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On Representing Disparity in Visual Cortex Populations in Mouse
On Representing Disparity in Visual Cortex Populations in Mouse  / Mandi C Severson
On Representing Disparity in Visual Cortex Populations in Mouse

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20260311091531.5
ISBN  
9798270231422
DDC  
519.5
저자명  
Severson, Mandi C.
서명/저자  
On Representing Disparity in Visual Cortex Populations in Mouse / Mandi C Severson
발행사항  
[Sl] : The University of Texas at Austin, 2025
형태사항  
1 electronic resource (90 pages)
주기사항  
Source: Dissertations Abstracts International, Volume: 87-06, Section: B.
주기사항  
Advisors: Priebe, Nicholas J. Committee members: Pierce, Jonathan T.; Glickfeld, Lindsey L.; Hayhoe, Mary M.; Geisler, Wilson S., III.
학위논문주기  
- Ph.D. : The University of Texas at Austin, 2025.
초록/해제  
요약The function of inhibition in disparity selectivity is not well understood. Disparity selectivity to correlated and anticorrelated random dot stereograms (RDS) in two of the major classes of inhibitory neurons, parvalbumin-expressing (PV) and somatostatin-expressing (SST), has not previously been characterized. We addressed the functional roles of different cortical circuit elements by first characterizing disparity selectivity in excitatory, PV, and SST neurons. We find that PV cell disparity tuning is broader than excitatory and SST cells, and it is highly correlated with the tuning of the summation of the activity of surrounding cells. In contrast, the disparity tuning of SST cells is not well predicted by surrounding activity. Additionally, we find that PV and SST cells also respond to anticorrelated RDS with an inversion in tuning, but the inversion is weak. Next we investigated the function of these inhibitory populations by optogenetic suppression of PV or SST cells. We hypothesized that if PV and SST cells are selectively suppressing responses to false matches in excitatory cells in anticorrelated RDS, optogenetic suppression of these populations would result in an increase in magnitude for disparity tuning to anticorrelated RDS. This is not what we found. We found that in response to correlated stimuli, tuning strength declines during suppression of both PV and SST cells, suggesting that they both play a role in enhancing selectivity to correlated RDS. In response to anticorrelated stimuli, PV suppression shows a slight decrease in tuning strength while SST suppression shows a slight increase in tuning strength, suggesting that SST cells may be involved in suppressing false matches. However, the effects in response to correlated RDS were much stronger than that of the anticorrelated RDS results, suggesting that both PV and SST cells are contributing to disparity tuning more by sharpening disparity selectivity for correlated stimuli. Lastly, we wanted to investigate disparity representation in a population-level analysis. We examined whether we could reliably represent disparity for correlated RDS and ignore false matches in anticorrelated RDS in excitatory populations using a Bayesian decoder. We find that the Bayesian decoder can reliably represent disparity for correlated RDS but does not reliably decode disparity in response to anticorrelated RDS.
언어주기  
English
일반주제명  
Physiology
일반주제명  
Statistics
일반주제명  
Neurosciences
키워드  
Random dot stereograms
키워드  
Parvalbumin-expressing
키워드  
SST cells
키워드  
Bayesian decoder
기타저자  
The University of Texas at Austin Neuroscience
기본자료저록  
Dissertations Abstracts International. 87-06B.
전자적 위치 및 접속  
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MARC

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■1001  ▼aSeverson,  Mandi  C.▼eauthor.
■24510▼aOn  Representing  Disparity  in  Visual  Cortex  Populations  in  Mouse  ▼cMandi  C  Severson
■260    ▼a[Sl]▼bThe  University  of  Texas  at  Austin▼c2025
■264  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a1  electronic  resource  (90  pages)
■336    ▼atext▼btxt▼2rdacontent
■337    ▼acomputer▼bc▼2rdamedia
■338    ▼aonline  resource▼bcr▼2rdacarrier
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-06,  Section:  B.
