Ubiquitin-specific protease 25 ameliorates ulcerative colitis by regulating the degradation of phosphor-STAT3

Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of...

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Published inCell death & disease Vol. 16; no. 1; pp. 5 - 14
Main Authors Liu, Zhengru, Liu, Jian, Wei, Yuping, Li, Jinting, Zhang, Jixiang, Yu, Rong, Yang, Qian, Miao, Yinglei, Dong, Weiguo
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 07.01.2025
Springer Nature B.V
Nature Publishing Group
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ISSN2041-4889
2041-4889
DOI10.1038/s41419-024-07315-z

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Abstract Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of USP25 in UC, bioinformatics analysis and research are conducted on clinical patients with UC, Usp25 knockout ( Usp25 −/− ) mice, intestinal epithelial cell-specific knockout signal transducer and activator of transcription 3 ( Stat3) (Villin-Cre Stat3 fl/fl ) mice, and human colonic epithelial cells. Results show that the expression of USP25 is decreased in patients with UC and mice with dextran sulfate sodium salt (DSS)-induced colitis and that USP25 deficiency exacerbates UC by destroying the intestinal mucosal barrier, however, overexpression of USP25 can alleviate colitis. Mechanistically, USP25 reduces the degradation of phosphor-STAT3 Y705 at lysine 409 by catalyzing K48-linked deubiquitination. Further, this study demonstrates the aggravation of DSS-induced colitis by intestinal epithelial cell-specific knockout Stat3 in mice, while Stat3 overexpression by adeno-associated virus attenuates colitis in DSS-induced Usp25 −/− mice. Together, these results showed that USP25 ameliorates UC by regulating the degradation of phosphor-STAT3. Collectively, USP25 is a specific STAT3 regulator that can be targeted in UC.
AbstractList Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of USP25 in UC, bioinformatics analysis and research are conducted on clinical patients with UC, Usp25 knockout (Usp25 ) mice, intestinal epithelial cell-specific knockout signal transducer and activator of transcription 3 (Stat3) (Villin-Cre Stat3 ) mice, and human colonic epithelial cells. Results show that the expression of USP25 is decreased in patients with UC and mice with dextran sulfate sodium salt (DSS)-induced colitis and that USP25 deficiency exacerbates UC by destroying the intestinal mucosal barrier, however, overexpression of USP25 can alleviate colitis. Mechanistically, USP25 reduces the degradation of phosphor-STAT3 at lysine 409 by catalyzing K48-linked deubiquitination. Further, this study demonstrates the aggravation of DSS-induced colitis by intestinal epithelial cell-specific knockout Stat3 in mice, while Stat3 overexpression by adeno-associated virus attenuates colitis in DSS-induced Usp25 mice. Together, these results showed that USP25 ameliorates UC by regulating the degradation of phosphor-STAT3. Collectively, USP25 is a specific STAT3 regulator that can be targeted in UC.
Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of USP25 in UC, bioinformatics analysis and research are conducted on clinical patients with UC, Usp25 knockout ( Usp25 −/− ) mice, intestinal epithelial cell-specific knockout signal transducer and activator of transcription 3 ( Stat3) (Villin-Cre Stat3 fl/fl ) mice, and human colonic epithelial cells. Results show that the expression of USP25 is decreased in patients with UC and mice with dextran sulfate sodium salt (DSS)-induced colitis and that USP25 deficiency exacerbates UC by destroying the intestinal mucosal barrier, however, overexpression of USP25 can alleviate colitis. Mechanistically, USP25 reduces the degradation of phosphor-STAT3 Y705 at lysine 409 by catalyzing K48-linked deubiquitination. Further, this study demonstrates the aggravation of DSS-induced colitis by intestinal epithelial cell-specific knockout Stat3 in mice, while Stat3 overexpression by adeno-associated virus attenuates colitis in DSS-induced Usp25 −/− mice. Together, these results showed that USP25 ameliorates UC by regulating the degradation of phosphor-STAT3. Collectively, USP25 is a specific STAT3 regulator that can be targeted in UC.
Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of USP25 in UC, bioinformatics analysis and research are conducted on clinical patients with UC, Usp25 knockout (Usp25−/−) mice, intestinal epithelial cell-specific knockout signal transducer and activator of transcription 3 (Stat3) (Villin-Cre Stat3fl/fl) mice, and human colonic epithelial cells. Results show that the expression of USP25 is decreased in patients with UC and mice with dextran sulfate sodium salt (DSS)-induced colitis and that USP25 deficiency exacerbates UC by destroying the intestinal mucosal barrier, however, overexpression of USP25 can alleviate colitis. Mechanistically, USP25 reduces the degradation of phosphor-STAT3Y705 at lysine 409 by catalyzing K48-linked deubiquitination. Further, this study demonstrates the aggravation of DSS-induced colitis by intestinal epithelial cell-specific knockout Stat3 in mice, while Stat3 overexpression by adeno-associated virus attenuates colitis in DSS-induced Usp25−/− mice. Together, these results showed that USP25 ameliorates UC by regulating the degradation of phosphor-STAT3. Collectively, USP25 is a specific STAT3 regulator that can be targeted in UC.
Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of USP25 in UC, bioinformatics analysis and research are conducted on clinical patients with UC, Usp25 knockout ( Usp25 −/− ) mice, intestinal epithelial cell-specific knockout signal transducer and activator of transcription 3 ( Stat3) (Villin-Cre Stat3 fl/fl ) mice, and human colonic epithelial cells. Results show that the expression of USP25 is decreased in patients with UC and mice with dextran sulfate sodium salt (DSS)-induced colitis and that USP25 deficiency exacerbates UC by destroying the intestinal mucosal barrier, however, overexpression of USP25 can alleviate colitis. Mechanistically, USP25 reduces the degradation of phosphor-STAT3 Y705 at lysine 409 by catalyzing K48-linked deubiquitination. Further, this study demonstrates the aggravation of DSS-induced colitis by intestinal epithelial cell-specific knockout Stat3 in mice, while Stat3 overexpression by adeno-associated virus attenuates colitis in DSS-induced Usp25 −/− mice. Together, these results showed that USP25 ameliorates UC by regulating the degradation of phosphor-STAT3. Collectively, USP25 is a specific STAT3 regulator that can be targeted in UC.
Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of USP25 in UC, bioinformatics analysis and research are conducted on clinical patients with UC, Usp25 knockout (Usp25-/-) mice, intestinal epithelial cell-specific knockout signal transducer and activator of transcription 3 (Stat3) (Villin-Cre Stat3fl/fl) mice, and human colonic epithelial cells. Results show that the expression of USP25 is decreased in patients with UC and mice with dextran sulfate sodium salt (DSS)-induced colitis and that USP25 deficiency exacerbates UC by destroying the intestinal mucosal barrier, however, overexpression of USP25 can alleviate colitis. Mechanistically, USP25 reduces the degradation of phosphor-STAT3Y705 at lysine 409 by catalyzing K48-linked deubiquitination. Further, this study demonstrates the aggravation of DSS-induced colitis by intestinal epithelial cell-specific knockout Stat3 in mice, while Stat3 overexpression by adeno-associated virus attenuates colitis in DSS-induced Usp25-/- mice. Together, these results showed that USP25 ameliorates UC by regulating the degradation of phosphor-STAT3. Collectively, USP25 is a specific STAT3 regulator that can be targeted in UC.Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of USP25 in UC, bioinformatics analysis and research are conducted on clinical patients with UC, Usp25 knockout (Usp25-/-) mice, intestinal epithelial cell-specific knockout signal transducer and activator of transcription 3 (Stat3) (Villin-Cre Stat3fl/fl) mice, and human colonic epithelial cells. Results show that the expression of USP25 is decreased in patients with UC and mice with dextran sulfate sodium salt (DSS)-induced colitis and that USP25 deficiency exacerbates UC by destroying the intestinal mucosal barrier, however, overexpression of USP25 can alleviate colitis. Mechanistically, USP25 reduces the degradation of phosphor-STAT3Y705 at lysine 409 by catalyzing K48-linked deubiquitination. Further, this study demonstrates the aggravation of DSS-induced colitis by intestinal epithelial cell-specific knockout Stat3 in mice, while Stat3 overexpression by adeno-associated virus attenuates colitis in DSS-induced Usp25-/- mice. Together, these results showed that USP25 ameliorates UC by regulating the degradation of phosphor-STAT3. Collectively, USP25 is a specific STAT3 regulator that can be targeted in UC.
