Tatjana Piotrowski

Assistant Professor of Neurobiology and Anatomy

Tatjana Piotrowski

B.A. University of Tubingen, Germany

Ph.D. Max-Planck-Institute for Developmental Biology, Germany

Research

References

 

Tatjana Piotrowski's Lab Page

Research

We are studying how the sensory lateral line develops in zebrafish by analyzing mutants that affect this process. It consists of hair cells, which functionally and morphologically are very similar to the hair cells of the inner ear of higher vertebrates. In fish, the lateral line and the ear serve to detect vibrational signals (including sounds), which helps the animal to orient itself in the environment. Because of the similarity of structure and function of the hair cells in the ear and lateral line, it is likely that their development is based on similar genetic mechanisms. A key difference between these two sensory systems is that unlike the hair cells of the inner ear, the hair cells of the lateral line system are directly exposed to the environment. This property makes this system well-suited for the study of cell migration, cell proliferation, pattern formation, and for the direct application of functional, and electrophysiological assays.

As yet, hardly anything is known about the molecular nature that underlies the development and function of this system. The sensory organs (neuromasts) and the nerves that innervate them are derived from cranial neurogenic placodes that deposit neuromast primordia as the placodes elongate or migrate. The direction of migration, position and number of neuromasts is an inherent property of the placode. It is not known how the placode "knows" where, when and how many neuromasts to deposit and whether neural crest cells play a role in this process. Our research focuses on the elucidation of these mechanisms by isolating the genes responsible for defects in these processes in mutants. We identified 26 mutants with defects in placode migration and patterning of neuromasts, or the function of the sensory organs proper. Tools that we are using to analyze the mutants involve meiotic mapping, transplantation experiments, misexpression studies, establishment of transgenic lines, comparison of gene expression (in situ hybridization) in mutant and wild-type larvae, confocal microscopy and classical embryological methods.
Piotrowski Figure

 

a. The posterior lateral line placode in a 35h old live larva stained with Bodipy. The placode drops off neuromast precursors as it migrates posteriorly on the trunk. b. Differentiated neuromast with hair bundles in a 4d old larva. c. 5d old live larva in which the neuromasts are stained with the fluorescent dye Daspei.

References

1. Grant K, Raible D, Piotrowski T (2005). Regulation of latent sensory hair cell precursors by glia in the zebrafish lateral line. Neuron, 45, 69-80. reviewed in: Preview in Neuron, 45, 3-5. L. Goodrich (2005). Hear, hear for the zebrafish.   Dispatch in Current Biology, 15, 67-70. T. Whitfield (2005). Precocious phenotypes and planar polarity.   BioEssays (in press). A. Ghysen. The three sided romance of the lateral line: glia love axons love precursors love glia.

2. Piotrowski T, Ahn D, Schilling TF, Nair S, Ruvinsky I, Geisler R, Rauch GJ, Haffter LP, Zon LI, Foott H, Dawid IB, Ho R (2003) The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans. Development 130:5043-5052.   Featured on "Most viewed Top 10" and "Hidden Jewel" in "Developmental Biology" on Faculty of 1000 (http://www.faculty of1000.com)

3. Chien C-B, Piotrowski T (2002) How the lateral line gets its glia.   Trends in Neurosciences Vol. 25:544-546

4. Grandel H, Lun K, Rauch GJ, Piotrowski T, Houart C, Sordino P, Kuechler AM, Schulte-Merker S, Geisler R, Holder N, Wilson S, Brand M (2002) Retinoic acid signaling in the zebrafish embryos is necessary to pattern the anterior-posterior axis of the CNS and to induce a pectoral fin bud.   Development 129:2851-2865

5. Piotrowski T, Nusslein-Volhard C (2000) The endomesoderm plays an important role in segmentation of the pharyngeal arches in the zebrafish (Danio rerio).   Dev. Biol. 225:339-356

6. Piotrowski T, Schilling TF, Brand M, Jiang YJ, Heisenberg CP, Beuchle D, Grandel H, van Eeden FJM, Furutani-Seiki M, Granato M, Haffter P, Hammerschmidt M, Kane DA, Kelsh RN, Mullins MC, Odenthal J, Warga RM, N¸sslein-Volhard C (1996) Jaw and branchial arch mutants in zebrafish II: anterior arches and cartilage differentiation.   Development 123:345-356

7. Schilling TF, Piotrowski T, Grandl H, Brand M, Jiang Y-J, Heisenberg C-P, Beuchle D, van Eeden FJM, Furutani-Seiki M, Granato M, Haffter P, Hammerschmidt M, Kane DA, Kelsh RN, Mullins MC, Odenthal J, N¸sslein-Volhard C (1996) Mutations affecting the development of the jaw and branchial arches I: Gill arches.   Development 123:329-344

8. Bartsch P, Gemballa S, Piotrowski T (1997) The embryonic development of Polypterus senegalus Cuvier, 1829: its staging with reference to external and skeletal features, behaviour and locomotory habits.   Acta Zoologica (Stockholm) 78, No. 4, pp.309-328

9. Piotrowski T, Northcutt RG (1996) The cranial nerves of the Senegal bichir, Polypterus senegalus (Osteichthyes; Actinopterygii, Cladistia).   Brain, Behavior and Evolution 47:55-102