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Transcript of By Sonali Dadoo School Pine-Richland High School Grade 11 Category Microbiology ADVIL EFFECTS ON 3T3...
![Page 1: By Sonali Dadoo School Pine-Richland High School Grade 11 Category Microbiology ADVIL EFFECTS ON 3T3 CELL PROLIFERATION, SURVIVORSHIP, AND REGENERATION.](https://reader035.fdocuments.us/reader035/viewer/2022062421/56649cfa5503460f949cb4ad/html5/thumbnails/1.jpg)
BySonali Dadoo
SchoolPine-Richland High School
Grade11
CategoryMicrobiology
ADVIL EFFECTS ON 3T3 CELL
PROLIFERATION, SURVIVORSHIP,
AND REGENERATION
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WOUND HEALING:“PATHOPHYSIOLOGY OF TISSUE REPAIR AND TRANSFER” BY
EDOARDO AUSTONI, V INCENZO GIANNOCCARO
Photo Credit to: Clini Medhttp://www.clinimed.co.uk/
Platelets, PMN
Macrophages, Fibroblasts, Capillaries
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What is a scar?Body’s natural healing mechanism in
response to injury, trauma, etc.Tissue formed during healing process
Scar Formation ComplicationsCollagen fibers arranged randomly as opposed
to linear, parallel formation
WOUND HEALING OVERPRODUCTION OF SCAR TISSUE
Photo Credit: wiseGEEK.com
Photo Credit: Schweiger Dermatology
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Myofibroblast TheoryFibroblast differentiation into myofibroblastsMyofibroblasts contract with alpha-smooth
muscle actinContracts edges of wound to repairLack of apoptosis leads to keloid and
hypertrophic scar
Fibronectin TheoryFibronectin structure precedes wound
contractionProvides structure for fibroblasts
CAUSES OF SCAR FORMATION COMPLICATIONS
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Corticosteroid Injections Reduce collagen synthesis,
infl ammatory mediators, and fi broblast proliferation
5-Fluorouracil Pyrimidine analogue with
antimetabolite activity Reduces fi broblastic proliferation in
tissue culture and postoperative scarring
Tamoxifen Nonsteroidal antiestrogen used to treat
breast cancer Inhibit proliferation of keloid
fi broblasts and their collagen synthesis
Manipulation Physically bending joint to break scar
tissue
SOME CURRENT TREATMENTS
Photo credit: Musculoskeletal Network
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Reduces inflammatory hormones in body
Generally given to patients in strong doses after surgery to reduce inflammation/trauma and restore joint mobility
Average dose 200mg – 1200mg
VARIABLEADVIL
Photo credit: Thisthatbynat
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Mouse derived fibroblastic cell line
Standard line used to simulate human fibroblasts
Cells proliferate extremely rapidly, but growth stops when cell-to-cell contacts are formed
Widely used cell line in research
Biologically immortalized cell line
3T3 CELLS
Photo credit: National Institute of Health
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To examine the effects of Advil on 3T3 cell proliferation, survivorship, and regeneration
PURPOSE
Photo credit: Advil.com
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Null HypothesisThe addition of Advil (Ibuprofen) will not affect the proliferation, survivorship, and regeneration of 3T3 cells
Alternate HypothesisThe addition of Advil (Ibuprofen) will significantly reduce the proliferation, survivorship, and regeneration of 3T3 cells
HYPOTHESES
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Cryotank One 75mm2 tissue
culture treated fl asks
Six 25 mm2 tissue culture treated fl asks
10% fetal bovine serum
3T3 Cell Line Trypsin-EDTA Pen/strep Macropipette +
sterile macropipette Tips (1 mL, 5 mL, 10, mL, 20 mL)
Micropipettes + sterile tips
DMEM media (4 mM L-glutamine,
4500 mg/L glucose, 1 mM sodium pyruvate, and 1500 mg/L sodium bicarbonate + [ 10% fetal bovine serum for complete])
Incubator Aspirating Vacuum
Line Nikon Inverted
Compound Optical Scope
Laminar Flow Hood Laminar Flow Hood
UV Sterilizing Lamp Labeling Tape Sterile PBS Ethanol (70% and
100%)
Distilled water Nikon Inverted
Microscope Aspirating Vacuum
Line Hemocytometer Permanent marker 24 well plate Test tube rack Sterile Filter Lint wipes Advil Capsules
MATERIALS
Photo credit: New York Microscope Company
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Liquified five 200mg capsules of Advil – about 1 gram total
X represents the average dose of Advil taken in a given day
= X100X stock solution of Advil was made and
purified
PROCEDURE: PREPARING VARIABLE STOCK
Photo credit: Advil.net
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A 1 mL sample of 3T3 cells from a Cryotank was used to inoculate 30 mL of 10% serum DMEM media in a 75mm2 culture flask.
The media was replaced with 15 mL of fresh media to remove cryo-freezing fluid and incubated (37° C, 5% CO2) for 2 days until a cell density of approximately 106 to 2x106 cells/mL was reached.
The culture was passed into 6 fl asks in preparation for experiment and incubated for 2 days at 37° C, 5% CO2.
