TY - JOUR
T1 - The interweaved signatures of common-gamma-chain cytokines across immunologic lineages
AU - The Immunological Genome Project Consortium
AU - Baysoy, Alev
AU - Seddu, Kumba
AU - Salloum, Tamara
AU - Dawson, Caleb A.
AU - Lee, Juliana J.
AU - Yang, Liang
AU - Gal-Oz, Shani
AU - Ner-Gaon, Hadas
AU - Tellier, Julie
AU - Millan, Alberto
AU - Sasse, Alexander
AU - Brown, Brian
AU - Lanier, Lewis L.
AU - Shay, Tal
AU - Nutt, Stephen
AU - Dwyer, Daniel
AU - Benoist, Christophe
N1 - Publisher Copyright:
© 2023 Benoist et al.
PY - 2023/7/3
Y1 - 2023/7/3
N2 - “γc” cytokines are a family whose receptors share a “common-gamma-chain” signaling moiety, and play central roles in differentiation, homeostasis, and communications of all immunocyte lineages. As a resource to better understand their range and specificity of action, we profiled by RNAseq the immediate-early responses to the main γc cytokines across all immunocyte lineages. The results reveal an unprecedented landscape: broader, with extensive overlap between cytokines (one cytokine doing in one cell what another does elsewhere) and essentially no effects unique to any one cytokine. Responses include a major downregulation component and a broad Myc-controlled resetting of biosynthetic and metabolic pathways. Various mechanisms appear involved: fast transcriptional activation, chromatin remodeling, and mRNA destabilization. Other surprises were uncovered: IL2 effects in mast cells, shifts between follicular and marginal zone B cells, paradoxical and cell-specific cross-talk between interferon and γc signatures, or an NKT-like program induced by IL21 in CD8+ T cells.
AB - “γc” cytokines are a family whose receptors share a “common-gamma-chain” signaling moiety, and play central roles in differentiation, homeostasis, and communications of all immunocyte lineages. As a resource to better understand their range and specificity of action, we profiled by RNAseq the immediate-early responses to the main γc cytokines across all immunocyte lineages. The results reveal an unprecedented landscape: broader, with extensive overlap between cytokines (one cytokine doing in one cell what another does elsewhere) and essentially no effects unique to any one cytokine. Responses include a major downregulation component and a broad Myc-controlled resetting of biosynthetic and metabolic pathways. Various mechanisms appear involved: fast transcriptional activation, chromatin remodeling, and mRNA destabilization. Other surprises were uncovered: IL2 effects in mast cells, shifts between follicular and marginal zone B cells, paradoxical and cell-specific cross-talk between interferon and γc signatures, or an NKT-like program induced by IL21 in CD8+ T cells.
UR - http://www.scopus.com/inward/record.url?scp=85151168115&partnerID=8YFLogxK
U2 - 10.1084/jem.20222052
DO - 10.1084/jem.20222052
M3 - Article
C2 - 36976164
AN - SCOPUS:85151168115
SN - 0022-1007
VL - 220
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 7
M1 - e20222052
ER -