Clifford Woolf

Clifford Woolf, MB, BCh, PhD

Professor of Neurology, Harvard Medical School

Adaptive and Maladaptive Plasticity in Sensory and Motor Systems

Neurons are subject to functional, chemical and structural plasticity. This plasticity is an important factor both in the normal function of the nervous system and in a vast range of neurological diseases.

The Woolf lab studies how different forms of neuronal plasticity contribute both to adaptive and maladaptive changes in the mammalian nervous system, particularly in relation to pain, regeneration and neurodegenerative diseases.

Most of our work is concentrated on primary sensory and motor neurons, and to the interaction of neurons and immune cells, using a multidisciplinary approach spanning stem cell, molecular and cell biology, electrophysiology, neuroanatomy, behavior and genetics. We have established functional and comparative genomic strategies using expression profiling, bioinformatics and gain- and loss-of-function approaches, to screen for novel genes that contribute to neuronal plasticity and disease phenotypes. Our group works closely with many academic groups and the pharmaceutical industry to model disease and identify molecular targets for novel analgesics, axonal growth determinants and neuroprotective agents.

Current research includes study of the transcriptional control and post-translational processing of receptors and ion channels that mediate pain hypersensitivity, selective silencing of defined neuronal populations, intracellular signal transduction cascades activated by peripheral inflammation and nerve injury, neuro-immune interactions, transcription factors as master regulators of pain, growth and survival programs, cell survival in injured sensory and motor neurons, and the contribution of intrinsic growth determinants in establishing regenerative capacity in the peripheral and central nervous system. We are an active part of the Harvard Stem Cell Institute and are investigating how sensory and motor neurons reprogrammed from patient fibroblasts can be used to study pain and motor neuron disease and to screen for new treatments.

Publications View
Neuronal plasticity: increasing the gain in pain.
Authors: Authors: Woolf CJ, Salter MW.
Science
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Putting the spinal cord together again.
Authors: Authors: Behar O, Mizuno K, Neumann S, Woolf CJ.
Neuron
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Diversity of expression of the sensory neuron-specific TTX-resistant voltage-gated sodium ion channels SNS and SNS2.
Authors: Authors: Amaya F, Decosterd I, Samad TA, Plumpton C, Tate S, Mannion RJ, Costigan M, Woolf CJ.
Mol Cell Neurosci
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Trigeminal neuralgia: opportunities for research and treatment.
Authors: Authors: Kitt CA, Gruber K, Davis M, Woolf CJ, Levine JD.
Pain
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The bigger the better or small but perfectly formed?
Authors: Authors: Woolf CJ.
Pain
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Silent NMDA receptor-mediated synapses are developmentally regulated in the dorsal horn of the rat spinal cord.
Authors: Authors: Baba H, Doubell TP, Moore KA, Woolf CJ.
J Neurophysiol
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Synaptic transmission and plasticity in the superficial dorsal horn.
Authors: Authors: Moore KA, Baba H, Woolf CJ.
Prog Brain Res
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Nociceptive-specific activation of ERK in spinal neurons contributes to pain hypersensitivity.
Authors: Authors: Ji RR, Baba H, Brenner GJ, Woolf CJ.
Nat Neurosci
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Semaphorin 3A growth cone collapse requires a sequence homologous to tarantula hanatoxin.
Authors: Authors: Behar O, Mizuno K, Badminton M, Woolf CJ.
Proc Natl Acad Sci U S A
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A role for HSP27 in sensory neuron survival.
Authors: Authors: Lewis SE, Mannion RJ, White FA, Coggeshall RE, Beggs S, Costigan M, Martin JL, Dillmann WH, Woolf CJ.
J Neurosci
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