HDAC10 deletion promotes Foxp3


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
16 01 2020
Historique:
received: 11 09 2019
accepted: 24 12 2019
entrez: 18 1 2020
pubmed: 18 1 2020
medline: 18 11 2020
Statut: epublish

Résumé

Foxp3

Identifiants

pubmed: 31949209
doi: 10.1038/s41598-019-57294-x
pii: 10.1038/s41598-019-57294-x
pmc: PMC6965082
doi:

Substances chimiques

FOXP3 protein, human 0
Forkhead Transcription Factors 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

424

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH108592
Pays : United States
Organisme : NIAID NIH HHS
ID : R56 AI095276
Pays : United States
Organisme : NIH HHS
ID : R01 OD010944
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI123241
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS021328
Pays : United States
Organisme : NIAID NIH HHS
ID : P01 AI073489
Pays : United States
Organisme : NIAID NIH HHS
ID : K08 AI095353
Pays : United States

Références

Feuerer, M., Hill, J. A., Mathis, D. & Benoist, C. Foxp3+ regulatory T cells: differentiation, specification, subphenotypes. Nat. Immunol. 10, 689–695, https://doi.org/10.1038/ni.1760 (2009).
doi: 10.1038/ni.1760 pubmed: 19536194
Yano, H., Andrews, L. P., Workman, C. J. & Vignali, D. A. A. Intratumoral regulatory T cells: markers, subsets and their impact on anti-tumor immunity. Immunology, https://doi.org/10.1111/imm.13067 (2019).
doi: 10.1111/imm.13067
van Loosdregt, J. et al. Regulation of Treg functionality by acetylation-mediated Foxp3 protein stabilization. Blood 115, 965–974, https://doi.org/10.1182/blood-2009-02-207118 (2010).
doi: 10.1182/blood-2009-02-207118 pubmed: 19996091
Liu, Y., Wang, L., Han, R., Beier, U. H. & Hancock, W. W. Two lysines in the forkhead domain of foxp3 are key to T regulatory cell function. PLoS One 7, e29035, https://doi.org/10.1371/journal.pone.0029035 (2012).
doi: 10.1371/journal.pone.0029035 pubmed: 22247766 pmcid: 3256141
Wang, L. et al. Histone/protein deacetylase inhibitor therapy for enhancement of Foxp3+ T-regulatory cell function posttransplantation. Am. J. Transpl. 18, 1596–1603, https://doi.org/10.1111/ajt.14749 (2018).
doi: 10.1111/ajt.14749
Tao, R. et al. Deacetylase inhibition promotes the generation and function of regulatory T cells. Nat. Med. 13, 1299–1307, https://doi.org/10.1038/nm1652 (2007).
doi: 10.1038/nm1652 pubmed: 17922010
de Zoeten, E. F., Wang, L., Sai, H., Dillmann, W. H. & Hancock, W. W. Inhibition of HDAC9 increases T regulatory cell function and prevents colitis in mice. Gastroenterology 138, 583–594, https://doi.org/10.1053/j.gastro.2009.10.037 (2010).
doi: 10.1053/j.gastro.2009.10.037 pubmed: 19879272
de Zoeten, E. F. et al. Histone deacetylase 6 and heat shock protein 90 control the functions of Foxp3(+) T-regulatory cells. Mol. Cell Biol. 31, 2066–2078, https://doi.org/10.1128/MCB.05155-11 (2011).
doi: 10.1128/MCB.05155-11 pubmed: 21444725 pmcid: 3133361
Beier, U. H. et al. Sirtuin-1 targeting promotes Foxp3+ T-regulatory cell function and prolongs allograft survival. Mol. Cell Biol. 31, 1022–1029, https://doi.org/10.1128/MCB.01206-10 (2011).
doi: 10.1128/MCB.01206-10 pubmed: 21199917 pmcid: 3067815
Beier, U. H. et al. Histone deacetylases 6 and 9 and sirtuin-1 control Foxp3+ regulatory T cell function through shared and isoform-specific mechanisms. Sci. Signal. 5, ra45, https://doi.org/10.1126/scisignal.2002873 (2012).
doi: 10.1126/scisignal.2002873 pubmed: 22715468 pmcid: 3603571
Beier, U. H. et al. Essential role of mitochondrial energy metabolism in Foxp3(+) T-regulatory cell function and allograft survival. FASEB J. 29, 2315–2326, https://doi.org/10.1096/fj.14-268409 (2015).
doi: 10.1096/fj.14-268409 pubmed: 25681462 pmcid: 4447222
Wang, L. et al. FOXP3+ regulatory T cell development and function require histone/protein deacetylase 3. J. Clin. Invest. 125, 1111–1123, https://doi.org/10.1172/JCI77088 (2015).
doi: 10.1172/JCI77088 pubmed: 25642770 pmcid: 4362235
Xiao, H. et al. HDAC5 controls the functions of Foxp3(+) T-regulatory and CD8(+) T cells. Int. J. Cancer 138, 2477–2486, https://doi.org/10.1002/ijc.29979 (2016).
