lunch & science journal club as part of the center scor award
DESCRIPTION
Lunch & Science Journal Club as part of the Center SCOR Award. July 10, 2013: “Progesterone Receptor (PR) Regulates Bone Growth, in Bone?” presented by Zhendong “Alex” Zhong, Ph.D. Peak bone mass (PBM) predicts osteoporosis. Peak bone mass (PBM). arthrolink.com. Estrogen deficiency. - PowerPoint PPT PresentationTRANSCRIPT
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Lunch & Science Journal Club as part of the Center SCOR Award
July 10, 2013: “Progesterone Receptor (PR) Regulates Bone Growth, in Bone?” presented by Zhendong “Alex” Zhong, Ph.D.
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Peak bone mass (PBM) predicts osteoporosis
arthrolink.com
Peak bone mass (PBM)
Estrogen deficiency
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Activity & apoptosis
Increase Osteoblast proliferation and differentiation
apoptosis
Gonads Sex steroids
Testis
Ovary
Androgens
Estrogens
Ovary orAdrenal glands
Progesterone
?
Sex hormones for bone homeostasis
osteoblastosteoclast
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Progesterone affects other sex hormones profoundly
Wikipedia
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Progesterone Receptor (PR)
Susan A. Leonhardt and Dean P. Edwards 2002
Female menstrual cycle (cyclical) Pregnancy (high, supports gestation) Embryogenesis Others (bone?)
Progesterone
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PR knockout (PRKO) mice show higher bone mass
Yao, PLoSONE, 2010
• Higher bone formation rate in females, lower bone resorption rate in males
• PR antagonist RU486 also enhanced bone formation in normal female mice• Higher Osteoblast maturation-related
genes, and lower apoptosis-related
• More dramatic HBM phenotype in females
BV/TV
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High bone mass
in PRKO mice ?
1. Which cell population is responsible?2. Which downstream signaling pathway of PR
is responsible?3. What is the mechanism of the sex
differences? 4. The timing of PR knockout
1. PR regulates bone homeostasis within bone
2. The regulation has sex differences
Hypothesis
Further questions
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Specific aims
Aim 1. To investigate the direct effects of PR deletion in osteoblasts on bone formation, and compare these effects in female and male mice
Aim 2. To determine time-dependent and tissue-specific PR inhibition on bone turnover and bone mass accrual
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Skeletal progenitor
Sox9+Runx2+ ??
Sox9+Col2α1+
Col2α1+
Runx2+ColXα1+
Chondrocyte Hypertrophicchondrocyte
Runx2+
Osteoblast progenitor
Osteoblast precursor
Osx1+
Osteoblast precursor
Oc+
Osteoblast
CapG+Dmp1+
Mineralizing osteocyte
SOST+FGF23+ORP150
Matureosteocyte
Figure adapted from Bonewald,2011, Vankoevering, 2008 and Rodda, S. J. 2006
Prx1-Cre Dermo1-Cre Col2α1-Cre Oc-Cre Dmp1-Cre Sox9-Cre Col1α1-Cre (3.6kb) Osx1-Cre
Adipocyte;
myocyte;
neuron
Col1α1-Cre (2.3kb)
Col10α1-CreOsx1-Cre Osteoclast
TRAP-CreCtsK-Cre
Skeletal primordium
Hematopoietic stem cell
MSC
Mx1-Cre
Bone Cell Differentiation
Mesenchymal Stem cell
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Cre-Tg/+
Generation of an inducible & bone-specific knockout of PR
X
XPR-flox/flox
Tg/+, flox/flox
Tg/+, flox/+
1. Mx1-Cre Osteoprogenitors 2. Col1a1-CreERT2Mature osteoblasts
PR is knocked out in “osteoprogenitors” or “mature osteoblasts”
Induce
pI-pC orTamoxifen
XMore tg/+, flox/flox +/+, flox/flox
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Mx1-Cre;PR-flox heterozygotes
Tg, flox/+, FemalepI-pC IP injection starts at 1 month of age
TV BV TV/BVwt 2.70 0.20 0.08
PRKO 2.41 0.61 0.25
3mo, Female
Bone volume (white) / Total volume (BV/TV)
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Challenges
• To induce PR gene knockout after 1 month of age Col1a1-CreERT2 does not respond well to Tamoxifen induction after 2 weeks of age
• How well is Cre activated in different compartments? Background activity? Specificities?
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ATG
loxPEGFP
loxPtdTomato
Stop codon Stop codon
×Col1a1-CreERT2
or Mx1-Cre
“mT/mG”
Determine the knockout efficiency using mT/mG model
Cell Stem Cell, 2012
Mx1-Cre; mTmG mice
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Bright fieldGreen: GFP /Mx1 activityRed: Tomato /all others
No induction
Induced in vivo
Bone marrow cells from the femurs, in vitro cultured for overnight
Osteoclastic differentiationBlue: DAPI/nuclei
Mx1-Cre; mTmG
Col1-Cre; mTmG
Mx1-Cre;mTmG mice, induced in vivo at 4 weeks of age
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Bone marrow stromal cells were differentiated into osteoblasts, for 7 days
Non-induced Induced
stromal cells were differentiated into osteoblasts
No differentiation 14d differentiation
1. Mx1-Cre is active in a part of osteoprogenitors before induction;
2. Mx1-Cre is harder to be activated in mineralized osteocytes?
Mx1-Cre;mTmG mice, induced in vivo at 4 weeks of age
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Ex vivo study on PR signaling
control
Induced(Mx1-Cre)
Induced(Col1-Cre)
Bone growth
PR protein
Mx1/Col1-Cre; PR-flox
Osteoblast differentiation, TGFβ/IHH/Wnt signaling changes
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Summary
• Generated conditional/inducible PR knockout mice,
measuring bone mass changes post induction
• Investigating the timing and dosage for TM/pl-pC induction
Next steps
• Measure bone mass in homozygotes
• New models: Prx1-Cre/ Oc-Cre
• Study Wnt/IHH/TGF pathways