Information

Name

Ma, Yong-Chao, PhD

Title

Assistant Professor

Email

ma@northwestern.edu

Office Phone

773-755-6393

Department

Pediatrics

Office

2430 North Halsted Street, Room C321L

Website

http://www.chicagochildrensresearch.org/ma

Areas of Research

Cell Biology, Computational Development, Molecular Neuroscience, Motor Control, Neurobiology of Disease, Signal Transduction

NU Scholar Profile

http://www.scholars.northwestern.edu/expert.asp?u_id=1470

Recent Publications on PubMed

http://www.ncbi.nlm.nih.gov/pubmed?term=Ma%2C%20Yong-Chao%5BFull%20Author%20Name%5D&cmd=DetailsSearch

Current Research

Current Research

Regulation of Motor Neuron and Dopaminergic Neuron Differentiation in Development and Disease

Spinal Motor Neurons and Spinal Muscular Atrophy (SMA). My laboratory is interested in studying the genetic and epigenetic mechanisms that regulate motor neuron differentiation and why only motor neurons degenerate in spinal muscular atrophy (SMA). To address these questions, we use a combination of genetic, biochemical and cell biological approaches, and utilize genetically modified mice, induced pluripotent stem (iPS) cells reprogrammed from fibroblasts, and embryonic chick neural tubes as model systems. Based on our findings, we develop new therapeutic strategies for treating SMA.

Dopaminergic Neurons and Parkinson’s Disease. Dopaminergic neurons located in the ventral midbrain control movement, emotional behavior and reward mechanisms. Dysfunction of dopaminergic neurons is implicated in Parkinson’s disease, drug addiction, depression, and schizophrenia. Generating dopaminergic neurons from stem cells offers a remarkable opportunity to treat these disorders by replacing sick/dead cells in patients and serving as a model system to study disease onset, progression and to perform drug screening. Realizing this opportunity requires understanding the mechanisms regulating dopaminergic neuron differentiation. My laboratory is interested in using basic helix-loop-helix transcription factor Neurogenin 2 (Ngn2), which was recently shown to be essential for dopaminergic neuron differentiation, as a molecular handle and entry point to investigate the underlying mechanisms. Using the Ngn2-EGFP knockin mouse line, in which the coding region of Ngn2 was replaced by EGFP to mark all Ngn2-expressing neural progenitors with EGFP, we isolated GFP positive neural progenitors from embryonic mouse ventral midbrain by microdissection and fluorescence-activated cell sorting (FACS), and performed gene expression profiling study using DNA microarray. This leads us to the identification of some novel transcription factors regulating dopaminergic fate specification. We are further investigating the roles of these factors by using genetically modified mice and embryonic chick neural tubes as model systems.

Cancer Stem Cells. We are also interested in characterizing cancer stem cells from various tumors including medulloblastoma, the most prevalent pediatric tumor, to facilitate the development of therapeutics capable of eliminating them. The traditional model of cancer development considers that tumors arise from a series of sequential mutations. More recently, a new model has been proposed that tissue stem cells undergo mutations that deregulate their self-renewal pathways, leading to tumor formation. We are interested in: 1. Isolating and characterizing cancer stem cells from solid tumors by using genetic cell-lineage tracing approach; 2. Identifying the defects that lead to the development of cancer stem cells; 3. Developing novel models that are capable of interrogating the effect of therapeutics on cancer stem cells.

Selected Publications

Selected Publications

Ma, Y. C., Song, M. R., Park, J. P., Ho, H. H., Hu, L., Kurtev, M., Zieg, J., Ma, Q., Pfaff, S. L., and Greenberg, M. E. 2008. Regulation of motor neuron specification by GSK3-mediated phosphorylation of Neurogenin 2. Neuron, 58:65-77.
Neuron Previews on this paper: Lai, H.C. and Johnson, J.E. 2008. Neurogenesis or Neuronal Specification: Phosphorylation Strikes Again! Neuron, 58:3-5.

Datta, S. R., Ranger, A. M., Lin, M. Z., Sturgill, J. F., Ma, Y. C., Cowan, C. W., Dikkes. P., Korsmeyer, S. J., and Greenberg, M. E. 2002. Survival factor-mediated BAD phosphorylation raises the mitochondrial threshold for apoptosis. Developmental Cell, 3(5): 631-43.

Lowry, W. E., Huang, J., Ma, Y. C., Ali, S., Wang, D., Williams, D. M., Okada, M., Cole, P. A., and Huang, X. Y. 2002. Csk, a critical link of protein signals to actin cytoskeletal reorganization. Developmental Cell, 2(6): 733-44.

Zheng, B.*, Ma, Y. C.*, Ostrom, R. S., Insel, P. A., Huang, X. Y. and Farquhar, M. G. 2001. RGS-PX1, a GAP for Gas and sorting nexin in vesicular trafficking. Science, 294:1939-42. (*Equal contribution)
Science Perspectives on this paper: Zastrow, M.V. and Mostov, K. 2001. A new thread in an intricate web. Science, 294:1845-47

Ma, Y. C., Huang, J., Ali, S., Lowry, W., and Huang, X. Y. 2000. Src tyrosine kinase is a novel direct effector of G proteins. Cell, 102: 635-646.

Ma, Y. C. and Huang, X. Y. 1998. Identification of the binding site for Gqa on its effector Bruton’s tyrosine kinase. Proc. Natl. Acad. Sci., USA 95:12197-12201.