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Calcium- and Integrin-Binding Protein 2 (CIB2) in Physiology and Disease: Bright and Dark Sides

Journal

Publisher

MDPI
DOI: 10.3390/ijms23073552

Keywords

non-syndromic deafness; Usher syndrome; hearing; integrin signaling; mechanoelectrical transduction

Funding

  1. Italian Ministry of University and Research [201744NR8S]

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CIB2 is a protein capable of binding calcium and magnesium ions, playing an important role in cochlear hair cells and being associated with non-syndromic deafness. Besides its involvement in auditory physiology, CIB2 has diverse functions in various processes.
Calcium- and integrin-binding protein 2 (CIB2) is a small EF-hand protein capable of binding Mg2+ and Ca2+ ions. While its biological function remains largely unclear, an increasing number of studies have shown that CIB2 is an essential component of the mechano-transduction machinery that operates in cochlear hair cells. Mutations in the gene encoding CIB2 have been associated with non-syndromic deafness. In addition to playing an important role in the physiology of hearing, CIB2 has been implicated in a multitude of very different processes, ranging from integrin signaling in platelets and skeletal muscle to autophagy, suggesting extensive functional plasticity. In this review, we summarize the current understanding of biochemical and biophysical properties of CIB2 and the biological roles that have been proposed for the protein in a variety of processes. We also highlight the many molecular aspects that remain unclarified and deserve further investigation.

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