Joanna Bakowska, PhD

Title/s:  <p>Associate Professor</p> <p>Molecular Pharmacology and Neuroscience</p>

Office #:  CTRE 422

Email: jbakowska@luc.edu

Research Interests

Genetic, behavioral and cellular approaches to study mechanisms in spastic paraplegias

Hereditary spastic paraplegias are a group of neurological disorders characterized by lower extremity spastic weakness, which is caused by distal axonal degeneration of the upper motor neurons with the longest axons. These disorders afflict tens of thousands of people in the United States. In the past several years, many genes have been shown to be responsible for different types of spastic paraplegias. My research has focused on examining the function of spartin protein, which gene mutation results in Troyer syndrome known also as hereditary spastic paraplegia type 20 (SPG20). Thus far, we discovered that spartin protein is an important component in the intracellular trafficking of receptors. Spartin plays a role in the internalization and sorting of epidermal growth factor receptor (ligand-induced receptor) but not in constitutively recycled receptors. Our studies using fibroblasts derived from patients with Troyer syndrome show that a premature stop codon in the spartin gene results in a complete loss of spartin rather than a truncated form of this protein.

Selected Publications