doi: 10.1002/ijc.29979 pubmed: 26704363 pmcid: 5484398
Hancock, W. W. Isoform-Selective HDAC Inhibitor Therapy for Transplantation: Are We Ready for HDAC6? Transplantation 100, 1597–1598, https://doi.org/10.1097/TP.0000000000001209 (2016).
doi: 10.1097/TP.0000000000001209 pubmed: 27222931 pmcid: 4961515
Qian, H. et al. HDAC6-mediated acetylation of lipid droplet-binding protein CIDEC regulates fat-induced lipid storage. J. Clin. Invest. 127, 1353–1369, https://doi.org/10.1172/JCI85963 (2017).
doi: 10.1172/JCI85963 pubmed: 28287402 pmcid: 5373879
Lieber, A. D. et al. Loss of HDAC6 alters gut microbiota and worsens obesity. FASEB J. 33, 1098–1109, https://doi.org/10.1096/fj.201701586R (2019).
doi: 10.1096/fj.201701586R pubmed: 30102568
Oehme, I. et al. Histone deacetylase 10 promotes autophagy-mediated cell survival. Proc. Natl Acad. Sci. USA 110, E2592–2601, https://doi.org/10.1073/pnas.1300113110 (2013).
doi: 10.1073/pnas.1300113110 pubmed: 23801752
Kao, H. Y., Lee, C. H., Komarov, A., Han, C. C. & Evans, R. M. Isolation and characterization of mammalian HDAC10, a novel histone deacetylase. J. Biol. Chem. 277, 187–193, https://doi.org/10.1074/jbc.M108931200 (2002).
doi: 10.1074/jbc.M108931200 pubmed: 11677242
Fischer, D. D. et al. Isolation and characterization of a novel class II histone deacetylase, HDAC10. J. Biol. Chem. 277, 6656–6666, https://doi.org/10.1074/jbc.M108055200 (2002).
doi: 10.1074/jbc.M108055200 pubmed: 11739383
Radhakrishnan, R. et al. Histone deacetylase 10 regulates DNA mismatch repair and may involve the deacetylation of MutS homolog 2. J. Biol. Chem. 290, 22795–22804, https://doi.org/10.1074/jbc.M114.612945 (2015).
doi: 10.1074/jbc.M114.612945 pubmed: 26221039 pmcid: 4566250
Yang, Y. et al. HDAC10 promotes lung cancer proliferation via AKT phosphorylation. Oncotarget 7, 59388–59401, https://doi.org/10.18632/oncotarget.10673 (2016).
doi: 10.18632/oncotarget.10673 pubmed: 27449083 pmcid: 5312319
Wang, B. et al. A Novel Role for Histone Deacetylase 10 (HDAC10) in the Regulation of PD-L1 Expression and Immune Tolerance Mediated By Antigen Presenting Cells (APCs). Blood 130, 3561 (2017).
Liu, Y. et al. Inhibition of p300 impairs Foxp3(+) T regulatory cell function and promotes antitumor immunity. Nat. Med. 19, 1173–1177, https://doi.org/10.1038/nm.3286 (2013).
doi: 10.1038/nm.3286 pubmed: 23955711 pmcid: 3793393
van Loosdregt, J. et al. Rapid temporal control of Foxp3 protein degradation by sirtuin-1. PLoS One 6, e19047, https://doi.org/10.1371/journal.pone.0019047 (2011).
doi: 10.1371/journal.pone.0019047 pubmed: 21533107 pmcid: 3080399
Osada, H. et al. Reduced expression of class II histone deacetylase genes is associated with poor prognosis in lung cancer patients. Int. J. Cancer 112, 26–32, https://doi.org/10.1002/ijc.20395 (2004).
doi: 10.1002/ijc.20395 pubmed: 15305372
Elstrom, R. L. et al. Akt stimulates aerobic glycolysis in cancer cells. Cancer Res. 64, 3892–3899, https://doi.org/10.1158/0008-5472.CAN-03-2904 (2004).
doi: 10.1158/0008-5472.CAN-03-2904 pubmed: 15172999
Gerriets, V. A. et al. Foxp3 and Toll-like receptor signaling balance Treg cell anabolic metabolism for suppression. Nat. Immunol. 17, 1459–1466, https://doi.org/10.1038/ni.3577 (2016).
doi: 10.1038/ni.3577 pubmed: 27695003 pmcid: 5215903
Angelin, A. et al. Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments. Cell Metab. 25, 1282–1293 e1287, https://doi.org/10.1016/j.cmet.2016.12.018 (2017).
doi: 10.1016/j.cmet.2016.12.018 pubmed: 28416194 pmcid: 5462872
Geraldy, M. et al. Selective Inhibition of Histone Deacetylase 10: Hydrogen Bonding to the Gatekeeper Residue is Implicated. J. Med. Chem. 62, 4426–4443, https://doi.org/10.1021/acs.jmedchem.8b01936 (2019).
doi: 10.1021/acs.jmedchem.8b01936 pubmed: 30964290
Uba, A. I. & Yelekci, K. Homology modeling of human histone deacetylase 10 and design of potential selective inhibitors. Journal of biomolecular structure & dynamics, 1–24, https://doi.org/10.1080/07391102.2018.1521747 (2018).
