Adhesive proteins linked with focal adhesion kinase regulate neurite outgrowth of PC12 cells.

Adhesive proteins existing in the extracellular matrix (ECM) play important roles in the regulation of neuronal cell behavior, including cell adhesion, motility and neurite outgrowth. Herein we show the effects of a series of adhesive proteins on the neurite outgrowth of PC12 cells and elucidate that this is closely related to the activation of focal adhesion kinase (FAK). For this we prepared culture substrates by coating tissue culture plastic with either collagen (Col), fibronectin (FN) or laminin (LN) and investigated the neurite outgrowth behavior. The results demonstrated that neurite outgrowth was highly dependent on the particular type of adhesive protein. While neurite number was comparable on all the coated surfaces, the length of neurites was greater on the FN- and LN-coated ones (greatest on the LN-coated one). In particular, FAK expression was highly up-regulated in the FN- and LN-coated surfaces, as revealed by Western blot analysis. A knock-down experiment further supported the idea that neurite outgrowth was largely suppressed in cells transfected with a FAK knock-down gene. Taken together, the neurite outgrowth of PC12 cells was greatly affected by adhesive proteins of the ECM, particularly FN and LN, and this is considered to be closely related to FAK intracellular signaling. This study may be useful in the consideration and design of nerve guidance and three-dimensional scaffolds which are appropriate to promote neuronal growth and nerve tissue regeneration.