Aberrant disulphide bonding contributes to the ER retention of alpha1-antitrypsin deficiency variants.

Abstract

Mutations in alpha1-antitrypsin (AAT) can cause the protein to polymerise and be retained in the endoplasmic reticulum (ER) of hepatocytes. The ensuing systemic AAT deficiency leads to pulmonary emphysema, while intracellular polymers are toxic and cause chronic liver disease. The severity of this process varies considerably between individuals, suggesting the involvement of mechanistic co-factors and potential for therapeutically beneficial interventions. We show in Hepa1.6 cells that the mildly polymerogenic I (Arg39Cys) AAT mutant forms aberrant inter- and intra-molecular disulphide bonds involving the acquired Cys39 and the only cysteine residue in the wild-type (M) sequence (Cys232). Substitution of Cys39 to serine partially restores secretion, showing that disulphide bonding contributes to the intracellular retention of I AAT. Covalent homodimers mediated by inter-Cys232 bonding alone are also observed in cells expressing the common Z and other polymerising AAT variants where conformational behaviour is abnormal, but not in those expressing M AAT. Prevention of such disulphide linkage through the introduction of the Cys232Ser mutation or by treatment of cells with reducing agents increases Z AAT secretion. Our results reveal that disulphide interactions enhance intracellular accumulation of AAT mutants and implicate the oxidative ER state as a pathogenic co-factor. Redox modulation, e.g. by anti-oxidant strategies, may therefore be beneficial in AAT deficiency-associated liver disease.

• Authors: Riccardo Ronzoni, Romina Berardelli, Daniela Medicina, Roberto Sitia, Bibek Gooptu, Anna Maria Fra
• Journal: Human molecular genetics (Hum Mol Genet) Vol. 25 Issue 4 Pg. 642-50 (Feb 15 2016) ISSN: 1460-2083 [Electronic] England
• PMID: 26647313 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected].

Chemical References

• Disulfides
• alpha 1-Antitrypsin

Topics

• Animals
• Cell Line, Tumor
• Disulfides (metabolism)
• Endoplasmic Reticulum (metabolism)
• Genotype
• Hepatocytes (metabolism)
• Humans
• Male
• Mice
• Mutation
• Polymerization
• alpha 1-Antitrypsin (genetics, metabolism)
• alpha 1-Antitrypsin Deficiency (genetics, metabolism)