doi: 10.1080/07391102.2018.1521747
Hai, Y., Shinsky, S. A., Porter, N. J. & Christianson, D. W. Histone deacetylase 10 structure and molecular function as a polyamine deacetylase. Nat. Commun. 8, 15368, https://doi.org/10.1038/ncomms15368 (2017).
doi: 10.1038/ncomms15368 pubmed: 28516954 pmcid: 5454378
Jin, Z. et al. Decreased expression of histone deacetylase 10 predicts poor prognosis of gastric cancer patients. Int. J. Clin. Exp. Pathol. 7, 5872–5879 (2014).
pubmed: 25337229 pmcid: 4203200
Oehme, I., Lodrini, M., Brady, N. R. & Witt, O. Histone deacetylase 10-promoted autophagy as a druggable point of interference to improve the treatment response of advanced neuroblastomas. Autophagy 9, 2163–2165, https://doi.org/10.4161/auto.26450 (2013).
doi: 10.4161/auto.26450 pubmed: 24145760
Ridinger, J. et al. Dual role of HDAC10 in lysosomal exocytosis and DNA repair promotes neuroblastoma chemoresistance. Sci. Rep. 8, 10039, https://doi.org/10.1038/s41598-018-28265-5 (2018).
doi: 10.1038/s41598-018-28265-5 pubmed: 29968769 pmcid: 6030077
Cicenas, J. The potential role of Akt phosphorylation in human cancers. Int. J. Biol. Markers 23, 1–9 (2008).
doi: 10.1177/172460080802300101
Tanaka, A. & Sakaguchi, S. Regulatory T cells in cancer immunotherapy. Cell Res. 27, 109–118, https://doi.org/10.1038/cr.2016.151 (2017).
doi: 10.1038/cr.2016.151 pubmed: 27995907
Song, C., Zhu, S., Wu, C. & Kang, J. Histone deacetylase (HDAC) 10 suppresses cervical cancer metastasis through inhibition of matrix metalloproteinase (MMP) 2 and 9 expression. J. Biol. Chem. 288, 28021–28033, https://doi.org/10.1074/jbc.M113.498758 (2013).
doi: 10.1074/jbc.M113.498758 pubmed: 23897811 pmcid: 3784715
Gialeli, C., Theocharis, A. D. & Karamanos, N. K. Roles of matrix metalloproteinases in cancer progression and their pharmacological targeting. FEBS J. 278, 16–27, https://doi.org/10.1111/j.1742-4658.2010.07919.x (2011).
doi: 10.1111/j.1742-4658.2010.07919.x pubmed: 21087457
Skarnes, W. C. et al. A conditional knockout resource for the genome-wide study of mouse gene function. Nature 474, 337–342, https://doi.org/10.1038/nature10163 (2011).
doi: 10.1038/nature10163 pubmed: 21677750 pmcid: 3572410
Akimova, T. et al. Targeting sirtuin-1 alleviates experimental autoimmune colitis by induction of Foxp3+ T-regulatory cells. Mucosal Immunol. 7, 1209–1220, https://doi.org/10.1038/mi.2014.10 (2014).
doi: 10.1038/mi.2014.10 pubmed: 24549276 pmcid: 4138288

Auteurs

Satinder Dahiya (S)

Division of Transplant Immunology, Department of Pathology and Laboratory Medicine, and Biesecker Center for Pediatric Liver Disease, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, 19104, USA.

Ulf H Beier (UH)

Division of Nephrology and Department of Pediatrics, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, 19104, USA.

Liqing Wang (L)

Division of Transplant Immunology, Department of Pathology and Laboratory Medicine, and Biesecker Center for Pediatric Liver Disease, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, 19104, USA.

Rongxiang Han (R)

Division of Transplant Immunology, Department of Pathology and Laboratory Medicine, and Biesecker Center for Pediatric Liver Disease, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, 19104, USA.

Jing Jiao (J)

Division of Nephrology and Department of Pediatrics, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, 19104, USA.

Tatiana Akimova (T)

Division of Transplant Immunology, Department of Pathology and Laboratory Medicine, and Biesecker Center for Pediatric Liver Disease, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, 19104, USA.

Alessia Angelin (A)

Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA.

Douglas C Wallace (DC)

Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA.

Wayne W Hancock (WW)

Division of Transplant Immunology, Department of Pathology and Laboratory Medicine, and Biesecker Center for Pediatric Liver Disease, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, 19104, USA. whancock@pennmedicine.upenn.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH