Clare Baker PhD
University
Lecturer
Tel: +44 (0)1223 333789, Fax: +44 (0)1223 333786, E-mail: cvhb1@cam.ac.uk
Neurogenic placodes and the neural crest: development and evolution of the vertebrate head
Neurogenic placodes and the neural crest are two distinct embryonic cell populations that are crucial for the development of the vertebrate head. Together, they give rise to the whole peripheral nervous system, i.e., all the sensory receptor cells, neurons (nerve cells) and glial cells (nerve-support cells) located outside the brain and spinal cord. Neural crest cells also build much of the craniofacial skeleton.
Neurogenic placodes (paired patches of thickened surface ectoderm in the embryonic head) give rise to the paired peripheral sense organs: the olfactory placodes form the olfactory receptor neurons in the nose that detect smells; the otic placodes form the inner ears, in which fluid movement (due to sound waves or head motion) stimulates mechanosensory hair cells, giving us our senses of hearing and balance; and a series of lateral line placodes forms the lateral line system of fish and aquatic-stage amphibians, in which mechanosensory hair cells (very like those in the inner ear), distributed in lines over the head and flank, detect local water movement for e.g. prey/predator detection and schooling behaviour. Neurogenic placodes also form the hormone-producing cells of the anterior pituitary gland, the eye lenses, and most of the peripheral sensory neurons of the head, collected in discrete cranial sensory ganglia.
Neural crest cells migrate out of the developing brain and spinal cord: they give rise to all the other neurons and all glial cells of the peripheral nervous system, plus a wide variety of other cell types including pigment cells, most of the cartilages and bones of the face and skull, and the dentine-producing cells of teeth.
We are investigating a
broad range of questions relating to
the development of
neurogenic placodes and the neural crest. Current projects
include:
-
the development of olfactory ensheathing
glia
-
the development and evolution of
electroreceptors
-
the role of Pax genes in neurogenic placode
development
-
the development and evolution of the neural
crest-derived
pharyngeal skeleton
Development of olfactory ensheathing glia: Using grafting techniques in chicken embryos and genetic lineage-tracing in mice, we have recently discovered that olfactory ensheathing cells (OECs, which ensheath and protect olfactory nerve fibres) are derived from the neural crest, like all other peripheral glial cells, and not from the olfactory placodes as previously thought (Barraud et al., 2010, Proc. Natl. Acad. Sci. USA). Excitingly, OECs can promote nerve repair when transplanted into the damaged spinal cord, but it has proved difficult to isolate them in large enough numbers from the nose for effective therapy. Neural crest stem cells persist in adult skin and hair follicles, and it is possible to isolate these stem cells and grow them in the lab. The next step is to work out how to turn these stem cells into OECs: to do this, we need to investigate how this process happens normally in the developing embryo. We are currently investigating this question, as well as the role of OECs during the embryonic development of the olfactory system.
Development and evolution of electroreceptors: Land vertebrates, as well as frogs and most modern bony fish, have lost one of the most ancient vertebrate senses, the ability to detect weak electric fields in water, used for finding prey and for orientation. Electroreceptors are modified hair cells, distributed in fields of “ampullary organs” on either side of the lateral lines of mechanosensory hair cells. They are found in all major aquatic vertebrate groups, including jawless fish (lampreys), cartilaginous fish (sharks, rays), primitive bony fish (e.g. sturgeon, paddlefish), and even some amphibians (salamanders). Although the ancestors of teleosts (modern bony fish) lost electroreceptors, so that most of these fish cannot detect electric fields, electroreceptors seem to have been independently "re-invented" at least twice in two different groupsof teleosts, including catfish and "electric fish". (For more information on vertebrate electroreception, see Map Of Life). Very little is known about electroreceptor development. We are investigating the embryological origins of electroreceptors, and the genes underlying their formation, in a wide range of vertebrate groups including shark, paddlefish, salamander and catfish.
Role of Pax genes in neurogenic placode development: Neurogenic placodes are relatively simple, accessible model systems for studying how cells adopt a specific sensory cell fate, since neurons arising from different placodes innervate different targets and transmit different kinds of sensory information. Different members of the Pax family of paired-box transcription factors are expressed in different placodes: Pax6 is required for the development of the olfactory and lens placodes; Pax3 is expressed in the ophthalmic trigeminal placode, while Pax2 is expressed in the epibranchial and otic placodes. We are interested in understanding the role of Pax genes in neurogenic placode development. The chicken embryo is our model system of choice for this work because it is readily accessible for microsurgery and cell-marking techniques, and gene expression can be manipulated both spatially and temporally by targeted in ovo electroporation.
Development and evolution of the neural crest-derived pharyngeal skeleton: Dr Andrew Gillis, a Royal Society Newton International Fellow in the lab, is working on a variety of questions relating to the formation of the neural crest-derived skeleton of the jaws and more posterior pharyngeal arches. For further details, please see his webpage.
