Literature DB >> 30737139

Murine models of the human porphyrias: Contributions toward understanding disease pathogenesis and the development of new therapies.

Makiko Yasuda1, Robert J Desnick2.   

Abstract

Mouse models of the human porphyrias have proven useful for investigations of disease pathogenesis and to facilitate the development of new therapeutic approaches. To date, mouse models have been generated for all major porphyrias, with the exception of X-linked protoporphyria (XLP) and the ultra rare 5-aminolevulinic acid dehydratase deficient porphyria (ADP). Mouse models have been generated for the three autosomal dominant acute hepatic porphyrias, acute intermittent porphyria (AIP), hereditary coproporphyria (HCP), and variegate porphyria (VP). The AIP mice, in particular, provide a useful investigative model as they have been shown to have acute biochemical attacks when induced with the prototypic porphyrinogenic drug, phenobarbital. In addition to providing important insights into the disease pathogenesis of the neurological impairment in AIP, these mice have been valuable for preclinical evaluation of liver-targeted gene therapy and RNAi-mediated approaches. Mice with severe HMBS deficiency, which clinically and biochemically mimic the early-onset homozygous dominant AIP (HD-AIP) patients, have been generated and were used to elucidate the striking phenotypic differences between AIP and HD-AIP. Mice modeling the hepatocutaneous porphyria, porphyria cutanea tarda (PCT), made possible the identification of the iron-dependent inhibitory mechanism of uroporphyrinogen decarboxylase (UROD) that leads to symptomatic PCT. Mouse models for the two autosomal recessive erythropoietic porphyrias, congenital erythropoietic porphyria (CEP) and erythropoeitic protoporphyria (EPP), recapitulate many of the clinical and biochemical features of the severe human diseases and have been particularly useful for evaluation of bone marrow transplantation and hematopoietic stem cell (HSC)-based gene therapy approaches. The EPP mice have also provided valuable insights into the underlying pathogenesis of EPP-induced liver damage and anemia.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Acute hepatic pophyrias; Erythropoietic porphyrias; Inborn errors of heme biosynthesis; Mouse models; Porphyrias

Mesh:

Substances:

Year:  2019        PMID: 30737139      PMCID: PMC6639143          DOI: 10.1016/j.ymgme.2019.01.007

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  91 in total

1.  Cytosolic persistence of mouse brain CYP1A1 in chronic heme deficiency.

Authors:  Ralf P Meyer; Raija L P Lindberg; Francine Hoffmann; Urs A Meyer
Journal:  Biol Chem       Date:  2005-11       Impact factor: 3.915

2.  Feline congenital erythropoietic porphyria: two homozygous UROS missense mutations cause the enzyme deficiency and porphyrin accumulation.

Authors:  Sonia Clavero; David F Bishop; Urs Giger; Mark E Haskins; Robert J Desnick
Journal:  Mol Med       Date:  2010-05-12       Impact factor: 6.354

3.  Porphyria.

Authors:  D Montgomery Bissell; Karl E Anderson; Herbert L Bonkovsky
Journal:  N Engl J Med       Date:  2017-11-23       Impact factor: 91.245

4.  Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyria.

Authors:  C Picat; M H Delfau; F W de Rooij; G J Beukeveld; B G Wolthers; S K Wadman; Y Nordmann; B Grandchamp
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

5.  Increased plasma transferrin, altered body iron distribution, and microcytic hypochromic anemia in ferrochelatase-deficient mice.

Authors:  Saïd Lyoumi; Marie Abitbol; Valérie Andrieu; Dominique Henin; Elodie Robert; Caroline Schmitt; Laurent Gouya; Hubert de Verneuil; Jean-Charles Deybach; Xavier Montagutelli; Carole Beaumont; Hervé Puy
Journal:  Blood       Date:  2006-09-26       Impact factor: 22.113

6.  Liver pathology and hepatocarcinogenesis in a long-term mouse model of erythropoietic protoporphyria.

Authors:  Louis Libbrecht; Leo Meerman; Folkert Kuipers; Tania Roskams; Valeer Desmet; Peter Jansen
Journal:  J Pathol       Date:  2003-02       Impact factor: 7.996

7.  AAV8-mediated gene therapy prevents induced biochemical attacks of acute intermittent porphyria and improves neuromotor function.

Authors:  Makiko Yasuda; David F Bishop; Mary Fowkes; Seng H Cheng; Lin Gan; Robert J Desnick
Journal:  Mol Ther       Date:  2009-10-27       Impact factor: 11.454

8.  An Inducible Promoter Responsive to Different Porphyrinogenic Stimuli Improves Gene Therapy Vectors for Acute Intermittent Porphyria.

Authors:  Irantzu Serrano-Mendioroz; Ana Sampedro; Manuel Alegre; Rafael Enríquez de Salamanca; Pedro Berraondo; Antonio Fontanellas
Journal:  Hum Gene Ther       Date:  2018-01-02       Impact factor: 5.695

9.  A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen.

Authors:  Ashlee J Conway; Fiona C Brown; Robert O Fullinfaw; Benjamin T Kile; Stephen M Jane; David J Curtis
Journal:  Dis Model Mech       Date:  2017-06-09       Impact factor: 5.758

10.  Preclinical Development of a Subcutaneous ALAS1 RNAi Therapeutic for Treatment of Hepatic Porphyrias Using Circulating RNA Quantification.

Authors:  Amy Chan; Abigail Liebow; Makiko Yasuda; Lin Gan; Tim Racie; Martin Maier; Satya Kuchimanchi; Don Foster; Stuart Milstein; Klaus Charisse; Alfica Sehgal; Muthiah Manoharan; Rachel Meyers; Kevin Fitzgerald; Amy Simon; Robert J Desnick; William Querbes
Journal:  Mol Ther Nucleic Acids       Date:  2015-11-03       Impact factor: 10.183

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  5 in total

Review 1.  Porphyrin-Induced Protein Oxidation and Aggregation as a Mechanism of Porphyria-Associated Cell Injury.

Authors:  Dhiman Maitra; Juliana Bragazzi Cunha; Jared S Elenbaas; Herbert L Bonkovsky; Jordan A Shavit; M Bishr Omary
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2019-06-21

Review 2.  Iron in Porphyrias: Friend or Foe?

Authors:  Elena Buzzetti; Paolo Ventura; Elena Corradini
Journal:  Diagnostics (Basel)       Date:  2022-01-21

3.  Mutation-Specific Guide RNA for Compound Heterozygous Porphyria On-target Scarless Correction by CRISPR/Cas9 in Stem Cells.

Authors:  Florence Prat; Jérôme Toutain; Julian Boutin; Samuel Amintas; Grégoire Cullot; Magalie Lalanne; Isabelle Lamrissi-Garcia; Isabelle Moranvillier; Emmanuel Richard; Jean-Marc Blouin; Sandrine Dabernat; François Moreau-Gaudry; Aurélie Bedel
Journal:  Stem Cell Reports       Date:  2020-08-13       Impact factor: 7.765

Review 4.  Kidney Involvement in Acute Hepatic Porphyrias: Pathophysiology and Diagnostic Implications.

Authors:  Andrea Ricci; Claudio Carmine Guida; Paola Manzini; Chiara Cuoghi; Paolo Ventura
Journal:  Diagnostics (Basel)       Date:  2021-12-10

Review 5.  Mechanisms of Neuronal Damage in Acute Hepatic Porphyrias.

Authors:  Andrea Ricci; Elena Di Pierro; Matteo Marcacci; Paolo Ventura
Journal:  Diagnostics (Basel)       Date:  2021-11-26
  5 in total

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