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
Utilization of an HSV-based amplicon vector encoding the axonal marker hPLAP to follow neurite outgrowth in cultured DRG neurons.
Authors: Authors: Seijffers R, Woolf CJ.
J Neurosci Methods
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Use and abuse of opioid analgesics: potential methods to prevent and deter non-medical consumption of prescription opioids.
Authors: Authors: Woolf CJ, Hashmi M.
Curr Opin Investig Drugs
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Cyclooxygenase 2 expression in the spared nerve injury model of neuropathic pain.
Authors: Authors: Broom DC, Samad TA, Kohno T, Tegeder I, Geisslinger G, Woolf CJ.
Neuroscience
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Development of neuropathic pain in the rat spared nerve injury model is not prevented by a peripheral nerve block.
Authors: Authors: Suter MR, Papaloïzos M, Berde CB, Woolf CJ, Gilliard N, Spahn DR, Decosterd I.
Anesthesiology
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Central sensitization and LTP: do pain and memory share similar mechanisms?
Authors: Authors: Ji RR, Kohno T, Moore KA, Woolf CJ.
Trends Neurosci
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Disruption of ErbB receptor signaling in adult non-myelinating Schwann cells causes progressive sensory loss.
Authors: Authors: Chen S, Rio C, Ji RR, Dikkes P, Coggeshall RE, Woolf CJ, Corfas G.
Nat Neurosci
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Removal of GABAergic inhibition facilitates polysynaptic A fiber-mediated excitatory transmission to the superficial spinal dorsal horn.
Authors: Authors: Baba H, Ji RR, Kohno T, Moore KA, Ataka T, Wakai A, Okamoto M, Woolf CJ.
Mol Cell Neurosci
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High basal expression and injury-induced down regulation of two regulator of G-protein signaling transcripts, RGS3 and RGS4 in primary sensory neurons.
Authors: Authors: Costigan M, Samad TA, Allchorne A, Lanoue C, Tate S, Woolf CJ.
Mol Cell Neurosci
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Selective up-regulation of the growth arrest DNA damage-inducible gene Gadd45 alpha in sensory and motor neurons after peripheral nerve injury.
Authors: Authors: Befort K, Karchewski L, Lanoue C, Woolf CJ.
Eur J Neurosci
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A conditional deletion of the NR1 subunit of the NMDA receptor in adult spinal cord dorsal horn reduces NMDA currents and injury-induced pain.
Authors: Authors: South SM, Kohno T, Kaspar BK, Hegarty D, Vissel B, Drake CT, Ohata M, Jenab S, Sailer AW, Malkmus S, Masuyama T, Horner P, Bogulavsky J, Gage FH, Yaksh TL, Woolf CJ, Heinemann SF, Inturrisi CE.
J Neurosci
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