Extracellular Vesicles and Endocannabinoid Signaling in Patients with COVID-19-Reference-Cited by-同舟云学术

Extracellular Vesicles and Endocannabinoid Signaling in Patients with COVID-19

Published:2023-09-14 Issue: Volume: Page:
ISSN:2578-5125
Container-title:Cannabis and Cannabinoid Research
language:en
Short-container-title:Cannabis and Cannabinoid Research

Author:

Brandes Florian¹,Keiler Annekathrin M.²,Kirchner Benedikt³,Borrmann Melanie¹,Billaud Jean-Noël⁴^ORCID,Reithmair Marlene⁵,Klein Matthias⁶,Campolongo Patrizia⁷^ORCID,Thieme Detlef²,Pfaffl Michael W.³,Schelling Gustav¹^ORCID,Meidert Agnes S.¹

Affiliation:

1. Department of Anesthesiology, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.

2. Institute of Doping Analysis and Sports Biochemistry, Kreischa, Germany.

3. Division of Animal Physiology and Immunology, School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.

4. QIAGEN Digital Insights, Redwood City, California, USA.

5. Institute of Human Genetics, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.

6. Department of Neurology, University Hospital, Ludwig-Maximilians-University of Munich, Munich, Germany.

7. Department of Physiology and Pharmacology «V. Erspamer», Sapienza University of Rome, Rome, Italy.

Publisher

Mary Ann Liebert Inc

Subject

Pharmacology (medical),Complementary and alternative medicine,Pharmacology

Link

https://www.liebertpub.com/doi/pdf/10.1089/can.2023.0040

Reference42 articles.

1. The Immunopathology of COVID-19 and the Cannabis Paradigm

2. Targeted deletion of cannabinoid receptors CB1and CB2produced enhanced inflammatory responses to influenza A/PR/8/34 in the absence and presence of Δ9-tetrahydrocannabinol

3. Active endocannabinoids are secreted on extracellular membrane vesicles

4. The biology , function , and biomedical applications of exosomes

5. Exosomes Recovered From the Plasma of COVID-19 Patients Expose SARS-CoV-2 Spike-Derived Fragments and Contribute to the Adaptive Immune Response

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