| Literature DB >> 26786105 |
Carla Reale1, Anna Iervolino1, Ivan Scudiero1, Angela Ferravante1, Luca Egildo D'Andrea1, Pellegrino Mazzone1, Tiziana Zotti2, Antonio Leonardi3, Luca Roberto1, Mariastella Zannini4, Tiziana de Cristofaro4, Muralitharan Shanmugakonar5, Giovambattista Capasso6, Manolis Pasparakis7, Pasquale Vito8, Romania Stilo9.
Abstract
The I-κB kinase (IKK) subunit NEMO/IKKγ (NEMO) is an adapter molecule that is critical for canonical activation of NF-κB, a pleiotropic transcription factor controlling immunity, differentiation, cell growth, tumorigenesis, and apoptosis. To explore the functional role of canonical NF-κB signaling in thyroid gland differentiation and function, we have generated a murine strain bearing a genetic deletion of the NEMO locus in thyroid. Here we show that thyrocyte-specific NEMO knock-out mice gradually develop hypothyroidism after birth, which leads to reduced body weight and shortened life span. Histological and molecular analysis indicate that absence of NEMO in thyrocytes results in a dramatic loss of the thyroid gland cellularity, associated with down-regulation of thyroid differentiation markers and ongoing apoptosis. Thus, NEMO-dependent signaling is essential for normal thyroid physiology.Entities:
Keywords: NF-kappaB; NF-kappaB transcription factor; apoptosis; signal transduction; thyroid; thyroid hormone
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Year: 2016 PMID: 26786105 PMCID: PMC4786713 DOI: 10.1074/jbc.M115.711697
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157