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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....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-8873364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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