Trans-activation of eotaxin-1 by Brg1 contributes to liver regeneration.


Journal

Cell death & disease
ISSN: 2041-4889
Titre abrégé: Cell Death Dis
Pays: England
ID NLM: 101524092

Informations de publication

Date de publication:
25 05 2022
Historique:
received: 03 09 2021
accepted: 12 05 2022
revised: 10 05 2022
entrez: 25 5 2022
pubmed: 26 5 2022
medline: 28 5 2022
Statut: epublish

Résumé

Infiltration of eosinophils is associated with and contributes to liver regeneration. Chemotaxis of eosinophils is orchestrated by the eotaxin family of chemoattractants. We report here that expression of eotaxin-1 (referred to as eotaxin hereafter), but not that of either eotaxin-2 or eotaxin-3, were elevated, as measured by quantitative PCR and ELISA, in the proliferating murine livers compared to the quiescent livers. Similarly, exposure of primary murine hepatocytes to hepatocyte growth factor (HGF) stimulated eotaxin expression. Liver specific deletion of Brahma-related gene 1 (Brg1), a chromatin remodeling protein, attenuated eosinophil infiltration and down-regulated eotaxin expression in mice. Brg1 deficiency also blocked HGF-induced eotaxin expression in cultured hepatocytes. Further analysis revealed that Brg1 could directly bind to the proximal eotaxin promoter to activate its transcription. Mechanistically, Brg1 interacted with nuclear factor kappa B (NF-κB)/RelA to activate eotaxin transcription. NF-κB knockdown or pharmaceutical inhibition disrupted Brg1 recruitment to the eotaxin promoter and blocked eotaxin induction in hepatocytes. Adenoviral mediated over-expression of eotaxin overcame Brg1 deficiency caused delay in liver regeneration in mice. On the contrary, eotaxin depletion with RNAi or neutralizing antibodies retarded liver regeneration in mice. More important, Brg1 expression was detected to be correlated with eotaxin expression and eosinophil infiltration in human liver specimens. In conclusion, our data unveil a novel role of Brg1 as a regulator of eosinophil trafficking by activating eotaxin transcription.

Identifiants

pubmed: 35614068
doi: 10.1038/s41419-022-04944-0
pii: 10.1038/s41419-022-04944-0
pmc: PMC9132924
doi:

Substances chimiques

Ccl11 protein, mouse 0
Chemokine CCL11 0
NF-kappa B 0
Nuclear Proteins 0
Transcription Factors 0
Smarca4 protein, mouse EC 3.6.1.-
DNA Helicases EC 3.6.4.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

495

Informations de copyright

© 2022. The Author(s).

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Auteurs

Zhiwen Fan (Z)

Department of Pathology, Nanjing Drum Tower Hospital Affiliated with Nanjing University School of Medicine, Nanjing, China.
Department of Gastroenterology, Nanjing Drum Tower Hospital Affiliated with Nanjing University School of Medicine, Nanjing, China.

Ming Kong (M)

Key Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysiology, Nanjing Medical University, Nanjing, China.

Wenhui Dong (W)

Key Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysiology, Nanjing Medical University, Nanjing, China.

Chunlong Dong (C)

Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital, Clinical College of Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China.

Xiulian Miao (X)

College of Life Sciences and Institute of Biomedical Research, Liaocheng University, Liaocheng, China.

Yan Guo (Y)

College of Life Sciences and Institute of Biomedical Research, Liaocheng University, Liaocheng, China.

Xingyu Liu (X)

College of Life Sciences and Institute of Biomedical Research, Liaocheng University, Liaocheng, China.

Shuying Miao (S)

Department of Pathology, Nanjing Drum Tower Hospital Affiliated with Nanjing University School of Medicine, Nanjing, China.

Lin Li (L)

Department of Pathology, Nanjing Drum Tower Hospital Affiliated with Nanjing University School of Medicine, Nanjing, China.

Tingting Chen (T)

Department of Pathology, Nanjing Drum Tower Hospital Affiliated with Nanjing University School of Medicine, Nanjing, China.

Yeqing Qu (Y)

Experimental Animal Center, Nanjing Drum Tower Hospital Affiliated with Nanjing University School of Medicine, Nanjing, China.

Fei Yu (F)

Experimental Animal Center, Nanjing Drum Tower Hospital Affiliated with Nanjing University School of Medicine, Nanjing, China.

Yunfei Duan (Y)

Department of Hepatobiliary Surgery, the First People's Hospital of Changzhou, the Third Hospital Affiliated with Soochow University, Changzhou, China.

Yunjie Lu (Y)

Department of Hepatobiliary Surgery, the First People's Hospital of Changzhou, the Third Hospital Affiliated with Soochow University, Changzhou, China. yjresearch@qq.com.

Xiaoping Zou (X)

Department of Gastroenterology, Nanjing Drum Tower Hospital Affiliated with Nanjing University School of Medicine, Nanjing, China. zouxp@nju.edu.cn.

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