Crosstalk of Humoral and Cell-Cell Contact-Mediated Signals in Postnatal Body Growth

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Abstract

The growth hormone (GH)-insulin-like growth factor 1 (IGF1) axis mediates postnatal body growth. The GH receptor has been regarded as the sole receptor that mediates the Janus kinase 2 (JAK2)/signal transducers and activators of the transcription 5B (STAT5B) signal toward IGF1 synthesis. Here, we report a signaling pathway that regulates postnatal body growth through EphA4, a member of the Eph family of receptor tyrosine kinases and a mediator of the cell-cell contact-mediated signaling. EphA4 forms a complex with the GH receptor, JAK2, and STAT5B and enhances Igf1 expression predominantly via the JAK2-dependent pathway, with some direct effect on STAT5B. Mice with a defective Epha4 gene have a gene dose-dependent short stature and low plasma IGF1 levels. Igf1 messenger RNA (mRNA) in the liver and many other tissues was also significantly reduced in Epha4-knockout mice, whereas pituitary Gh mRNA and plasma GH levels were not. These findings suggest that the local cell-cell contact-mediated ephrin/EphA4 signal is as important as the humoral GH signal in IGF1 synthesis and body size determination

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APA

Jing, X., Miyajima, M., Sawada, T., Chen, Q., Iida, K., Furushima, K., … Sakaguchi, K. (2012). Crosstalk of Humoral and Cell-Cell Contact-Mediated Signals in Postnatal Body Growth. Cell Reports, 2(3), 652–665. https://doi.org/10.1016/j.celrep.2012.08.021

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