Nek5, a novel substrate for caspase-3, promotes skeletal muscle differentiation by up-regulating caspase activity

• Published in: FEBS letters 2013-07, Vol.587 (14), p.2219-2225
• Main Authors: Shimizu, Kouhei, Sawasaki, Tatsuya
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Amino Acid Substitution; Animals; C2C12 myoblast; Caspase 3 - chemistry; Caspase 3 - metabolism; Caspase-3; Cell Differentiation; Cell Line; differentiation medium; Enzyme Induction; growth medium; MHC; Mice; MRFs; Muscle Development; Muscle differentiation; Myoblasts - physiology; myogenic regulatory factors; myosin heavy chain; Nek5; NIMA-Related Kinases; Protein Kinases - chemistry; Protein Kinases - genetics; Protein Kinases - metabolism; RNA, Messenger - genetics; RNA, Messenger - metabolism; Up-Regulation
• ISSN: 0014-5793; 1873-3468
• DOI: 10.1016/j.febslet.2013.05.049

•We present first evidence for the function of mammalian Nek5.•Nek5 is a novel substrate for caspase-3.•Nek5 promotes myogenic differentiation of C2C12 myoblasts.•The mRNA encoding Nek5 is up-regulated during myogenic differentiation.•Nek5 up-regulates caspase-3 activity during myogenic differentiation. Accumulating evidence suggests that caspase-3-mediated cleavage of protein kinase could be a key event to regulate cell differentiation. In this study, we investigated the role of Nek5 kinase, identified as a novel substrate for caspase-3, in skeletal muscle differentiation. Up-regulation of Nek5 mRNA expression was accompanied by cell differentiation. Myotube formation was promoted in Nek5 expressing cells, and was conversely inhibited in Nek5 knockdown cells. Furthermore, we found that caspase-3 activity, an important factor for myogenic differentiation, was enhanced by Nek5 cleavage. Although caspase-3-cleaved Nek5 partially exerted a promyogenic effect, it tended to induce apoptotic cell death. In summary, our findings suggest that Nek5 promotes myogenic differentiation through up-regulation of caspase activity.