Kelly L. Jordan-Sciutto, Ph.D
Assitant Professor, Dept of Pathology

Cancer Biology Program

Address

240 S. 40th St
Rm 312-314 Levy Bldg (Lab)
Philadelphia, PA 19104-6030

Office tel.: 215 898-4196
Lab tel.: 215 898-4514
Fax: 215 573-2050
E-mail: Jordan@path.dental.upenn.edu

Link(s)

Dr. Jordan-Sciutto's Penn Dental webpage
Microbiology, Virology & Parastiology

Villanova University: BS (Cumulative Science), 1991.

Thomas Jefferson University: PhD (Biochemistry and Molecular Biology), 1996.

University of Pittsburgh Medical Center: Postdoctoral Research (Neuropathology), 1996-2001.

Research Interests

• Assessing mechanisms of neuronal death (apoptosis vs necrosis) in response to neuroinflammatory stimuli (i.e. oxidative stress, cytokines, excitotoxicity).
• Determining mechanisms of protection by neurotrophins and chemokines.
• Molecular mechanisms underlying neuronal loss in neurodegenerative disorders (i.e. Alzheimer’s Disease, Parkinson’s disease, and HIV encephalitis). We are specifically interested in the role of cell cycle proteins and transcriptional regulators in neuronal survival decisions.

Key words: Cell Cycle, Oxidative Stress Response, Antioxidant Response, Neurodegeneration, Transcription, Primary Culture, HIV encephalitis, Alzheimer Disease, Parkinson disease, Retinoblastoma, E2F1.

Description of Research

Our laboratory investigates molecular mechanisms underlying neurodegenerative processes in the hopes of identifying common and unique players in determining neuronal survival among several neurodegenerative diseases. Currently we are focusing our research efforts on the role of cell cycle proteins, the endogenous antioxidant response and unfolded protein response in three neurodegenerative disorders: HIV encephalitis (HIVE), Alzheimer’s disease (AD), and Parkinson’s disease (PD).

While HIVE, AD, and PD exhibit different pathologic features, theories as to their etiology share common molecular mechanisms including changes in the trophic factor environment, oxidative stress, and activation of CNS inflammatory components. We hypothesize that neuronal response to these neurodegenerative stimuli includes alterations in expression and/or activity of cell cycle proteins. To this end, we and others have shown that key regulators of cell cycle progression, Retinoblastoma susceptibility gene (pRb), E2F1, and/or p53, exhibit altered levels and patterns of expression in HIVE, PD, and AD. These changes are associated with areas of pathology suggesting a role in degenerative processes. In vitro models of neurodegeneration in each of these diseases also exhibit alterations in cell cycle protein subcellular localization. We are using both human tissue and in vitro models to uncover the role of cell cycle proteins, E2F1, MDMx (a p53 and E2F1 regulatory protein), and pRb in interpreting neuroprotective vs neurotoxic stimuli in primary human, rat, and mouse neuroglial cultures stimulated with trophic factors, chemokines, dopamine, free radicals, beta-amyloid, and HIV-infected macrophage supernatant. These studies are aimed at determining how cell cycle proteins regulate neuronal survival in response to varied and conflicting stimuli. In vitro findings are then used to assess potential roles for these proteins in animal models as well as autopsy tissue relevant to each neurodegenerative condition. Our investigation of E2F1 has resulted in the discovery of a role for this protein in activation of a calpain-dependent death pathway which has not been previously described. Interestingly, neurons responding to HIV-infected macrophage supernatants (our in vitro model of neuronal response to inflammatory infiltrate which mediates HIV encephalitis) activate calpain and increase E2F1 protein levels. One of our immediate lines of investigation is testing the hypothesis that E2F1 induces neuronal death in HIV encephalitis via calpain activation, a novel pathway.

A second area of research in our laboratory is the study of the endogenous anti-oxidant response and its failure to prevent accumulation of oxidative damage and neuronal loss in neurodegenerative disorders. The two proteins of direct interest to the laboratory are Keap1 and Nrf2. Nrf2 is a transcription factor that regulates the expression of the enzymes responsible for the antioxidant response. Normally, Nrf2 is bound in the cytoplasm by the Kelch ECH associated protein 1(Keap1). However, in response to oxidative stress, sulfhydryl groups on Keap1 become oxidized releasing Nrf2 for translocation into the nucleus. We have recently shown that Nrf2 is aberrantly expressed in AD indicating it is not responding to oxidative stress in neurons of affected brain regions. Interestingly, Nrf2 does appear to be responding appropriately in neurons affected in PD. This has led us to hypothesize that the endogenous antioxidant response is aberrant in AD, but insufficient in PD. Our current studies focus on identifying differences in regulation of the endogenous antioxidant response in AD and PD. The goal of these studies is to explore this pathway as a therapeutic target for neurodegenerative conditions. By enhancing the endogenous anti-oxidant response, neuronal toxicity may decrease leading to increased neuronal function in these patients.

