Proteomic profiling of adipose tissue from Zmpste24-/- mice, a model of lipodystrophy and premature aging, reveals major changes in mitochondrial function and vimentin processing.

Abstract

Lipodystrophy is a major disease involving severe alterations of adipose tissue distribution and metabolism. Mutations in genes encoding the nuclear envelope protein lamin A or its processing enzyme, the metalloproteinase Zmpste24, cause diverse human progeroid syndromes that are commonly characterized by a selective loss of adipose tissue. Similarly to humans, mice deficient in Zmpste24 accumulate prelamin A and display phenotypic features of accelerated aging, including lipodystrophy. Herein, we report the proteome and phosphoproteome of adipose tissue as well as serum metabolome in lipodystrophy by using Zmpste24(-/-) mice as experimental model. We show that Zmpste24 deficiency enhanced lipolysis, fatty acid biogenesis and β-oxidation as well as decreased fatty acid re-esterification, thus pointing to an increased partitioning of fatty acid toward β-oxidation and away from storage that likely underlies the observed size reduction of Zmpste24-null adipocytes. Besides the mitochondrial proteins related to lipid metabolism, other protein networks related to mitochondrial function, including those involved in tricarboxylic acid cycle and oxidative phosphorylation, were up-regulated in Zmpste24(-/-) mice. These results, together with the observation of an increased mitochondrial response to oxidative stress, support the relationship between defective prelamin A processing and mitochondrial dysfunction and highlight the relevance of oxidative damage in lipoatrophy and aging. We also show that absence of Zmpste24 profoundly alters the processing of the cytoskeletal protein vimentin and identify a novel protein dysregulated in lipodystrophy, High-Mobility Group Box-1 Protein. Finally, we found several lipid derivates with important roles in energy balance, such as Lysophosphatidylcholine or 2-arachidonoylglycerol, to be dysregulated in Zmpste24(-/-) serum. Together, our findings in Zmpste24(-/-) mice may be useful to unveil the mechanisms underlying adipose tissue dysfunction and its overall contribution to body homeostasis in progeria and other lipodystrophy syndromes as well as to develop novel strategies to prevent or ameliorate these diseases.

• Authors: Juan R Peinado, Pedro M Quirós, Marina R Pulido, Guillermo Mariño, Maria L Martínez-Chantar, Rafael Vázquez-Martínez, José M P Freije, Carlos López-Otín, María M Malagón
• Journal: Molecular & cellular proteomics : MCP (Mol Cell Proteomics) Vol. 10 Issue 11 Pg. M111.008094 (Nov 2011) ISSN: 1535-9484 [Electronic] United States
• PMID: 21828285 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Biomarkers
• Blood Glucose
• HMGB1 Protein
• Lamin Type A
• Lipids
• Membrane Proteins
• Nuclear Proteins
• Phosphoproteins
• Protein Precursors
• Proteome
• Vimentin
• prelamin A
• Metalloendopeptidases
• Zmpste24 protein, mouse

Topics

• Aging, Premature (genetics, metabolism)
• Animals
• Biomarkers (blood)
• Blood Glucose (metabolism)
• Gene Expression Regulation
• HMGB1 Protein (genetics, metabolism)
• Intra-Abdominal Fat (metabolism, pathology)
• Lamin Type A
• Lipid Metabolism
• Lipids (blood)
• Lipodystrophy (genetics, metabolism)
• Male
• Membrane Proteins (genetics)
• Metabolome
• Metalloendopeptidases (genetics)
• Mice
• Mice, Knockout
• Mitochondria (enzymology, metabolism)
• Nuclear Proteins (metabolism)
• Oxidation-Reduction
• Phosphoproteins (metabolism)
• Protein Interaction Maps
• Protein Precursors (metabolism)
• Proteome (genetics, metabolism)
• Vimentin (metabolism)