Research Team
Dr Perrine Barraud
Jim Blundell (PhD Student)
Umut Dursun (PhD Student)
Dr Andrew Gillis
Dorit Hockman (PhD Student)
Sophie Miller (PhD Student)
Dr Melinda Modrell
Connie Rich (PhD Student)
Adam Hunt (undergraduate research project student)
Former Members of
Research Team
Carolynn Dude (PhD awarded
May 2008), currently a medical student at the University
of Wisconsin, Madison
Dr Kelly Kuan, currently a Molecular & Cell
Biologist at Pfizer UK
Ruth McCole, currently a postdoc with
Prof Ting Wu, Department of
Genetics, Harvard Medical School
Dr Paul O'Neill, currently a RIKEN postdoctoral fellow at the RIKEN Centre
for Developmental Biology, Kobe, Japan
Anastasia Seferiadis (MPhil awarded April 2007), currently a Junior
Researcher in the Department of Biology and Society, Vrije
Universiteit, Amsterdam
Hong Xu (PhD awarded May 2008), currently an R&D
Manager at COFCO Corporation, China
Former
rotation students (Wellcome Trust 4-year PhD Programme in
Developmental Biology)
Philippe Loiseau, Will Mifsud, Vincent Pasque, Maarten Zwart,
Dorit Hockman, Jonathan Lawson, Alexis Hazbun
Former undergraduate research project students
Eleanor Bates, Katie Birley, Jason George, Harry Gibson, Haseeb
Rahman, Luke Tyson, Jiexin Zheng, Rob Walsh, Nicola Xiang, Fern
Adams, Sophie Miller
Nuffied
Undergraduate Research
Bursaries in Science
Summer 2010: Sophie Miller, University of Cambridge
Nuffield
Science Bursary - Schools and Colleges
Summer 2009: Susannah Worster, Hills Road Sixth Form College, Cambridge
Summer 2010: Andrew Gvozdanovic, The Leventhorpe School,
Sawbridgeworth, Herts.
Summer 2011: Danielle Lis, Saffron Walden County High School, Essex
Amgen
Scholars Programme, University of Cambridge
Summer 2011: Patrick Kennedy (University of Oxford)
Main
Collaborators
Professor Marianne Bronner-Fraser, California Institute of
Technology, USA
Dr Alan Burns, UCL Institute of Child Health, London
Dr Marcus Davis, Kennesaw State University, USA
Dr Raj Ladher, RIKEN Centre for Developmental Biology, Kobe, Japan
Dr Sylvie Mazan, Station Biologique, Roscoff, France
Dr Filippo Rijli, Friedrich Miescher Institute for Biomedical
Research, Basel,
Switzerland
Dr Andrea Streit, King's College London
Professor Eric Turner, Seattle Children's Research Institute, USA
Sources of funding: BBSRC, March of Dimes (Basil O'Connor Starter Scholar Award), Isaac Newton Trust, Wellcome Trust
External Teaching: I run the chick embryo module and lecture on the summer Embryology Course for advanced graduate students and postdocs at the Marine Biological Laboratory, Woods Hole, Massachusetts.
Selected Publications:
Sabado, V., Barraud, P., Baker, C. V. H. and Streit, A. (2012) Specification of GnRH-1 neurons by antagonistic FGF and retinoic acid signalling. Dev. Biol. 362: 254-262 (ref.)
Modrell, M. S., Bemis, W. E., Northcutt, R. G., Davis, M. C. and Baker, C. V. H. (2011) Electrosensory ampullary organs are derived from lateral line placodes in bony fishes. Nature Communications 2: 496, DOI:10.1038/ncomms1502) (ref.)
Gillis, J. A.*, Rawlinson, K. A., Bell, J., Lyon, W. S., Baker, C. V. H. and Shubin N. H.* (2011) Holocephalan embryos provide evidence for gill arch appendage reduction and opercular evolution in cartilaginous fishes. Proc. Natl. Acad. Sci. U.S.A. 108: 1507-12 (ref.) *Joint corresponding authors.
Modrell, M. S., Buckley, D. and Baker, C. V. H.* (2011) Molecular analysis of neurogenic placode development in a basal ray-finned fish. Genesis 49: 278-94 (ref.)
Barraud P., Seferiadis A. A., Tyson L. D., Zwart M. F., Szabo-Rogers H. L., Ruhrberg C., Liu K. J., Baker C. V. H.* (2010) Neural crest origin of olfactory ensheathing glia. Proc. Natl. Acad. Sci. U.S.A. 107: 21040-5 (ref.)
Dude, C. M., Kuan, C.-Y. K., Bradshaw, J. R., Greene, N. D. E., Relaix, F., Stark, M. R.*, Baker, C. V. H.* (2009). Activation of Pax3 target genes is necessary but not sufficient for neurogenesis in the ophthalmic trigeminal placode. Dev. Biol. 326: 314-26 (ref.) *Joint corresponding authors
Baker, C. V. H. (2008) The evolution and elaboration of vertebrate neural crest cells. Curr. Op. Gen. Dev. 18: 536-43 (ref.)