Abstract Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation, and immune regulation. However, the role and mechanism of USP25 in ulcerative colitis (UC) remain unclear. To study the role and mechanism of USP25 in UC, bioinformatics analysis and research are conducted on clinical patients with UC, Usp25 knockout (Usp25 −/− ) mice, intestinal epithelial cell-specific knockout signal transducer and activator of transcription 3 (Stat3) (Villin-Cre Stat3fl/fl) mice, and human colonic epithelial cells. Results show that the expression of USP25 is decreased in patients with UC and mice with dextran sulfate sodium salt (DSS)-induced colitis and that USP25 deficiency exacerbates UC by destroying the intestinal mucosal barrier, however, overexpression of USP25 can alleviate colitis. Mechanistically, USP25 reduces the degradation of phosphor-STAT3Y705 at lysine 409 by catalyzing K48-linked deubiquitination. Further, this study demonstrates the aggravation of DSS-induced colitis by intestinal epithelial cell-specific knockout Stat3 in mice, while Stat3 overexpression by adeno-associated virus attenuates colitis in DSS-induced Usp25 −/− mice. Together, these results showed that USP25 ameliorates UC by regulating the degradation of phosphor-STAT3. Collectively, USP25 is a specific STAT3 regulator that can be targeted in UC.
ArticleNumber 5
Author Yang, Qian
Yu, Rong
Li, Jinting
Liu, Zhengru
Liu, Jian
Zhang, Jixiang
Dong, Weiguo
Miao, Yinglei
Wei, Yuping
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Cites_doi 10.1038/s41423-021-00810-9
10.1007/s00535-005-1744-3
10.1053/j.gastro.2017.11.276
10.1158/0008-5472.CAN-20-0447
10.2147/OTT.S194917
10.1016/j.bbagrm.2018.08.001
10.1073/pnas.0237137100
10.1038/ni.3230
10.1038/nature13150
10.1126/scisignal.2003708
10.1084/jem.20082683
10.1016/S0140-6736(17)32448-0
10.1002/advs.201901261
10.1038/nature16460
10.1016/j.bbamem.2020.183399
10.1016/j.immuni.2016.04.003
10.1016/j.molcel.2019.02.030
10.1146/annurev-biochem-061516-044916
10.1038/s41590-020-0681-x
10.3389/fphar.2020.00106
10.14309/ajg.0000000000000152
10.1053/j.gastro.2016.09.032
10.1002/path.5358
10.1172/JCI152170
10.1038/s41580-019-0099-1
10.1038/s41385-022-00487-x
10.1007/s12104-013-9495-1
10.1038/nrgastro.2016.169
10.1038/s41586-019-0992-y
10.1053/j.gastro.2007.09.001
10.1101/gad.300889.117
10.1016/j.immuni.2022.02.003
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References S Nikolaus (7315_CR24) 2007; 133
J Ahlers (7315_CR9) 2022; 15
7315_CR11
7315_CR12
CL Zindl (7315_CR10) 2022; 55
Y Chen (7315_CR31) 2020; 250
T Hibi (7315_CR3) 2006; 41
G Pickert (7315_CR28) 2009; 206
MJ Clague (7315_CR26) 2019; 20
L Shi (7315_CR14) 2014; 8
C Long (7315_CR15) 2018; 1861
SC Ng (7315_CR2) 2017; 390
DT Rubin (7315_CR1) 2019; 114
7315_CR6
P Li (7315_CR22) 2019; 12
MA Odenwald (7315_CR27) 2017; 14
F Rouaud (7315_CR29) 2020; 1862
TET Mevissen (7315_CR25) 2017; 86
M Sandip (7315_CR7) 2020; 21
M Gersch (7315_CR13) 2019; 74
K Sugimoto (7315_CR19) 2008; 118
JK Nelson (7315_CR16) 2022; 13
P Cao (7315_CR32) 2020; 11
T Welte (7315_CR18) 2003; 100
Q Zheng (7315_CR17) 2022; 132
F Yuan (7315_CR4) 2020; 80
SR Brant (7315_CR5) 2017; 152
CA Lindemans (7315_CR20) 2015; 528
D Sharma (7315_CR23) 2018; 154
C Zhang (7315_CR8) 2016; 44
T Olszak (7315_CR21) 2014; 509
K Parikh (7315_CR30) 2019; 567
D Xu (7315_CR33) 2017; 31
B Zhong (7315_CR34) 2013; 6
40140356 - Cell Death Dis. 2025 Mar 26;16(1):207. doi: 10.1038/s41419-025-07491-6.
