Functions of the bone morphogenetic protein signaling pathway through microRNAs (Review)

  • Authors:
    • Akiko Hata
    • Hara Kang
  • View Affiliations

  • Published online on: January 2, 2015     https://doi.org/10.3892/ijmm.2015.2060
  • Pages: 563-568
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Abstract

MicroRNAs (miRNAs or miRs) have emerged as key regulators of gene expression in essential cellular processes, such as cell growth, differentiation and development. Recent findings have established that the levels of miRNAs are modulated by cell signaling mechanisms, including the bone morphogenetic protein (BMP) signaling pathway. The BMP signaling pathway controls diverse cellular activities by modulating the levels of miRNAs, indicating the complexity of gene regulation by the BMP signaling pathway. The tight regulation of the levels of miRNAs is critical for maintaining normal physiological conditions, and dysregulated miRNA levels contribute to the development of diseases. In the present review, we discuss different insights (provided over the past decade) into the regulation of miRNAs governed by the BMP signaling pathway and the implications of this regulation on the understanding of the cellular differentiation of vascular smooth muscle cells (VSMCs), osteoblasts and neuronal cells.
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March-2015
Volume 35 Issue 3

Print ISSN: 1107-3756
Online ISSN:1791-244X

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Spandidos Publications style
Hata A and Kang H: Functions of the bone morphogenetic protein signaling pathway through microRNAs (Review). Int J Mol Med 35: 563-568, 2015.
APA
Hata, A., & Kang, H. (2015). Functions of the bone morphogenetic protein signaling pathway through microRNAs (Review). International Journal of Molecular Medicine, 35, 563-568. https://doi.org/10.3892/ijmm.2015.2060
MLA
Hata, A., Kang, H."Functions of the bone morphogenetic protein signaling pathway through microRNAs (Review)". International Journal of Molecular Medicine 35.3 (2015): 563-568.
Chicago
Hata, A., Kang, H."Functions of the bone morphogenetic protein signaling pathway through microRNAs (Review)". International Journal of Molecular Medicine 35, no. 3 (2015): 563-568. https://doi.org/10.3892/ijmm.2015.2060