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Transplant Surgery »  Meet the Team »  Basic Scientists »  Holger Willenbring, M.D., Ph.D.
Holger Willenbring, M.D., Ph.D.

Holger Willenbring, M.D., Ph.D.

  • Professor of Surgery
  • Member, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research
  • Associate Director, Liver Center

Contact Information

(415) 476-2417 Office
(415) 514-2346 Facsimile
[email protected]
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  • Medical University Lübeck, Germany, 10/1989 - 07/1995
  • Harvard Medical School, Boston, MA 08/1995 - 04/1996
  • University of Münster, Germany, 05/1996 - 12/1996
  • University of Münster, Germany, Department of Pediatrics, Medical Intern, 02/1997 - 07/1998
  • University of Münster, Germany, Department of Pediatrics, Medical Resident, 08/1998 - 09/2001
  • Oregon Health & Science University, Portland, Oregon, Department of Molecular and Medical Genetics, 10/2001 -10/2005
  • Liver Cell Therapy
  • LIver Development
  • Liver Regeneration

Our research is aimed at developing new therapies for patients with severe liver diseases. To restore liver function in patients with liver failure, we are working on generating hepatocytes from human pluripotent stem cells or by reprogramming of readily accessible human cell types. To be therapeutically effective, these cells need to replicate both function and the ability to proliferate of primary human hepatocytes. To establish and improve protocols for the production of such cells, we have been working on obtaining a detailed molecular understanding of hepatocyte differentiation and regeneration. For this, we are using mouse models for liver cell lineage tracing developed in our laboratory. In addition, we are using rigorous animal models of human liver failure to test the therapeutic efficacy of our surrogate hepatocytes. While developing novel liver cell therapies is our main focus, we are also using hepatocytes derived from human pluripotent stem cells or by reprogramming to generate in vitro and in vivo liver disease models. Another goal of our laboratory is to determine the origin and follow the fate of liver cancer-initiating cells with the goal to identify the molecular mechanisms that drive liver cancer formation and progression. For this, we are using new mouse models generated in our laboratory. By obtaining an improved understanding of hepatocarcinogenesis, we hope to contribute to the development of strategies for early detection and effective eradication of liver cancer. 

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  • Next-generation human liver gene therapy
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    Sep 2021
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    Jun 2026
    Principal Investigator
  • Targeting AAV vectors to cell types involved in alcohol-induced liver injury
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    Sep 2018
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    May 2023
    Principal Investigator
  • Building a functional biliary system from hepatocytes
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    Sep 2016
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    Jul 2021
    Co-Principal Investigator
  • Microphysiological systems to interrogate the Islet-Liver-Adipose Axis in normal physiology and Type-2 Diabetes Mellitus
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    Sep 2018
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    Jul 2020
    Co-Principal Investigator
  • Myofibroblast-to-hepatocyte conversion as a therapy for alcoholic liver disease
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    Sep 2013
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    Aug 2015
    Principal Investigator
  • Liver regeneration with stems cells of uniparental origin
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    Apr 2008
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    Aug 2013
    Co-Principal Investigator
MOST RECENT PUBLICATIONS FROM A TOTAL OF 70
Data provided by UCSF Profiles, powered by CTSI
  1. Groeger M, Matsuo K, Heidary Arash E, Pereira A, Le Guillou D, Pino C, Telles-Silva KA, Maher JJ, Hsiao EC, Willenbring H. Modeling and therapeutic targeting of inflammation-induced hepatic insulin resistance using human iPSC-derived hepatocytes and macrophages. Nat Commun. 2023 07 03; 14(1):3902. View in PubMed
  2. Qi L, Matsuo K, Pereira A, Lee YT, Zhong F, He Y, Zushin PH, Gröger M, Sharma A, Willenbring H, Hsiao EC, Stahl A. Human iPSC-Derived Proinflammatory Macrophages cause Insulin Resistance in an Isogenic White Adipose Tissue Microphysiological System. Small. 2023 08; 19(34):e2203725. View in PubMed
  3. Laemmle A, Häberle J, Willenbring H. Reply. Hepatology. 2022 04; 75(4):1059-1060. View in PubMed
  4. Laemmle A, Poms M, Hsu B, Borsuk M, Rüfenacht V, Robinson J, Sadowski MC, Nuoffer JM, Häberle J, Willenbring H. Aquaporin 9 induction in human iPSC-derived hepatocytes facilitates modeling of ornithine transcarbamylase deficiency. Hepatology. 2022 09; 76(3):646-659. View in PubMed
  5. Lee-Montiel FT, Laemmle A, Charwat V, Dumont L, Lee CS, Huebsch N, Okochi H, Hancock MJ, Siemons B, Boggess SC, Goswami I, Miller EW, Willenbring H, Healy KE. Integrated Isogenic Human Induced Pluripotent Stem Cell-Based Liver and Heart Microphysiological Systems Predict Unsafe Drug-Drug Interaction. Front Pharmacol. 2021; 12:667010. View in PubMed
  6. View All Publications

 

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