Associated PDFs

Progress Report 2007
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Nervous System Injuries

The common theme that arises from central nervous system (CNS) injury research is how basic studies can inform the development of therapies. In each of the primary CNS injuries—spinal cord injury, stroke, and brain tumors—treatments are lacking, in large part because of the complexity of the underlying processes.

Research has therefore mainly focused on unraveling the processes of cell death, nerve regeneration, and tumor genesis, with the ever-present goal of translating that knowledge into molecularly targeted treatments that prevent or repair nervous system damage.

Harnessing Thoughts

In one of the year’s biggest headline grabbers, a paralyzed man controlled a computer using thoughts. This advance is the culmination of decades of basic research on the brain’s motor control center (also discussed in the Neuroethics section, page 36). A pilot study on this one patient, reported in Nature by John Donoghue of Brown University and a Harvard-based team of collaborators, proved the concept that a brain-computer interface can record neural activity from a person’s primary motor cortex and translate it into specific actions on external devices.1

 boy in wheel chair 
Brain-computer interface: In a pilot study, a brain-computer interface allowed a single patient with paralysis to operate a computer using only his thoughts. Paired with a muscle stimulator system, such technology may one day allow people who are paralyzed to move their limbs again. (Illustration courtesy of Cyberkinetics Neurotechnology Systems, Inc.)

The man in the study, paralyzed from the neck down in a spinal cord injury three years ago, was able to open e-mail messages, operate a television and light switches, open and close a prosthetic hand, and perform rudimentary actions with a multijointed arm. The work represents an early step toward thought-powered robotics, which are envisioned as tools to help restore some degree of independence to people paralyzed by central nervous system damage. The authors were careful to note that the technology requires further refinement before it can be practically applied beyond a research setting. 

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References

1. Hochberg LR, Serruva MD, Friehs GM, Mukand JA, Saleh M, Caplan AH, Branner A, Chen D, Penn RD, and Donoghue JP. Neuronal ensemble control of prosthetic devices by a human with tetraplegia. Nature 2006 442(7099):164–171.

2. Massey JM, Hubscher CH, Wagoner MR, Decker JA, Amps J, Silver J, and Onifer SM. Chondroitinase ABC digestion of the perineuronal net promotes functional collateral sprouting in the cuneate nucleus after cervical spinal cord injury. Journal of Neuroscience 2006 26(16):4406–4414.

3. Yang LJ, Lorenzini I, Vajn K, Mountney A, Schramm P, Schnaar RL. Sialidase enhances spinal axon outgrowth in vivo. Proceedings of the National Academy of Sciences USA 2006 103(29):11057–11062.

4. Yin Y, Henzl MT, Lorber B, Nakazawa T, Thomas TT, Jiang F, Langer R, and Benowitz LI. Oncomodulin is a macrophage-derived signal for axon regeneration in retinal ganglion cells. Nature Neuroscience 2006 9(6):843–852.

5. Shirasaki R, Lewcock JW, Lettieri K, and Pfaff SL. FGF as a target-derived chemoattractant for developing motor axons genetically programmed by the LIM code. Neuron 2006 15(50):841–853.

6. Medeiros NA, Burnette DT, and Forscher P. Myosin II functions in actin-bundle turnover in neuronal growth cones. Nature Cell Biology 2006 8(3):215–226.

7. Houle JD, Tom VJ, Mayes D, Wagoner G, Phillips N, and Silver J. Combining an autologous peripheral nervous system “bridge” and matrix modification by chondroitinase allows robust, functional regeneration beyond a hemisection lesion of the adult rat spinal cord. Journal of Neuroscience 2006 12(28):7405–7415.

8. Deshpande DM, Kim YS, Martinez T, Carmen J, Dike S, Shats I, Rubin LL, Drummond J, Krishnan C, Hoke A, Maragakis N, Shefner J, Rothstein JD, and Kerr DA. Recovery from paralysis in adult rats using embryonic stem cells. Annals of Neurology 2006 60(1):32–44.

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10. Lees KR, Zivin JA, Ashwood T, Davalos A, Davis SM, Diener HC, Grotta J, Lyden P, Shuaib A, Hardemark HG, and Wasiewski WW for the Stroke-Acute Ischemic NXY Treatment (SAINT I) Trial Investigators. NXY-059 for acute ischemic stroke. New England Journal of Medicine 354(6):588–600.

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12. Sun L, Hui AM, Su Q, Vortmeyer A, Kotliarov Y, Pastorino S, Passaniti A, Menon J, Walling J, Bailey R, Rosenblum M, Mikkelsen T, and Fine HA. Neuronal and glioma-derived stem cell factor induces angiogenesis within the brain. Cancer Cell 2006 9(4):287–300.

13. Jackson EL, Garcia-Verdugo JM, Gil-Perotin S, Roy M, Quinones-Hinojosa A, VandenBerg S, and Alvarez-Buylla A. PDGRR alpha-positive B cells are neural stem cells in the adult SVZ that form glioma-like growths in response to increased PDGF signaling. Neuron 2006 51(2):187–199.