PROCEDURE: PREPARING THE CELLS
Photo credit: BioResource
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Seeded 15 fl asks with 3T3 cells from the original flasks in 5mL of 10% DMEM media each
Allowed cells to incubate in CO2 incubator overnight and adhere to bottom of flask
Allowed fl asks to proliferate in incubator overnight
PROCEDURE: PROLIFERATION
Control group:
• 5 flasks
Low concentration of variable group:• 5 flasks• Removed
5μL media• Added 5μL
variable
High concentration of variable group:• 5 flasks• Removed
50μL media• Added
50μL variable
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Next day, trypsinized cells and performed cell counts on the cell suspension Rinsed with 1mL of trypsin, pipetted out Added 1mL trypsin, incubate for 5 minutes Slap flask and confirm with microscope that cells are no longer
adhered to bottom of flask Quenched reaction with 5mL media. Re-added variable. Re-suspended cells with 1mL trypsin wash before taking counts
using pipetteLoaded hemocytometer with 25uL from fl askTook 8 counts per fl askCounted cells in fi eld of view of hemocytometer under
Nikon inverted microscope and multiplied count by 10 3 for total cells/mL
Repeated on Day 3
PROCEDURE: PROLIFERATION (CONTINUED)
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Seeded 15 wells: 1mL of 3T3 cell suspension in 10% DMEM media Allowed cells to proliferate until reached 80%
confluenceMade scratch in all plates
WellScratch
Kept 5 control wellsTook images of plates with Nikon Inverted
Microscope Day 1, Day 3 and Day 5 of scratchCompared regeneration over scratch on each well
PROCEDURE: REGENERATION
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Fixed and stained each plate after imagingRemoved media1mL PBS Wash1mL Ethanol Wash for 2 minutesAdded 0.5mL of Toluidine Blue StainRemoved Stain1mL PBS Wash
Compared regeneration over scratch on each well and re-imaged on Day 1, Day 3, and Day 5
PROCEDURE: REGENERATION (CONTINUED)
Photo credit: Shutterstock.com
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PROLIFERATION RESULTS
Control Low High0
5
10
15
20
25
30
Proliferation Cell Counts
Day 1Day 3
Concentration of VariableCell C
ou
nts
(in
th
ou
san
ds)
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Day 1 p-value: 2.16E-07
Day 3 p-value: 0.000259
PROLIFERATION RESULTS (CONTINUED)
ANOVA
Con-trol
Low High05
1015202530
Proliferation Cell Counts
Day 1Day 3
Concentration of VariableC
ell C
ou
nts
(in
th
ou
san
ds)
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PROLIFERATION RESULTS (CONTINUED)
DUNNETT’S TEST
T-Value
Difference of Average of Experimental Group and Average of Control Group
Square Root of two times the MS Value divide by the number of replicates
Concentration
T-Value T-Critical Significance
Low – 0.1X 6.63 2.42 Yes
High - X 1.64 2.42 NoConcentration
T-Value T-Critical Significance
Low – 0.1X 2.12 2.42 No
High - X 2.54 2.42 Yes
Day 1
Day 3
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REGENERATION RESULTSDAY 1
Control Group
Low Concentration Group
High Concentration Group
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REGENERATION RESULTS (CONTINUED)DAY 3 CONTROL GROUP
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REGENERATION RESULTS (CONTINUED)
DAY 3 LOW CONCENTRATION OF VARIABLE
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REGENERATION RESULTS (CONTINUED)
DAY 3 HIGH CONCENTRATION OF VARIABLE
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REGENERATION RESULTS (CONTINUED)DAY 5 CONTROL GROUP
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REGENERATION RESULTS (CONTINUED)
DAY 5 LOW CONCENTRATION OF VARIABLE
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REGENERATION RESULTS (CONTINUED)
DAY 5 HIGH CONCENTRATION OF VARIABLE
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ProliferationAdvil significantly reduced 3T3 cell growth by
Day 3 of the High Concentration and significantly increased proliferation for the Low Concentration on Day 1. The High Concentration on Day 1 and the Low Concentration on Day 3 both appeared to have no significant effect when compared to the control.
RegenerationAdvil appeared to have little eff ect on 3T3
cell regeneration based on qualitative analysis of images
CONCLUSION
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LimitationsTwo concentrations of variable usedTwo days of cell counting Cell counts have small, inherent errorsRegeneration analysis was qualitative
ExtensionsWider range of variable concentrationsEarlier exposure to test eff ects on cell attachmentCount cells using time lapse imagingExplore synergistic eff ects of Advil with other
drugs
LIMITATIONS AND EXTENSIONS
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Mr. Mark KrotecPittsburgh Tissue Engineering InitiativeConrad M. Zapanta, Ph.D. Biomedical Engineering
Laboratory, Carnegie Mellon University
"Hypertrophic Scarring and Keloids." Medscape . N.p., 2013. Web. 25 Jan. 2013. <http://emedicine.medscape.com/>.
"Keloids & Hypertrophic Scars." DermNet NZ . N.p., n.d. Web. 25Jan. 2013. <http://www.dermnetnz.org/>.
"Keloid Scars." Schweiger Dermatology . N.p., n.d. Web. 25 Jan.2013. <http://www.nyccosmeticdermatology.com/>.
Knapp, Daniels, and Kaplan. "Pathologic Scar Formation." National Center for Biotechnology Information . U.S. National Library of Medicine, Jan. 1977.Web. 25 Jan. 2013. <http://www.ncbi.nlm.nih.gov/>.
"Scar Tissue Formation." Breastcancer.org . Breastcancer.org, 17Sept. 2012. Web. 25 Jan. 2013.
http://www.breastcancer.org/>.
ACKNOWLEDGMENTS AND REFERENCES