Myosin X (Myo10) with pleckstrin homology (PH) domains is a motor protein acting in filopodium initiation and extension. However, its potential role has not been fully understood, especially in neuronal development. In the present study the preferential accumulation of Myo10 in axon tips has been revealed in primary culture of hippocampal neurons with the aid of immunofluorescence from anti-Myo10 antibody in combination with anti-Tuj1 antibody as specific marker. Knocking down Myo10 gene transcription impaired outgrowth of axon with loss of Tau-1-positive phenotype. Interestingly, inhibition of actin polymerization by cytochalasin D rescued the defect of axon outgrowth. Furthermore, ectopic expression of Myo10 with enhanced green fluorescence protein (EGFP) labeled Myo10 mutants induced multiple axon-like neurites in a motor-independent way. Mechanism studies demonstrated that the recruitment of Myo10 through its PH domain to phosphatidylinositol (3,4,5)-trisphosphate (PtdIns (3,4,5) P3) was essential for axon formation. In addition, in vivo studies confirmed that Myo10 was required for neuronal morphological transition during radial neuronal migration in the developmental neocortex.
References
[1]
Barnes AP, Polleux F (2009) Establishment of axon-dendrite polarity in developing neurons. Annu Rev Neurosci 32: 347–381.
[2]
Dotti CG, Sullivan CA, Banker GA (1988) The establishment of polarity by hippocampal neurons in culture. J Neurosci 8(4): 1454–1468.
[3]
Suter DM, Miller KE (2011) The emerging role of forces in axonal elongation. Prog Neurobiol 94(2): 91–101.
[4]
Menager C, Arimura N, Fukata Y, Kaibuchi K (2004) PIP3 is involved in neuronal polarization and axon formation. J Neurochem 89(1): 109–118.
[5]
Shi SH, Jan LY, Jan YN (2003) Hippocampal neuronal polarity specified by spatially localized mPar3/mPar6 and PI 3-kinase activity. Cell 112(1): 63–75.
[6]
Yoshimura T, Arimura N, Kawano Y, Kawabata S, Wang S, et al. (2006) Ras regulates neuronal polarity via the PI3-kinase/Akt/GSK-3beta/CRMP-2 pathway. Biochem Biophys Res Commun 340(1): 62–68.
[7]
Cosker KE, Shadan S, van Diepen M, Morgan C, Li M, et al. (2008) Regulation of PI3K signalling by the phosphatidylinositol transfer protein PITPalpha during axonal extension in hippocampal neurons. J Cell Sci 121(Pt 6): 796–803.
[8]
Schwamborn JC, Puschel AW (2004) The sequential activity of the GTPases Rap1B and Cdc42 determines neuronal polarity. Nat Neurosci 7(9): 923–929.
[9]
Garvalov BK, Flynn KC, Neukirchen D, Meyn L, Teusch N, et al. (2007) Cdc42 regulates cofilin during the establishment of neuronal polarity. J Neurosci 27(48): 13117–13129.
[10]
Bradke F, Dotti CG (1999) The role of local actin instability in axon formation. Science 283(5409): 1931–1934.
[11]
Witte H, Bradke F (2008) The role of the cytoskeleton during neuronal polarization. Curr Opin Neurobiol 18(5): 479–487.
[12]
Flynn KC, Pak CW, Shaw AE, Bradke F, Bamburg JR (2009) Growth cone-like waves transport actin and promote axonogenesis and neurite branching. Dev Neurobiol 69(12): 761–779.
[13]
Kollins KM, Hu J, Bridgman PC, Huang YQ, Gallo G (2009) Myosin-II negatively regulates minor process extension and the temporal development of neuronal polarity. Dev Neurobiol 69(5): 279–298.
[14]
Korobova F, Svitkina T (2008) Arp2/3 complex is important for filopodia formation, growth cone motility, and neuritogenesis in neuronal cells. Mol Biol Cell 19(4): 1561–1574.
[15]
Kwiatkowski AV, Rubinson DA, Dent EW, Edward van Veen J, Leslie JD, et al. (2007) Ena/VASP Is Required for neuritogenesis in the developing cortex. Neuron 56(3): 441–455.
[16]
Bohil AB, Robertson BW, Cheney RE (2006) Myosin-X is a molecular motor that functions in filopodia formation. Proc Natl Acad Sci U S A 103(33): 12411–12416.