References_xml – ident: 7315_CR11
  doi: 10.1038/s41423-021-00810-9
– volume: 41
  start-page: 10
  year: 2006
  ident: 7315_CR3
  publication-title: J Gastroenterol
  doi: 10.1007/s00535-005-1744-3
– volume: 154
  start-page: 948
  year: 2018
  ident: 7315_CR23
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2017.11.276
– volume: 80
  start-page: 4004
  year: 2020
  ident: 7315_CR4
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-20-0447
– volume: 12
  start-page: 1603
  year: 2019
  ident: 7315_CR22
  publication-title: Onco Targets Ther
  doi: 10.2147/OTT.S194917
– volume: 1861
  start-page: 773
  year: 2018
  ident: 7315_CR15
  publication-title: Biochim Biophys Acta Gene Regul Mech
  doi: 10.1016/j.bbagrm.2018.08.001
– volume: 100
  start-page: 1879
  year: 2003
  ident: 7315_CR18
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.0237137100
– ident: 7315_CR12
  doi: 10.1038/ni.3230
– volume: 509
  start-page: 497
  year: 2014
  ident: 7315_CR21
  publication-title: Nature
  doi: 10.1038/nature13150
– volume: 6
  start-page: ra35
  year: 2013
  ident: 7315_CR34
  publication-title: Sci Signal
  doi: 10.1126/scisignal.2003708
– volume: 206
  start-page: 1465
  year: 2009
  ident: 7315_CR28
  publication-title: J Exp Med
  doi: 10.1084/jem.20082683
– volume: 390
  start-page: 2769
  year: 2017
  ident: 7315_CR2
  publication-title: Lancet
  doi: 10.1016/S0140-6736(17)32448-0
– ident: 7315_CR6
  doi: 10.1002/advs.201901261
– volume: 118
  start-page: 534
  year: 2008
  ident: 7315_CR19
  publication-title: J Clin Invest
– volume: 528
  start-page: 560
  year: 2015
  ident: 7315_CR20
  publication-title: Nature
  doi: 10.1038/nature16460
– volume: 1862
  year: 2020
  ident: 7315_CR29
  publication-title: Biochim Biophys Acta Biomembr
  doi: 10.1016/j.bbamem.2020.183399
– volume: 44
  start-page: 913
  year: 2016
  ident: 7315_CR8
  publication-title: Immunity
  doi: 10.1016/j.immuni.2016.04.003
– volume: 74
  start-page: 436
  year: 2019
  ident: 7315_CR13
  publication-title: Mol Cell
  doi: 10.1016/j.molcel.2019.02.030
– volume: 86
  start-page: 159
  year: 2017
  ident: 7315_CR25
  publication-title: Annu Rev Biochem
  doi: 10.1146/annurev-biochem-061516-044916
– volume: 21
  start-page: 626
  year: 2020
  ident: 7315_CR7
  publication-title: Nat Immunol
  doi: 10.1038/s41590-020-0681-x
– volume: 11
  start-page: 106
  year: 2020
  ident: 7315_CR32
  publication-title: Front Pharmacol
  doi: 10.3389/fphar.2020.00106
– volume: 114
  start-page: 384
  year: 2019
  ident: 7315_CR1
  publication-title: Am J Gastroenterol
  doi: 10.14309/ajg.0000000000000152
– volume: 152
  start-page: 206
  year: 2017
  ident: 7315_CR5
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2016.09.032
– volume: 250
  start-page: 170
  year: 2020
  ident: 7315_CR31
  publication-title: J Pathol
  doi: 10.1002/path.5358
– volume: 132
  start-page: e152170
  year: 2022
  ident: 7315_CR17
  publication-title: J Clin Invest
