Leukocytes mediate disease pathogenesis in the Ndufs4(KO) mouse model of Leigh syndrome

JCI insight - Tập 7 Số 5 - 2022
Julia Stokes1, Rebecca Bornstein1,2, Katerina James1, Kyung Yeon Park1, Kira A. Spencer1, Katie Vo1, John Snell1, Brittany Johnson3, Philip G. Morgan1,4, Margaret M. Sedensky1,4, Nathan A. Baertsch1,5, Simon C. Johnson1,4,2,3
1Center for Integrative Brain Research, Seattle Children’s Research Institute, Seattle, Washington, USA
2Department of Laboratory Medicine and Pathology
3Department of Neurology
4Department of Anesthesiology and Pain Medicine and
5Department of Pediatrics, University of Washington, Seattle, Washington USA

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10.1148/rg.2020200052

10.1002/path.5641

10.1097/NEN.0000000000000195

Johnson, 2015, Dose-dependent effects of mTOR inhibition on weight and mitochondrial disease in mice, Front Genet, 6, 10.3389/fgene.2015.00247

10.1126/science.1244360

10.1016/j.kint.2018.08.038

10.1002/acn3.50846

10.1016/j.ymgme.2020.03.007

10.3389/fgene.2017.00221

10.1038/s41598-019-39419-4

10.1038/s42255-020-00319-x

10.1073/pnas.0808594106

10.1158/1535-7163.MCT-13-0865

10.1186/s13058-016-0697-1

10.1093/neuonc/nox181

10.1158/0008-5472.CAN-16-2534

Bornstein, 2021, Differential effects of mTOR inhibition and dietary ketosis in a mouse model of subacute necrotizing encephalomyelopathy, Neurobiol Dis, 163

10.1073/pnas.0607899103

10.1021/ml200156t

10.1186/s13023-020-1297-9

10.1158/1078-0432.CCR-12-3110

10.1080/13543776.2021.1839414

10.1172/JCI62923

10.3389/fphys.2019.01113

10.1016/j.pediatrneurol.2011.04.008

10.1016/j.ejpn.2015.05.002

10.1038/jhg.2015.57

10.5692/clinicalneurol.cn-000834

10.1016/j.braindev.2011.08.004

10.1016/j.jcma.2011.05.006

10.1016/j.mri.2019.01.010

Nafisinia, 2017, Whole exome sequencing identifies the genetic basis of late-onset Leigh syndrome in a patient with MRI but little biochemical evidence of a mitochondrial disorder, JIMD Rep, 32, 117, 10.1007/8904_2016_541

10.1016/j.redox.2013.12.026

10.1213/ANE.0000000000005430

10.1097/00000542-199902000-00031

10.1213/00000539-200009000-00042

10.1002/onco.13629

10.1182/blood-2009-06-222943

10.1186/s40425-018-0457-0

10.7554/eLife.47163

10.1073/pnas.1006214107

10.1136/jnnp.14.3.216

10.1007/s00441-007-0474-7

10.1016/j.jcpa.2014.07.003

Kaiser, 2019, Tmem119-EGFP and Tmem119-CreERT2 transgenic mice for labeling and manipulating microglia, eNeuro, 6, ENEURO.0448, 10.1523/ENEURO.0448-18.2019

10.1186/s40478-019-0850-z

Johnson, 2014, Translational medicine. A target for pharmacological intervention in an untreatable human disease, Science, 346, 10.1126/science.aaa1811

10.1093/hmg/ddx341

Civiletto, 2018, Rapamycin rescues mitochondrial myopathy via coordinated activation of autophagy and lysosomal biogenesis, EMBO Mol Med, 10, 10.15252/emmm.201708799

10.1016/j.molmet.2018.05.002

10.18632/oncotarget.12560

10.1016/j.heliyon.2019.e01217

10.1111/cts.12501

Gopal-Srivastava, 2017, Facilitating clinical studies in rare diseases, Adv Exp Med Biol, 1031, 125, 10.1007/978-3-319-67144-4_6

10.1186/s13023-018-0936-x

10.1186/s13063-017-2287-7

10.1097/MD.0000000000018634

10.1002/jimd.12281

10.1111/cge.13713

10.1016/j.cmet.2013.07.002

10.1016/j.yjmcc.2018.08.022

Chiao, 2021, NAD+ Redox imbalance in the heart exacerbates diabetic cardiomyopathy, Circ Heart Fail, 14, 10.1161/CIRCHEARTFAILURE.120.008170

10.1001/archotol.128.4.355

10.3346/jkms.2019.34.e143

10.1159/000446586

10.1515/jpem-2020-0139

Wang, 2001, Acute necrotizing encephalopathy of childhood, Chang Gung Med J, 24, 1

10.1007/s10072-018-3541-9

Wu, 1993, Leigh disease (subacute necrotizing encephalomyelopathy): report of one case, Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi, 34, 301

10.1126/science.aad9642

10.3389/fimmu.2021.753789

10.1186/s12943-019-1087-y