Wnt signaling in zebrafish fin regeneration : chemical biology using a GSK3β inhibitor

dc.contributor.advisorMarrs, James
dc.contributor.authorCurtis, Courtney L.
dc.contributor.otherSkalnik, David Gordon
dc.contributor.otherLi, Jiliang
dc.contributor.otherAtkinson, Simon
dc.date.accessioned2014-07-31T20:06:19Z
dc.date.available2014-07-31T20:06:19Z
dc.date.issued2014-07-31
dc.degree.date2013en_US
dc.degree.disciplineDepartment of Biologyen
dc.degree.grantorPurdue Universityen_US
dc.degree.levelM.S.en_US
dc.descriptionIndiana University-Purdue University Indianapolis (IUPUI)en_US
dc.description.abstractBone growth can be impaired due to disease, such as osteoporosis. Currently, intermittent parathyroid hormone (PTH) treatment is the only approved therapy in the United States for anabolic bone growth in osteoporosis patients. The anabolic effects of PTH treatment are due, at least in part, to modulation of the Wnt/β-catenin pathway. Activation of the Wnt/ β-catenin pathway using a small molecule inhibitor of GSK3β was previously shown to increase markers of bone formation in vitro. Our study utilized a zebrafish model system to study Wnt activated fin regeneration and bone growth. Wnt signaling is the first genetically identified step in fin regeneration, and bony rays are the main structure in zebrafish fins. Thus, zebrafish fin regeneration may be a useful model to study Wnt signaling mediated bone growth. Fin regeneration experiments were conducted using various concentrations of a GSK3β inhibitor compound, LSN 2105786, for different treatment periods and regenerative outgrowth was measured at 4 and 7 days post amputation. Experiments revealed continuous low concentration (4-5 nM) treatment to be most effective at increasing regeneration. Higher concentrations inhibited fin growth, perhaps by excessive stimulation of differentiation programs. In situ hybridization experiments were performed to examine effects of GSK3β inhibitor on Wnt responsive gene expression. Experiments showed temporal and spatial changes on individual gene markers following GSK3β inhibitor treatment. Additionally, confocal microscopy and immunofluorescence labeling data indicated that the Wnt signaling intracellular signal transducer, β-catenin, accumulates throughout GSK3β inhibitor treated tissues. Finally, experiments revealed increased cell proliferation in fin regenerates following LSN 2105786 treatment. Together, these data indicate that bone growth in zebrafish fin regeneration is improved by activating Wnt signaling. Zebrafish Wnt signaling experiments provide a good model to study bone growth and bone repair mechanisms, and may provide an efficient drug discovery platform.en_US
dc.identifier.urihttps://hdl.handle.net/1805/4835
dc.identifier.urihttp://dx.doi.org/10.7912/C2/2156
dc.language.isoen_USen_US
dc.subjectzebrafish, Wnt, regeneration, boneen_US
dc.subject.lcshBones -- Growthen_US
dc.subject.lcshBone regenerationen_US
dc.subject.lcshZebra danio -- Physiologyen_US
dc.subject.lcshWnt genesen_US
dc.subject.lcshGenetic markersen_US
dc.subject.lcshWnt proteinsen_US
dc.subject.lcshRegeneration (Biology)en_US
dc.subject.lcshGene expression -- Methodologyen_US
dc.subject.lcshFish as laboratory animals -- Researchen_US
dc.subject.lcshFins (Anatomy)en_US
dc.subject.lcshIn situ hybridizationen_US
dc.subject.lcshCellular signal transductionen_US
dc.subject.lcshCell differentiationen_US
dc.subject.lcshBones -- Diseasesen_US
dc.subject.lcshTissue engineeringen_US
dc.subject.lcshOsteoporosisen_US
dc.titleWnt signaling in zebrafish fin regeneration : chemical biology using a GSK3β inhibitoren_US
dc.typeThesisen
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Courtney Curtis Final Thesis.pdf
Size:
1.4 MB
Format:
Adobe Portable Document Format
Description:
Thesis
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.88 KB
Format:
Item-specific license agreed upon to submission
Description: