NIAID and NIDDK Workshop May 10 , 2016tandem-fp7.eu/fileadmin/tandem/downloads/workshop/... ·...
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Developing a Comprehensive Therapeutic Research Strategy for the Converging Epidemics of TB, T2DM, and HIV
NIAID and NIDDK WorkshopMay 10th, 2016
Metabolite-Induced ROS Overproduction Activates the Diverse Biochemical and Molecular Mechanisms Underlying Diabetic
Complications
Michael Brownlee, M.D.Anita and Jack Saltz Chair in Diabetes Research
Associate Director for Biomedical Sciences,Einstein Diabetes Research Center
Professor of Medicine and Pathology Albert Einstein College of Medicine
New York
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Physiologic ROS production is essential for normal intracellular signaling and cellular homeostasis
Holmström, K.M. & Finkel, T. Nature Reviews Molecular Cell Biology 15, 411-421, 2014
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Current view of ROS stress
Nathan, C., and Cunningham-Bussel, A. Nat Rev Immunol 13:349-361, 2013
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The diabetic complications epidemic
DiabeticRetinopathy
Leading causeof blindness
in working ageadults
Stroke
2- to 4- fold increase in stroke and dementia
DiabeticNeuropathy
Leading cause of non-traumatic lower extremity amputations
CardiovascularDisease
CVD: 2/3 of heart attack pts. have diabetes or IGT
Diabetic NephropathyLeading cause of
end-stage renal disease
20-50% of T2D, 33% of T1DIncreased risk of CVD and death
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Hyperglycemia- and FFA-induced overproduction of ROS activates all major pathways of diabetic cellular damage
↑ Polyol PW flux
↑PKC ↑Hexosamine PW flux
Cytoplasm
↑ Glucose/FFA
Modified from Brownlee M., Nature, 2001; 4104:813-82
↑Methylglyoxal
↑ NFκB↑RAGE & RAGE ligands
↑ AGE
↑ PARP
Nucleus↓ GAPDH
↑ ROS
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Superoxide also inhibits critical endothelial enzymes
Endothelial nitric oxide synthase (eNOS) KD
Zhao, H.J., et al. J. Am. Soc Nephrol 17:2664-2669, 2006 ; Nasu, T., et al., Am J Phys Renal Phys 302:F1616-F1629, 2012
Prostacyclin synthase (PGI2) KD
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Recently described mechanisms of diabetic tissue damage activated by metabolite-induced overproduction of ROS
• Nuclear import of NFAT transcription factors• Nuclear translocation of FOXO transcription factors• PPARα nuclear receptor expression• CaMKII activation/increased intracellular Ca++
• Decreased sirtuin 1, PGC1α, AMPK expression• Downregulation and mismatching of specific miRNAs• NRLP3 inflammasome activation• Neutrophil extracellular trap formation/mφ priming
Shah, M.S., and Brownlee, M. Circ Res in press, 2016
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Transgenic expression of the antioxidant enzyme superoxide dismutase prevents each
complication in experimental diabetes
Diabetic retinopathy Diabetic nephropathy
Diabetic cardiomyopathyDiabetic neuropathy
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Post-translational modifications of histones cause chromatin remodeling and changes in levels of gene expression
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Hyperglycemia-induced ROS cause activating modifications of histone 3 lysine 4 and de-repressing modifications of histone 3 lysine 9 at the
NFκB p65 proximal promoter
El-Osta, A., et al. J Exp Med, 2008, 205:2409
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In non-diabetic mice, transient hyperglycemia induces a long-term increase in H3K4me1 at the NFκB p65 promoter
by recruiting the histone methyltransferase Set 7
El-Osta, A., et al. J Exp Med, 2008, 205:2409
0
100
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qPCR
for N
FκB
p65 p
rom
oter
afte
r LCM
and
cChI
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H3K
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(Arb
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HG(6h)+LG(4d) HG(6h)+LG(6d) LG(6d)
* **
*
Treatment Group (clamped mice)
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In non-diabetic mice, six hours of transient hyperglycemia causes a six DAY increase in NFκB expression, a master
regulator of inflammatory genes
El-Osta, A., et al. J Exp Med, 2008, 205:2409
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000
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6h 6h 6h+vector 6h+MnSOD 6h+2d 6h+5d
RO
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5mM glucose 25mM glucose 25mM glucose + 5mM glucose
After transient hyperglycemia, elevated mitochondrial ROS production persists for days
Ferdinando Giacco et al. Diabetes 2015;64:3273-328
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Transient exposure to hyperglycemia above a critical threshold level activates a multi-component positive feedback loop
Ferdinando Giacco et al. Diabetes 2015;64:3273-3284
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ROS-induced methylglyoxal adducts accumulate in TB lesions of patients
Rachman H, Kim N, Ulrichs T, Baumann S, Pradl L, et al. (2006) . PLoS ONE 1(1): e29. doi:10.1371/journal.pone.0000029
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Van Heijst, H.W.J, and Pamer, E.G. Cell 153:507-508, 2013
TNF-induced mitochondrial ROS in TB-infected macrophages increases killing of mycobacteria, but increases necroptosis and mycobacterial release
into the extracellular milieu and bacterial dissemination
Roca, F.J and Ramakrishnan, L. Cell 153:521-534, 2013;
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Colleagues who contributed to the work presented today
CollaboratorsNaila Ahmed Angelika BierhausMark CooperStephanie DimmelerAjit S. DivakaruniAssam El-OstaHans-Peter HammesAnne N.MurphyPeter NawrrothAlessandro PocaiRobert RoederVijay P. SarthyPhilip SchererGuntram SuskePaul ThornalleyCsabo SzaboMark Yorek
Brownlee LabAnna CarratuXueliang DuDiane EdelsteinIda GiardinoFerdinando GiaccoQida JuTakeshi MatsumuraTakeshi NishikawaManasi ShahGuanghi SuiTetsuya Taguchi
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