The SWI/SNF chromatin-remodeling subunit DPF2 regulates macrophage inflammation in intestinal injury via the CACNA1D-mediated MAPK pathway
Abstract
The immune system plays a pivotal role in pathogenesis of intestinal injury and subsequent regenerative processes, particularly macrophages, orchestrate the inflammatory response and tissue repair. Here, we identified that loss of double PHD fingers 2 (DPF2) enhances intestinal regeneration and reduces inflammation. Using a combination of mouse genetics, single cell RNA sequencing, and spatial transcriptomics, we found that Dpf2 loss in macrophage modulates inflammatory polarization, thus protecting against intestinal injury. Mechanistically, Dpf2 deficiency leads to loss of H3K27ac and H3K4me1 marks at Cacna1d enhancer, impairing Cacna1d messenger RNA (mRNA) expression and reducing intracellular calcium. Consequently, loss of Dpf2 attenuates mitogen-activated protein kinases signaling activity, promoting an anti-inflammatory macrophage polarization. Finally, through analysis of clinical inflammatory bowel disease (IBD) single cell RNA and spatial transcriptome data, patient-derived organoids and clinical samples, we validated a positive correlation between DPF2, CACNA1D, and intestinal inflammation. Our findings establish an essential role for DPF2 in facilitating CACNA1D expression in macrophages to regulate intestinal inflammation and regeneration.
Article Details
Journal Info
Proceedings of the National Academy of Sciences
National Academy of Sciences
Authors (17)
Mintao Ji
Institute of Radiation Medicine, Shanghai Medical College, Fudan University
Haisheng Liang
Institute of Radiation Medicine, Shanghai Medical College, Fudan University
Shuai Dong
Southeast University , , ,
Yuhan Guo
State Key Laboratory of Radiation Medicine and Protection, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Jiangsu Key Laboratory of Infection and Immunity, School of Radiation Medicine and Protection, Suzhou Medical College of Soochow University
Yiping Lin
State Key Laboratory of Radiation Medicine and Protection, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Jiangsu Key Laboratory of Infection and Immunity, School of Radiation Medicine and Protection, Suzhou Medical College of Soochow University
Hong Zhang
Yuhong Wang
Department of Pathology, The First Affiliated Hospital of Soochow University
Zhe Lei
Department of Pathology, The First Affiliated Hospital of Soochow University
Xiaoya Xu
Institute of Radiation Medicine, Shanghai Medical College, Fudan University
Yinyin Shu
Institute of Radiation Medicine, Shanghai Medical College, Fudan University
Zhisen Zhang
State Key Laboratory of Radiation Medicine and Protection, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Jiangsu Key Laboratory of Infection and Immunity, School of Radiation Medicine and Protection, Suzhou Medical College of Soochow University
Xiaoni Jin
State Key Laboratory of Radiation Medicine and Protection, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Jiangsu Key Laboratory of Infection and Immunity, School of Radiation Medicine and Protection, Suzhou Medical College of Soochow University
Shuangshuang Lu
State Key Laboratory of Radiation Medicine and Protection, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Jiangsu Key Laboratory of Infection and Immunity, School of Radiation Medicine and Protection, Suzhou Medical College of Soochow University
Wensheng Zhang
Lingchuan Guo
Department of Pathology, The First Affiliated Hospital of Soochow University
Chunlin Shao
Institute of Radiation Medicine, Shanghai Medical College, Fudan University
Lei Chang
Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.