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HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory disease

Authors :
Baoyu Chen
Susan Price
Moza Al Hassani
M. Cecilia Poli
Ivan K. Chinn
Zeynep H. Coban-Akdemir
Tram N. Cao
Sarah Cook
Sylvain Latour
Gehad ElGhazali
Geoffrey D.E. Cuvelier
Jason W. Caldwell
Sheng Yang
D. Eric Anderson
Jordan S. Orange
Douglas B. Kuhns
Lisa R. Forbes
Alexander Vargas-Hernández
Soma Jyonouchi
Nikita Raje
Aiman J. Faruqi
V. Koneti Rao
Michael J. Lenardo
Benjamin Fournier
Alexandre F. Carisey
Donna M. Muzny
Shalini N. Jhangiani
James R. Lupski
Morgan Similuk
Wadih Abou Chahla
Janis K. Burkhardt
Yanping Huang
Nawal Al Kaabi
William A. Comrie
Richard A. Gibbs
Margery G. Smelkinson
Emily M. Mace
Zain Al Yafei
Andrew J. Oler
Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP)
Source :
Science, Science, American Association for the Advancement of Science, 2020, 369 (6500), pp.202-207. ⟨10.1126/science.aay5663⟩, BASE-Bielefeld Academic Search Engine
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

An inherited disorder makes WAVEs The WAVE regulatory complex (WRC) is a multiunit complex that regulates actin cytoskeleton formation. Although other actin-regulatory proteins modulate human immune responses, the precise role for the WRC has not yet been established. Cook et al. studied five patients from four unrelated families who harbor missense variants of the gene encoding the WRC component HEM1. These patients presented with recurrent infections and poor antibody responses, along with enhanced allergic and autoimmune disorders. HEM1 was found to be required for the regulation of cortical actin and granule release in T cells and also interacted with a key metabolic signaling complex contributing to the disease phenotype. By linking these interactions to immune function, this work suggests potential targets for future immunotherapies. Science , this issue p. 202

Details

Language :
English
ISSN :
00368075 and 10959203
Database :
OpenAIRE
Journal :
Science, Science, American Association for the Advancement of Science, 2020, 369 (6500), pp.202-207. ⟨10.1126/science.aay5663⟩, BASE-Bielefeld Academic Search Engine
Accession number :
edsair.doi.dedup.....234bbc7516711e8791b736237bbbf410
Full Text :
https://doi.org/10.1126/science.aay5663⟩