Baker, C. V. H., O'Neill, P. and McCole, R. B. (2008) Lateral line, otic and epibranchial placodes: developmental and evolutionary links? J. Exp. Zool. B Mol. Dev. Evol. 310B: 370-383 (ref.)
Xu, H., Dude, C. M. and Baker, C. V. H. (2008) Fine-grained fate maps for the ophthalmic and maxillomandibular trigeminal placodes in the chick embryo. Dev. Biol. 317:174-86 (ref.)
Lassiter, R. N., Dude, C. M., Reynolds, S. B., Winters, N. I., Baker, C. V. H., and Stark, M. R. (2007). Canonical Wnt signaling is required for ophthalmic trigeminal placode cell fate determination and maintenance. Dev. Biol. 308: 392-406 (ref.)
O'Neill, P., McCole, R. B. and Baker, C. V. H. (2007) A molecular analysis of neurogenic placode and cranial sensory ganglion development in the shark, Scyliorhinus canicula. Dev. Biol. 304: 156-181 (ref.)
Baker, C. V. H. and Schlosser, G. (2005) Editorial: the evolutionary origin of neural crest and placodes. J. Exp. Zool. B Mol. Dev. Evol. 304: 269-273 (ref.)
Lee, V. M.,
Bronner-Fraser, M. and Baker, C. V. H. (2005) Restricted
response of mesencephalic
neural crest to sympathetic differentiation
signals in the trunk.
Dev. Biol. 278: 175-192 (ref.)
Baker, C. V. H., Stark, M. R. and Bronner-Fraser, M. (2002). Pax3-expressing
trigeminal placode cells can localize to trunk neural crest sites
but are committed
to a cutaneous sensory neuron fate. Dev.
Biol. 249, 219-236 (ref.)
Baker, C. V. H. and Bronner-Fraser, M. (2001) Vertebrate cranial placodes.
Part I. Embryonic induction. Dev.
Biol. 232: 1-61 (ref.)
Baker, C. V. H. and Bronner-Fraser, M. (2000) Establishing neuronal identity
in vertebrate neurogenic placodes. Development 127:
3045-3056 (ref.)
Baker, C. V. H.*, Stark, M. R.*, Marcelle, C. and Bronner-Fraser, M. (1999)
Competence, specification and induction of Pax-3 in the trigeminal
placode. Development 126:
147-156 (ref.)
*Joint first authors.
Baker, C. V. H., Bronner-Fraser, M., Le Douarin, N. M. and
Teillet, M.-A. (1997)
Early- and late-migrating cranial neural crest cell populations
have equivalent
developmental potential in vivo. Development 124:
3077-3087 (ref.)
Baker, C. V. H. and Bronner-Fraser, M. (1997) The origins of the
neural crest.
Part I: Embryonic induction. Mech.
Dev. 69: 3-11 (ref.)
Baker, C. V. H. and Bronner-Fraser, M. (1997) The origins of the
neural crest.
Part II: An evolutionary perspective. Mech.
Dev. 69: 13-29 (ref.)
Baker, C. V. H., Sharpe, C. R., Torpey, N. P., Heasman, J. and Wylie, C. C. (1995) A Xenopus c-kit-related receptor tyrosine kinase expressed in migrating stem cells of the lateral line system. Mech. Dev. 50: 217-228 (ref.)
Book Chapters
Baker, C. V. H. (2005) Neural Crest and Cranial Ectodermal Placodes. In "Developmental Neurobiology", 4th edition (M. S. Rao and M. Jacobson, Eds.), pp. 67-127. Springer, New York.
Baker, C. V. H. (2005). The Embryology of Vagal Sensory Neurons. In "Advances in Vagal Afferent Neurobiology" (B. J. Undem and D. Weinreich, Eds.), pp. 3-26. CRC Press, Boca Raton.
Above: Cross-section of the embryonic chicken olfactory bulb showing neural crest-derived olfactory ensheathing cells (green). (Blue, axons; red, low-affinity neurotrophin receptor.) Dr Perrine Barraud
Above: Head of a paddlefish (Polyodon) embryo stained for Sytox green, showing fields of rosette-like ampullary organs (containing electroreceptors) on either side of lines of mechanosensory hair cells. Dr Melinda Modrell
Above: Scanning electron micrograph of a frog (Xenopus) mechanosensory lateral line organ showing the long kinocilia of the mechanosensory hair cells that make up the neuromast. The kinocilia are deflected by water movements. Dr Clare Baker & Dr Jeremy Skepper

Above: Neurons (red) in the developing trigeminal ganglion derive from two distinct placodes and the neural crest. Only the ophthalmic trigeminal placode-derived neurons (top) express Pax3 (green). The non-neuronal Pax3-positive cells are neural crest cells. Dr Clare Baker
Above: Section showing sensory neurons (red nuclei; blue axons) formed by an epibranchial placode (thickened surface ectoderm), which expresses Pax2 (green nuclei). Dr Paul O'Neill
Above: A holocephalan (elephant fish) embryo, showing expression of the Sonic hedgehog gene (dark purple staining) in the developing operculum and gill arches. Dr Andrew Gillis.




