Glia promote local synaptogenesis through UNC-6 (netrin) signaling in C. elegans

Science

Volumn 318, Issue 5847, 2007, Pages 103-106

  Colón Ramos, Daniel A ^a   Margeta, Milica A ^a   Shen, Kang ^a  

^a STANFORD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NETRIN; NETRIN RECEPTOR; RECEPTOR; UNCLASSIFIED DRUG;

CANCER; GENE EXPRESSION; NEMATODE; NERVOUS SYSTEM; PROTEIN;

ARTICLE; CAENORHABDITIS ELEGANS; CELL GROWTH; COLORECTAL CANCER; CONTROLLED STUDY; GLIA; GLIA CELL; INTERNEURON; NERVE TRACT; NONHUMAN; POSTSYNAPTIC POTENTIAL; PRESYNAPTIC NERVE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; SIGNAL TRANSDUCTION; SYNAPTOGENESIS;

ANIMALS; ANIMALS, GENETICALLY MODIFIED; AXONS; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; CELL ADHESION MOLECULES; INTERNEURONS; NERVE TISSUE PROTEINS; NEUROGLIA; SIGNAL TRANSDUCTION; SYNAPSES;

CAENORHABDITIS ELEGANS;

EID: 35148813033     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1143762     Document Type: Article

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29. We thank G. Wang, C. Johnson, J. Audhya, M. Nonet, Y. Kohara, J. Kaplan, G. Garriga, E. Lundquist, the Caenorhabditis Genetic Center, and the Japanese National BioResource Project for strains and reagents; D. Hall and Z. Altun for diagrams used in the figures; C. Bargmann for helpful discussions and generous sharing of advice and reagents; C. Gao and Frank Chen for technical assistance; and S. Margolis, L. Looger, J. Irazoqui, B. Barres, and members of the Shen lab for thoughtful comments on the manuscript. This work was funded by grants to K.S. from the following: the McKnight Endowment Fund, the W. M. Keck Foundation, and the Searle Scholar program. M.A.M. was supported by the Stanford Medical Scientist Training Program and NIH grant GM007365. D.A.C.-R. was supported by the Damon Runyon Foundation and NIH grant K99 NS057931-01.