Caroline Enns, Ph.D
- Professor of Cell, Developmental and Cancer Biology, School of Medicine
- Cancer Biology Graduate Program, School of Medicine
- Cell and Developmental Biology Graduate Program, School of Medicine
- Program in Molecular and Cellular Biosciences, School of Medicine
Biography
The cell is a highly organized and dynamic structure. Most proteins are found exclusively in one compartment of the cell and are only transported to other locations as a result of intra- or extra-cellular signaling pathways. For the most part, proteins are synthesized in the cytoplasm and targeted either co- or post-translationally to their particular destination. Recently, an increasing number of human diseases have been attributed to mutations which result in the mistargeting of essential proteins. The signals responsible for the targeting membrane proteins in the biosynthetic and endocytic pathways are of particular interest to my laboratory. In addition to studying the basic cell biology of protein trafficking within the cell, we have begun to examine the trafficking and function of the protein implicated in hemochromatosis, the most common hereditary disease of people of European ancestry. Malfunctioning of this protein results in the abnormal accumulation of iron in the body. Iron uptake into the body is highly regulated. Although it is essential for life, too much iron is toxic and results in heart failure, adult onset diabetes, arthritis, and cirrhosis of the liver. We are examining the intracellular trafficking of this protein and how it participates in the control of iron uptake and egress.
Education and training
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Degrees
- Ph.D., 1976, University of Oregon
Areas of interest
- cell biology protein trafficking hereditary hemochromatosis cellular basis of human disease structure function of membrane proteins cancer
Additional information
Publications
Publications
Hepcidin expression is associated with increased γ-secretase–mediated cleavage of neogenin in the liver
Journal of Biological ChemistryMatriptase-2 regulates iron homeostasis primarily by setting the basal levels of hepatic hepcidin expression through a nonproteolytic mechanism
Journal of Biological ChemistryHepatocyte neogenin is required for hemojuvelin-mediated hepcidin expression and iron homeostasis in mice
BloodExtrahepatic deficiency of transferrin receptor 2 is associated with increased erythropoiesis independent of iron overload
Journal of Biological ChemistryThe ectodomain of matriptase-2 plays an important nonproteolytic role in suppressing hepcidin expression in mice
BloodImaging viper-labeled cellular proteins by correlative light and electron microscopy
Bio-protocolImplementing viper for imaging cellular proteins by fluorescence microscopy
Bio-protocolThe catalytic, stem, and transmembrane portions of matriptase-2 are required for suppressing the expression of the iron-regulatory hormone hepcidin
Journal of Biological ChemistryThe hemochromatosis protein HFE signals predominantly via the BMP type I receptor ALK3 in vivo
Communications BiologyTransferrin Receptors TfR1 and TfR2 Bind Transferrin through Differing Mechanisms
BiochemistryUltrafiltered recombinant AAV8 vector can be safely administered in vivo and efficiently transduces liver
PloS oneVIPER is a genetically encoded peptide tag for fluorescence and electron microscopy
Proceedings of the National Academy of Sciences of the United States of AmericaMatriptase-2 suppresses hepcidin expression by cleaving multiple components of the hepcidin induction pathway
Journal of Biological ChemistryThe tumor suppressor, P53, decreases the metal transporter, ZIP14
NutrientsVersatile Interacting Peptide (VIP) Tags for Labeling Proteins with Bright Chemical Reporters
ChemBioChemMutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia
Nature communicationsNeogenin facilitates the induction of hepcidin expression by hemojuvelin in the liver
Journal of Biological ChemistryCD81 Promotes both the degradation of transferrin receptor 2 (TfR2) and the Tfr2-mediated maintenance of hepcidin expression
Journal of Biological ChemistryLow intracellular iron increases the stability of Matriptase-2
Journal of Biological ChemistryAn iron-regulated and glycosylation-dependent proteasomal degradation pathway for the plasma membrane metal transporter ZIP14
Proceedings of the National Academy of Sciences of the United States of AmericaFerristatin II Promotes Degradation of Transferrin Receptor-1 In Vitro and In Vivo
PloS oneIncreased Iron Loading Induces Bmp6 Expression in the Non-Parenchymal Cells of the Liver Independent of the BMP-Signaling Pathway
PloS oneIron regulation by hepcidin
Journal of Clinical InvestigationN-linked glycosylation is required for transferrin-induced stabilization of transferrin receptor 2, but not for transferrin binding or trafficking to the cell surface
BiochemistryThe First Transmembrane Domain of Lipid Phosphatase SAC1 Promotes Golgi Localization
PloS one