@article{7dc720b6bad942779ea25a76964a994a,
title = "Lipin-1 Contributes to IL-4 Mediated Macrophage Polarization",
abstract = "Macrophage responses contribute to a diverse array of pathologies ranging from infectious disease to sterile inflammation. Polarization of macrophages determines their cellular function within biological processes. Lipin-1 is a phosphatidic acid phosphatase in which its enzymatic activity contributes to macrophage pro-inflammatory responses. Lipin-1 also possesses transcriptional co-regulator activity and whether this activity is required for macrophage polarization is unknown. Using mice that lack only lipin-1 enzymatic activity or both enzymatic and transcriptional coregulator activities from myeloid cells, we investigated the contribution of lipin-1 transcriptional co-regulator function toward macrophage wound healing polarization. Macrophages lacking both lipin-1 activities did not elicit IL-4 mediated gene expression to levels seen in either wild-type or lipin-1 enzymatically deficient macrophages. Furthermore, mice lacking myeloid-associated lipin-1 have impaired full thickness excisional wound healing compared to wild-type mice or mice only lacking lipin-1 enzymatic activity from myeloid cell. Our study provides evidence that lipin-1 transcriptional co-regulatory activity contributes to macrophage polarization and influences wound healing in vivo.",
keywords = "lipin-1, macrophage, polarization, transcriptional coregulator, wound healing",
author = "Sunitha Chandran and Schilke, \{Robert M.\} and Blackburn, \{Cassidy M.R.\} and Aila Yurochko and Rusella Mirza and Scott, \{Rona S.\} and Finck, \{Brian N.\} and Woolard, \{Matthew D.\}",
note = "Funding Information: This work was supported by the National Heart, Lung, and Blood Institute R01 HL131844 (MW) and R01 HL119225 (BF). Malcolm Feist Predoctoral Fellowship (CB). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Funding Information: We would like to thank David Custis for his help with running samples related to flow cytometric experiments, Deshawn Blankenship for sectioning all tissues used in this study, and Gabrielle Gahn for determining genotypes of all mice. This manuscript has been released as a preprint at BioRxiv (42 ). Funding. This work was supported by the National Heart, Lung, and Blood Institute R01 HL131844 (MW) and R01 HL119225 (BF). Malcolm Feist Predoctoral Fellowship (CB). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Publisher Copyright: {\textcopyright} Copyright {\textcopyright} 2020 Chandran, Schilke, Blackburn, Yurochko, Mirza, Scott, Finck and Woolard.",
year = "2020",
month = may,
day = "5",
doi = "10.3389/fimmu.2020.00787",
language = "English",
volume = "11",
journal = "Frontiers in immunology",
issn = "1664-3224",
}