Quick Project Snapshot

How can Ndfip1 reduce brain damage following stroke?

Stroke is the third most common cause of death.  After the onset of cerebral ischemia, about 2 million neurons die per minute, mostly from brain tissue surrounding the hemorrhage.  We have discovered that if neurons in these areas increase their levels of Ndfip1, they are protected from death during the vulnerable period.  In this project, we aim to test a number of factors that are known to increase Ndfip1 in neurons.  We will discover the molecular pathways that allow these factors to upregulate Ndfip1, and therefore increase the number of surviving neurons following stroke.


  1. Howitt, J., Putz, U., Lackovic, J., Doan, A., Dorstyn, L., Cheng, H., Yang, B., Chan-Ling, T., Silke, J., Kumar, S. and Tan, S-S (2009)Divalent  metal transporter 1 (DMT1) regulation by Ndfip1 prevents metal toxicity in  human neurons.  Proc. Natl. Acad. Sci. USA 106:15489-15494  
  2. Schieber, C., Howitt, J., Putz, U., White, J.M., Parish, C.L., Donnelly,  P.S. and Tan, S-S (2011)  Cellular upregulation  of Nedd4-family interacting protein 1 (Ndfip1) using low levels of bioactive cobalt complexes.  J. Biol. Chem 286:8555-8564  
  3. Howitt, J., Lackovic, J., Low, L-H.,  Naguib,  A.,  Macintyre,  A., Goh, C-P.,  Callaway, J.K., Hammond V., Thomas, T., Dixon, M., Putz, U. Silke, J., Bartlett, P., Yang, B., Kumar, S., Trotman, L.C., Tan, S-S. (2012).     Ndfip1 regulates nuclear Pten import in vivo to promote neuronal survival following cerebral ischemia  J. Cell Biol. 196:29-36  
  4. Lackovic, J., Howitt, J., Callaway, J.K., Silke, J., Bartlett, P., and Tan, S-S. (2012)  Differential regulation of Nedd4 ubiquitin ligases and their adaptor protein Ndfip1 in a rat model of ischemic stroke.  Exp. Neurol. 235:326-335  
  5. Goh, C.P., Putz, U., Howitt, J., Low, L.H., Gunnersen, J., Bye, N., Morganti-Kossmann, C. and Tan, S-S. (2014)  Nuclear trafficking of Pten after brain injury leads to neuron survival not death  Exp. Neurol 252:37-46


Prof Seong-Seng Tan

Exosome Biology Laboratory

Brain cells are in constant communication with each other for transmitting electrical and chemical signals during mental activity. However, we believe that certain chemicals are also exchanged between brain cells for purposes that are not related to sensory and motor activity, for example for brain repair after injury.  Brain communication is also important for protection of nerve cells against brain stress.  We are currently engaged in discovering the nature of these communications and the circumstances behind their transmission.

We have been engaged in studying this natural method of communication using vesicles called exosomes.    The exchanged material contains important messages (proteins, nucleic acids) that can have important consequences for cells that receive them.  For example, in cancer, the spread of cancerous cells can be either hastened or retarded depending on the nature of these messages.  Recently, we found out how to include certain additional messages that are normally not found in these exosomes. We are excited to study how these new messages can be used to repair brain cells after injury by boosting levels of repair proteins.  In addition, we are enthusiastic about using these exosomes for transferring anti-cancer messages into brain tumours for reversing cancerous growth.  

All Projects by this Lab

Investigating interneuron migration and placement into cortical circuitsControl of protein transport in exosomes by Ndfip1How can Ndfip1 reduce brain damage following stroke?How does the brain protect itself during injury?Protein trafficking in neurodegenerative diseases.

Prof Seong-Seng Tan


Brain Development & Regeneration

Our group is interested in the self-defence mechanisms that operate in the brain when something goes wrong.  This may take the form of degenerative disease (Parkinson's, Alzheimer's) or cancer (brain tumours) due to gene mutations and ageing.  As a result, mutant or toxic proteins accumulate in brain cells, causing them to degenerate or proliferate. We have been working with one system of self-defence called protein ubiquitination which allows harmful proteins in brain cells to be removed and in the process, halt or reverse the disease process. We are particularly interested in finding how to accelerate beneficial ubiquitination in neurones using the Nedd4/Ndfip1 proteins.  Our studies so far demonstrate that these proteins can halt cell death following injury and stroke, and slow down the division of brain cancer cells.

All Labs that operate in this Division

Exosome Biology Laboratory