Education
- 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
In the News
Grants and Funding
- Next-generation human liver gene therapy | NIH | 2021-09-30 - 2026-06-30 | Role: Principal Investigator
- Microphysiological systems to interrogate the Islet-Liver-Adipose Axis in normal physiology and Type-2 Diabetes Mellitus | NIH | 2018-09-20 - 2023-07-31 | Role: Co-Principal Investigator
- Targeting AAV vectors to cell types involved in alcohol-induced liver injury | NIH | 2018-09-01 - 2023-05-31 | Role: Principal Investigator
- Building a functional biliary system from hepatocytes | NIH | 2016-09-01 - 2021-07-31 | Role: Co-Principal Investigator
- Microphysiological systems to interrogate the Islet-Liver-Adipose Axis in normal physiology and Type-2 Diabetes Mellitus | NIH | 2018-09-20 - 2020-07-31 | Role: Co-Principal Investigator
- Myofibroblast-to-hepatocyte conversion as a therapy for alcoholic liver disease | NIH | 2013-09-01 - 2016-08-31 | Role: Principal Investigator
- Liver regeneration with stems cells of uniparental origin | NIH | 2008-04-01 - 2013-08-31 | Role: Co-Principal Investigator
Research Narrative
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.
Research Interests
Liver Regeneration
Liver Cell Therapy
LIver Development
Research Pathways
Publications
- Resolving fibrosis by stimulating HSC-dependent extracellular matrix degradation.| | PubMed PubMed
- Identification of a robust promoter in mouse and human hepatocytes by in vivo biopanning of a barcoded AAV library.| | PubMed PubMed
- AAV capsid prioritization in normal and steatotic human livers maintained by machine perfusion.| | PubMed PubMed
- Pervasive and programmed nucleosome distortion patterns on single mammalian chromatin fibers.| | PubMed PubMed
- Adipocyte inflammation is the primary driver of hepatic insulin resistance in a human iPSC-based microphysiological system.| | PubMed PubMed
- Human Hepatocytes Can Give Rise to Intrahepatic Cholangiocarcinomas.| | PubMed PubMed
- Modeling and therapeutic targeting of inflammation-induced hepatic insulin resistance using human iPSC-derived hepatocytes and macrophages.| | PubMed PubMed
- Human iPSC-Derived Proinflammatory Macrophages cause Insulin Resistance in an Isogenic White Adipose Tissue Microphysiological System.| | PubMed PubMed
- Reply.| | PubMed PubMed
- Aquaporin 9 induction in human iPSC-derived hepatocytes facilitates modeling of ornithine transcarbamylase deficiency.| | PubMed PubMed
- Integrated Isogenic Human Induced Pluripotent Stem Cell-Based Liver and Heart Microphysiological Systems Predict Unsafe Drug-Drug Interaction.| | PubMed PubMed
- Induced Pluripotent Stem Cell-derived Hepatocytes From Patients With Nonalcoholic Fatty Liver Disease Display a Disease-specific Gene Expression Profile.| | PubMed PubMed
- Emerging cell therapy for biliary diseases.| | PubMed PubMed
- Transcriptomic Traces of Adult Human Liver Progenitor Cells.| | PubMed PubMed
- Broad Distribution of Hepatocyte Proliferation in Liver Homeostasis and Regeneration.| | PubMed PubMed
- Hepatocyte Nuclear Factor 4 Alpha Activation Is Essential for Termination of Liver Regeneration in Mice.| | PubMed PubMed
- De novo formation of the biliary system by TGFβ-mediated hepatocyte transdifferentiation.| | PubMed PubMed
- Postnatal Organogenesis by Transdifferentiation.| | UCSF Research Profile
- Advances in cholangiocarcinoma research: report from the third Cholangiocarcinoma Foundation Annual Conference.| | PubMed PubMed
- In Vivo Hepatic Reprogramming of Myofibroblasts with AAV Vectors as a Therapeutic Strategy for Liver Fibrosis.| | PubMed PubMed
- Assessing the therapeutic potential of lab-made hepatocytes.| | PubMed PubMed
- Physiological ranges of matrix rigidity modulate primary mouse hepatocyte function in part through hepatocyte nuclear factor 4 alpha.| | PubMed PubMed
- A screen in mice uncovers repression of lipoprotein lipase by microRNA-29a as a mechanism for lipid distribution away from the liver.| | PubMed PubMed
- AAV8-mediated in vivo overexpression of miR-155 enhances the protective capacity of genetically attenuated malarial parasites.| | PubMed PubMed
- Evidence against a Stem Cell Origin of New Hepatocytes in a Common Mouse Model of Chronic Liver Injury.| | UCSF Research Profile
- Evidence against a stem cell origin of new hepatocytes in a common mouse model of chronic liver injury.| | PubMed PubMed
- Brief report: Parthenogenetic embryonic stem cells are an effective cell source for therapeutic liver repopulation.| | PubMed PubMed
