Literature DB >> 20193006

Transcriptional regulation of bone and joint remodeling by NFAT.

Despina Sitara1, Antonios O Aliprantis.   

Abstract

Osteoporosis and arthritis are highly prevalent diseases and a significant cause of morbidity and mortality worldwide. These diseases result from aberrant tissue remodeling leading to weak, fracture-prone bones or painful, dysfunctional joints. The nuclear factor of activated T cells (NFAT) transcription factor family controls diverse biologic processes in vertebrates. Here, we review the scientific evidence that links NFAT-regulated gene transcription to bone and joint pathology. A particular emphasis is placed on the role of NFATs in bone resorption and formation by osteoclasts and osteoblasts, respectively. In addition, emerging data that connect NFATs with cartilage biology, angiogenesis, nociception, and neurogenic inflammation are explored. The goal of this article is to highlight the importance of tissue remodeling in musculoskeletal disease and situate NFAT-driven cellular responses within this context to inspire future research endeavors.

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Year:  2010        PMID: 20193006      PMCID: PMC2904911          DOI: 10.1111/j.0105-2896.2009.00849.x

Source DB:  PubMed          Journal:  Immunol Rev        ISSN: 0105-2896            Impact factor:   12.988


  145 in total

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Review 3.  Notch regulation of bone development and remodeling and related skeletal disorders.

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6.  STAT3 controls osteoclast differentiation and bone homeostasis by regulating NFATc1 transcription.

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7.  Osteopontin signals through calcium and nuclear factor of activated T cells (NFAT) in osteoclasts: a novel RGD-dependent pathway promoting cell survival.

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Journal:  Arthritis Rheumatol       Date:  2016-12       Impact factor: 10.995

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