (PrPTSE) in extracellular vesicles from plasma of mice infected with mouse-adapted variant Creutzfeldt-Jakob disease by in vitro amplification.

Review 2. Cellular mechanisms responsible for cell-to-cell spreading of prions.

Review 3. Anchorless risk or released benefit? An updated view on the ADAM10-mediated shedding of the prion protein.

4. A Soluble PrPC Derivative and Membrane-Anchored PrPC in Extracellular Vesicles Attenuate Innate Immunity by Engaging the NMDA-R/LRP1 Receptor Complex.

Review 5. Salivary biomarkers in cancer detection.

Review 6. Exosome analysis: a promising biomarker system with special attention to saliva.

7. Plasma soluble prion protein, a potential biomarker for sport-related concussions: a pilot study.

8. Salivary exosomal PSMA7: a promising biomarker of inflammatory bowel disease.

9. The Biological Function of the Prion Protein: A Cell Surface Scaffold of Signaling Modules.

Review 10. Salivary Exosomes: Emerging Roles in Systemic Disease.

4. A Soluble PrP^C Derivative and Membrane-Anchored PrP^C in Extracellular Vesicles Attenuate Innate Immunity by Engaging the NMDA-R/LRP1 Receptor Complex.