Co-option of neutrophil fates by tissue environments

Classically considered short-lived and purely defensive leukocytes, neutrophils are unique in their fast and moldable response to stimulation. This plastic behavior may underlie variable and even antagonistic functions during inflammation or cancer, yet the full spectrum of neutrophil properties as...

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Main Authors: Ballesteros, I, Rubio-Ponce, A, Genua, M, Lusito, E, Kwok, I, Fernández-Calvo, G, Khoyratty, TE, van Grinsven, E, González-Hernández, S, Nicolás-Ávila, JÁ, Vicanolo, T, Maccataio, A, Benguría, A, Li, JL, Adrover, JM, Aroca-Crevillen, A, Quintana, JA, Martín-Salamanca, S, Mayo, F, Ascher, S, Barbiera, G, Soehnlein, O, Gunzer, M, Ginhoux, F, Sánchez-Cabo, F, Nistal-Villán, E, Schulz, C, Dopazo, A, Reinhardt, C, Udalova, IA, Ng, LG, Ostuni, R, Hidalgo, A
Format: Journal article
Language:English
Published: Cell Press 2020
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author Ballesteros, I
Rubio-Ponce, A
Genua, M
Lusito, E
Kwok, I
Fernández-Calvo, G
Khoyratty, TE
van Grinsven, E
González-Hernández, S
Nicolás-Ávila, JÁ
Vicanolo, T
Maccataio, A
Benguría, A
Li, JL
Adrover, JM
Aroca-Crevillen, A
Quintana, JA
Martín-Salamanca, S
Mayo, F
Ascher, S
Barbiera, G
Soehnlein, O
Gunzer, M
Ginhoux, F
Sánchez-Cabo, F
Nistal-Villán, E
Schulz, C
Dopazo, A
Reinhardt, C
Udalova, IA
Ng, LG
Ostuni, R
Hidalgo, A
author_facet Ballesteros, I
Rubio-Ponce, A
Genua, M
Lusito, E
Kwok, I
Fernández-Calvo, G
Khoyratty, TE
van Grinsven, E
González-Hernández, S
Nicolás-Ávila, JÁ
Vicanolo, T
Maccataio, A
Benguría, A
Li, JL
Adrover, JM
Aroca-Crevillen, A
Quintana, JA
Martín-Salamanca, S
Mayo, F
Ascher, S
Barbiera, G
Soehnlein, O
Gunzer, M
Ginhoux, F
Sánchez-Cabo, F
Nistal-Villán, E
Schulz, C
Dopazo, A
Reinhardt, C
Udalova, IA
Ng, LG
Ostuni, R
Hidalgo, A
author_sort Ballesteros, I
collection OXFORD
description Classically considered short-lived and purely defensive leukocytes, neutrophils are unique in their fast and moldable response to stimulation. This plastic behavior may underlie variable and even antagonistic functions during inflammation or cancer, yet the full spectrum of neutrophil properties as they enter healthy tissues remains unexplored. Using a new model to track neutrophil fates, we found short but variable lifetimes across multiple tissues. Through analysis of the receptor, transcriptional, and chromatin accessibility landscapes, we identify varying neutrophil states and assign non-canonical functions, including vascular repair and hematopoietic homeostasis. Accordingly, depletion of neutrophils compromised angiogenesis during early age, genotoxic injury, and viral infection, and impaired hematopoietic recovery after irradiation. Neutrophils acquired these properties in target tissues, a process that, in the lungs, occurred in CXCL12-rich areas and relied on CXCR4. Our results reveal that tissues co-opt neutrophils en route for elimination to induce programs that support their physiological demands.
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spelling oxford-uuid:e5351e91-776c-42c3-a50c-5a43d2c068f22022-03-27T10:22:24ZCo-option of neutrophil fates by tissue environmentsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e5351e91-776c-42c3-a50c-5a43d2c068f2EnglishSymplectic ElementsCell Press2020Ballesteros, IRubio-Ponce, AGenua, MLusito, EKwok, IFernández-Calvo, GKhoyratty, TEvan Grinsven, EGonzález-Hernández, SNicolás-Ávila, JÁVicanolo, TMaccataio, ABenguría, ALi, JLAdrover, JMAroca-Crevillen, AQuintana, JAMartín-Salamanca, SMayo, FAscher, SBarbiera, GSoehnlein, OGunzer, MGinhoux, FSánchez-Cabo, FNistal-Villán, ESchulz, CDopazo, AReinhardt, CUdalova, IANg, LGOstuni, RHidalgo, AClassically considered short-lived and purely defensive leukocytes, neutrophils are unique in their fast and moldable response to stimulation. This plastic behavior may underlie variable and even antagonistic functions during inflammation or cancer, yet the full spectrum of neutrophil properties as they enter healthy tissues remains unexplored. Using a new model to track neutrophil fates, we found short but variable lifetimes across multiple tissues. Through analysis of the receptor, transcriptional, and chromatin accessibility landscapes, we identify varying neutrophil states and assign non-canonical functions, including vascular repair and hematopoietic homeostasis. Accordingly, depletion of neutrophils compromised angiogenesis during early age, genotoxic injury, and viral infection, and impaired hematopoietic recovery after irradiation. Neutrophils acquired these properties in target tissues, a process that, in the lungs, occurred in CXCL12-rich areas and relied on CXCR4. Our results reveal that tissues co-opt neutrophils en route for elimination to induce programs that support their physiological demands.
spellingShingle Ballesteros, I
Rubio-Ponce, A
Genua, M
Lusito, E
Kwok, I
Fernández-Calvo, G
Khoyratty, TE
van Grinsven, E
González-Hernández, S
Nicolás-Ávila, JÁ
Vicanolo, T
Maccataio, A
Benguría, A
Li, JL
Adrover, JM
Aroca-Crevillen, A
Quintana, JA
Martín-Salamanca, S
Mayo, F
Ascher, S
Barbiera, G
Soehnlein, O
Gunzer, M
Ginhoux, F
Sánchez-Cabo, F
Nistal-Villán, E
Schulz, C
Dopazo, A
Reinhardt, C
Udalova, IA
Ng, LG
Ostuni, R
Hidalgo, A
Co-option of neutrophil fates by tissue environments
title Co-option of neutrophil fates by tissue environments
title_full Co-option of neutrophil fates by tissue environments
title_fullStr Co-option of neutrophil fates by tissue environments
title_full_unstemmed Co-option of neutrophil fates by tissue environments
title_short Co-option of neutrophil fates by tissue environments
title_sort co option of neutrophil fates by tissue environments
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