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Single-cell analysis of skin immune cells reveals an Angptl4-ifi20b axis that regulates monocyte differentiation during wound healing

The persistent inflammatory response at the wound site is a cardinal feature of nonhealing wounds. Prolonged neutrophil presence in the wound site due to failed clearance by reduced monocyte-derived macrophages delays the transition from the inflammatory to the proliferative phase of wound healing....

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Autores principales: Wee, Wei Kiat Jonathan, Low, Zun Siong, Ooi, Chin Kiat, Henategala, Benjamin Patrana, Lim, Zhi Guang Ridley, Yip, Yun Sheng, Vos, Marcus Ivan Gerard, Tan, William Wei Ren, Cheng, Hong Sheng, Tan, Nguan Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873364/
https://www.ncbi.nlm.nih.gov/pubmed/35210411
http://dx.doi.org/10.1038/s41419-022-04638-7
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author Wee, Wei Kiat Jonathan
Low, Zun Siong
Ooi, Chin Kiat
Henategala, Benjamin Patrana
Lim, Zhi Guang Ridley
Yip, Yun Sheng
Vos, Marcus Ivan Gerard
Tan, William Wei Ren
Cheng, Hong Sheng
Tan, Nguan Soon
author_facet Wee, Wei Kiat Jonathan
Low, Zun Siong
Ooi, Chin Kiat
Henategala, Benjamin Patrana
Lim, Zhi Guang Ridley
Yip, Yun Sheng
Vos, Marcus Ivan Gerard
Tan, William Wei Ren
Cheng, Hong Sheng
Tan, Nguan Soon
author_sort Wee, Wei Kiat Jonathan
collection PubMed
description The persistent inflammatory response at the wound site is a cardinal feature of nonhealing wounds. Prolonged neutrophil presence in the wound site due to failed clearance by reduced monocyte-derived macrophages delays the transition from the inflammatory to the proliferative phase of wound healing. Angiopoietin-like 4 protein (Angptl4) is a matricellular protein that has been implicated in many inflammatory diseases. However, its precise role in the immune cell response during wound healing remains unclear. Therefore, we performed flow cytometry and single-cell RNA sequencing to examine the immune cell landscape of excisional wounds from Angptl4(+/+) and Angptl4(−/−) mice. Chemotactic immune cell recruitment and infiltration were not compromised due to Angptl4 deficiency. However, as wound healing progresses, Angptl4(−/−) wounds have a prolonged neutrophil presence and fewer monocyte-derived macrophages than Angptl4(+/+) and Angptl4(LysM−/−) wounds. The underlying mechanism involves a novel Angptl4-interferon activated gene 202B (ifi202b) axis that regulates monocyte differentiation to macrophages, coordinating neutrophil removal and inflammation resolution. An unbiased kinase inhibitor screen revealed an Angptl4-mediated kinome signaling network involving S6K, JAK, and CDK, among others, that modulates the expression of ifi202b. Silencing ifi202b in Angptl4(−/−) monocytes, whose endogenous expression was elevated, rescued the impaired monocyte-to-macrophage transition in the in vitro reconstituted wound microenvironment using wound exudate. GSEA and IPA functional analyses revealed that ifi202b-associated canonical pathways and functions involved in the inflammatory response and monocyte cell fate were enriched. Together, we identified ifi202b as a key gatekeeper of monocyte differentiation. By modulating ifi202b expression, Angptl4 orchestrates the inflammatory state, innate immune landscape, and wound healing process.
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spelling pubmed-88733642022-03-17 Single-cell analysis of skin immune cells reveals an Angptl4-ifi20b axis that regulates monocyte differentiation during wound healing Wee, Wei Kiat Jonathan Low, Zun Siong Ooi, Chin Kiat Henategala, Benjamin Patrana Lim, Zhi Guang Ridley Yip, Yun Sheng Vos, Marcus Ivan Gerard Tan, William Wei Ren Cheng, Hong Sheng Tan, Nguan Soon Cell Death Dis Article The persistent inflammatory response at the wound site is a cardinal feature of nonhealing wounds. Prolonged neutrophil presence in the wound site due to failed clearance by reduced monocyte-derived macrophages delays the transition from the inflammatory to the proliferative phase of wound healing. Angiopoietin-like 4 protein (Angptl4) is a matricellular protein that has been implicated in many inflammatory diseases. However, its precise role in the immune cell response during wound healing remains unclear. Therefore, we performed flow cytometry and single-cell RNA sequencing to examine the immune cell landscape of excisional wounds from Angptl4(+/+) and Angptl4(−/−) mice. Chemotactic immune cell recruitment and infiltration were not compromised due to Angptl4 deficiency. However, as wound healing progresses, Angptl4(−/−) wounds have a prolonged neutrophil presence and fewer monocyte-derived macrophages than Angptl4(+/+) and Angptl4(LysM−/−) wounds. The underlying mechanism involves a novel Angptl4-interferon activated gene 202B (ifi202b) axis that regulates monocyte differentiation to macrophages, coordinating neutrophil removal and inflammation resolution. An unbiased kinase inhibitor screen revealed an Angptl4-mediated kinome signaling network involving S6K, JAK, and CDK, among others, that modulates the expression of ifi202b. Silencing ifi202b in Angptl4(−/−) monocytes, whose endogenous expression was elevated, rescued the impaired monocyte-to-macrophage transition in the in vitro reconstituted wound microenvironment using wound exudate. GSEA and IPA functional analyses revealed that ifi202b-associated canonical pathways and functions involved in the inflammatory response and monocyte cell fate were enriched. Together, we identified ifi202b as a key gatekeeper of monocyte differentiation. By modulating ifi202b expression, Angptl4 orchestrates the inflammatory state, innate immune landscape, and wound healing process. Nature Publishing Group UK 2022-02-24 /pmc/articles/PMC8873364/ /pubmed/35210411 http://dx.doi.org/10.1038/s41419-022-04638-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wee, Wei Kiat Jonathan
Low, Zun Siong
Ooi, Chin Kiat
Henategala, Benjamin Patrana
Lim, Zhi Guang Ridley
Yip, Yun Sheng
Vos, Marcus Ivan Gerard
Tan, William Wei Ren
Cheng, Hong Sheng
Tan, Nguan Soon
Single-cell analysis of skin immune cells reveals an Angptl4-ifi20b axis that regulates monocyte differentiation during wound healing
title Single-cell analysis of skin immune cells reveals an Angptl4-ifi20b axis that regulates monocyte differentiation during wound healing
title_full Single-cell analysis of skin immune cells reveals an Angptl4-ifi20b axis that regulates monocyte differentiation during wound healing
title_fullStr Single-cell analysis of skin immune cells reveals an Angptl4-ifi20b axis that regulates monocyte differentiation during wound healing
title_full_unstemmed Single-cell analysis of skin immune cells reveals an Angptl4-ifi20b axis that regulates monocyte differentiation during wound healing
title_short Single-cell analysis of skin immune cells reveals an Angptl4-ifi20b axis that regulates monocyte differentiation during wound healing
title_sort single-cell analysis of skin immune cells reveals an angptl4-ifi20b axis that regulates monocyte differentiation during wound healing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873364/
https://www.ncbi.nlm.nih.gov/pubmed/35210411
http://dx.doi.org/10.1038/s41419-022-04638-7
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