Literature DB >> 28752458

Measuring the Effect of Histone Deacetylase Inhibitors (HDACi) on the Secretion and Activity of Alpha-1 Antitrypsin.

Chao Wang1, Marion Bouchecareilh2, William E Balch3.   

Abstract

Alpha-1 antitrypsin deficiency (AATD) is a protein conformational disease with the most common cause being the Z-variant mutation in alpha-1 antitrypsin (Z-AAT). The misfolded conformation triggered by the Z-variant disrupts cellular proteostasis (protein folding) systems and fails to meet the endoplasmic reticulum (ER) export metrics, leading to decreased circulating AAT and deficient antiprotease activity in the plasma and lung. Here, we describe the methods for measuring the secretion and neutrophil elastase (NE) inhibition activity of AAT/Z-AAT, as well as the response to histone deacetylase inhibitor (HDACi), a major proteostasis modifier that impacts the secretion and function of AATD from the liver to plasma. These methods provide a platform for further therapeutic development of proteostasis regulators for AATD.

Entities:  

Keywords:  Alpha-1 antitrypsin deficiency; Cellular proteostasis; Histone deacetylase inhibitor; Proteostasis regulators

Mesh:

Substances:

Year:  2017        PMID: 28752458      PMCID: PMC5535769          DOI: 10.1007/978-1-4939-7163-3_18

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  28 in total

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4.  Histone deacetylase inhibitor (HDACi) suberoylanilide hydroxamic acid (SAHA)-mediated correction of α1-antitrypsin deficiency.

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Journal:  J Biol Chem       Date:  2012-09-20       Impact factor: 5.157

5.  Myogenin and class II HDACs control neurogenic muscle atrophy by inducing E3 ubiquitin ligases.

Authors:  Viviana Moresi; Andrew H Williams; Eric Meadows; Jesse M Flynn; Matthew J Potthoff; John McAnally; John M Shelton; Johannes Backs; William H Klein; James A Richardson; Rhonda Bassel-Duby; Eric N Olson
Journal:  Cell       Date:  2010-10-01       Impact factor: 41.582

Review 6.  Liver disease in alpha-1 antitrypsin deficiency: current understanding and future therapy.

Authors:  Jeffrey H Teckman
Journal:  COPD       Date:  2013-03       Impact factor: 2.409

Review 7.  Recent advances in α-1-antitrypsin deficiency-related lung disease.

Authors:  Judith A Brebner; Robert A Stockley
Journal:  Expert Rev Respir Med       Date:  2013-06       Impact factor: 3.772

Review 8.  Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease.

Authors:  Raafe Ghouse; Andrew Chu; Yan Wang; David H Perlmutter
Journal:  Dis Model Mech       Date:  2014-04       Impact factor: 5.758

Review 9.  The molecular and cellular pathology of α₁-antitrypsin deficiency.

Authors:  Bibek Gooptu; Jennifer A Dickens; David A Lomas
Journal:  Trends Mol Med       Date:  2013-12-25       Impact factor: 11.951

Review 10.  The potential of epigenetic therapies in neurodegenerative diseases.

Authors:  Fabio Coppedè
Journal:  Front Genet       Date:  2014-07-14       Impact factor: 4.599

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Journal:  J Biol Chem       Date:  2020-04-30       Impact factor: 5.157

2.  HDAC inhibitors rescue multiple disease-causing CFTR variants.

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3.  Secretion of functional α1-antitrypsin is cell type dependent: Implications for intramuscular delivery for gene therapy.

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4.  Quantitating the epigenetic transformation contributing to cholesterol homeostasis using Gaussian process.

Authors:  Chao Wang; Samantha M Scott; Kanagaraj Subramanian; Salvatore Loguercio; Pei Zhao; Darren M Hutt; Nicole Y Farhat; Forbes D Porter; William E Balch
Journal:  Nat Commun       Date:  2019-11-07       Impact factor: 14.919

5.  Hepatocyte proteomes reveal the role of protein disulfide isomerase 4 in alpha 1-antitrypsin deficiency.

Authors:  Esra Karatas; Anne-Aurélie Raymond; Céline Leon; Jean-William Dupuy; Sylvaine Di-Tommaso; Nathalie Senant; Sophie Collardeau-Frachon; Mathias Ruiz; Alain Lachaux; Frédéric Saltel; Marion Bouchecareilh
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  5 in total

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