Jennifer Wood, Ph.D. Dept. of Animal Science, UNL
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Transcript of Jennifer Wood, Ph.D. Dept. of Animal Science, UNL
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Jennifer Wood, Ph.D.Dept. of Animal Science, UNL
Nebraska Center for the Prevention of Obesity Diseases through Dietary
Molecules (NPOD):
Abnormalities in Regulation of Myocyte versus Adipocyte Differentiation by Maternal Obesity
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Significance
The economic cost of obesity is estimated at 147 billion dollars which is > 9% of national health expenditures and is comparable to health care costs associated with smoking
Finkelstein et al. (2009) Health Aff; NIH (1998) Obesity Research
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Visceral Adipose
FreeFatty Acids
Pro-InflammatoryCytokines
InsulinResistance
DyslipidemiaHypertension
Type 2Diabetes
CardiovascularDisease
MetabolicSyndrome
SedentaryLifestyle
Nutrient-DenseFood
Genetic Predisposition
Metabolic Syndrome
Criteria (3 of 5)• Elevated Waist Circumference• Elevated Triglycerides• Reduced HDL-C• Elevated Blood Pressure• Elevated Fasting Glucose
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Significance
Children of obese mothers are at increased risk of becoming obese and developing metabolic syndrome
Bruce et al. (2010) J Nutr.; Power et al. (2011) Physiol Behav; Heerwagen et al. (2010) Am J Physiol Regul Integr Comp Physiol
Approximately 22% of obstetric patients are obeseKim et al. (2007) Obesity
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SignificanceIn a sheep model of maternal obesity, fetal muscle mass is decreased due to increased signaling of AMP kinase and activation of FOXO3a and NFkB p65 transcription factors
Zhu et al (2008) J Physiol; Tong et al (2009) Am J Physiol Endocrinol Metab; Du et al (2010) Biol Reprod
Sarcopenic obesity is the loss of muscle mass in combination with increases in visceral fat resulting in the development of metabolic syndrome in 1/3 of the female population and 2/3 of the male population >60 years old in the US
Stenholm et al. (2008) Curr Opin Clin Nutr Metab Care; Jensen (2008) J Parenter Enteral Nutr
Epigenetic modifications of the embryonic genome determine cell fate during normal development and therefore changes in these modifications due to maternal obesity may contribute to the “programming” of decreased fetal muscle mass and the development of sarcopenic obesityHeerwagen et al. (2010) Am J Physiol Regul Integr Comp Physiol; Gluckman (2009)
Nat Rev Endocrinol; Campion (2009) Obes Rev
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Developmental Trajectory of Mesenchymal Stem Cells
Gesta et al (2007) Cell
Pref-1CEBPb
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Mesodermal Cell
ROSPlacenta
Maternal Obesity
TNFa
BMPTNFa
TNFR1Wnt
SMAD 2/3
SMAD 4
NFkBp65/p50
Myf5, Pax3, Pax7;
JNK
b-catenin
FOXOTCF
TrxPrx
Pref-1, CEBPb
Adipoblasts
Myoblasts
Omega-3Fatty Acids
Central Hypothesis
Curcumin
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InnovationBiochemical studies → altered insulin signaling
Genetic studies → insulin resistance is highly heritable (above 40%)
However, genetic loci only account for ~10% of the obese population and the success of current therapeutic interventions based on biochemical studies are limited.
Novel hypothesis → children of obese mothers develop sarcopenic obesity at an early age due to decreased programming of myoblasts and increased programming of adipoblasts.
Novel Experimental Model → obese mouse model which expresses a phenotype consistent with human metabolic syndrome.
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B6
LY
Lethal Yellow (LY) mice Mimics human obesity
Merc
1Ay 1A 1A’ 1B 1C 2
AgoutiAgouti
Merc/agouti fusion
1Ay 1A 1A’ 1B 1C 2
Agouti
( 120 kb Ay deletion )
Blood Hypothalamus
ME Arcuate
ααα-MSHCART Satiety
Insulin
Leptin-
Agouti (Ay)
+ MC4R
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Yang et al. 2011, Mol Reprod Dev
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Maternal Obesity Decreases Growth and Development of Embryos
Norwood et al., unpublished data
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Specific Aim 1: Identify TNFa-dependent mechanisms of decreased myogenic and increased adiopogenic regulatory factor expression.
Somite
Placenta
TNFa
BMPTNFa
TNFR1
SMAD 2/3
SMAD 4
NFkBp65/p50
Myf5, Pax3, Pax7; Pref-1, CEBPb
Omega-3Fatty Acids
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NFkB-dependent regulation of gene expression
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Massagué J et al. Genes Dev. 2005;19:2783-2810
Smad-dependent regulation of gene expression
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Experimental DesignYear 1:
–Establish somite explant cultures from E8.5 CF-1 mouse embryos–Treat with increasing concentration of TNFa, collect protein, and carry out Western blot analysis using antibodies against JNK, NFkB, Smad–Monitor TNFa-dependent increases in Pax3, Pax7, Myf5, Pref1, and Cebpb mRNAs in the absence or presence of JNK inhibitor or Smad siRNA
Year 2: –Carry out ChIP assays using antibodies against NFkB, Smads, HDAC, p300/CBP coupled to QPCR at the promoter of Pax3, Pax7, Myf5, Pref1, Cebpb in TNFa-treated somites OR somites collected from embryos developed in an obese (LY) compared to lean (B6) in utero environment (E10.5)–Alternatively, use Chromosome Conformation Capture assays (3C) to determine long-range regulation of Pax3, Pax7, Myf5, Pref1, or Cebpb by NFkB or Smad transcription factors
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Experimental DesignYear 3:
–Supplement dams with omega 3 fatty acid–Collect somites from E10.5 embryos developed in obese (LY) or lean (B6) dams without or with supplement–Collect protein and carry out Western blot analyses using antibodies against JNK, NFkB, Smad–Monitor supplement-dependent changes in Pax3, Pax7, Myf5, Pref1, and Cebpb mRNAs
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Somite
ROS
Placenta
Wnt
Myf5, Pax3, Pax7;
JNK
b-catenin
FOXOTCF
TrxPrx
Pref-1
Curcumin
Specific Aim 2: Identify ROS-dependent mechanisms of decreased myogenic and increased adiopogenic regulatory factor expression.
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FOXO-dependent regulation of gene expression
Huang et al. (2007) J Cell Sci
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Experimental DesignYear 1:
–Establish somite explant cultures from E8.5 CF-1 mouse embryos–Treat with increasing concentration of H2O2, collect protein, and carry out Western blot analysis using antibodies against JNK, b-catenin, TCF, FOXO–Monitor H2O2 -dependent increases in Pax3, Pax7, Myf5, Pref1, and Cebpb mRNAs in the absence or presence of JNK inhibitor or FOXO siRNA
Year 2: –Carry out ChIP assays using antibodies against b-catenin, TCF, FOXO, SIRT1, or p300/CBP coupled to QPCR at the promoter of Pax3, Pax7, Myf5, Pref1, Cebpb in H2O2 -treated somites OR somites collected from embryos developed in an obese (LY) compared to lean (B6) in utero environment (E10.5)–Alternatively, use Chromosome Conformation Capture assays (3C) to determine long-range regulation of Pax3, Pax7, Myf5, Pref1, or Cebpb by FOXO or TCF transcription factors
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Experimental DesignYear 3:
–Supplement dams with curcumin–Collect somites from E10.5 embryos developed in obese (LY) or lean (B6) dams without or with supplement–Collect protein and carry out Western blot analyses using antibodies against JNK, b-catenin, TCF, FOXO –Monitor supplement-dependent changes in Pax3, Pax7, Myf5, Pref1, and Cebpb mRNAs
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Mesenchymal Stem Cell Niche
Maternal Obesity
Adipoblasts
Myoblasts
Omega-3Fatty Acids
Curcumin
Specific Aim 3: Identify maternal-obesity dependent decreases in myoblast and increases in adipoblast populations in the mesenchymal stem cell niche within adipose tissue, skeletal muscle, and bone marrow
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Experimental DesignYear 2 and 3:
–Collect mesenchymal stem cells (adipose, bone marrow, muscle) from 6 and 12 week old B6 males developed in an obese (LY) or lean (B6) in utero environment in the absence or presence of an anti-inflammatory (omega-3 fatty acids) or an anti-oxidant (curcumin)–Carry out QPCR using primers against Pax3, Pax7, Myf5, Pref1, and Cebpb –Carry out ChIP analyses coupled to QPCR in mesenchymal stem cells using antibodies against transcription factors (NFkB, FOXO, Smads) and coactivators (HDAC, SIRT, p300/CBP) associated with the promoter of Pax3, Pax7, Myf5, Pref1, and Cebpb–Determine differences in body fat composition in 6 and 12 week old B6 males developed in an obese (LY) or lean (B6) in utero environment using DEXA. The effect of in utero exposure to an anti-inflammatory (omega-3 fatty acids) or an anti-oxidant (curcumin) as well as the response to a dietary challenge (high fat diet) on body fat composition will also be measured using DEXA
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Expected Outcomes• Identify signaling pathways and transcription factors activated by the
inflammatory response, oxidative stress, or both which regulate the expression of myogenic and adipogenic regulatory factors
• Determine the ability of omega-3 fatty acids or curcumin to modify or reverse TNFa- and ROS dependent regulation of mesodermal cell differentiation
• Determine the effect of maternal obesity on the phenotype of mesenchymal stem cell niches in the bone marrow, adipose tissue, and skeletal muscle
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Environment and Mentors• Core Facilities:
– Epigenetics– Biostatistics
• Mentors– John Davis: cell signaling, reproductive physiology– Andrea Cupp: growth factor signaling, stem cell biology,
reproductive physiology– Robert Powers: