Investigating the role of EphAl ephrin-a signalling during trigeminal ganglion axon guidance

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Investigating the role of EphAl ephrin-a signalling during trigeminal ganglion axon guidance A thesis submitted for the degree of Doctor of Philosophy Molecular and Biomedical Science (Discipline of Genetics), University of Adelaide By Chathurani S. Jayasena, B.Sc. (Hons.) December 2004

Table of Contents Table of Contents... i List of Figures and Tables... vi Declaration... ix Abstract... xi Acknowledgements... xiii Personal bibliography... xv Chapter 1: Introduction......... 1 1.1 Axon guidance...................... 3...................................................................... 1.1.1 Types of guidance cues........ 4 1.1.2 Growth cone machinery and dynamics. 1.1.2.1 Structure of the growth cone................................................................ 7................................................ 7............................. 1.1.2.2 Guidance cues and the growth cone cytoskeleton.. 8 1.1.2.3 Rho GTPases and axon guidance. 1.1.2.4 Overview...................................................... 8........................................................................................... 8 1.2 The trigeminal ganglion- a model system?...... 11 1.2.1 Morphology of the trigeminal ganglion. 1.2.2 Dual embryonic origin of the trigeminal ganglion.. 1.2.2.1 Neural crest.. 1.2.2.2 Epidermal neurogenic placode................................................... 11.................................. 12...................................................................................... 12......................................................... 12 1.2.2.3 Requirement for both neural crest and placode components............. 17 1.3 The trigeminal ganglion and axon guidance...... 18 1.3.1 The placode and axon pathfinding. 1.3.2 Trigeminal ganglion guidance cues............................................................ 18...................................................... 19................................. 1.3.3 Trigeminal ganglion lobe specific guidance cues?.. 20 1.4 Ephs and ephrins as candidates...... 25 1.4.1 Eph receptor structure. 1.4.2 Signalling mechanisms......................... 1.4.2.1 Eph kinase "forward" signalling................................................... 26............................................................................ 26......................................................... 31................... 1.4.2.2 ephrin "reverse" / Eph-kinase independent signalling.... 31 1.4.2.3 Adhesive/ attractive and repulsive Eph/ ephrin interactions............... 37 1.4.2.4 Modulation of Eph signalling by co-expressed ephrins...................... 47 1.4.3 Examples of Eph/ ephrin interactions during development of the nervous system...................................................................................................... 48 1.4.3.1 Axon pathfinding- roles during optic nerve formation and during................................................. commissural axon tract formation.............. 48 1.4.3.2 Axon fasciculation......................... 51................................................ 1.4.3.3 Roles during anterior-posterior retinotectal topographic mapping...... 55 1.5 Summary: EphAs and ephrinas- possible candidates for lobe specific trigeminal ganglion axon guidance?.................. 65 1.5.1 Project Aims.......................................................................................... 66

Chapter 2: Materials and methods..................................................... 71 2.1 Abbreviations............,... 73 2.2 Materials................................................... 73 2.1.1 Chemicals......... 73 2.1.2 Enzymes... 74 2.1.3 DNA plasmids................. 74 2.1.3 RNA in situ hybridisation probes...... 74 2.1.4 Antibodies/ Fc-fusion chimeras...... 74 2.1.6 Chick embryos......... 75 2.3 Methods........................... 76 2.3.1 Chick embryos... 76 2.3.2 Bacteriological techniques... 76 2.3.2.1 Bacterial culture... 76 2.3.2.2 Bacterial stains...... 76 2.3.2.3 Preparation of electrocompetent DH5a cells... 76 2.3.2.4 Transformation of DH5a cells... 77 2.3.2.5 Plasmid screening for transformed recombinant clones- cracking... 77 2.3.2.6 Plasmid screening for transformed recombinant clones- alkaline lysis....................................................................................................................... 78 2.3.3 DNA techniques...................................... 79 2.3.3.1 Plasmid preparations................ 79 2.3.3.2 Electrophoretic separation of DNA...... 79 2.3.3.3 DNA modifying enzyme reactions... 79 2.3.3.4 Preparation of DNA for ligations... 79 2.3.3.5 Cleanup of ligation products for transformation into DH5a cells... 79 2.3.3.6 Cleanup of cdna for real-time PCR... 80 2.3.3.7 Real-time PCR... 80 2.3.3.8 Automated DNA sequencing... 81 2.3.4 RNA techniques........ 81 2.3.4.1 Total RNA extraction from trigeminal ganglion lobes...... 81 2.3.4.2 Reverse transcription... "."."... '" '"... 82 2.3.4.3 Transcription of RNA probes for in situ hybridisation... 83 2.3.5 Embryo/ Trigeminal ganglion harvesting... 84 2.3.5.2 Chick embryos... 84 2.3.5.1 Trigeminal ganglia and trigeminal ganglion lobes... 84 2.3.6 Tissue sectioning... 85 2.3.6.1 Vibratome sections...... 85 2.3.6.2 Cryostat sections... 85 2.3."1 Whole-mount RNA in situ hybridisation......... 85 2.3.8 Antibody/ Fc-Fusion techniques............. 86 2.3.8.1 Antibody staining......... :... 86 2.3.8.2 Eph and ephrin-fc staining......... 87 2.3.8.3 Microscopy...... "... '"... 87 2.3.8.4 Whole-mount EphA3 trigeminal ganglion intensity readings... 88 2.3.8.5 EphA3 growth cone intensity readings... '... '"... 88 2.3.9 Trigeminal ganglion culture...... 88 2.3.9.1 Antibody/ Fc-fusion staining of cultures... 89 2.3.10 In vitro assays, analysis and statistics... 89 2.3.10.1 Substratum choice assay and uniform substrate assay... 89 2.3.10.2 Analysis of neurite parameters. Rq

2.3.10.3 Analysis of growth cone parameters... 89 2.3.10.4 Data processing and statistics... 90 Chapter 3: EphA and ephrin-a expression analysis in the trigeminal ganglion peripheral targets.......... 91 3.1 Introduction.................. 92 3.2 Results...................... 97 3.2.1 EphA- and ephrin-a-fc staining during trigeminal ganglion axon guidance.......................................................................................................................... 97 3.2.1.1 Complementary and overlapping EphA and ephrin-a expression in the trigeminal ganglion target fields....... 97 3.2.1.2 Differential Eph/ ephrin-a expression in the trigeminal ganglion... 98 3.2.2 EphA expression in the trigeminal ganglion peripheral target fields... 103 3.2.2.1 EphA3 is expressed in the ophthalmic process and is expressed in the trigeminal ganglion... 103 3.2.2.2 EphA4 is expressed in the ophthalmic process during ophthalmic trigeminal ganglion axon growth at stage 13... 109 3.2.2.3 EphA5, EphA7 and EphA9 are not candidate guidance cues for trigeminal ganglion axons... 112 3.2.3 ephrin-a expression in the trigeminal ganglion peripheral target fields... 117 3.2.3.1 ephrin-a2 is expressed in the maxillary and mandibular processes. 117 3.2.3.2 ephrin-a5 is expressed in the maxillary and mandibular processes and in the trigeminal ganglion... 119 3.3 Summary and discussion.................. 125 3.3.1 Complementary expression of EphA3/A4 and ephrin-a2/a5 at stages 13 and 15 when trigeminal axons are pathfinding... 125 3.3.2 Similar EphAi ephrin-a expression patterns are observed for mouse and chick...... 126 3.3.3 Conclusion... 127 Chapter 4: EphA and ephrin-a expression in the trigeminal ganglion... 131 4.1 Introduction................... 132 4.2 Results.................. 133 4.2.1 EphA4, A5, A7, A9 and ephrin-a2 are not expressed in the trigeminal ganglion... 133 4.2.2 EphA3 is differentially expressed in the trigeminal ganglion... 133 4.2.2.1 EphA3 localises to the ophthalmic placode and trigeminal ganglion neurons at stages 13 and 15... 133 4.2.2.2 The ophthalmic lobe expresses high levels EphA3 transcript and protein at stage 20... 135 4.2.3 ephrin-a5 is not differentially expressed in the trigeminal ganglion... 149 4.2.3.1 ephrin-a5 localises to the ophthalmic placode and trigeminal ganglion neurons at stages 13 and 15... 149 4.2.3.2 The trigeminal ganglion at stage 20 non-differentially expresses ephrin-a5... 157 4.2.4 Differential co-expression of EphA3 and ephrin-a5 in the maxillomandibular lobe... 157 4.3 Summary and discussion.............. 161