[17]
Sousa AD, Cheney RE (2005) Myosin-X: a molecular motor at the cell's fingertips. Trends Cell Biol 15(10): 533–539.
[18]
Bennett RD, Caride AJ, Mauer AS, Strehler EE (2008) Interaction with the IQ3 motif of myosin-10 is required for calmodulin-like protein-dependent filopodial extension. FEBS Lett 582(16): 2377–2381.
[19]
Cox D, Berg JS, Cammer M, Chinegwundoh JO, Dale BM, et al. (2002) Myosin X is a downstream effector of PI(3)K during phagocytosis. Nat Cell Biol 4(7): 469–477.
[20]
Woolner S, O'Brien LL, Wiese C, Bement WM (2008) Myosin-10 and actin filaments are essential for mitotic spindle function. J Cell Biol 182(1): 77–88.
[21]
Tokuo H, Ikebe M (2004) Myosin X transports Mena/VASP to the tip of filopodia. Biochem Biophys Res Commun 319(1): 214–220.
[22]
Zhang H, Berg JS, Li Z, Wang Y, Lang P, et al. (2004) Myosin-X provides a motor-based link between integrins and the cytoskeleton. Nat Cell Biol 6(6): 523–531.
[23]
Zhu XJ, Wang CZ, Dai PG, Xie Y, Song NN, et al. (2007) Myosin X regulates netrin receptors and functions in axonal path-finding. Nat Cell Biol 9(2): 184–192.
[24]
Pi X, Ren R, Kelley R, Zhang C, Moser M, et al. (2007) Sequential roles for myosin-X in BMP6-dependent filopodial extension, migration, and activation of BMP receptors. J Cell Biol 179(7): 1569–1582.
[25]
Almagro S, Durmort C, Chervin-Petinot A, Heyraud S, Dubois M, et al. (2010) The motor protein myosin-X transports VE-cadherin along filopodia to allow the formation of early endothelial cell-cell contacts. Mol Cell Biol 30(7): 1703–1717.
[26]
Plantard L, Arjonen A, Lock JG, Nurani G, Ivaska J, et al. (2010) PtdIns(3,4,5)P is a regulator of myosin-X localization and filopodia formation. J Cell Sci 123(Pt 20): 3525–3534.
[27]
Zhang X, Zhu J, Yang GY, Wang QJ, Qian L, et al. (2007) Dishevelled promotes axon differentiation by regulating atypical protein kinase C. Nat Cell Biol 9(7): 743–754.
[28]
Dent EW, Kwiatkowski AV, Mebane LM, Philippar U, Barzik M, et al. (2007) Filopodia are required for cortical neurite initiation. Nat Cell Biol 9(12): 1347–1359.
[29]
Sousa AD, Berg JS, Robertson BW, Meeker RB, Cheney RE (2006) Myo10 in brain: developmental regulation, identification of a headless isoform and dynamics in neurons. J Cell Sci 119(Pt 1): 184–194.
[30]
Jiang H, Guo W, Liang X, Rao Y (2005) Both the establishment and the maintenance of neuronal polarity require active mechanisms: critical roles of GSK-3beta and its upstream regulators. Cell 120(1): 123–135.
[31]
Umeki N, Jung HS, Sakai T, Sato O, Ikebe R, et al. (2011) Phospholipid-dependent regulation of the motor activity of myosin X. Nat Struct Mol Biol 18(7): 783–788.
[32]
Stiess M, Bradke F (2011) Neuronal polarization: The cytoskeleton leads the way. Dev Neurobiol 71(6): 430–444.
[33]
Brajenovic M, Joberty G, Kuster B, Bouwmeester T, Drewes G (2004) Comprehensive proteomic analysis of human Par protein complexes reveals an interconnected protein network. J Biol Chem 279(13): 12804–12811.
[34]
Mendoza-Naranjo A, Gonzalez-Billault C, Maccioni RB (2007) Abeta1-42 stimulates actin polymerization in hippocampal neurons through Rac1 and Cdc42 Rho GTPases. J Cell Sci 120(Pt 2): 279–288.
[35]
Lim KB, Bu W, Goh WI, Koh E, Ong SH, et al. (2008) The Cdc42 effector IRSp53 generates filopodia by coupling membrane protrusion with actin dynamics. J Biol Chem 283(29): 20454–20472.
[36]
Neukirchen D, Bradke F (2011) Cytoplasmic linker proteins regulate neuronal polarization through microtubule and growth cone dynamics. J Neurosci 31(4): 1528–1538.