retinal regeneration in larval zebrafish...retinal regeneration in larval zebrafish noah wille 1 ,...

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Introduction Approximately 3 million people over the age of 40 suffer from glaucoma, a blinding disease. By 2050, that number will rise to 6 million. 1 This disorder, along with age-related macular degeneration and retinitis pigmentosa, affect the most important part of the eye, the retina. Presently, there are no known cures for these diseases. 2 The retina possesses a similar structure in all vertebrates, although cold blooded vertebrates are able to regenerate the retina whereas warm blooded mammals such as humans cannot. 3 Understanding how this process occurs could lead to cures for retinal degenerative diseases. Zebrafish provide a valuable model to study these diseases due to several factors such as large clutch size, transparency for the first few days of life, and quick development. 4 Zebrafish retinal proliferation occurs at two locations. The CMZ is the site of ongoing proliferation during development and through adulthood. 5 The INL, however, contains specialized cells known as Müller glia. These cells are thought to de- differentiate and act as neural progenitors to replace all of the cell types of the retina after injury(see figure 1A). 5 By studying larval zebrafish regeneration, cells may be observed as they migrate and differentiate. In order to study repair responses using larval zebrafish, it must be confirmed that the mechanism for regeneration is the same as observed in adult fish. Experimental Q uestions When do retinal cells respond to an injury in larval zebrafish? Which cell types are induced to proliferate following injury? Methods & Materials Zebrafish Preparation Tuba1a:GFP transgenic zebrafish were bred with WT zebrafish for study. At 3 dpf the fish were anaesthetized by being placed in a tricaine solution. (500mg/L) A small probe was used to pierce the top part of the fish’s right eye. Fish were then transferred to a 24-well plate containing a 0.5x penicillin and streptomycin solution. Immunohistochemistry- Zebrafish were fixed at 6, 24, and 48 hpl in 4% paraformaldehyde and cryosectioned Incubated with blocking buffer PBS-T, 10% BSA, and 1% normal donkey serum 0 dpl tissue sections were labeled using Rabbit anti-PH3 primary antibodies. 1 dpl and 2 dpl tissue sections were labeled using Rat anti-BrdU and Rabbit anti-GFP primary antibodies. Tissues were labeled with Donkey anti-Rabbit Cy3, Donkey anti-Rabbit AF488, and Donkey anti-Rat Cy3 secondary antibodies and DAPI. Imaging and Analysis Imaging was performed using a fluorescence microscope (Nikon Microphot FXA, Tokyo, Japan), equipped with a Retiga 2000R digital camera and Zeiss LSM700 Confocal microscope. Images were captured using QCapture software, colorized with Photoshop, and analyzed using ImageJ Data was graphed using ANOVA and Sidak’s Multiple comparisons test Conclusions Proliferation in the INL increases from time of injury until at least 2dpl. Müller glia activation begins at 2dpl. Proliferation of the Müller glia is minimal at 1dpl. At 2dpl most Müller glia proliferate. More proliferation occurs in the lesioned eyes than the left eyes at 2dpl. The mechanism for retinal regeneration appears to be the same in both adult and larval fish Future Directions Use of live imaging on larval zebrafish would be beneficial to see migrating cells and neural progenitors. Study progeny of the neural progenitors and migration of those cells Use of a larger sample size for quantification purposes References 1 (Learn About Glaucoma. (n.d.). Retrieved July 20, 2017, from https://nei.nih.gov/nehep/programs/glaucoma/learn-about)) 2 Facts About Age-Related Macular Degeneration. (2015, September 01). Retrieved July 21, 2017, from https://nei.nih.gov/health/maculardegen/armd_facts 3 Than-Trong, E., & Bally-Cuif, L. (2015).. Glia, 63(8), 1406-1428. doi:10.1002/glia.22856 4 Kimmel, C. B., Ballard, W. W., Kimmel, S. R., Ullmann, B., & Schilling, T. F. (1995). Developmental Dynamics,203(3), 253-310. doi:10.1002/aja.1002030302 5 Wilson, S. G., Wen, W., Pillai-Kastoori, L., & Morris, A. C. (2016). Experimental Eye Research, 145, 75-87. doi:10.1016/j.exer.2015.11.002 Retinal Regeneration in L arval Zebrafish Noah Wille 1 , Alex Conyers 2 , Alison Nevin 3 , Elizabeth Sandquist 4 , Jeffrey Essner 4 , Donald Sakaguchi 4 1 North Polk High School, 2 Waterloo West High School, 3 University of Northwestern-St Paul, 4 Genetics, Development, and Cell Biology, Iowa State University Results Fig. 2 At 0dpl there is no proliferation in the INL and no activated Müller glia. The injury site is visible at 0 days post lesion as marked by the arrow. Red=PH3, Blue=DAPI, Green= Tuba1. IHC performed by Anna Zmich. Fig. 3 At 1dpl Müller glia are activated with very little proliferation. Red=BrdU, Blue=DAPI, Green= Tuba1 Fig. 4 At 2dpl many Müller glia are activated and proliferating. A) 20X image of lesioned eye, B) 40x confocal image of proliferating Müller glia. Red=BrdU, Blue=DAPI, Green= Tuba1 Discussion Fig. 5 Quantification of Müller Glia activation and labeling for proliferation. Graph A shows no significant difference between the amount of GFP+ cells in either time point or either eye. Graph B shows no significant difference between the amount of GFP+ cells that are co-labeled with BrdU between 1dpl and 2dpl. Graph C shows a significant difference between both the lesioned eyes (1dpl and 2 dpl) and the lesion and control eyes of the 2dpl fish. N=2-3 Acknowledgements A big thank you to Adah Leshem, Jennifer Lillo, and Maureen Griffin and anyone who helped to organize the YES program. Thank you to the McGrail and Essner labs for providing the Zebrafish and Antibodies used in our lab. Thanks to Anna Zmich for the images and data for our poster. Thanks to all of those in the lab who helped support me throughout my experience. Thanks to my parents Jason and Suzanne for always being there to support me. And finally, thanks to my high school Chemistry and Biology teachers; Kim Kult, and Rosalie Eimers, for giving me the experience to participate in the YES program. 1 dpl 2 dpl 0 50 100 % of BrdU+ that are GFP+ 1 dpl 2 dpl 0 5 10 15 # of GFP+ cells / Section 1 dpl 2 dpl 0 5 10 15 Ave # of BrdU+ / Section *** *** Control Eye Lesion Eye Fig. 1 A) Image of the lesion site of the eye marked by an arrow. B) Diagram of a zebrafish retina. A B A C B A B

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Page 1: Retinal Regeneration in Larval Zebrafish...Retinal Regeneration in Larval Zebrafish Noah Wille 1 , Alex Conyers 2 , Alison Nevin 3 , Elizabeth Sandquist 4 , Jeffrey Essner 4 , Donald

Introduction

Approximately3millionpeopleovertheageof40sufferfromglaucoma,ablindingdisease.By2050,thatnumberwillriseto6million.1 Thisdisorder,alongwithage-relatedmaculardegenerationandretinitispigmentosa,affectthemostimportantpartoftheeye,theretina.Presently,therearenoknowncuresforthesediseases.2

Theretinapossessesasimilarstructureinallvertebrates,althoughcoldbloodedvertebratesareabletoregeneratetheretinawhereaswarmbloodedmammalssuchashumanscannot.3 Understandinghowthisprocessoccurscouldleadtocuresforretinaldegenerativediseases.Zebrafishprovideavaluablemodeltostudythesediseasesduetoseveralfactorssuchaslargeclutchsize,transparencyforthefirstfewdaysoflife,andquickdevelopment.4

Zebrafishretinalproliferationoccursattwolocations.TheCMZisthesiteofongoingproliferationduringdevelopmentandthroughadulthood.5 TheINL,however,containsspecializedcellsknownasMüllerglia.Thesecellsarethoughttode-differentiateandactasneuralprogenitorstoreplaceallofthecelltypesoftheretinaafterinjury(seefigure1A).5 Bystudyinglarvalzebrafishregeneration,cellsmaybeobservedastheymigrateanddifferentiate.Inordertostudyrepairresponsesusinglarvalzebrafish,itmustbeconfirmedthatthemechanismforregenerationisthesameasobservedinadultfish.

ExperimentalQuestionsWhendoretinalcellsrespondtoaninjuryinlarvalzebrafish?Whichcelltypesareinducedtoproliferatefollowinginjury?

Methods&MaterialsZebrafishPreparation• Tuba1a:GFPtransgeniczebrafishwerebredwithWTzebrafishforstudy.• At3dpf thefishwereanaesthetizedbybeingplacedinatricaine solution.(500mg/L)• Asmallprobewasusedtopiercethetoppartofthefish’srighteye.• Fishwerethentransferredtoa24-wellplatecontaininga0.5xpenicillinand

streptomycinsolution.Immunohistochemistry-• Zebrafishwerefixedat6,24,and48hpl in4%paraformaldehydeandcryosectioned• IncubatedwithblockingbufferPBS-T,10%BSA,and1%normaldonkeyserum• 0dpl tissuesectionswerelabeledusingRabbitanti-PH3primaryantibodies.• 1dpl and2dpl tissuesectionswerelabeledusingRatanti-BrdU andRabbitanti-GFP

primaryantibodies.• TissueswerelabeledwithDonkeyanti-RabbitCy3,Donkeyanti-RabbitAF488,and

Donkeyanti-RatCy3secondaryantibodiesandDAPI.ImagingandAnalysis• Imagingwasperformedusingafluorescencemicroscope(NikonMicrophot FXA,

Tokyo,Japan),equippedwithaRetiga 2000RdigitalcameraandZeissLSM700Confocalmicroscope.

• ImageswerecapturedusingQCapture software,colorizedwithPhotoshop,andanalyzedusingImageJ

• DatawasgraphedusingANOVAandSidak’s Multiplecomparisonstest

Conclusions• ProliferationintheINLincreasesfromtime

ofinjuryuntilatleast2dpl.

• Müllergliaactivationbeginsat2dpl.

• ProliferationoftheMüllergliaisminimalat1dpl.At2dplmostMüllergliaproliferate.

• Moreproliferationoccursinthelesionedeyesthanthelefteyesat2dpl.

• Themechanismforretinalregenerationappearstobethesameinbothadultandlarvalfish

FutureDirections• Useofliveimagingonlarvalzebrafish

wouldbebeneficialtoseemigratingcellsandneuralprogenitors.

• Studyprogenyoftheneuralprogenitorsandmigrationofthosecells

• Useofalargersamplesizeforquantification purposes

References1(LearnAboutGlaucoma.(n.d.).RetrievedJuly20,2017,fromhttps://nei.nih.gov/nehep/programs/glaucoma/learn-about))2FactsAboutAge-RelatedMacularDegeneration.(2015,September01).RetrievedJuly21,2017,fromhttps://nei.nih.gov/health/maculardegen/armd_facts3Than-Trong,E.,&Bally-Cuif,L.(2015)..Glia, 63(8),1406-1428.doi:10.1002/glia.228564Kimmel,C.B.,Ballard,W.W.,Kimmel,S.R.,Ullmann,B.,&Schilling,T.F.(1995). DevelopmentalDynamics,203(3),253-310.doi:10.1002/aja.10020303025Wilson,S.G.,Wen,W.,Pillai-Kastoori,L.,&Morris,A.C.(2016). ExperimentalEyeResearch, 145,75-87.doi:10.1016/j.exer.2015.11.002

RetinalRegenerationinLarvalZebrafishNoahWille1,AlexConyers2,AlisonNevin3,ElizabethSandquist4,JeffreyEssner4,DonaldSakaguchi4

1NorthPolkHighSchool,2WaterlooWestHighSchool,3UniversityofNorthwestern-StPaul,4Genetics,Development,andCellBiology,IowaStateUniversity

Results

Fig.2At0dplthereisnoproliferationintheINLandnoactivatedMüllerglia.Theinjurysiteisvisibleat0dayspostlesionasmarkedbythearrow.Red=PH3,Blue=DAPI,Green=Tuba1.IHCperformedbyAnnaZmich.

Fig.3At1dplMüllergliaareactivatedwithverylittleproliferation.Red=BrdU,Blue=DAPI,Green=Tuba1

Fig.4At2dplmanyMüllergliaareactivatedandproliferating.A)20Ximageoflesionedeye,B)40xconfocalimageofproliferatingMüllerglia.Red=BrdU,Blue=DAPI,Green=Tuba1

Discussion

Fig.5QuantificationofMüllerGliaactivationandlabelingforproliferation.GraphAshowsnosignificantdifferencebetweentheamountofGFP+cellsineithertimepointoreithereye.GraphBshowsnosignificantdifferencebetweentheamountofGFP+cellsthatareco-labeledwithBrdU between1dpland2dpl.GraphCshowsasignificantdifferencebetweenboththelesionedeyes(1dpland2dpl)andthelesionandcontroleyesofthe2dplfish.N=2-3

AcknowledgementsAbigthankyoutoAdahLeshem,JenniferLillo,andMaureenGriffinandanyonewhohelpedtoorganizetheYESprogram.ThankyoutotheMcGrail andEssner labsforprovidingtheZebrafishandAntibodiesusedinourlab.ThankstoAnnaZmich fortheimagesanddataforourposter.Thankstoallofthoseinthelabwhohelpedsupportmethroughoutmyexperience.ThankstomyparentsJasonandSuzanneforalwaysbeingtheretosupportme.Andfinally,thankstomyhighschoolChemistryandBiologyteachers;KimKult,andRosalieEimers,forgivingmetheexperiencetoparticipateintheYESprogram.

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