4.3.1 Insights into intra-ganglionic EphA3/ ephrin-a5 interactions...... 161 4.3.2 EphA3 is differentially expressed within the ganglion... 162 4.3.3 Significance of EphA3 and ephrin-a5 expression in the placode during axon guidance......... 162 4.3.4 Conclusion... 163 Chapter 5: In vitro analysis of trigeminal ganglion EphA3 forward signalling... 5.1 Introduction.......... 169........................... 170 5.2 Results.................. 175 5.2.1 Trigeminal ganglion explant axons express EphA(s)... 175 5.2.2 A sub-population of trigeminal ganglion axons are sensitive to substratum bound ephrin-a5... 175 5.2.3 Trigeminal ganglion ophthalmic lobe axons are sensitive to substratumbound ephrin-a5...... 179 5.2.4 Axons and growth cones from Ophthalmic and maxillomandibular lobe explants express EphA3... 184 5.3 Summary and discussion................. 188 5.3.1 Ephrin-A5 as a guidance cue... 188 5.3.2 Ephrin-A5-Fc and the differential guidance of ophthalmic versus maxillomandibular lobe axons... '.............................. 189 5.3.3 EphA3 expressing maxillomandibular axons are not responsive to ephrin- A5-Fc............................................................................................................... 193 5.3.4 Conclusion... 195 Chapter 6: In vitro analysis of trigeminal ganglion ephrin reverse signalling.................. 197 6.1 Introduction............................................. 198 6.2 Results.......................................... 199 6.2.1 Trigeminal ganglion explants express ephrin-a5... 199 6.2.2 Trigeminal ganglion axons are not responsive to EphA4-Fc... 200 6.2.3 EphA4-Fc does not promote neurite growth... 203 6.2.4 EphA4-Fc influences growth cone morphology... 207 6.2.5 Trigeminal ganglion explants express ephrin-b2... 209 6.3 Summary and discussion........................................ 211 6.3.1 In vivo EphA3/ A4 expression patterns correlate with in vitro substratum choice assay results...... 211 6.3.2 ephrin-a5 reverse signalling and the growth cone... 212 6.3.3 Is there convergence of ephrin-a5 and ephrin-b2 reverse signalling?... 214 6.3.4 Is EphA4 Fc permissive or adhesive to trigeminal ganglion growth cones/ axons?... 215 6.4.5 EphAs are pathfinding cues to trigeminal ganglion growth cones?... 215 6.3.6 Conclusion...... 217 Chapter 7: General discussion and future directions...... 221 7.1 Similarities and differences between trigeminal ganglion lobe guidance and motor axon hindlimb innervation..... 7.2 Suggested model of trigeminal ganglion axon guidance............................. 227....... 230

7.3 In vivo examination of EphAl ephrin-a interactions during trigeminal ganglion axon guidance... 233 7.3.1 Elucidating in vivo trigeminal axonal-epha3 and first branchial arch-ephrin- A2/A5 interactions in the chick embryo... 233 7.3.2 Elucidating in vivo EphA! ephrin-a interactions in the mouse embryo... 234 7.4 In vivo elucidation of guidance cue interactions during trigeminal ganglion axon guidance... 235 7.5 What signals lie downstream of EphA3 activation in trigeminal ganglion axonsl growth cones?... 236 7.6 Other roles for ganglionic EphA31 ephrin-a5 interactions during trigeminal ganglion development?... 237 7.7 Conclusion............ 239 References........... 240

Abstract The ophthalmic, maxillary and mandibular axon branches of the trigeminal ganglion (TG) provide cutaneous sensory innervation to the vertebrate face, and multiple families of guidance cues amalgamate to direct the navigation of these branches. However, target tissue specific guidance cues that discriminately guide the three TG axon branches are unknown. Prior work demonstrated that EphAs and ephrin-as could discriminately direct dorsal versus ventral motor axon projections into the hindlimb. Similarly, do EphA tyrosine kinases and ephrin-a ligands discriminately guide trigeminal ganglion ophthalmic (TGop) lobe versus maxillomandibular (TGmm) axon projections into the chick embryo face? The aims of this work were two-fold: (1) to identify candidate EphA and ephrin-a molecules during TG axon guidance, and (2) to detennine the functional significance of TG axon EphA and ephrin-a signalling in vitro. This study identified EphA3, EphA4, ephrin-a2 and ephrin-a5 at stages 13, IS and 20, as putative guidance cues to TG axons. TG-EphA3 and -ephrin-a5 were identified as putative receptors to guidance cues expressed in the target fields. EphA3 receptor was differentially expressed, with the TGop lobe expressing higher levels compared to the TGmm lobe. However, ephrin-a5 transcript was not differentially expressed between the two ganglion lobes. In a substratum choice in vitro assay, ephrin-as-fc was found to repel approximately 50 % of axons growing from stage 20 whole TG explants. This population of axons was identified to be from the TGop lobe. The in vitro data supports the contention that during facial development there may be trigeminal ganglion lobe specific guidance of TGop in comparison to TGmm peripheral sensory axonal projections to target fields coordinated through EphA3 and ephrin-a2/as repulsive interactions. In vitro, EphA4-Fc caused morphological changes to TG growth cones, which is likely mediated through TG ephrin-as reverse signaling. Furthennore, this study provided in vitro evidence that trigeminal ganglion axons were not responsive to EphA4-Fc, possibly implying that EphAs expressed in the target fields were not repulsive to ganglionic axons during pathfinding. The data suggests that EphN ephrin-a interactions may specifically guide TGop projections into the ophthalmic process similar to lateral motor axon guidance into the hindlimb. For the first time, a model of how EphN ephrin-a interactions and other families of guidance cues may act in concert to guide trigeminal ganglion axons is suggested.