■500    ▼aAdvisors:  Priebe,  Nicholas  J.    Committee  members:  Pierce,  Jonathan  T.;  Glickfeld,  Lindsey  L.;  Hayhoe,  Mary  M.;  Geisler,  Wilson  S.,  III.
■5021  ▼bPh.D.▼cThe  University  of  Texas  at  Austin▼d2025.
■520    ▼aThe  function  of  inhibition  in  disparity  selectivity  is  not  well  understood.  Disparity  selectivity  to  correlated  and  anticorrelated  random  dot  stereograms  (RDS)  in  two  of  the  major  classes  of  inhibitory  neurons,  parvalbumin-expressing  (PV)  and  somatostatin-expressing  (SST),  has  not  previously  been  characterized.    We  addressed  the  functional  roles  of  different  cortical  circuit  elements  by  first  characterizing  disparity  selectivity  in  excitatory,  PV,  and  SST  neurons.  We  find  that  PV  cell  disparity  tuning  is  broader  than  excitatory  and  SST  cells,  and  it  is  highly  correlated  with  the  tuning  of  the  summation  of  the  activity  of  surrounding  cells.  In  contrast,  the  disparity  tuning  of  SST  cells  is  not  well  predicted  by  surrounding  activity.  Additionally,  we  find  that  PV  and  SST  cells  also  respond  to  anticorrelated  RDS  with  an  inversion  in  tuning,  but  the  inversion  is  weak.  Next  we  investigated  the  function  of  these  inhibitory  populations  by  optogenetic  suppression  of  PV  or  SST  cells.  We  hypothesized  that  if  PV  and  SST  cells  are  selectively  suppressing  responses  to  false  matches  in  excitatory  cells  in  anticorrelated  RDS,  optogenetic  suppression  of  these  populations  would  result  in  an  increase  in  magnitude  for  disparity  tuning  to  anticorrelated  RDS.  This  is  not  what  we  found.  We  found  that  in  response  to  correlated  stimuli,  tuning  strength  declines  during  suppression  of  both  PV  and  SST  cells,  suggesting  that  they  both  play  a  role  in  enhancing  selectivity  to  correlated  RDS.  In  response  to  anticorrelated  stimuli,  PV  suppression  shows  a  slight  decrease  in  tuning  strength  while  SST  suppression  shows  a  slight  increase  in  tuning  strength,  suggesting  that  SST  cells  may  be  involved  in  suppressing  false  matches.  However,  the  effects  in  response  to  correlated  RDS  were  much  stronger  than  that  of  the  anticorrelated  RDS  results,  suggesting  that  both  PV  and  SST  cells  are  contributing  to  disparity  tuning  more  by  sharpening  disparity  selectivity  for  correlated  stimuli.  Lastly,  we  wanted  to  investigate  disparity  representation  in  a  population-level  analysis.  We  examined  whether  we  could  reliably  represent  disparity  for  correlated  RDS  and  ignore  false  matches  in  anticorrelated  RDS  in  excitatory  populations  using  a  Bayesian  decoder.  We  find  that  the  Bayesian  decoder  can  reliably  represent  disparity  for  correlated  RDS  but  does  not  reliably  decode  disparity  in  response  to  anticorrelated  RDS.
■546    ▼aEnglish
■590    ▼aSchool  code:  0227
■650  4▼aPhysiology
■650  4▼aStatistics
■650  4▼aNeurosciences
■653    ▼aRandom  dot  stereograms
■653    ▼aParvalbumin-expressing
■653    ▼aSST  cells
■653    ▼aBayesian  decoder
■7102  ▼aThe  University  of  Texas  at  Austin▼bNeuroscience.▼edegree  granting  institution.
■7201  ▼aPriebe,  Nicholas  J.▼edegree  supervisor.
■7730  ▼tDissertations  Abstracts  International▼g87-06B.
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17361192▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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