Extracellular muscle myosin II promotes sensory axon formation

DNA and Cell Biology

Volumn 24, Issue 7, 2005, Pages 438-445

  Silver, Lee ^a   Gallo, Gianluca ^a  

^a DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LAMININ; MYOSIN II; NEUROTROPHIN; PROTEOCHONDROITIN SULFATE; SEMAPHORIN 3A;

ANIMAL TISSUE; ARTICLE; CELL SURVIVAL; CHICK EMBRYO; CONTROLLED STUDY; EMBRYO; EXTRACELLULAR MATRIX; GROWTH CONE; GROWTH STIMULATION; NERVE FIBER GROWTH; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SENSORY NERVE CELL; SPINAL GANGLION;

ANIMALS; AXONS; CELL ADHESION; CELLS, CULTURED; CHICK EMBRYO; DOSE-RESPONSE RELATIONSHIP, DRUG; EXTRACELLULAR MATRIX; GANGLIA, SPINAL; IMMUNOHISTOCHEMISTRY; LAMININ; MICROSCOPY, VIDEO; MUSCLE, SKELETAL; MYOSIN TYPE II; NERVE GROWTH FACTORS; NEURONS, AFFERENT; ORGAN CULTURE TECHNIQUES; PROTEOCHONDROITIN SULFATES; SEMAPHORIN-3A; SUBSTRATE SPECIFICITY; TIME FACTORS;

EID: 22244491300     PISSN: 10445498     EISSN: None     Source Type: Journal    
DOI: 10.1089/dna.2005.24.438     Document Type: Article

References (28)

