The School of Molecular and Cellular Biology at the University of Illinois at Urbana-Champaign

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Department of Molecular and Integrative Physiology
Richard Kollmar

rkollmar@uiuc.edu

427A Burrill Hall
Office: (217) 333-9861
Lab: (217) 244-6294

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Department of Molecular and Integrative Physiology
427A Burrill Hall
407 S. Goodwin Ave.
Urbana, IL 61801

Richard Kollmar

Assistant Professor of Molecular and Integrative Physiology and Neuroscience

Education

Dipl. Chem. 1988 Ludwigs-Maximilians Universität München
Ph.D. 1993 University of Wisconsin-Madison
Postdoc 1993-1995 University of Texas Southwestern Medical Center at Dallas
Postdoc 1995-2003 Rockefeller University

Teaching Interests

Molecular Genetics of Hearing and Balance in the Zebrafish

Disorders of hearing and balance, which restrict our ability to communicate and to move about, afflict a significant percentage of our population: 30 million Americans have impaired hearing, and about two million are profoundly deaf. One in a thousand children is born with a deafness that impedes language development; another one in a thousand are stricken by heritable deafness before adulthood. One-third of those over 65 years of age have suffered a handicapping hearing loss; more than half of those over 70 experience balance problems. Environmental influences, such as noise, play an important role in hearing loss, but most of these ailments are due to genetic predisposition or disease. So far, however, we know only a small fraction of the several hundred genes that are likely to be important.

To investigate the genetic basis of the ear's operation, our group works primarily with the zebrafish, Danio rerio. Because it is also a vertebrate, its internal ears are very similar to those of humans: They exhibit the same elaborate anatomy, called the labyrinth, with distinct organs that detect sound or accelerations. They employ the same type of sensory cell, the so-called hair cell, that converts these mechanical stimuli into electrical signals. In the few known instances, they also express the same or similar genes. Furthermore, the zebrafish offers a unique combination of experimental advantages: simple husbandry, a short generation time, and large clutches of embryos; external development and optical transparency that facilitate imaging, electrophysiology, and behavioral studies; efficient methods for mutagenesis, transgenesis, and the manipulation of gene expression; and an advanced genomics infrastructure (see http://zfin.org/).

Our research focuses on two unique and essential elements of the internal ear, the otoliths and the hair bundle:

  • Otoliths of ray-finned fish, like otoconia of tetrapods, are acellular composites of proteins and calcium carbonate that convey linear accelerations to sensory hair cells. Otoliths nucleate early during ear development and grow throughout life; their extravagant shapes differ substantially among otolithic organs and among species. How and why do these differences arise in the same fluid compartment?
  • The hair bundle is the hair cell's eponymous mechano-sensitive organelle whose deflection initiates mechano-electrical transduction. Its "hairs", the so-called stereocilia, are supported by actin filaments whose number, length, and arrangement vary in a systematic and stereotypic fashion within each bundle, within and among the organs of the labyrinth, and among species. The resulting changes in stiffness and viscous drag optimize the hair cells' sensitivity and frequency selectivity. How is the hair bundle's intricate cytoskeleton assembled?

To answer these questions, we apply techniques from a variety of disciplines, such as biochemistry, molecular genetics, embryology, and physiology, to wildtype, mutant, and transgenic zebrafish.

Representative Publications

Vieira, M., Christensen, B.L., Wheeler, B.C., Feng, A.S., Kollmar, R. 2007. Survival and stimulation of neurite outgrowth in a serum-free culture of spiral ganglion neurons from adult mice. Hear. Res., 230:17–23. [Abstract] [Manuscript available at http://hdl.handle.net/2142/1353]

Asai, Y., Chan, D.K., Starr, C.J., Kappler, J.A., Kollmar, R., and Hudspeth, A.J. 2006. Mutation of the atrophin2 gene in the zebrafish disrupts signaling by fibroblast growth factor during development of the inner ear. Proc. Natl. Acad. Sci. USA, 103:9069–74. [Abstract]

Lopez-Schier, H., Starr, C.J., Kappler, J.A., Kollmar, R., and Hudspeth, A.J. 2004. Directional cell migration establishes the axes of planar polarity in the posterior lateral-line organ of the zebrafish. Dev. Cell, 7:401–12. [Abstract]

Kappler, J.A., Starr, C.J., Chan, D.K., Kollmar, R., and Hudspeth, A.J. 2004. A nonsense mutation in the gene encoding a zebrafish myosin VI isoform causes defects in hair-cell mechanotransduction. Proc. Natl. Acad. Sci. USA., 101:13056–61. [Abstract]

Starr, C.J., Kappler, J.A., Chan, D.K., Kollmar, R., and Hudspeth, A.J. 2004. Mutation of the zebrafish choroideremia gene encoding Rab escort protein 1 devastates hair cells. Proc. Natl. Acad. Sci. USA., 101:2572–7. [Abstract]

Kollmar, R., Nakamura, S.K., Kappler, J.A., and Hudspeth, A.J. 2001. Expression and phylogeny of claudins in vertebrate primordia. Proc. Natl. Acad. Sci. USA., 98(18): 10196–201. [Abstract]

Kollmar, R. 1999. Who does the hair cell's 'do? Rho GTPases and hair-bundle morphogenesis. Curr. Opin. Neurobiol., 9(4): 394–8. [Abstract]

Kollmar, R., Fak, J., Montgomery, L.G., and Hudspeth, A.J. 1997. Hair cell-specific splicing of mRNA for the alpha1D subunit of voltage-gated Ca2+ channels in the chicken's cochlea. Proc. Natl. Acad. Sci. USA., 94(26): 14889–93. [Abstract]

PubMed