The Economist - USA (2022-02-26)

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TheEconomistFebruary26th 2022 Science&technology 75

hasgrown,evenasthenumberoffactory
robotsincreased(seechart).
Thereisa similarfearinhealthcarethat
robotswilldestroyjobs.Butthisisa myth,
Michelle Johnson told the meeting. Dr
JohnsonisthedirectoroftheRehabilita­
tionRoboticsLabattheUniversityofPenn­
sylvania,andcurrentlyworksinBotswana
onwaystouserobotstohelppeoplerecov­
erfromillnessandinjury.EveninAmeri­
ca, let aloneAfrica, “there are just not
enoughclinicianstodothejob,”sheadds.
DrJohnsonhasa particularinterestin
helpingpeoplerecoverfromstrokes.This
sometimesrequiresintensivetherapyfor
longperiods.Butpublichealth­caresys­
temsareoftentoostretchedtoofferany­
thingbutlimited treatment.Robotscan
helphere,andinsomecircumstancesmay
bebetter,even,thanhumanphysiothera­
pists,sincetheyarebothtirelessandreli­
able.Theycan exerciseaperson’slimbs
withconsistentmovementsandtakeob­
jective measurements of recovery.This,
saysDrJohnson,allowsa singleoccupa­
tionaltherapist,assistedbya technician,
tolookafter,atthesametime,half­a­doz­
enor sopatients who would otherwise
needone­to­oneattention.
Robotsthatworkwithpeopleinsuch
waysdo,though,requirespecialtraining.
Andthereisa longwaytogotoimprove
thatsaysJulieShah,wholeadstheInterac­
tiveRoboticsGroupattheMassachusetts
InstituteofTechnology.Mostrobotsper­
formnarrowlydefinedtasks,withmobile
onesusingtheirsensorstoavoidbumping
intopeople.“Robotsneedtoseeusasmore
than just an obstacle to manoeuvre
around,”addsDrShah.“Theyneedtowork
withusandanticipatewhatweneed.”
Studying what happens in factories
showsthatthemostsuccessfulapplica­
tionsemployrobots programmedby an
engineerwhoisworkingside­by­sidewith
someone(aso­called“domainexpert”)ful­
lyversedinthetasksathand.Tomakethat
easier,sheandhercolleaguesaredevelop­
ingaisystemswhichcanschoola robot
usingnatural­languagecommands.


Althoughallthreeexpertsbelievero­
botswillenhancehumancapability,one
problemisthatregulationlagstechnology.
Withcovid­19,saysDrJohnson,somecli­
niciansworriedthateventhespreadofte­
lemedicine mightaffecttheirindemnity
insurance,letalonerobots.Andalthougha
longroadremainsaheadforthedevelop­
ment ofautonomous deliveryvans and
lorries,DrChristensenfindsit“ludicrous”
thatatestvehicledrivingacrossastate
borderinAmericamaythereafterhaveto
complywitha completelydifferentsetof
regulationsfromthosewhichpertainedin
theplacewhenceitcame.Itseemsanaw­
fullotofmeetingslieaheadforroboticists
and regulators to determine how ma­
chinesandpeoplewillworktogether.n

Bots at work
United States

Sources:UniversityofCalifornia,SanDiego;International
FederationofRobotics;BureauofLabourStatistics

50
40
30
20
0
0
19152010

Robot sales,
’000
3.0
2.5
2.0
.5
.0

19152010

Manufacturing
employment, m

Neuroscience

From here to


humanity


S


tudying thehuman brain is hard. Oth­
er  animals’  brains  provide  clues.  But
they cannot reveal the special essence that
makes human brains different. Nor, often,
do  they  make  good  models  for  neurologi­
cal conditions that affect human beings. 
Recently,  however,  two  halfway­house
approaches have been developed. One is to
grow  so­called  brain  organoids  from  hu­
man tissue. The other is to create animals
with  human­derived  neurons  in  their  bo­
dies.  As  the  aaasheard,  both  approaches
are yielding results. But they also raise eth­
ical questions of their own.
Organoids  are  usually  grown  from  in­
duced  pluripotent  stem  cells—artificial
equivalents  of  embryonic  cells.  The  pro­
cess  is  now  sufficiently  well  understood
for them to be mass produced and Paola Ar­
lotta of Harvard University described ways
they  are  being  put  to  use.  These  include
studying  brain  development,  examining
the pathology and genetics of disease, and
screening  potential  drugs.  A  particularly
exciting  idea  is  to  grow  organoids  using
cells from people with known, genetically
related  problems.  That  will  allow  specific
instances of disease to be investigated.
Dr Arlotta herself employs organoids to
study  autistic­spectrum  disorders  (asds),
using  versions  which  incorporate  muta­
tions  of  three  genes  seemingly  linked  to
those  conditions.  Though  these  genes
work in different ways, she found that mu­
tating  any  one  of  them  induces  the  same
effects. These include accelerated develop­
ment of cells called gabaergic neurons and
a consequent slowing of the rate, and dimi­

nution of the amplitude, of electrical spik­
ing. This is of interest because other stud­
ies  suggest  that  disrupted  gabaergic  sig­
nalling is indeed associated with asds.
Dr Arlotta also described how it is now
possible to make organoids that resemble,
in their mix of cells, different parts of the
central  nervous  system  (for  example,  the
cerebral cortex and the spinal cord) and to
link these together, and also to muscle or­
ganoids,  to  create  what  are  known  as  as­
sembloids.  That  permits  preliminary  in­
vestigation of how different regions of the
brain  connect  up,  and  how  the  brain  con­
nects with the rest of the body.
A  thoughtful  individual  might,  at  this
point, be tempted to stop and ask whether
brain  organoids  themselves  can  do  any­
thing  remotely  like  thinking.  At  the  mo­
ment, the answer to that is a pretty defini­
tive  “no”.  Those  currently  emerging  from
the culture tanks are under 5mm across, so
have less than a ten­thousandth of the vol­
ume of an adult human brain. More impor­
tantly,  microscopic  examination  shows
that they have little of the complex organi­
sation found in real brains. And they have
no sensory connections through which to
learn  about  the  world.  But  technology
moves  on.  As  Bernard  Lo,  a  medical  ethi­
cist  at  the  University  of  California,  San
Francisco,  told  the  meeting,  “this  science
is  developing  rapidly,  and  we  don’t  know
what will be possible in a decade.”
The  second  approach,  putting  human
neurons into living animals, was outlined
by  Joshua  Sanes,  who  also  works  at  Har­
vard.  Dr  Sanes  came  to  public  attention  a
few years ago as co­inventor of “Brainbow
mice”—creatures that have had individual
neurons  in  their  brains  “painted”  using
proteins  that  fluoresce  in  different  col­
ours. Recently, though, he has found him­
self  struggling  against  the  limits  of  what
can  be  learned  from  laboratory  animals,
and  has  become  interested  in  the  idea  of
partly “humanising” them.
Transplanting  neurons  is  an  old  tech­
nique, and is even being tested therapeuti­
cally  for  the  treatment  of  Parkinson’s  dis­
ease. But they can also be transplanted be­
tween  species,  and  human  neurons  have,
indeed,  been  transplanted  into  mice.
Some,  though,  talk  of  going  further,  and
transplanting human neural stem cells in­
to embryonic mouse brains. The intention
would  be  to  create  a  “chimera”  in  which
brain  cells  from  both  sources  were  inter­
mixed and interfunctional. 
At  the  moment,  formidable  technical
obstacles  stand  in  the  way  of  doing  this.
But  Dr  Lo’s  observation  about  scientific
progress  is  equally  applicable  here.  And
chimeric animals of this sort, which might
even exhibit humanlike behaviours, are an
idea  at  least  as  disturbing  as  brain  orga­
noids’  becoming  conscious.  In  2020,
therefore,  America’s  scientific  establish­

Organoids and neuron transplants give
new ways to study the brain
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