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The Fine Balance of Esophageal Homeostasis: The Role of Unique Cells
The Fine Balance of Esophageal Homeostasis: The Role of Unique Cells
The Fine Balance of Esophageal Homeostasis: The Role of Unique Cells

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자료유형  
 학위논문 서양
최종처리일시  
20250211151336
ISBN  
9798382830667
DDC  
574.191
저자명  
Reyes Hueros, Raul A.
서명/저자  
The Fine Balance of Esophageal Homeostasis: The Role of Unique Cells
발행사항  
[Sl] : University of Pennsylvania, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
107 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-12, Section: B.
주기사항  
Advisor: Shaffer, Sydney M.
학위논문주기  
Thesis (Ph.D.)--University of Pennsylvania, 2024.
초록/해제  
요약This study explores the intricacies of cellular variability and expression in the context of in vitro models of esophageal epithelial cells (EPC2-hTERT) and Barrett's Esophagus (BE), shedding light on the diverse growth dynamics and cellular states within these systems. Esophageal epithelial cells highlighted remarkable growth variability, with approximately 10% of clones exhibiting exponential growth, while the majority displayed logistic growth patterns or halted growth due to non-proliferative cells. Through clonal tracing, mathematical modeling, and cellular barcoding, we elucidated the heritability of growth tendencies and the impact of environmental conditions, such as plating density, on proliferative capabilities. Combining barcoding with single-cell RNA-sequencing (scRNA-seq), we identified the cellular states associated with the highly proliferative clones, which include genes in the WNT and PI3K pathways. Finally, we identified an enrichment of cells resembling the highly proliferative cell state in the proliferating healthy human esophageal epithelium. In BE, advanced spatial transcriptomics revealed a detailed cellular architecture along glandular structures, pinpointing various cell types including previously unidentified ones like tuft and ciliated cells. Notably, ciliated cells at the transitional zone between squamous and columnar epithelium suggest a potential role in the early stages of BE development.
일반주제명  
Biophysics
일반주제명  
Molecular biology
일반주제명  
Cellular biology
일반주제명  
Biochemistry
키워드  
Epithelial cells
키워드  
RNA sequencing
키워드  
Logistic growth
키워드  
Glandular structures
기타저자  
University of Pennsylvania Biochemistry and Molecular Biophysics
기본자료저록  
Dissertations Abstracts International. 85-12B.
전자적 위치 및 접속  
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■1001  ▼aReyes  Hueros,  Raul  A.
■24510▼aThe  Fine  Balance  of  Esophageal  Homeostasis:  The  Role  of  Unique  Cells
■260    ▼a[Sl]▼bUniversity  of  Pennsylvania▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
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■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-12,  Section:  B.
■500    ▼aAdvisor:  Shaffer,  Sydney  M.
■5021  ▼aThesis  (Ph.D.)--University  of  Pennsylvania,  2024.
■520    ▼aThis  study  explores  the  intricacies  of  cellular  variability  and  expression  in  the  context  of  in  vitro  models  of  esophageal  epithelial  cells  (EPC2-hTERT)  and  Barrett's  Esophagus  (BE),  shedding  light  on  the  diverse  growth  dynamics  and  cellular  states  within  these  systems.  Esophageal  epithelial  cells  highlighted  remarkable  growth  variability,  with  approximately  10%  of  clones  exhibiting  exponential  growth,  while  the  majority  displayed  logistic  growth  patterns  or  halted  growth  due  to  non-proliferative  cells.  Through  clonal  tracing,  mathematical  modeling,  and  cellular  barcoding,  we  elucidated  the  heritability  of  growth  tendencies  and  the  impact  of  environmental  conditions,  such  as  plating  density,  on  proliferative  capabilities.  Combining  barcoding  with  single-cell  RNA-sequencing  (scRNA-seq),  we  identified  the  cellular  states  associated  with  the  highly  proliferative  clones,  which  include  genes  in  the  WNT  and  PI3K  pathways.  Finally,  we  identified  an  enrichment  of  cells  resembling  the  highly  proliferative  cell  state  in  the  proliferating  healthy  human  esophageal  epithelium.  In  BE,  advanced  spatial  transcriptomics  revealed  a  detailed  cellular  architecture  along  glandular  structures,  pinpointing  various  cell  types  including  previously  unidentified  ones  like  tuft  and  ciliated  cells.  Notably,  ciliated  cells  at  the  transitional  zone  between  squamous  and  columnar  epithelium  suggest  a  potential  role  in  the  early  stages  of  BE  development.
■590    ▼aSchool  code:  0175.
■650  4▼aBiophysics
■650  4▼aMolecular  biology
■650  4▼aCellular  biology
■650  4▼aBiochemistry
■653    ▼aEpithelial  cells
■653    ▼aRNA  sequencing
■653    ▼aLogistic  growth
■653    ▼aGlandular  structures
■690    ▼a0786
■690    ▼a0307
■690    ▼a0379
■690    ▼a0487
■71020▼aUniversity  of  Pennsylvania▼bBiochemistry  and  Molecular  Biophysics.
■7730  ▼tDissertations  Abstracts  International▼g85-12B.
■790    ▼a0175
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17161298▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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