Ben BarresAcademic Appointments
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Professor
Professor
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Professor
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Administrative Appointments
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Associate Chair
Stanford University School of Medicine - Neurobiology
2004
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Research Interests
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.
(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
- Stevens B, Allen NJ, Vazquez LE, Howell GR, Christopherson KS, Nouri N, Micheva KD, Mehalow AK, Huberman AD, Stafford B, Sher A, Litke AM, Lambris JD, Smith SJ, John SW, Barres BA "The classical complement cascade mediates CNS synapse elimination." Cell 2007; 131: 6: 1164-78 More »
- Cahoy JD, Emery B, Kaushal A, Foo LC, Zamanian JL, Christopherson KS, Xing Y, Lubischer JL, Krieg PA, Krupenko SA, Thompson WJ, Barres BA "A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function." J Neurosci 2008; 28: 1: 264-78 More »
- Dugas JC, Ibrahim A, Barres BA "A crucial role for p57(Kip2) in the intracellular timer that controls oligodendrocyte differentiation." J Neurosci 2007; 27: 23: 6185-96 More »
- Wang JT, Kunzevitzky NJ, Dugas JC, Cameron M, Barres BA, Goldberg JL "Disease gene candidates revealed by expression profiling of retinal ganglion cell development." J Neurosci 2007; 27: 32: 8593-603 More »
- Dugas JC, Tai YC, Speed TP, Ngai J, Barres BA "Functional genomic analysis of oligodendrocyte differentiation." J Neurosci 2006; 26: 43: 10967-83 More »
45 publications: view full list
