Key Documents
Ben Barres
- Professor, Neurobiology
- Professor, Neurology & Neurological Sciences
- Professor (By courtesy), Ophthalmology
- Member, Bio-X
- Professor, Developmental Biology
Contact Information
- Clinical Offices
Administrative Appointments
- Chair, Stanford University School of Medicine - Neurobiology , (2008– present )
Postdoctoral Advisees
Research Interests
THE MYSTERY AND MAGIC OF GLIA
We are interested in the development and function of glial cells in the mammalian central nervous system. To understand the interactions between neurons and glial cells we have developed methods to highly purify and culture retinal ganglion cells (neurons) as well as the glial cell types they interact with, oligodendrocytes and astrocytes, from the rodent optic nerve. We are using a large variety of methods to address these issues including cell purification by immunopanning, tissue culture, patch clamping, immunohistochemistry and molecular biology. Currently, we are focusing on several questions:
(1) What are the cell-cell interactions that control myelination and node of Ranvier formation?
(2) Do glial cells play a role in synapse formation and function?
(3) What are the signals that promote the survival and growth of retinal ganglion cells and can we use this knowledge to promote their survival and regeneration after injury?
(4) How do protoplasmic astrocytes, the main glial cell type in gray matter, develop and what is their function?.
We have found evidence of several novel glial signals that induce the onset of myelination, the clustering of axonal sodium channels, the survival and growth of retinal ganglion cells, and the formation of synapses. We are characterizing these processes and are attempting to identify these glial-derived molecules.
Publications
- PLoS Biol. 2009; (8): e1000185
- Proc Natl Acad Sci U S A. 2009; (2): 641-6
- Neuron. 2009; (3): 327-34
- Cell. 2009; (1): 172-85
- Cell. 2009; (2): 380-92
- Cell. 2008; (4): 596-8
- Neuron. 2008; (4): 555-69
- J Neurosci. 2008; (1): 264-78
- Neuron. 2008; (3): 425-38
- J Neurosci. 2008; (33): 8294-305
- Neuron. 2008; (3): 430-40
- Annu Rev Neurosci. 2007; 153-79
- J Neurosci. 2007; (32): 8593-603
- J Neurosci. 2007; (23): 6185-96
- Cell. 2007; (6): 1164-78
- J Neurosci. 2006; (43): 10967-83
- Cell. 2005; (1): 9-12
- Cell. 2005; (3): 421-33
- Curr Biol. 2005; (8): R302-5
- Curr Opin Neurobiol. 2005; (5): 542-8
- Mol Cell Neurosci. 2004; (2): 241-51
- J Neurosci. 2004; (21): 4989-99
- Glia. 2004; (3): 209-16
- Mol Cell Neurosci. 2004; (4): 544-57
- Neuron. 2004; (2): 183-91
- J. NEUROSCI. 2004; 4989-99
- Glia. 2003; (1): 4-5
- Neuron. 2003; (5): 897-904
- SCIENCE. 2002; 1860-4
- Neuron. 2002; (5): 689-702
- Curr Biol. 2002; (19): R654-6
- Science. 2002; (5574): 1860-4
- Neuron. 2001; (3): 603-14
- Neuron. 2001; (1): 105-19
- Science. 2001; (5545): 1296-7
- J Neurosci. 2001; (5): 1538-47
- Science. 2001; (5504): 657-61
- Annu Rev Neurosci. 2000; 579-612
- Neuron. 2000; (2): 197-200
- Curr Opin Neurobiol. 2000; (5): 642-8
- Mol Cell Neurosci. 1999 Oct-Nov; (4-5): 385-97
- J Neurosci. 1999; (3): 1049-61
- Cell. 1999; (6): 667-70
- J Cell Biol. 1999; (6): 1123-8
- Neuron. 1998; (4): 651-2
- J Neurosci. 1998; (18): 7361-71
- Curr Biol. 1998; (9): R310-2
- J Neurosci. 1998; (12): 4627-36
- Curr Biol. 1997; (7): R433-6
- Mol Cell Neurosci. 1996; (2-3): 146-56
- Mol Cell Neurosci. 1996; (2/3): 146-56
- Curr Opin Neurobiol. 1996; (5): 615-21
- Cell. 1995; (5): 671-4
- Neuron. 1995; (4): 805-19
- Curr Biol. 1994; (9): 847-50