- Failure to achieve normal metabolic response in non-obese diabetic mice and streptozotocin-induced diabetic mice after transplantation of primary murine hepatocytes electroporated with the human proinsulin gene (p3MTChins).| | PubMed PubMed
- Inhibition of microRNA-24 expression in liver prevents hepatic lipid accumulation and hyperlipidemia.| | PubMed PubMed
- Mouse liver repopulation with hepatocytes generated from human fibroblasts.| | PubMed PubMed
- Addendum: A reproducible and well-tolerated method for 2/3 partial hepatectomy in mice.| | PubMed PubMed
- Human induced pluripotent stem cell-based microphysiological tissue models of myocardium and liver for drug development.| | PubMed PubMed
- MicroRNA-494 within an oncogenic microRNA megacluster regulates G1/S transition in liver tumorigenesis through suppression of mutated in colorectal cancer.| | PubMed PubMed
- Transplantable liver organoids made from only three ingredients.| | PubMed PubMed
- Highly efficient differentiation of functional hepatocytes from human induced pluripotent stem cells.| | PubMed PubMed
- A therapy for liver failure found in the JNK yard.| | PubMed PubMed
- Akt/Notch activation drives rapid cholangiocarcinoma development originating from mature hepatocytes in the mouse.| | UCSF Research Profile
- Cholangiocarcinomas can originate from hepatocytes in mice.| | PubMed PubMed
- A ZFN/piggyBac step closer to autologous liver cell therapy.| | PubMed PubMed
- A microRNA-21 surge facilitates rapid cyclin D1 translation and cell cycle progression in mouse liver regeneration.| | PubMed PubMed
- Stem cells in liver diseases and cancer: recent advances on the path to new therapies.| | PubMed PubMed
- Fate tracing of mature hepatocytes in mouse liver homeostasis and regeneration.| | PubMed PubMed
- A simple code for installing hepatocyte function.| | PubMed PubMed
- Mouse chimeras as a system to investigate development, cell and tissue function, disease mechanisms and organ regeneration.| | PubMed PubMed
- Core promoter recognition complex changes accompany liver development.| | PubMed PubMed
- The MAP3K TAK1: a chock block to liver cancer formation.| | PubMed PubMed
- Induced pluripotent stem cell-derived hepatocytes have the functional and proliferative capabilities needed for liver regeneration in mice.| | PubMed PubMed
- Transplanted nonviable human hepatocytes produce appreciable serum albumin levels in mice.| | PubMed PubMed
- miRNAs regulate SIRT1 expression during mouse embryonic stem cell differentiation and in adult mouse tissues.| | PubMed PubMed
- Therapeutic liver reconstitution with murine cells isolated long after death.| | PubMed PubMed
- MicroRNAs control hepatocyte proliferation during liver regeneration.| | PubMed PubMed
- Loss of p21 permits carcinogenesis from chronically damaged liver and kidney epithelial cells despite unchecked apoptosis.| | PubMed PubMed
- ????????in vitro???.| | UCSF Research Profile
- A reproducible and well-tolerated method for 2/3 partial hepatectomy in mice.| | PubMed PubMed
- On the origin of the term "stem cell".| | PubMed PubMed
- Myeloid lineage progenitors give rise to vascular endothelium.| | PubMed PubMed
- Bone marrow-derived cells fuse with normal and transformed intestinal stem cells.| | PubMed PubMed
- Sustained phosphorylation of Bid is a marker for resistance to Fas-induced apoptosis during chronic liver diseases.| | PubMed PubMed
- Myeloid Lineage-Restricted Progenitors Contribute to Vascular Endothelium.| | UCSF Research Profile
- In vivo genetic selection of renal proximal tubules.| | PubMed PubMed
- Therapeutic cell fusion.| | PubMed PubMed
- Delineating the hepatocyte's hematopoietic fusion partner.| | PubMed PubMed
- Myelomonocytic cells are sufficient for therapeutic cell fusion in liver.| | PubMed PubMed
- Embryonic versus adult stem cell pluripotency: in liver only fusion matters.| | PubMed PubMed
- Cell fusion is the principal source of bone-marrow-derived hepatocytes.| | PubMed PubMed
- Argininosuccinate lyase (ASL) deficiency: mutation analysis in 27 patients and a completed structure of the human ASL gene.| | PubMed PubMed
- Genomic structure and transcript variants of the human methylenetetrahydrofolate reductase gene.| | PubMed PubMed
- Telomerase activity distinguishes between neuroblastomas with good and poor prognosis.| | PubMed PubMed
- Telomerase activity in human proliferative breast lesions.| | PubMed PubMed
- Nonisotopic single strand conformation analysis of the 5 alpha-reductase type 2 gene for the diagnosis of 5 alpha-reductase deficiency.| | PubMed PubMed
- Molecular genetic analysis and human chorionic gonadotropin stimulation tests in the diagnosis of prepubertal patients with partial 5 alpha-reductase deficiency.| | PubMed PubMed
 
    