{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,6,19]],"date-time":"2024-06-19T01:32:59Z","timestamp":1718760779411},"reference-count":33,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2010,2,22]],"date-time":"2010-02-22T00:00:00Z","timestamp":1266796800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Biomedical Materials Res"],"published-print":{"date-parts":[[2010,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>In this study, we modified poly(ethylene\u2010<jats:italic>co<\/jats:italic>\u2010vinyl alcohol) (EVAL) membranes by the covalent bonding of diamines via epoxidation of surface hydroxyl groups of EVAL to analyze the effect of immobilized diamines with different carbon chain length on the cultured cerebellar granule neurons. Morphological studies showed that neurons seeded on the diamine\u2010immobilized EVAL membrane were able to survive and regenerate with formation of an extensive neuritic network. Furthermore, cultured neurons showed that the presence of diamine with different carbon chain length was able to effectively regulate the neuron adhesion, migration, aggregation, and neurite growth pattern, but mediated neuronal activity with equal efficacy. The short\u2010chain amine stimulated neuron migration, aggregation, and neurite fasciculation, whereas the long carbon chain diamine maintained single neuron distribution with the defasciculated feature of the neurite. Although it is known that positively charged amine molecules can interact directly with cell surface proteoglycans to mediate cell attachment, this study further demonstrated that the terminal primary amine with different carbon chain length is involved in mediating cell\u2013substrate interaction to further regulate neuron aggregation and neurite fasciculation. This indicates a delicate interaction of neuron with the immobilized diamine molecules on the EVAL membrane surface. This work is encouraging because the diamine\u2010 immobilized EVAL membranes can be applied for the establishment of different neural culture systems useful for future investigations of neuron biology under <jats:italic>in vitro<\/jats:italic> conditions. \u00a9 2010 Wiley Periodicals, Inc. 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