The 20 S proteasome core, active within apoptotic exosome-like vesicles, induces autoantibody production and accelerates rejection

Author:

Dieudé Mélanie12,Bell Christina23,Turgeon Julie12,Beillevaire Deborah12,Pomerleau Luc12,Yang Bing12,Hamelin Katia12,Qi Shijie12,Pallet Nicolas1,Béland Chanel1,Dhahri Wahiba1,Cailhier Jean-François12,Rousseau Matthieu24,Duchez Anne-Claire24,Lévesque Tania24,Lau Arthur25,Rondeau Christiane6,Gingras Diane6,Muruve Danie25,Rivard Alain1,Cardinal Héloise12,Perreault Claude23,Desjardins Michel6,Boilard Éric24,Thibault Pierre23,Hébert Marie-Josée12

Affiliation:

1. Research Centre, Centre hospitalier de l’Université de Montréal (CRCHUM), Montréal, Québec G1V 4G2, Canada.

2. Canadian National Transplantation Research Program, Edmonton, Alberta T6G 2E1, Canada.

3. Institute for Research in Immunology and Cancer (IRIC), Montréal, Québec H3T 1JA, Canada.

4. Centre de Recherche du CHU de Québec, Québec, Québec G1V 4G2, Canada.

5. University of Calgary, Calgary, Alberta T2N 1N4, Canada.

6. Université de Montréal, Montréal, Québec H3T 1J4, Canada.

Abstract

Exosome-like vesicles containing an active 20 S proteasome core contribute to autoimmunity and vascular allograft inflammation.

Funder

Canadian Cancer Society Research Institute (CCSRI)

Canadian Institutes of Health Research (CIHR)

Natural Sciences and Engineering Research Council of Canada (NSERC)

NSERC

Kidney Foundation of Canada

Canadian National Transplantation Research Program (CNTRP)

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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