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
Pain
Authors: Authors: The stereospecific effect of naloxone on rat dorsal horn neurones; inhibition in superficial laminae and excitation in deeper laminae
1980 Dec; 9(3):293-306.
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Nature
Authors: Authors: Nociceptor neurons affect cancer immunosurveillance
2022 Nov; 611(7935):405-412.
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Pain
Authors: Authors: Sensitization of high mechanothreshold superficial dorsal horn and flexor motor neurones following chemosensitive primary afferent activation
1994 Aug; 58(2):141-155.
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J Neurosci Methods
Authors: Authors: Characterization of the cutaneous input to the ventral horn in vitro using the isolated spinal cord-hind limb preparation
1990 Oct; 35(1):39-46.
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Neuroscience
Authors: Authors: Axotomy increases glycogen phosphorylase activity in motoneurones
1984 Aug; 12(4):1261-9.
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Pflugers Arch
Authors: Authors: The effect of an inhibitor of adenylate cyclase on the development of pyrogen, prostaglandin and cyclic AMP fevers in the rabbit
1976 Dec 28; 367(2):177-81.
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Brain Res
Authors: Authors: Morphological and membrane properties of young rat lumbar and thoracic dorsal root ganglion cells with unmyelinated axons
1993 Apr 23; 609(1-2):193-200.
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J Neurophysiol
Authors: Authors: Physiology and morphology of multireceptive neurons with C-afferent fiber inputs in the deep dorsal horn of the rat lumbar spinal cord
1987 Sep; 58(3):460-79.
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J Physiol
Authors: Authors: Effects of cutaneous nerve and intraspinal conditioning of C-fibre afferent terminal excitability in decerebrate spinal rats
1981 Sep; 318:25-39.
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Eur J Neurosci
Authors: Authors: Morphine selectively depresses the slowest, NMDA-independent component of C-fibre-evoked synaptic activity in the rat spinal cord in vitro
1995 Jan 01; 7(1):12-8.
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