  doi: 10.1172/JCI152170
– volume: 20
  start-page: 338
  year: 2019
  ident: 7315_CR26
  publication-title: Nat Rev Mol Cell Biol
  doi: 10.1038/s41580-019-0099-1
– volume: 15
  start-page: 480
  year: 2022
  ident: 7315_CR9
  publication-title: Mucosal Immunol
  doi: 10.1038/s41385-022-00487-x
– volume: 8
  start-page: 255
  year: 2014
  ident: 7315_CR14
  publication-title: Biomol NMR Assign
  doi: 10.1007/s12104-013-9495-1
– volume: 14
  start-page: 9
  year: 2017
  ident: 7315_CR27
  publication-title: Nat Rev Gastroenterol Hepatol
  doi: 10.1038/nrgastro.2016.169
– volume: 567
  start-page: 49
  year: 2019
  ident: 7315_CR30
  publication-title: Nature
  doi: 10.1038/s41586-019-0992-y
– volume: 133
  start-page: 1670
  year: 2007
  ident: 7315_CR24
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2007.09.001
– volume: 31
  start-page: 1024
  year: 2017
  ident: 7315_CR33
  publication-title: Genes Dev
  doi: 10.1101/gad.300889.117
– volume: 13
  year: 2022
  ident: 7315_CR16
  publication-title: Nat Commun
– volume: 55
  start-page: 494
  year: 2022
  ident: 7315_CR10
  publication-title: Immunity
  doi: 10.1016/j.immuni.2022.02.003
– reference: 40140356 - Cell Death Dis. 2025 Mar 26;16(1):207. doi: 10.1038/s41419-025-07491-6.
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Snippet Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation, inflammation,...
Abstract Ubiquitin-specific protease 25 (USP25), a member of the deubiquitination family, plays an important role in protein ubiquitination, degradation,...
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StartPage 5
SubjectTerms 13
13/21
13/51
14
14/35
38
631/136/1425
692/699/1503/257/1389
Animals
Antibodies
Biochemistry
Bioinformatics
Biomedical and Life Sciences
Cell Biology
Cell Culture
Colitis, Ulcerative - chemically induced
Colitis, Ulcerative - genetics
Colitis, Ulcerative - metabolism
Colitis, Ulcerative - pathology
Degradation
Dextran
Dextran Sulfate
Epithelial cells
Humans
Immunology
Immunoregulation
Inflammatory bowel disease
Intestinal Mucosa - metabolism
Intestinal Mucosa - pathology
Intestine
Life Sciences
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Phosphorylation
Proteolysis
Stat3 protein
STAT3 Transcription Factor - metabolism
Ubiquitin Thiolesterase - genetics
Ubiquitin Thiolesterase - metabolism
Ubiquitin-specific proteinase
Ubiquitination
Ulcerative colitis
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Title Ubiquitin-specific protease 25 ameliorates ulcerative colitis by regulating the degradation of phosphor-STAT3
URI https://link.springer.com/article/10.1038/s41419-024-07315-z
https://www.ncbi.nlm.nih.gov/pubmed/39773987
https://www.proquest.com/docview/3152366508
https://www.proquest.com/docview/3153873192
https://pubmed.ncbi.nlm.nih.gov/PMC11707020
https://doaj.org/article/bbbce7a537d94d5c848c5ba392b561e9
Volume 16
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