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Quantification and Analysis of Spatio-Temporal Waves in Dynamic Cellular Systems.- [electronic resources]
Quantification and Analysis of Spatio-Temporal Waves in Dynamic Cellular Systems. - [elect...
Quantification and Analysis of Spatio-Temporal Waves in Dynamic Cellular Systems.- [electronic resources]

상세정보

자료유형  
 학위논문(국외)
자관 청구기호  
기본표목-개인명  
표제와 책임표시사항  
Quantification and Analysis of Spatio-Temporal Waves in Dynamic Cellular Systems. - [electronic resources]
발행, 배포, 간사 사항  
발행, 배포, 간사 사항  
Ann Arbor : ProQuest Dissertations & Theses , 2025
    형태사항  
    140 p.
    일반주기  
    Source: Dissertations Abstracts International, Volume: 87-03, Section: B.
    일반주기  
    Advisor: Losert, Wolfgang.
    학위논문주기  
    Thesis (Ph.D.)--University of Maryland, College Park, 2025.
    요약 등 주기  
    요약Rhythms are signatures of life. From the nanoscopic flicker of molecular switches to the metronomic beating of the heart, internally generated clocks regulate virtually every aspect of physiology, thereby shaping the very essence of living systems. This dissertation addresses two interrelated questions: How can such biological rhythms be captured and quantified with sufficient resolution, and do common design principles underlie their organization across different biological scales? This work follows a cohesive narrative that investigates rhythmic phenomena across progressively smaller spatial and temporal domains, while concurrently developing novel analytical tools to advance their characterization.We begin with a survey of oscillatory phenomena spanning multiple orders of magnitude, introducing multiscale modeling as a unifying framework for integrating diverse biological rhythms. With this broad context established, we turn to specific experimental systems, starting with gut motility in an ex vivo crayfish model. By isolating central, myogenic, and serotonergic inputs, we find that chemical cues can restore contraction strength but reduce spatial synchrony in the absence of central control. These results suggest that local sensing mechanisms may be essential for coordinating large-scale motor patterns.The focus then shifts to a finer spatial scale: actin dynamics in astrocytes, a type of glial cell. Using a custom optical-flow analysis pipeline, we identify recurrent actin "hotspots" whose activity is suppressed by engineered nanotopographies but enhanced in the presence of neighboring neurons. These findings suggest that the cytoskeleton itself functions as a dynamic sensor of mechanical and biochemical cues. Building on this insight into cellular sensing, we next examine how cells interact with their environment during development. In growing cortical neurons, actin wave tracks and growth-cone trajectories initially align with nanotopographic cues; however, this influence diminishes as axons mature. The observed decline points to age-dependent cytoskeletal plasticity as a potential factor limiting regenerative capacity in adult neurons.In the final part of this work, we extend our analysis from two-dimensional imaging to the three-dimensional microenvironments in which cells naturally reside. As most, if not all tissues function in three dimensions, spatial depth fundamentally alters how motion is encoded and perceived. To address this complexity, we adapt the optical-flow framework to volumetric datasets. Applications to actin dynamics in Dictyostelium and axonal growth in Drosophila pupal wings reveal spatial patterns obscured in two-dimensional projections. Complementary experiments involving calcium imaging and electrophysiological recordings in the gut further link local intracellular activity with large-scale contractions, thereby reinforcing the broader theme of wave propagation across scales.Overall, this work aims to bridge wave phenomena across diverse spatial and temporal domains, unifying them under the central theme of local versus global control in the coordination of biological rhythms.
    주제명부출표목-일반주제명  
    주제명부출표목-일반주제명  
    주제명부출표목-일반주제명  
    비통제 색인어  
    비통제 색인어  
    비통제 색인어  
    비통제 색인어  
    비통제 색인어  
    비통제 색인어  
    부출표목-단체명  
    기본자료저록  
    Dissertations Abstracts International. 87-03B.
    전자적 위치 및 접속  
     원문정보보기