1. BARRES, B.A., and BARDE, Y. (2000). Neuronal and glial cell biology. Curr. Opin. Neurobiol. 10, 642-648.
2. BRIDGMAN, P.C., DAVE, S., ASNES, C.F., TULLIO, A.N., and ADELSTEIN, R.S. (2001). Myosin IIB is required for growth cone motility. J. Neurosci. 21, 6159-6169.
3. BROWN, J., and BRIDGMAN, P.C. (2003). Role of myosin II in axon outgrowth. J. Histochem. Cytochem. 51, 421-428.
4. DONTCHEV, V.D., and LETOURNEAU, P.C. (2003). Growth cones integrate signaling from multiple guidance cues. J. Histochem. Cytochem. 51, 435-444.
5. GALLO, G., and LETOURNEAU, P.C. (1999). Different contributions of microtubule dynamics and transport to the growth of axons and collateral sprouts. J. Neurosci. 19, 3860-3873.
6. HUANG, C.L., and KEYNES, R.J. (1983). Terminal sprouting of mouse motor nerves when the post-synaptic membrane degenerates. Brain Res. 274, 225-229.
7. KOLLER, A., MAIR, J., SCHOBERSBERGER, W., WOHLFARTER, T., HAID, C., MAYR, M., VILLIGER, B., FREY, W., and PUSCHENDORF, B. (1998). Effects of prolonged strenuous endurance exercise on plasma myosin heavy chain fragments and other muscular proteins. Cycling vs running. J. Sports Med. Phys. Fitness 38, 10-17.
8. KUHN, T.B., BROWN, M.D., and BAMBURG, J.R. (1998). Rac1-dependent actin filament organization in growth cones is necessary for beta1-integrin-mediated advance but not for growth on poly-D-lysine. J. Neurobiol. 37, 524-540.
9. LAMOUREUX, P., RUTHEL, G., BUXBAUM, R.E., and HEIDEMANN, S.R. (2002). Mechanical tension can specify axonal fate in hippocampal neurons. J. Cell. Biol. 159, 499-508.
10. LEMMON, V., BURDEN, S.M., PAYNE, H.R., ELMSLIE, G.J., and HLAVIN, M.L. (1992). Neurite growth on different substrates: Permissive versus instructive influences and the role of adhesive strength. J. Neurosci. 12, 818-826.
11. LIAO, L., SINDHWANI, R., ROJKIND, M., FACTOR, S., LEINWAND, L., and DIAMOND, B. (1995) Antibody-mediated autoimmune myocarditis depends on genetically determined target organ sensitivity. J. Exp. Med. 181, 1123-1131.
12. LIN, C.H., ESPREAFICO, E.M., MOOSEKER, M.S., and FORSCHER, P. (1997). Myosin drives retrograde F-actin flow in neuronal growth cones. Biol. Bull. 192, 183-185.
13. MAIR, J., KOLLER, A., ARTNER-DWORZAK, E., HAID, C., WICKE, K., JUDMAIER, W., and PUSCHENDORF, B. (1992). Effects of exercise on plasma myosin heavy chain fragments and MRI of skeletal muscle. J. Appl. Physiol. 72, 656-663.
14. MAIR, J., MAYR, M., MULLER, E., KOLLER, A., HAID, C., ARTNER-DWORZAK, E., CALZOLARI, C., LARUE, C., and PUSCHENDORF, B. (1995). Rapid adaptation to eccentric exercise-induced muscle damage. Int. J. Sports Med. 16, 352-356.
15. MEDINA, M.B. (2004). Binding interaction studies of the immobilized Salmonella typhimurium with extracellular matrix and muscle proteins, and polysaccharides. Int. J. Food Microbiol. 93, 63-72.
16. ONUOHA, G.N., ALPAR, E.K., LAPRADE, M., RAMA, D., and PAU, B. (1999). Effects of bone fracture and surgery on plasma myosin heavy chain fragments of skeletal muscle. Clin. Invest. Med. 22, 180-184.
17. ONUOHA, G.N., ALPAR, E.K., LAPRADE, M., RAMA, D., and PAU, B. (2001). Levels of myosin heavy chain fragment in patients with tissue damage. Arch. Med. Res. 32, 27-29.
18. PECOT-DECHAVASSINE, M. (1986). Increase in polyneuronal innervation in frog muscle after muscle injury. J. Physiol. 371, 167-177.
19. POLLACK, E.D., and LIEBIG, V. (1990). Stage-dependent spontaneous frog dorsal root ganglion neuritogenesis on polylysine in vitro. Anat. Rec. 228, 220-224.
20. RAVKILDE, J. (1998). Creatine kinase isoenzyme MB mass, cardiac troponin T, and myosin light chain isotype 1 as serological markers of myocardial injury and their prognostic importance in acute coronary syndrome. Dan. Med. Bull. 45, 34-50.
21. SANDVIG, A., BERRY. M., BARRETT, L.B., BUTT. A., and LOGAN, A. (2004). Myelin-, reactive glia-, and scar-derived CNS axon growth inhibitors, expression, receptor signaling, and correlation with axon regeneration. Glia 46, 225-251.
22. SMALHEISER, N.R. (1996). Proteins in unexpected locations. Mol. Biol. Cell. 7, 1003-1014.
23. SMITH, C.L. (1994). Cytoskeletal movements and substrate interactions during initiation of neurite outgrowth by sympathetic neurons in vitro. J. Neurosci. 14, 384-398.
24. SUMMERS, P.J., and ASHMORE, C.R. (1983). Regeneration and reinnervation of the dystrophic mouse soleus muscle. A light- and electron-microscopic study. Acta Neuropathol. (Berl.) 59, 207-215.
25. TULLIO, A.N., BRIDGMAN, P.C., TRESSER, N.J., CHAN, C.C., CONTI, M.A., ADELSTEIN, R.S., and HARA, Y. (2001). Structural abnormalities develop in the brain after ablation of the gene encoding nonmuscle myosin II-B heavy chain. J. Comp. Neurol. 433, 62-74.
26. WYLIE, S.R., and CHANTLER, P.D. (2001). Separate but linked functions of conventional myosins modulate adhesion and neurite outgrowth. Nat. Cell. Biol. 3, 88-92.
27. WYLIE, S.R., and CHANTLER, P.D. (2003). Myosin IIA drives neurite retraction. Mol. Biol. Cell 14, 4654-4666.
28. WYLIE, S.R., WU, P.J., PATEL, H., and CHANTLER, P.D. (1998). A conventional myosin motor drives neurite outgrowth. Proc. Natl. Acad. Sci. USA 95, 12967-12972.