2. Academic Validation
  3. Macrophage autophagy deficiency-induced CEBPB accumulation alleviates atopic dermatitis via impairing M2 polarization

Macrophage autophagy deficiency-induced CEBPB accumulation alleviates atopic dermatitis via impairing M2 polarization

  • Cell Rep. 2023 Nov 13;42(11):113430. doi: 10.1016/j.celrep.2023.113430.
Yongcheng Zhu 1,  Yunyao Liu 2,  Yuxiang Ma 3,  Liu Chen 1,  He Huang 4,  Siting Huang 1,  Huiling Zhang 1,  Yuying He 5,  Cheng Tan 6,  Yuan He 7,  Lei Qiang 8
Affiliations

Affiliations

  • 1 State Key Laboratory of Natural Medicines, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
  • 2 State Key Laboratory of Natural Medicines, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing 211198, China; Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing 210042, China.
  • 3 Department of Pharmacology, Guilin Medical University, Guilin 541199, China.
  • 4 Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201213, China. Electronic address: hhuang@simm.ac.cn.
  • 5 Department of Medicine, Section of Dermatology, University of Chicago, Chicago, IL, USA.
  • 6 Department of Dermatology, Affiliated Hospital of Nanjing University of Chinese Medicine, 155 Hanzhong Road, Nanjing 210029, China. Electronic address: tancheng@yeah.net.
  • 7 State Key Laboratory of Natural Medicines, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing 211198, China. Electronic address: yuanhe0822@cpu.edu.cn.
  • 8 State Key Laboratory of Natural Medicines, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing 211198, China; Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and STIs, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing 210042, China. Electronic address: lqiang@cpu.edu.cn.
PMID: 37963021 DOI: 10.1016/j.celrep.2023.113430
Abstract

Macroautophagy/Autophagy plays a pivotal role in immune regulation. Its significance is evident in modulation of immune cell differentiation and maturation, physiologically and pathologically. Here, we investigate the role of macrophage Autophagy on the development of atopic dermatitis (AD). By employing an MC903-induced AD mice model, we observe reduced cutaneous inflammation in macrophage Atg5 cKO mice compared with WT mice. Notably, there is a decreased infiltration of M2 macrophages in lesional skin from Atg5 cKO mice. Furthermore, impaired STAT6 phosphorylation and diminished expression of M2 markers are detected in autophagy-deficient macrophages. Our mechanistic exploration reveals that CEBPB drives the transcription of SOCS1/3 and SQSTM1/p62-mediated Autophagy degrades CEBPB normally. Autophagy deficiency leads to CEBPB accumulation, and further promotes the expression of SOCS1/3. This process inhibits JAK1-STAT6 pathway activation and M2 marker expression. Together, our study indicates that Autophagy is required for M2 activation and macrophage Autophagy may be a promising target for AD intervention.

Keywords

CEBPB; CP: Immunology; M2 activation; SOCS1 and SOCS3; SQSTM1/p62; atopic dermatitis; autophagy.

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