Characterization of Tusc5, an adipocyte gene co-expressed in peripheral neurons
Autor: | Craig H Warden, Sean H. Adams, Thomas K. Baumann, Trina A. Knotts, Pieter J. Oort |
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Rok vydání: | 2007 |
Předmět: |
medicine.medical_specialty
Molecular Sequence Data Peroxisome proliferator-activated receptor Adipose tissue White adipose tissue Biology Biochemistry Transcriptome Benzophenones Mice chemistry.chemical_compound Endocrinology 3T3-L1 Cells Ganglia Spinal Internal medicine Adipocyte Brown adipose tissue Adipocytes medicine Animals Humans Amino Acid Sequence Lactic Acid RNA Messenger Molecular Biology Oligonucleotide Array Sequence Analysis Neurons chemistry.chemical_classification Sequence Homology Amino Acid Gene Expression Profiling Tumor Suppressor Proteins Membrane Proteins Cell Differentiation Protein Structure Tertiary PPAR gamma Glucose medicine.anatomical_structure Gene Expression Regulation Trigeminal Ganglion chemistry Adipogenesis biology.protein Tyrosine GLUT4 |
Zdroj: | Molecular and Cellular Endocrinology. 276:24-35 |
ISSN: | 0303-7207 |
Popis: | Tumor suppressor candidate 5 (Tusc5, also termed brain endothelial cell derived gene-1 or BEC-1), a CD225 domain-containing, cold-repressed gene identified during brown adipose tissue (BAT) transcriptome analyses was found to be robustly-expressed in mouse white adipose tissue (WAT) and BAT, with similarly high expression in human adipocytes. Tusc5 mRNA was markedly increased from trace levels in pre-adipocytes to significant levels in developing 3T3-L1 adipocytes, coincident with several mature adipocyte markers (phosphoenolpyruvate carboxykinase 1, GLUT4, adipsin, leptin). The Tusc5 transcript levels were increased by the peroxisome proliferator activated receptor- (PPAR) agonist GW1929 (1g/mL, 18 h) by >10-fold (pre-adipocytes) to ∼1.5-fold (mature adipocytes) versus controls (p < 0.0001). Taken together, these results suggest an important role for Tusc5 in maturing adipocytes. Intriguingly, we discovered robust co-expression of the gene in peripheral nerves (primary somatosensory neurons). In light of the marked repression of the gene observed after cold exposure, these findings may point to participation of Tusc5 in shared adipose–nervous system functions linking environmental cues, CNS signals, and WAT–BAT physiology. Characterization of such links is important for clarifying the molecular basis for adipocyte proliferation and could have implications for understanding the biology of metabolic disease-related neuropathies. Published by Elsevier Ireland Ltd. |
Databáze: | OpenAIRE |
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