David Van Vactor

David Van Vactor, Ph.D.

Professor of Cell Biology
Director, Biological and Biomedical Sciences Graduate Program (HMS)
Director, Curriculum Fellows Program (HMS)

David Van Vactor, Ph.D. is a Professor of Cell Biology in the Blavatnik Institute at Harvard Medical School (HMS) and a member of the Program in Neuroscience and the DFCI/Harvard Cancer Center. He is the Faculty Director of the HMS Curriculum Fellows program and Director/PI of Harvard’s Molecular, Cellular and Developmental Dynamics (MCD2) T32 PhD training program. He is also a Visiting Professor at the Okinawa Institute of Science and Technology (OIST) Graduate University in Japan.  Dr. Van Vactor received his B.A. in Behavioral Biology at the Johns Hopkins University and his Ph.D. from the Department of Biological Chemistry at the University of California, Los Angeles (UCLA), before post-doctoral research at the University of California, Berkeley.

The Van Vactor Lab is focused on understanding the development, maintenance and plasticity of neuromuscular connectivity in the model organism Drosophila. The coordinated morphogenesis of the synapse, fundamental unit of cell-cell communication in neural networks, requires many layers of regulatory mechanisms.  Genome-wide enhancer/suppressor screens to define the molecular machinery controlling neuromuscular junction development (NMJ) led us to multiple translational regulators, including a number of microRNA (miR) genes. Because the fly NMJ has served so well for genetic analysis of synapse development and function in many labs, we have a sophisticated knowledge of underling pathways and gene networks, thus making this a system particularly well suited to explore upstream regulatory logic. Using conditional genetic tools to manipulate the function of conserved miRs and their target genes, we have identified several novel regulatory pathways.  In addition, through a close and long-term collaboration with the Artavanis-Tsakonas Lab, we have worked to better understand developmental and age-dependent degeneration of the neuromuscular system using a variety of models for human disease in Drosophila.

Harvard Medical School

Dept. of Cell Biology, LHRRB 314

240 Longwood Avenue

Boston, MA 02115

Lab telephone: 617-432-2195

Axonal heparan sulfate proteoglycans regulate the distribution and efficiency of the repellent slit during midline axon guidance.
Authors: Authors: Johnson KG, Ghose A, Epstein E, Lincecum J, O'Connor MB, Van Vactor D.
Curr Biol
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Functions of the ectodomain and cytoplasmic tyrosine phosphatase domains of receptor protein tyrosine phosphatase Dlar in vivo.
Authors: Authors: Krueger NX, Reddy RS, Johnson K, Bateman J, Kaufmann N, Scalice D, Van Vactor D, Saito H.
Mol Cell Biol
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Neurons take shape.
Authors: Authors: Lee H, Van Vactor D.
Curr Biol
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Receptor protein tyrosine phosphatases in nervous system development.
Authors: Authors: Johnson KG, Van Vactor D.
Physiol Rev
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A Drosophila homolog of cyclase-associated proteins collaborates with the Abl tyrosine kinase to control midline axon pathfinding.
Authors: Authors: Wills Z, Emerson M, Rusch J, Bikoff J, Baum B, Perrimon N, Van Vactor D.
Neuron
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Robo is Abl to block N-Cadherin function.
Authors: Authors: Emerson MM, Van Vactor D.
Nat Cell Biol
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GAPs in Slit-Robo signaling.
Authors: Authors: Ghose A, Van Vactor D.
Bioessays
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Axon guidance: the cytoplasmic tail.
Authors: Authors: Patel BN, Van Vactor DL.
Curr Opin Cell Biol
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Drosophila liprin-alpha and the receptor phosphatase Dlar control synapse morphogenesis.
Authors: Authors: Kaufmann N, DeProto J, Ranjan R, Wan H, Van Vactor D.
Neuron
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Induction of cell fate in the Drosophila retina: the bride of sevenless protein is predicted to contain a large extracellular domain and seven transmembrane segments.
Authors: Authors: Hart AC, Krämer H, Van Vactor DL, Paidhungat M, Zipursky SL.
Genes Dev
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