Tenascin-R induces actin-rich microprocesses and branches along neurite shafts

被引:20
作者
Zacharias, U [1 ]
Leuschner, R [1 ]
Nörenberg, U [1 ]
Rathjen, FG [1 ]
机构
[1] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
关键词
D O I
10.1006/mcne.2002.1203
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The formation of protrusions along the shaft of neurites might be important in the establishment and refinement of neuronal connections during development. In a search for extracellular signals that affect the formation of microprocesses along neurites we found that the ECM glycoprotein tenascin-R (TN-R) but not other ECM glycoproteins increased the percentage of tectal neurons with actin-rich microprocesses and side branches. Longer actin-based microprocesses were also invaded by microtubuli in their proximal part. The formation of microprocesses by TN-R extending laterally along the neuritic shaft was time- and dose-dependent. In addition to the induction of microprocesses, TN-R increased the size of the growth cone of tectal neurons. A cross-species experiment in combination with blocking antibodies demonstrated that the TN-R-induced effects are mediated by the Ig superfamily member contactin. These observations suggest that TN-R via its neuronal receptor contactin might induce a transition from long-distance growth of tectal interneurons to differentiation, including the formation of microprocesses.
引用
收藏
页码:626 / 633
页数:8
相关论文
共 37 条
[21]   Mobilization of the cell adhesion glycoprotein F3/contactin to axonal surfaces is activity dependent [J].
Pierre, K ;
Dupouy, B ;
Allard, M ;
Poulain, DA ;
Theodosis, DT .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 14 (04) :645-656
[22]  
RATHJEN FG, 1991, DEVELOPMENT, V113, P151
[23]   MEMBRANE-GLYCOPROTEINS INVOLVED IN NEURITE FASCICULATION [J].
RATHJEN, FG ;
WOLFF, JM ;
FRANK, R ;
BONHOEFFER, F ;
RUTISHAUSER, U ;
SCHOEFFSKI, A .
JOURNAL OF CELL BIOLOGY, 1987, 104 (02) :343-353
[24]   The interaction between F3 immunoglobulin domains and protein tyrosine phosphatases ζ/β triggers bidirectional signalling between neurons and glial cells [J].
Revest, JM ;
Faivre-Sarrailh, C ;
Maeda, N ;
Noda, M ;
Schachner, M ;
Rougon, G .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (04) :1134-1147
[25]  
Saito Y, 1997, J NEUROSCI, V17, P8792
[26]   Induction of neurite outgrowth through contactin and Nr-CAM by extracellular regions of glial receptor tyrosine phosphatase beta [J].
Sakurai, T ;
Lustig, M ;
Nativ, M ;
Hemperly, JJ ;
Schlessinger, J ;
Peles, E ;
Grumet, M .
JOURNAL OF CELL BIOLOGY, 1997, 136 (04) :907-918
[27]   Fibroblast growth factor-2 promotes axon branching of cortical neurons by influencing morphology and behavior of the primary growth cone [J].
Szebenyi, G ;
Dent, EW ;
Callaway, JL ;
Seys, C ;
Lueth, H ;
Kalil, K .
JOURNAL OF NEUROSCIENCE, 2001, 21 (11) :3932-3941
[28]   LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite [J].
Toni, N ;
Buchs, PA ;
Nikonenko, I ;
Bron, CR ;
Muller, D .
NATURE, 1999, 402 (6760) :421-425
[29]   Neurofascin induces neurites by heterophilic interactions with axonal NrCAM while NrCAM requires F11 on the axonal surface to extend neurites [J].
Volkmer, H ;
Leuschner, R ;
Zacharias, U ;
Rathjen, FG .
JOURNAL OF CELL BIOLOGY, 1996, 135 (04) :1059-1069
[30]   Dissection of complex molecular interactions of neurofascin with axonin-1, F11, and tenascin-R, which promote attachment and neurite formation of tectal cells [J].
Volkmer, H ;
Zacharias, U ;
Nörenberg, U ;
Rathjen, FG .
JOURNAL OF CELL BIOLOGY, 1998, 142 (04) :1083-1093