Eming, Sabine | Fabri, Mario - C 04

Unlocking tissue protective and regenerative functions of myeloid cells by metabolic reprograming

Prof. Dr. Sabine Eming
Prof. Dr. Sabine Eming

Clinic of Dermatology and Venereology

CMMC - Vice Chair
CMMC - PI - C 04

Clinic of Dermatology and Venereology

Kerpener Str. 62

50937 Cologne

Prof. Dr. Mario Fabri
Prof. Dr. Mario Fabri

Clinic of Dermatology and Venereology

CMMC - Co-PI - C 04

Clinic of Dermatology and Venereology

Kerpener Str. 62

50931 Cologne

Introduction

The laboratory is localized in the Department of Dermatology at the University of Cologne. The group has a longstanding expertise in the understanding of cell-cell and cell-matrix interactions relevant to different aspects of tissue remodeling and repair. Research involves a broad range of in vitro and in vivo models to analyze the function of diverse types of skin cells. These include a number of cellular systems (monolayer cultures, complex co-cultures), but also the investigation of genetically modified mouse models. In cooperation with other investigators the group also studies cellular communications in Drosophila and Zebrafish. State of the art technologies for molecular and cell biology are in place (FACS analysis, microarray analysis, time labs video microscopy, confocal microscopy) or are accessible through the Service Laboratory of the CMMC or close collaborations with other groups at the Campus of the University (MPI for Biology of Ageing, MPI for Metabolism Research, Excellence Cluster Cellular Stress Responses in Ageing-Associated Diseases).

Lab website

For information about Prof. Eming's and Prof. Fabri's research and work, please visit the following page: Eming Group and Fabri Lab

2024 (up to June)
  • Bopp L, Martinez ML, Schumacher C, Seitz R, Arana MH, Klapproth H, Lukas D, Oh JH, Neumayer D, Lackmann JW, Mueller S, von Stebut E, Brachvogel B, Brodesser S, Klein Geltink RI, and Fabri M (2024). Glutamine promotes human CD8(+) T cells and counteracts imiquimod-induced T cell hyporesponsiveness. iScience27, 109767. doi:10.1016/j.isci.2024.109767.
     
  • Injarabian L, Willenborg S, Welcker D, Sanin DE, Pasparakis M, Kashkar H, and Eming SA (2024). FADD- and RIPK3-Mediated Cell Death Ensures Clearance of Ly6C(high) Wound Macrophages from Damaged Tissue. J Invest Dermatol144, 152-164 e157. doi:10.1016/j.jid.2023.06.203.
     
  • Klapproth H, Rauterberg J, Shabli S, Silling S, Böttcher S, von Stebut E, Fabri M. Papulo-vesicular eruption and profound unilateral hearing loss in a 20-year-old man. J Dtsch Dermatol Ges. 2024 May;22(5):720-723. doi: 10.1111/ddg.15363. Epub 2024 Apr 6. PMID: 38581347.
     
  • Willenborg S, Satzinger S, and Eming SA (2024). [Skin fibrosis : Novel insights in pathophysiology and treatment]. Dermatologie (Heidelb)75, 218-224. doi:10.1007/s00105-024-05299-7.
2023
  • Hadrian K, Musial G, Schonberg A, Georgiev T, Kuper C, Bock F, Jantsch J, Cursiefen C, Eming SA, and Hos D (2023). The role of the osmosensitive transcription factor NFAT5 in corneal edema resorption after injury. Exp Mol Med 55, 565-573. doi:10.1038/s12276-023-00954-w.
     
  • Injarabian L, Willenborg S, Welcker D, Sanin DE, Pasparakis M, Kashkar H, and Eming SA (2024). FADD- and RIPK3-Mediated Cell Death Ensures Clearance of Ly6C(high) Wound Macrophages from Damaged Tissue. J Invest Dermatol 144, 152-164 e157. doi:10.1016/j.jid.2023.06.203.
     
  • Riehl DR, Sharma A, Roewe J, Murke F, Ruppert C, Eming SA, Bopp T, Kleinert H, Radsak MP, Colucci G, Subramaniam S, Reinhardt C, Giebel B, Prinz I, Guenther A, Strand D, Gunzer M, Waisman A, Ward PA, Ruf W, Schafer K, and Bosmann M (2023). Externalized histones fuel pulmonary fibrosis via a platelet-macrophage circuit of TGFbeta1 and IL-27. Proc Natl Acad Sci U S A 120, e2215421120. doi:10.1073/pnas.2215421120.
     
  • Satzinger S, Willenborg S, Ding X, Klose CSN, Radtke D, Voehringer D, and Eming SA (2023). Type 2 Immunity Regulates Dermal White Adipose Tissue Function. J Invest Dermatol 143, 2456-2467 e2455. doi:10.1016/j.jid.2023.05.017.