Myosin IIB is required for growth cone motility

被引:173
作者
Bridgman, PC
Dave, S
Asnes, CF
Tullio, AN
Adelstein, RS
机构
[1] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
[3] NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
关键词
growth cones; motility; myosin; actin; traction force; knock-out mice;
D O I
10.1523/JNEUROSCI.21-16-06159.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Growth cones are required for the forward advancement and navigation of growing axons. Modulation of growth cone shape and reorientation of the neurite are responsible for the change of outgrowth direction that underlies navigation. Change of shape involves the reordering of the cytoskeleton. Reorientation of the neurite requires the generation of tension, which is supplied by the ability of the growth cone to crawl on a substrate. The specific molecular mechanisms responsible for these activities are unknown but are thought to involve actomyosin-generated force combined with linkage to the cell surface receptors that are responsible for adhesion (Heidemann and Buxbaum, 1998). To test whether myosin IIB is responsible for the force generation, we quantified shape dynamics and filopodial-mediated traction force in growth cones from myosin IIB knock-out (KO) mice and compared them with neurons from normal littermates. Growth cones from the KO mice spread less, showed alterations in shape dynamics and actin organization, and had reduced filopodial-mediated traction force. Although peak traction forces produced by filopodia of KO cones were decreased significantly, KO filopodia occasionally developed forces equivalent to those in the wild type. This indicates that other myosins participate in filopodial-dependent traction force. Therefore, myosin IIB is necessary for normal growth cone spreading and the modulation of shape and traction force but acts in combination with other myosins for some or all of these activities. These activities are essential for growth cone forward advancement, which is necessary for outgrowth. Thus outgrowth is slowed, but not eliminated, in neurons from the myosin IIB KO mice.
引用
收藏
页码:6159 / 6169
页数:11
相关论文
共 47 条
[1]   DISORIENTED PATHFINDING BY PIONEER NEURON GROWTH CONES DEPRIVED OF FILOPODIA BY CYTOCHALASIN TREATMENT [J].
BENTLEY, D ;
TOROIANRAYMOND, A .
NATURE, 1986, 323 (6090) :712-715
[2]   Keratocytes generate traction forces in two phases [J].
Burton, K ;
Park, JH ;
Taylor, DL .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (11) :3745-3769
[3]   NAVIGATIONAL ERRORS MADE BY GROWTH CONES WITHOUT FILOPODIA IN THE EMBRYONIC XENOPUS BRAIN [J].
CHIEN, CB ;
ROSENTHAL, DE ;
HARRIS, WA ;
HOLT, CE .
NEURON, 1993, 11 (02) :237-251
[4]   MYOSIN IS INVOLVED IN POSTMITOTIC CELL SPREADING [J].
CRAMER, LP ;
MITCHISON, TJ .
JOURNAL OF CELL BIOLOGY, 1995, 131 (01) :179-189
[5]   Imaging the traction stresses exerted by locomoting cells with the elastic substratum method [J].
Dembo, M ;
Oliver, T ;
Ishihara, A ;
Jacobson, K .
BIOPHYSICAL JOURNAL, 1996, 70 (04) :2008-2022
[6]  
Evans LL, 1997, J CELL SCI, V110, P439
[7]   Cell crawling: First the motor, now the transmission [J].
Heidemann, SR ;
Buxbaum, RE .
JOURNAL OF CELL BIOLOGY, 1998, 141 (01) :1-4
[8]   GROWTH CONE BEHAVIOR AND PRODUCTION OF TRACTION FORCE [J].
HEIDEMANN, SR ;
LAMOUREUX, P ;
BUXBAUM, RE .
JOURNAL OF CELL BIOLOGY, 1990, 111 (05) :1949-1957
[9]   NEURONAL CELL EXPRESSION OF INSERTED ISOFORMS OF VERTEBRATE NONMUSCLE MYOSIN HEAVY-CHAIN II-B [J].
ITOH, K ;
ADELSTEIN, RS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14533-14540
[10]  
JAY PY, 1995, J CELL SCI, V108, P387