Ronald E. Kalil

 

 

Neural Stem Cells, Adult Neurogenesis and the Injured Brain

E-mail: rekalil@wisc.edu

Research Strength: Development: Plasticity and Repair

When the brain is damaged, injured neurons die and typically are not replaced. This cell death frequently results in a loss of function by the affected region of the brain. However, if neurons that have died could be replaced and their connections rebuilt, normal function might be restored. There are two possible approaches available to achieve this goal. One involves transplanting neural stem cells to the injured brain, and then coaxing them to differentiate into new, functionally appropriate neurons and glial cells. The second approach acknowledges that new neurons are produced in the brain throughout life, and endeavors to encourage these newly generated neurons to replace those that have died. We are investigating both of these approaches.

In previous work, we have shown that embryonic neural stem cells transplanted to the injured adult brain will survive and differentiate into neurons and glial cells. Currently, we are studying methods to enhance the survival and integration of transplanted cells. In parallel with this research, we have discovered that cells in several areas of the adult brain express the cytoskeletal protein nestin. This suggests that these cells may be neural stem cells or have stem cell-like properties. We now are characterizing these nestin-positive cells in detail as a first step in determining whether they may be capable of functioning as endogenous neural stem cells.

The research underway is conducted in vitro and in vivo, and spans molecular neurobiology to systems neuroscience. However, all of it converges on a common goal; to restore behavioral function that has been compromised or lost because of brain injury by replacing cells that have died and rebuilding appropriate neural connections.

Lab Website:

http://www.keck.bioimaging.wisc.edu/

Selected Publications:

• Dean O. Smith, Julie L. Rosenheimer, R.E. Kalil. 2008. Delayed Rectifier and A-Type Potassium Channels Associated with Kv 2.1 and Kv 4.3 Expression in Embryonic Rat Neural Progenitor Cells. PLoS ONE, Vol. 3. [PDF]
• Wyatt Potter, R.E. Kalil, and Weiyuan J. Kao. 2008. Biomimetic material systems for neural progenitor cell-based therapy. Frontiers in Bioscience, 13: 806-821. [PDF] .
• Rao, A.J. M.L. Hendrickson, S. Salamat, and R.E. Kalil. 2005. Nestin expression by terminally differentiated neurons in the adult human brain. Soc. Neurosci. Abstr., Vol. 31. Online.
• Hendrickson, M.L., A.J. Rao, and R.E. Kalil. 2005. Nestin Expression by neurons in the dorsal neocortex of the early postnatal rat brain. Soc. Neurosci. Abstr., Vol. 31 Online.
• Rao, A.J., O.N. Demerdash, M.L. Hendrickson, and R.E. Kalil. 2004. Nestin expression by terminally differentiated neurons in the adult brain. Soc. Neurosci. Abstr., Vol. 30. Online.
• Hendrickson, M.L. and R.E. Kalil. 2003. Labeling of Neural Progenitor Cells Transplanted to the Adult Brain with CFDA, SE. Society for Neuroscience, 2003. Online.
• Demerdash, O., J. Paulus, and R.E. Kalil. 2002. Widespread Expression of Nestin By Cells in the Adult Brain. Society for Neuroscience, 2002. Online.
• Stein, T., J. Fedynyshyn, and R.E. Kalil. 2002. Circulating autoantibodies recognize and bind dying neurons following injury to the brain. J. Neuropath and Exp. Neurol., 61: 1100-1108. [PDF]