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Kai Markus Schneider Group

Experimental Gastroenterology and Organ Crosstalk

Portrait Kai Markus Schneider

The scientific focus of Prof. Schneider’s group is in the field of molecular gastroenterology and hepatology, in particular the molecular circuitry of cellular and inter-organ communication. Using recent breakthroughs in functional genomics, metabolomics and computational biology, we focus on understanding the interactions between the gut, microbiome, liver and nervous system and how these influence disease processes. We are investigating how neuroimmune signals drive the development of chronic inflammation and how the nervous and immune systems interact in this context.

A key example is our work on the relationship between psychological stress and the enteric nervous system. In this study, we uncovered a previously unknown molecular mechanism by which psychological stress amplifies inflammatory responses in inflammatory bowel disease. In addition, we identified a novel glial cell population that promotes inflammation through its interaction with monocytes.

In recent years, our research has also contributed significantly to the understanding of the gut-liver axis, demonstrating the close link between liver disease and alterations in the gut environment. We aim to identify new therapeutic targets using modern omics approaches, advanced imaging strategies and bioinformatics analysis, for example by studying the nervous system and neuro-immune interactions at the single cell level. Furthermore, we are also applying neuroscience techniques to the gastrointestinal tract. Using chemogenetics, we can selectively activate or inhibit specific neuronal populations to gain mechanistic insights into neuro-immune interactions.

Future Projects and Goals

Many of our projects are inspired by clinical challenges and unmet needs and are designed to provide new mechanistic insights and therapeutic approaches. To this end, our research includes analyses of both large clinical datasets (e.g. UK Biobank, Penn Medicine Biobank, All of Us) and human tissue samples, as well as experimental studies using in-vivo and in-vitro models.

Methodological and Technical Expertise

  • Experimental models of disease
    • HCC/CCA Models
    • Models of cholestatic liver disease
    • Metabolic dysfunction-associated Steatotic Liver Disease (MASLD)
    • Liver fibrosis models
    • Acute/Chronic liver injury models
    • Colitis Models
  • Single-cell and spatial transcriptomics
  • Microbiome analyses (16s gene amplicon & metagenomics)
  • Confocal microscopy
    • Intestinal whole mount
    • Tissue clearing
  • Flow cytometry analysis

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Kai Markus Schneider is recruiting in the PhD Summer Selection 2025

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CV

Since October 2024
Full Professor (W3) of Molecular Gastroenterology and Hepatology and Research Group leader at the Center for Regenerative Therapies Dresden (CRTD) and Else Kröner Fresenius Center (EKFZ) for Digital Health

Since October 2024
Senior Physician, Department of Medicine I, University Hospital Dresden

2023–2024
Assistant Professor (W1, tenure Track) of Experimental Gastroenterology and Organ Crosstalk, RWTH Aachen University Medical School

2022–2024
Physician Scientist and Junior Research group leader, Division of Gastroenterology and Hepatology, University Hospital RWTH Aachen, Germany

2020–2022
Postdoctoral Fellow at Christoph Thaiss’ lab, Dept. of Microbiology, University of Pennsylvania, USA. Topic: Neuro-immune interactions and gut-brain axis.

2016–2020
Resident Physician, Division of Gastroenterology, RWTH Aachen, Germany

Selected Publications

Jaeger JW, Brandt A, Gui W, Yergaliyev T, Hernández-Arriaga A, Muthu MM, Edlund K, Elashy A, Molinaro A, Möckel D, Sarges J, Halibasic E, Trauner M, Kahles F, Rolle-Kampczyk U, Hengstler J, Schneider CV, Lammers T, Hanns-Marschall U, von Bergen M, Camarinha-Silva A, Bergheim I, Trautwein C, Schneider KM
Microbiota modulation by dietary oat beta-glucan prevents steatotic liver disease progression
JHEP Reports 6, 100987 (2024)

Schneider KM, Blank N, Alvarez Y, Thum K, Lundgren P, Litichevskiy L, Sleeman M, Bahnsen K, Kim J, Kardo S, Patel S, Dohnalová L, Uhr GT, Descamps HC, Kircher S, McSween AM, Ardabili AR, Nemec KM, Jimenez MT, Glotfelty LG, Eisenberg JD, Furth EE, Henao-Mejia J, Bennett FC, Pierik MJ, Romberg-Camps M, Mujagic Z, Prinz M, Schneider CV, Wherry EJ, Bewtra M, Heuckeroth RO, Levy M, Thaiss CA
The enteric nervous system relays psychological stress to intestinal inflammation
Cell 186, 2823–2838.e20 (2023)

Gui W, Hole MJ, Molinaro A, Edlund K, Jørgensen KK, Su H, Begher-Tibbe B, Gaßler N, Schneider CV, Muthukumarasamy U, Mohs A, Liao L, Jaeger J, Mertens CJ, Bergheim I, Strowig T, Hengstler JG, Hov JR, Marschall, H-U, Trautwein C, Schneider KM
Colitis ameliorates cholestatic liver disease via suppression of bile acid synthesis
Nat Commun 14, 3304 (2023)

Schneider KM, Mohs A, Gui W, Galvez EJC, Candels LS, Hoenicke L, Muthukumarasamy U, Holland CH, Elfers C, Kilic K, et al.
Imbalanced gut microbiota fuels hepatocellular carcinoma development by shaping the hepatic inflammatory microenvironment
Nat. Commun. 13, 3964 (2022)

Schneider KM, Candels LS, Hov JR, Myllys M, Hassan R, Schneider CV, Wahlström A, Mohs A, Zühlke S, Liao L, Elfers C, Kilic K, Henricsson M, Molinaro A, Hatting M, Zaza A, Drasdo D, Frissen M, Devlin AS, Gálvez EJC, Strowig T, Karlsen TH, Hengstler JG, H.-Marschall U, Ghallab A, Trautwein C
Gut microbiota depletion exacerbates cholestatic liver injury via loss of FXR signalling
Nat. Metab. 3, 1228–1241 (2021)