Deletion of Wiskott–Aldrich syndrome protein triggers Rac2 activity and increased cross-presentation by dendritic cells
Wiskott–Aldrich syndrome (WAS) is a severe X-linked primary immunodeficiency syndrome. Here, the authors show that loss of WAS gene in dendritic cells results in increased activity of Rac2, increase of phagosomal pH, and more efficient cross-presentation.
Enregistré dans:
Auteurs principaux: | Marisa A. P. Baptista, Marton Keszei, Mariana Oliveira, Karen K. S. Sunahara, John Andersson, Carin I. M. Dahlberg, Austen J. Worth, Agne Liedén, I-Chun Kuo, Robert P. A. Wallin, Scott B. Snapper, Liv Eidsmo, Annika Scheynius, Mikael C. I. Karlsson, Gerben Bouma, Siobhan O. Burns, Mattias N. E. Forsell, Adrian J. Thrasher, Susanne Nylén, Lisa S. Westerberg |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2016
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/b30cb5531b534a4c9f3e0c5bebf69da8 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Wiskott-Aldrich syndrome protein regulates autophagy and inflammasome activity in innate immune cells
par: Pamela P. Lee, et autres
Publié: (2017) -
Wiskott Aldrich syndrome: healthcare utilizations and disparities in transplant care
par: Nikki Agarwal, et autres
Publié: (2021) -
Targeted gene correction of human hematopoietic stem cells for the treatment of Wiskott - Aldrich Syndrome
par: Rajeev Rai, et autres
Publié: (2020) -
Analysis of clinical and molecular genetic characteristics of Wiskott-Aldrich syndrome and X-linked thrombocytopenia
par: Doina TURCAN, et autres
Publié: (2021) -
Trasplante alogénico de precursores hematopoyéticos en pacientes con síndrome de Wiskott-Aldrich
par: Wietstruck P,María Angélica, et autres
Publié: (2007)