    MARC

     008260219s2025        us            s          000c||eng  d
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    ■006m          o    d                
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    ■020    ▼a9798293832859
    ■035    ▼a(MiAaPQ)AAI32044082
    ■040    ▼aMiAaPQ▼cMiAaPQ
    ■0820  ▼a574.191
    ■090    ▼a전자자료
    ■1001  ▼aPathak,  Spandan.▼0(orcid)0000-0001-7866-2096
    ■24510▼aQuantification  and  Analysis  of  Spatio-Temporal  Waves  in  Dynamic  Cellular  Systems.▼h[electronic  resources]
    ■260    ▼a[S.l.]▼bUniversity  of  Maryland,  College  Park.  ▼c2025
    ■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
    ■300    ▼a140  p.
    ■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-03,  Section:  B.
    ■500    ▼aAdvisor:  Losert,  Wolfgang.
    ■5021  ▼aThesis  (Ph.D.)--University  of  Maryland,  College  Park,  2025.
    ■520    ▼aRhythms  are  signatures  of  life.  From  the  nanoscopic  flicker  of  molecular  switches  to  the  metronomic  beating  of  the  heart,  internally  generated  clocks  regulate  virtually  every  aspect  of  physiology,  thereby  shaping  the  very  essence  of  living  systems.  This  dissertation  addresses  two  interrelated  questions:  How  can  such  biological  rhythms  be  captured  and  quantified  with  sufficient  resolution,  and  do  common  design  principles  underlie  their  organization  across  different  biological  scales?  This  work  follows  a  cohesive  narrative  that  investigates  rhythmic  phenomena  across  progressively  smaller  spatial  and  temporal  domains,  while  concurrently  developing  novel  analytical  tools  to  advance  their  characterization.We  begin  with  a  survey  of  oscillatory  phenomena  spanning  multiple  orders  of  magnitude,  introducing  multiscale  modeling  as  a  unifying  framework  for  integrating  diverse  biological  rhythms.  With  this  broad  context  established,  we  turn  to  specific  experimental  systems,  starting  with  gut  motility  in  an  ex  vivo  crayfish  model.  By  isolating  central,  myogenic,  and  serotonergic  inputs,  we  find  that  chemical  cues  can  restore  contraction  strength  but  reduce  spatial  synchrony  in  the  absence  of  central  control.  These  results  suggest  that  local  sensing  mechanisms  may  be  essential  for  coordinating  large-scale  motor  patterns.The  focus  then  shifts  to  a  finer  spatial  scale:  actin  dynamics  in  astrocytes,  a  type  of  glial  cell.  Using  a  custom  optical-flow  analysis  pipeline,  we  identify  recurrent  actin  "hotspots"  whose  activity  is  suppressed  by  engineered  nanotopographies  but  enhanced  in  the  presence  of  neighboring  neurons.  These  findings  suggest  that  the  cytoskeleton  itself  functions  as  a  dynamic  sensor  of  mechanical  and  biochemical  cues.  Building  on  this  insight  into  cellular  sensing,  we  next  examine  how  cells  interact  with  their  environment  during  development.  In  growing  cortical  neurons,  actin  wave  tracks  and  growth-cone  trajectories  initially  align  with  nanotopographic  cues;  however,  this  influence  diminishes  as  axons  mature.  The  observed  decline  points  to  age-dependent  cytoskeletal  plasticity  as  a  potential  factor  limiting  regenerative  capacity  in  adult  neurons.In  the  final  part  of  this  work,  we  extend  our  analysis  from  two-dimensional  imaging  to  the  three-dimensional  microenvironments  in  which  cells  naturally  reside.  As  most,  if  not  all  tissues  function  in  three  dimensions,  spatial  depth  fundamentally  alters  how  motion  is  encoded  and  perceived.  To  address  this  complexity,  we  adapt  the  optical-flow  framework  to  volumetric  datasets.  Applications  to  actin  dynamics  in  Dictyostelium  and  axonal  growth  in  Drosophila  pupal  wings  reveal  spatial  patterns  obscured  in  two-dimensional  projections.  Complementary  experiments  involving  calcium  imaging  and  electrophysiological  recordings  in  the  gut  further  link  local  intracellular  activity  with  large-scale  contractions,  thereby  reinforcing  the  broader  theme  of  wave  propagation  across  scales.Overall,  this  work  aims  to  bridge  wave  phenomena  across  diverse  spatial  and  temporal  domains,  unifying  them  under  the  central  theme  of  local  versus  global  control  in  the  coordination  of  biological  rhythms.
    ■590    ▼aSchool  code:  0117.
    ■650  4▼aBiophysics.
    ■650  4▼aNeurosciences.
    ■650  4▼aCellular  biology.
    ■653    ▼aBiological  rhythms
    ■653    ▼aCytoskeletal  dynamics
    ■653    ▼aMultiscale  analysis
    ■653    ▼aNeuronal  development
    ■653    ▼aOptical  flow
    ■653    ▼aWave  propagation
    ■690    ▼a0786
    ■690    ▼a0317
    ■690    ▼a0379
    ■71020▼aUniversity  of  Maryland,  College  Park▼bBiophysics  (BIPH).
    ■7730  ▼tDissertations  Abstracts  International▼g87-03B.
    ■790    ▼a0117
    ■791    ▼aPh.D.
    ■792    ▼a2025
    ■793    ▼aEnglish
    ■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17357891▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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