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Stem-cell therapies here to stay–but from where?
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Transcript of Stem-cell therapies here to stay–but from where?
For personal use. Only reproduce with permission from The Lancet Publishing Group.
that the field is too new to know whichcell source ultimately will be mostappropriate. “Our work shows that wecan mimic normal development of the
midbrain in tissue culture”, notesMcKay. “Perhaps the adult cells canreach the same endpoint. We don’tknow yet.”
For Sanberg, the debate needs toinclude embryonic and post-birthtissues, such as umbilical-cord blood. “Ihave no doubt that we will continue tobe able to translate findings andtechniques discovered in embryoniccells to post-birth and adult cells, andvice versa”, he says, pointing to recentreports in a special neuroscience issue ofCell Transplantation (2002; 4: issue 3).“That is why research in both areasneeds to continue.”Kelly Morris
THE LANCET Neurology Vol 1 August 2002 http://neurology.thelancet.com204
Never before have prospects for stem-cell therapies looked so good,particularly to replace or regenerateneural tissue. But despite the recentsurge in scientific reports (LancetNeurology 2002; 1: 144), experts arekeeping an open mind on the source ofstem cells for clinical purposes.
Current research focuses on stemcells from embryonic tissue (ES cells) oradult tissue, including bone marrowand brain. Recent research is expectedto rekindle the debate on the relativemerits of adult stem cells versus ES cells.
Catherine Verfaillie and colleagues(University of Minnesota, Minneapolis,MN, USA) report the presence of rarecells in adult mouse bone marrow thatseem to respond to organ-specific cues,just like ES cells. These multipotentadult progenitor cells “proliferateextensively without obvious senescenceor loss of differentiation potential”, saythe authors, so “they may be an ideal cellsource for therapy of inherited ordegenerative disease” (Nature 2002; 418:41–49).
Meanwhile, a group led by RonMcKay (National Institute ofNeurological Disorders and Stroke,Bethesda, MD, USA) show thatdopaminergic neurons generated fromcultured ES cells can fully restoreelectrophysiological and motor functionin Parkinson’s disease, at least in a ratmodel. The group says these findings“encourage the use of ES cells in cell-replacement therapy for Parkinson’sdisease” (Nature 2002; 418: 50–56), and,says McKay, are also important in awider context: “They imply that stem-cell manipulation in vitro will become atool used in many fields of medicine.”
According to Paul Sanberg(University of South Florida, Tampa,FL, USA), another encouraging aspectof these findings is that “they continueto support the view that once a neuralstem or progenitor cell is differentiated,they do not form tumours or teratomasfollowing transplantation”. He believessuch evidence “will be supportive inbringing these therapies to the clinic”.
McKay responds pragmatically tothe issue of embryonic versus adult stemcells: “We need cells that work whatevertheir source.” Expert opinion suggests
Stem-cell therapies here to stay—but from where?
Technology for telekinesis
Newsdesk
Catherine Verfaillie
Cou
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Monkeys can be trained to move acursor on a computer screen bythought alone, according to USresearchers. This technology mayenable patients with paralysed oramputated limbs to control roboticprostheses neurally.
Dawn Taylor and co-workers(Arizona State University, Tempe, AZ,USA) implanted electrodes into thecerebral cortex of macaque monkeysto measure activity of neurons thatcontrol arm movements. First, themonkeys guided a cursor towardstargets on a computer screen withtheir arm movements and theresearchers recorded the neuralactivity. Next, the monkeys’ arms wererestrained and first set of measure-ments used to convert neural activitydirectly into on-screen movement ofthe cursor. The monkeys tried to movetheir arms at first but eventuallyrealised they could move the cursor bythought alone.
Calibration of actual movementwith neural activity would not bepossible in patients who do not havethe use of their limbs. However, theauthors report that they have“developed a ‘coadaptive’ movementprediction algorithm that does notrequire physical limb movements orany a priori knowledge of cell tuningproperties”, which could be used in
patients with paralysed or amputatedlimbs (Science 2002; 296: 1829–32).
The most encouraging finding isthat the monkeys processed visualfeedback quickly enough to change thedirection of cursor movement duringeach task; they also improved betweentasks. This is the first time thatindividual neurons have been shownto adapt and improve performanceduring task.
This improvement suggests thatcontrolling the cursor is a new skillthat must be learnt. “Further studiesare needed to explore the long-termdevelopment and maintenance of thisnew skill”, says John Wolpaw (NewYork State Department of Health, NY,USA), “which depends on continuedeffective interaction between twoadaptive controllers—the user’s brainand the system that is processing thebrain signals.”
Taylor’s team plans to investigatewhether monkeys can control a robotarm in this way. This technology couldlead to brain-controlled prostheses.Eventually, stimulation of patients’muscles may help restore function totheir own limbs. However, as Wolpawwarns, “the clinical practicality and theapplicability of systems based oninvasively recorded brain signalsremain to be explored”.Peter Hayward
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