Lorraine Iacovitti, PhD
Philadelphia, PA 19107
(215) 955-2992 fax
Most Recent Peer-reviewed Publications
- Evolutionary conservation of an atypical glucocorticoid-responsive element in the human tyrosine hydroxylase gene
- BMP and TGF-Β pathway mediators are critical upstream regulators of Wnt signaling during midbrain dopamine differentiation in human pluripotent stem cells
- Tracking Transplanted Bone Marrow Stem Cells and Their Effects in the Rat MCAO Stroke Model
- Gremlin is a novel VTA derived neuroprotective factor for dopamine neurons
- Changes in host blood factors and brain glia accompanying the functional recovery after systemic administration of bone marrow stem cells in ischemic stroke rats
B.S., Monmouth College, (Biology) - 1973
Ph.D., Cornell University Medical College, (Neurobiology) - 1979
Post-Doctoral, Washington University-St. Louis, (Anatomy & Neurobiology) - 1979-81
Research and Clinical Interests
Neurodegenerative Diseases, Stem Cells, Parkinson's Disease
Research in my laboratory is aimed at understanding how neurons differentiate into dopamine neurons during development of the brain and how that information may be useful for the treatment of neurodegenerative diseases such as Parkinson's. A major goal of our studies has been defining the key fate determinant genes and lineage stages in the development of human dopamine neurons. Our hope is that an understanding of those mechanisms that first direct expression of neurotransmitter genes during differentiation will provide a molecular blueprint that can be used to intentionally target the differentiation of cells, such as human embryonic stem or precursor cells, toward that phenotype. Using an approach that combines cell culture and genetic engineering, our aim is to induce dopaminergic traits in human stem/progenitor cells and devise ways to amplify and purify prospective human dopamine neurons for study after transplantation into rat and monkey models of Parkinson's disease.
In our laboratory, we use a multidisciplinary approach, employing tissue culture (primary and cell lines), molecular (qPCR, microarray, gene cloning, transfection, transduction), anatomical (immunocytochemistry, confocal) biochemical (HPLC), surgical (stereotaxic brain surgery, arterial occlusion), imaging (PET, spect) and behavioral (sensory and motor skills tests).
The overall goal of our studies is take what we have learned about the differentiation of dopamine neurons from human stem cells and translate that into a cell replacement treatment for Parkinson's disease.