A final area of interest on which our other two lines of investigation has converged is the role of the unfolded protein response (UPR). Induction of the unfolded protein response results in activation of Nrf2 and calpain, proteins activated in response to the endogenous antioxidant response and the E2F1 cell cycle protein respectively. This has led to our investigation of the UPR in neurodegenerative conditions. We are currently looking at pathways activated by the UPR in our various models of HIVE, AD, and PD. The key regulators of this response include pancreatic endoplasmic reticulum kinase (PERK), IRE1, and ATF6. We have already identified increased PERK and phosphorylation of PERK substrate eukaryotic initiation factor 2 ? in AD tissue and an in vitro model of HIVE. This is consistent with findings by Ryu, E. J., et al. (2002, J. Neuroscience 22:10690) indicating a role for UPR in an in vitro PD model. However, our results indicate that Nrf2 a PERK substrate is not activated in AD suggesting the pathway is compromised in AD. Our future investigations are to determine what parts of the pathway are aberrant in disease progression and identify small molecule inhibitors to block chronic UPR pathway activation which is contributing to neuronal dysfunction and loss.

By assessing the interaction of these three convergent pathways in neurons responding to neurodegenerative stimuli such as oxidative damage, misfolded proteins, and inflammation, we hope to gain a greater understanding of the basic mechanisms underlying neuronal damage, dysfunction and loss in neurodegenerative diseases and identify drugable targets for treatment of AD, PD, and HIVE.

Selected Publications

Strachan, G.D., Koike, M.A., Siman, R., Hall, D.J., and Jordan-Sciutto, K.L. E2F1 induces cell death, calpain activation, and MDMX degradation in a transcription independent manner implicating a novel role for E2F1 in neuronal loss in SIV encephalitis. 2005. Journal of Cellular Biochemistry. 96(4):728-40.

Ramsey, C.P.&, Glass, C.A.&, Montgomery, M.B., Lindl, K.A., Ritson, G.P., Chia, L.A., Hamilton, R.L., Chu, C.T., and Jordan-Sciutto, K.L. Expression of Nrf2 in Neurodegenerative Diseases. 2007. Journal of Neuropathology and Experimental Neurology. 66(1):75-85.

Wang, Y., White, M.G., Akay, C., Chodroff, R.A., Robinson, J., Lindl, K.A., Dichter, M.A., Qian, Y., Mao, Z., Kolson, D.L., and Jordan-Sciutto, K.L. Activation of cyclin dependent kinase 5 by calpains contributes to human immunodeficiency virus-induced neurotoxicity. 2007. Journal of Neurochemistry. 103(2):439-55.

Chu, C.T., Plowey, E. Wang, Y., Patel, V., and Jordan-Sciutto, K.L. Location, Location, Location: Altered transcription factor trafficiking in neurodegeneration. 2007. Journal of Neuropathology and Experimental Neurology. 66(10):873-883

Lindl, K.A., Akay, C., Wang, Y., White, M.G., and Jordan-Sciutto, K.L. Expression of the Endoplasmic Reticulum Stress Response marker, BiP in the Central Nervous System of Human Immunodeficiency Virus Positive Individuals. 2007. Neuropathology and Applied Neurobiology. 33:658-669.

Search PubMed for more articles

Lab

Rotation Projects

1. Effect of calpain cleaved E2F1 on neuronal viability
2. Identification of RNA species bound by E2F1
3. Differential binding of E2F1 and E2F4 to promoters in differentiated neurons
4. Identification of the E2F1 RNA binding domain
5. Identification of pro-survival pRb binding partners in neurons
6. Determination of pro-survival vs pro-toxic phospho-isoforms of pRb
7. Determination of ER stress pathways involved in neuronal survival during HIV-induced neurodegeneration
8. Please contact me for other available projects

Personnel:

Cagla Akay, M.D. Post-doctoral Researcher
David Marks, Ph.D., Post-doctoral Researcher
Ying Wang, M.D., Ph.D., Post-doctoral Researcher
Michael G. White, Ph.D., Post-doctoral Researcher
Kathryn A. Lindl, A.B., Graduate Student
Jenhao Harry Ting, B.A., Graduate Student
Galina Grigoriev, undergraduate research assistant
Alyssa Yeager, undergraduate research assistant
Lwin Khine, lab assistant