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The Role of Interleukin-10 in Sex Differences in Pain and Long-Term Suppression of Pain
The Role of Interleukin-10 in Sex Differences in Pain and Long-Term Suppression of Pain
The Role of Interleukin-10 in Sex Differences in Pain and Long-Term Suppression of Pain

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20260202105301
ISBN  
9798263301408
DDC  
616.079
저자명  
Sim, Jaewon.
서명/저자  
The Role of Interleukin-10 in Sex Differences in Pain and Long-Term Suppression of Pain
발행사항  
[Sl] : Michigan State University, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
150 p
주기사항  
Source: Dissertations Abstracts International, Volume: 87-05, Section: B.
주기사항  
Advisor: Laumet, Geoffroy.
학위논문주기  
Thesis (Ph.D.)--Michigan State University, 2025.
초록/해제  
요약Chronic pain is a prevalent disorder that compromises quality of life and imposes a burden on society. Increasing evidence indicates that the immune system can cause, worsen, prolong, or, conversely, resolve pain. In particular, interleukin (IL)-10 is a potent anti-inflammatory cytokine produced by immune cells including monocytes, macrophages, T cells, and B cells. Although IL-10 has been implicated in pain inhibition in both animals and humans, its pain-resolving mechanisms or cellular sources under pain conditions remain to be further elucidated. In my Ph.D. dissertation, I investigated the role of IL-10 in 1) sex differences in pain resolution in an inflammatory pain model and 2) long-term pain suppression in chemotherapy-induced neuropathic pain. 1) During skin inflammation, IL-10 in the inflamed skin resolves pain by signaling through IL-10R1+ sensory nerves innervating the skin. IL-10 is primarily produced by infiltrating monocytes, and IL-10+ monocytes serve as potent drivers of pain resolution. These cells are more abundant in males than females, which contributes to sex differences in pain resolution. The male predominance of IL-10+ monocytes is regulated by sex hormones, particularly androgen signaling, which promotes IL-10 production in monocytes. Altogether, androgen signaling enables the greater abundance of IL-10+ monocytes in males resulting in faster pain resolution compared with females. 2) In chemotherapy-induced neuropathic pain model, I found that pain is being actively suppressed by IL-10 during ostensible pain recovery. IL-10 is continuously produced from spinal meningeal resident macrophages. Especially, IL-10R signaling in DRG sensory neurons is crucial to maintain IL-10-driven pain suppression. I further identified that long-term pain suppression is driven by upregulation of δOR in DRG neurons, driven by IL-10. Collectively, my result shows that IL-10 upregulated δOR in DRG to maintain remission of pain. Overall, these dissertation studies advance our understanding of IL-10-mediated crosstalk between immune cells and pain-sensing neurons, providing new insights into promising therapeutic strategies for the treatment of chronic pain.
일반주제명  
Immunology
일반주제명  
Neurosciences
일반주제명  
Cellular biology
일반주제명  
Molecular biology
키워드  
Interleukin
키워드  
Monocytes
키워드  
Chronic pain
키워드  
Testosterone
기타저자  
Michigan State University Cell and Molecular Biology - Doctor of Philosophy
기본자료저록  
Dissertations Abstracts International. 87-05B.
전자적 위치 및 접속  
로그인 후 원문을 볼 수 있습니다.

MARC

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■1001  ▼aSim,  Jaewon.▼0(orcid)0009-0007-4560-3525
■24510▼aThe  Role  of  Interleukin-10  in  Sex  Differences  in  Pain  and  Long-Term  Suppression  of  Pain
■260    ▼a[Sl]▼bMichigan  State  University▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a150  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-05,  Section:  B.
■500    ▼aAdvisor:  Laumet,  Geoffroy.
■5021  ▼aThesis  (Ph.D.)--Michigan  State  University,  2025.
■520    ▼aChronic  pain  is  a  prevalent  disorder  that  compromises  quality  of  life  and  imposes  a  burden  on  society.  Increasing  evidence  indicates  that  the  immune  system  can  cause,  worsen,  prolong,  or,  conversely,  resolve  pain.  In  particular,  interleukin  (IL)-10  is  a  potent  anti-inflammatory  cytokine  produced  by  immune  cells  including  monocytes,  macrophages,  T  cells,  and  B  cells.  Although  IL-10  has  been  implicated  in  pain  inhibition  in  both  animals  and  humans,  its  pain-resolving  mechanisms  or  cellular  sources  under  pain  conditions  remain  to  be  further  elucidated.  In  my  Ph.D.  dissertation,  I  investigated  the  role  of  IL-10  in  1)  sex  differences  in  pain  resolution  in  an  inflammatory  pain  model  and  2)  long-term  pain  suppression  in  chemotherapy-induced  neuropathic  pain.  1)  During  skin  inflammation,  IL-10  in  the  inflamed  skin  resolves  pain  by  signaling  through  IL-10R1+  sensory  nerves  innervating  the  skin.  IL-10  is  primarily  produced  by  infiltrating  monocytes,  and  IL-10+  monocytes  serve  as  potent  drivers  of  pain  resolution.  These  cells  are  more  abundant  in  males  than  females,  which  contributes  to  sex  differences  in  pain  resolution.  The  male  predominance  of  IL-10+  monocytes  is  regulated  by  sex  hormones,  particularly  androgen  signaling,  which  promotes  IL-10  production  in  monocytes.  Altogether,  androgen  signaling  enables  the  greater  abundance  of  IL-10+  monocytes  in  males  resulting  in  faster  pain  resolution  compared  with  females.  2)  In  chemotherapy-induced  neuropathic  pain  model,  I  found  that  pain  is  being  actively  suppressed  by  IL-10  during  ostensible  pain  recovery.  IL-10  is  continuously  produced  from  spinal  meningeal  resident  macrophages.  Especially,  IL-10R  signaling  in  DRG  sensory  neurons  is  crucial  to  maintain  IL-10-driven  pain  suppression.  I  further  identified  that  long-term  pain  suppression  is  driven  by  upregulation  of  δOR  in  DRG  neurons,  driven  by  IL-10.  Collectively,  my  result  shows  that  IL-10  upregulated  δOR  in  DRG  to  maintain  remission  of  pain.  Overall,  these  dissertation  studies  advance  our  understanding  of  IL-10-mediated  crosstalk  between  immune  cells  and  pain-sensing  neurons,  providing  new  insights  into  promising  therapeutic  strategies  for  the  treatment  of  chronic  pain.
■590    ▼aSchool  code:  0128.
■650  4▼aImmunology
■650  4▼aNeurosciences
■650  4▼aCellular  biology
■650  4▼aMolecular  biology
■653    ▼aInterleukin
■653    ▼aMonocytes
■653    ▼aChronic  pain
■653    ▼aTestosterone
■690    ▼a0982
■690    ▼a0317
■690    ▼a0379
■690    ▼a0307
■71020▼aMichigan  State  University▼bCell  and  Molecular  Biology  -  Doctor  of  Philosophy.
■7730  ▼tDissertations  Abstracts  International▼g87-05B.
■790    ▼a0128
■791    ▼aPh.D.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17360083▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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