본문

서브메뉴

Role of Alveolar Epithelial Cells and Macrophages in the Pathogenesis of Respiratory Viral Infections: Computational Approach Using Transcriptomics
Role of Alveolar Epithelial Cells and Macrophages in the Pathogenesis of Respiratory Viral...
Role of Alveolar Epithelial Cells and Macrophages in the Pathogenesis of Respiratory Viral Infections: Computational Approach Using Transcriptomics

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20250211151016
ISBN  
9798382762845
DDC  
574
저자명  
Anekalla, Kishore Reddy.
서명/저자  
Role of Alveolar Epithelial Cells and Macrophages in the Pathogenesis of Respiratory Viral Infections: Computational Approach Using Transcriptomics
발행사항  
[Sl] : Northwestern University, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
172 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-11, Section: B.
주기사항  
Advisor: Ridge, Karen M.
학위논문주기  
Thesis (Ph.D.)--Northwestern University, 2024.
초록/해제  
요약This study utilizes RNA sequencing (RNA-seq) to probe the juvenile response to influenza A virus (IAV) infection, with a specific focus on key cellular groups: Alveolar Epithelial Cells (AECs), Tissue Resident Alveolar Macrophages (TRAMs), and Monocyte-Derived Alveolar Macrophages (MoAMs). Although the impact of IAV in adults has been extensively studied, the response in juveniles remains less characterized. We aimed to unravel the transcriptional dynamics and intercellular communication of these cells during juvenile IAV infection to identify unique molecular signatures and pathways.Challenging the conventional use of plaque assays as the primary method for measuring viral titers, our study combines this technique with viral transcript measurements. This dual approach not only provides a more comprehensive understanding of the viral presence in the host but also emphasizes the necessity for broader metrics in viral infection assessment. Our comprehensive RNA-seq analysis uncovered distinct, time-specific transcriptomic responses in juveniles, underscoring critical pathways and regulatory networks vital for counteracting IAV. A key finding is the intricate cell-to-cell communication within the Type-1 IFN-related pathway, which plays a crucial role in the juvenile immune response. Disruption of Type-1 IFN signaling in MoAMs through the IFN receptor significantly improved survival rates in juvenile mice, opening up promising avenues for therapeutic intervention.This research advances our understanding of pediatric influenza, highlighting the complexity of the juvenile immune response to IAV and advocating for more nuanced and expansive approaches in viral infection studies. The insights gained from our study have important implications for developing targeted treatments to alleviate the effects of IAV in younger populations.
일반주제명  
Bioinformatics
일반주제명  
Biomedical engineering
일반주제명  
Molecular biology
일반주제명  
Genetics
일반주제명  
Pathology
키워드  
RNA sequencing
키워드  
Influenza A virus
키워드  
Tissue Resident Alveolar Macrophages
키워드  
Alveolar Epithelial Cells
키워드  
Monocyte-Derived Alveolar Macrophages
기타저자  
Northwestern University Driskill Graduate Training Program in Life Sciences
기본자료저록  
Dissertations Abstracts International. 85-11B.
전자적 위치 및 접속  
로그인 후 원문을 볼 수 있습니다.

MARC

 008250123s2024        us                              c    eng  d
■001000017160418
■00520250211151016
■006m          o    d                
■007cr#unu||||||||
■020    ▼a9798382762845
■035    ▼a(MiAaPQ)AAI30995869
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a574
■1001  ▼aAnekalla,  Kishore  Reddy.
■24510▼aRole  of  Alveolar  Epithelial  Cells  and  Macrophages  in  the  Pathogenesis  of  Respiratory  Viral  Infections:  Computational  Approach  Using  Transcriptomics
■260    ▼a[Sl]▼bNorthwestern  University▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a172  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-11,  Section:  B.
■500    ▼aAdvisor:  Ridge,  Karen  M.
■5021  ▼aThesis  (Ph.D.)--Northwestern  University,  2024.
■520    ▼aThis  study  utilizes  RNA  sequencing  (RNA-seq)  to  probe  the  juvenile  response  to  influenza  A  virus  (IAV)  infection,  with  a  specific  focus  on  key  cellular  groups:  Alveolar  Epithelial  Cells  (AECs),  Tissue  Resident  Alveolar  Macrophages  (TRAMs),  and  Monocyte-Derived  Alveolar  Macrophages  (MoAMs).  Although  the  impact  of  IAV  in  adults  has  been  extensively  studied,  the  response  in  juveniles  remains  less  characterized.  We  aimed  to  unravel  the  transcriptional  dynamics  and  intercellular  communication  of  these  cells  during  juvenile  IAV  infection  to  identify  unique  molecular  signatures  and  pathways.Challenging  the  conventional  use  of  plaque  assays  as  the  primary  method  for  measuring  viral  titers,  our  study  combines  this  technique  with  viral  transcript  measurements.  This  dual  approach  not  only  provides  a  more  comprehensive  understanding  of  the  viral  presence  in  the  host  but  also  emphasizes  the  necessity  for  broader  metrics  in  viral  infection  assessment. Our  comprehensive  RNA-seq  analysis  uncovered  distinct,  time-specific  transcriptomic  responses  in  juveniles,  underscoring  critical  pathways  and  regulatory  networks  vital  for  counteracting  IAV.  A  key  finding  is  the  intricate  cell-to-cell  communication  within  the  Type-1  IFN-related  pathway,  which  plays  a  crucial  role  in  the  juvenile  immune  response.  Disruption  of  Type-1  IFN  signaling  in  MoAMs  through  the  IFN  receptor  significantly  improved  survival  rates  in  juvenile  mice,  opening  up  promising  avenues  for  therapeutic  intervention.This  research  advances  our  understanding  of  pediatric  influenza,  highlighting  the  complexity  of  the  juvenile  immune  response  to  IAV  and  advocating  for  more  nuanced  and  expansive  approaches  in  viral  infection  studies.  The  insights  gained  from  our  study  have  important  implications  for  developing  targeted  treatments  to  alleviate  the  effects  of  IAV  in  younger  populations.
■590    ▼aSchool  code:  0163.
■650  4▼aBioinformatics
■650  4▼aBiomedical  engineering
■650  4▼aMolecular  biology
■650  4▼aGenetics
■650  4▼aPathology
■653    ▼aRNA  sequencing
■653    ▼aInfluenza  A  virus
■653    ▼aTissue  Resident  Alveolar  Macrophages
■653    ▼aAlveolar  Epithelial  Cells
■653    ▼aMonocyte-Derived  Alveolar  Macrophages
■690    ▼a0715
■690    ▼a0541
■690    ▼a0369
■690    ▼a0307
■690    ▼a0571
■71020▼aNorthwestern  University▼bDriskill  Graduate  Training  Program  in  Life  Sciences.
■7730  ▼tDissertations  Abstracts  International▼g85-11B.
■790    ▼a0163
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17160418▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

미리보기

내보내기

chatGPT토론

Ai 추천 관련 도서


    신착도서 더보기
    최근 3년간 통계입니다.

    소장정보

    • 예약
    • 소재불명신고
    • 나의폴더
    • 우선정리요청
    • 비도서대출신청
    • 야간 도서대출신청
    소장자료
    등록번호 청구기호 소장처 대출가능여부 대출정보
    TF10854 전자도서 대출가능 마이폴더 부재도서신고 비도서대출신청 야간 도서대출신청

    * 대출중인 자료에 한하여 예약이 가능합니다. 예약을 원하시면 예약버튼을 클릭하십시오.

    해당 도서를 다른 이용자가 함께 대출한 도서

    관련 인기도서

    로그인 후 이용 가능합니다.