TMEM120A and B: Nuclear Envelope Transmembrane Proteins Important for Adipocyte Differentiation

• Published in: PloS one 2015-05, Vol.10 (5), p.e0127712-e0127712
• Main Authors: Batrakou, Dzmitry G, de Las Heras, Jose I, Czapiewski, Rafal, Mouras, Rabah, Schirmer, Eric C
• Format: Article
• Language: English
• Subjects: 3T3-L1 Cells; Adipocytes; Adipocytes - metabolism; Adiponectin - genetics; Adiponectin - metabolism; Animals; Biology; Cell Differentiation; Cloning; Coding; Coherent scattering; Diabetes; Differentiation; GATA-3 protein; GATA3 Transcription Factor - genetics; GATA3 Transcription Factor - metabolism; Gene expression; Gene Knockdown Techniques; Genes; Genetic aspects; Genomes; Genomics; Glucose Transporter Type 4 - genetics; Glucose Transporter Type 4 - metabolism; Insulin; Kinases; Lipid metabolism; Lipids; Membrane proteins; Membrane Proteins - genetics; Membrane Proteins - metabolism; Metabolism; Mice; Microscopy; Mutation; Nuclear Envelope - genetics; Nuclear Envelope - metabolism; Obesity; Obesity - genetics; Obesity - metabolism; Peroxisome proliferator-activated receptors; Pharmacology; Physiological aspects; PPAR gamma - genetics; PPAR gamma - metabolism; Proteins; Raman scattering; Raman spectra; Signaling; Transmembrane proteins
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0127712

Recent work indicates that the nuclear envelope is a major signaling node for the cell that can influence tissue differentiation processes. Here we present two nuclear envelope trans-membrane proteins TMEM120A and TMEM120B that are paralogs encoded by the Tmem120A and Tmem120B genes. The TMEM120 proteins are expressed preferentially in fat and both are induced during 3T3-L1 adipocyte differentiation. Knockdown of one or the other protein altered expression of several genes required for adipocyte differentiation, Gata3, Fasn, Glut4, while knockdown of both together additionally affected Pparg and Adipoq. The double knockdown also increased the strength of effects, reducing for example Glut4 levels by 95% compared to control 3T3-L1 cells upon pharmacologically induced differentiation. Accordingly, TMEM120A and B knockdown individually and together impacted on adipocyte differentiation/metabolism as measured by lipid accumulation through binding of Oil Red O and coherent anti-Stokes Raman scattering microscopy (CARS). The nuclear envelope is linked to several lipodystrophies through mutations in lamin A; however, lamin A is widely expressed. Thus it is possible that the TMEM120A and B fat-specific nuclear envelope transmembrane proteins may play a contributory role in the tissue-specific pathology of this disorder or in the wider problem of obesity.