Src-related nonreceptor protein tyrosine kinases in nerve growth cones (p59fyn, pp60c-src, and pp62c-yes) are potential intracellular signaling molecules for cell adhesion molecule-directed axonal growth. To determine whether src-related tyrosine kinases mediate NCAM-dependent neurite outgrowth, cultures of cerebellar and sensory neurons from fyn-, src-, and yes- minus mice were analyzed for neurite outgrowth on monolayers of NCAM140-transfected L fibroblasts. NCAM-dependent neurite outgrowth was selectively inhibited in cultures of cerebellar and dorsal root ganglion neurons from fyn-, but not src- or yes- mice. Neurite outgrowth by fyn-, src-, or yes- neurons on untransfected fibroblast monolayers was unaffected, indicating that these kinases do not contribute significantly to axon growth on at least some integrins or other adhesive substrates present on fibroblasts. This study demonstrates that p59fyn is an essential component of the NCAM signaling pathway leading to axonal growth.
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1 November 1994
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November 01 1994
NCAM-dependent neurite outgrowth is inhibited in neurons from Fyn-minus mice.
H E Beggs,
H E Beggs
Department of Biochemistry, University of North Carolina School of Medicine, Chapel Hill 27599-7260.
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P Soriano,
P Soriano
Department of Biochemistry, University of North Carolina School of Medicine, Chapel Hill 27599-7260.
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P F Maness
P F Maness
Department of Biochemistry, University of North Carolina School of Medicine, Chapel Hill 27599-7260.
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H E Beggs
Department of Biochemistry, University of North Carolina School of Medicine, Chapel Hill 27599-7260.
P Soriano
Department of Biochemistry, University of North Carolina School of Medicine, Chapel Hill 27599-7260.
P F Maness
Department of Biochemistry, University of North Carolina School of Medicine, Chapel Hill 27599-7260.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1994) 127 (3): 825–833.
Citation
H E Beggs, P Soriano, P F Maness; NCAM-dependent neurite outgrowth is inhibited in neurons from Fyn-minus mice.. J Cell Biol 1 November 1994; 127 (3): 825–833. doi: https://doi.org/10.1083/jcb.127.3.825
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