Modulation of microtubule dynamics by the microtubule-associated protein 1a

• Published in: Journal of neuroscience research Vol. 87; no. 5; pp. 1080 - 1089
• Main Authors: Faller, Elliott M., Brown, David L.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.04.2009
• Subjects: Animals; Blotting, Western; Cell Line; Gene Expression; Green Fluorescent Proteins - metabolism; Humans; MAP1a; MAP2c; Mice; Microscopy, Fluorescence; microtubule dynamics; Microtubule-Associated Proteins - metabolism; microtubules; Microtubules - metabolism; neuronal microtubule-associated proteins; Swine; Transfection; Tubulin - metabolism
• ISSN: 0360-4012; 1097-4547
• DOI: 10.1002/jnr.21920

Structural microtubule‐associated proteins (MAPs) interact with microtubules to regulate the various dynamic stages of microtubules. The purpose of this study was to measure the impact of myc‐tagged MAP1a fragments on microtubule dynamic phases in vivo. Cells from an epithelial kidney cell line (LLCPK1) that had been permanently transfected with human green fluorescent protein (GFP)‐α‐tubulin were transiently transfected with myc‐tagged MAP1a fragments. Cells expressing MAP1a fragments were used to make direct observations of microtubule dynamics in living cells using fluorescence microscopy. All truncated MAP1a heavy chain fragments that contained the microtubule‐binding domain were shown to associate with microtubules. Truncated fragments containing different regions of the projection domain of MAP1a demonstrated variations in their impact on microtubule dynamic events by promoting growth or inhibition of shortening phases. In contrast to MAP1a, MAP2c bundled microtubules and resulted in a complete arrest of microtubule motility. Results from the present study suggest that MAP1a promotes slow, stable growth of microtubules. This type of growth may be important in the maintenance and restructuring of adult neurons. © 2008 Wiley‐Liss, Inc.