USC logo
University of Southern California
PIBBS Online ApplicationPIBBS CalendarContact PIBBSPIBBS Faculty DirectoryPIBBS Site Index
PIBBS Home PageFaculty ResearchFaculty DirectoryPhD ProgramsOnline Application
Research Centers and Institutes Faculty Research Support PIBBS Faculty in the News


Le Ma

Assistant Professor

Cell & Neurobiology
Zilkha Neurogenetic Institute
Keck School of Medicine

Send E-mail to:   le.ma@usc.edu 
Telephone: 323-442-2484Fax: 323-442-2448
Office: ZNI 441Mail Code: 2821 HSC

Education:
BS 1989 - Fudan University
MS 1992 - University of Hawaii
PhD 1999 - Harvard University, Cambridge, Massachusettes

Postdoctoral Research Fellowship:
2005 HHMI, UCSF, Stanford

Started at USC: 2005

Research Topics: Cellular Neurobiology, Developmental Biology, Cell Structure & Organization, Neurogenetics, Human/Mammalian Genetics

Click here for:PubMed Search NIH GrantsSearch USC for Professor Ma

See also:     All USC Research GrantsAll HSC Research Grants

Research Description

Much like the computer, our brain relies on the electricity for its function. However, the electricity in the brain is conducted by axons and dendrites, the long and thin extensions from the nerve cell body that form synaptic connections with one another. In addition, much unlike the computer, the circuits made from billions of nerve cells are assembled during embryonic development and any misregulation in establishing proper connections could lead to early childhood diseases such as mental retardation. Furthermore, many synaptic connections can be remodeled even after the circuits are established, yet such ability appears to be diminished over time, contributing to the great medical challenge in adult nerve regeneration.

The research in my laboratory attempts to understand the general principles underlying neurite growth, guidance and branching, three key steps in establishing synaptic connection during development. Our current effort devotes to the understanding of branching, a process that is common to almost every nerve cell yet the mechanism of which is not well understood. How does the neuron decide when and where to make branches? What controls the branch number and pattern? How is it regulated coordinately with neurite growth and guidance to produce many striking cell morphologies in the brain? How are they modified by neuronal activities? To explore these questions, we use vertebrate sensory neurons in the dorsal root ganglion as a model and study their branch formation by combining a variety of approaches, including transgenic mice, primary cell culture and live cell imaging.

Using these modern tools, we recently discovered that the secreted molecule Slit and its cell surface receptor Robo play an important role in regulating arborization and bifurcation, two forms of branching of sensory neurons at different embryonic stages. This opens the door to further identifying the signaling network and studying the branching machinery inside the cell. In addition, it provides us a unique opportunity to understand the interplay between branching and neurite growth and guidance, two steps that are intimately associated with branching. We hope that our research on developing sensory neurons will not only help us uncover the wiring mechanisms of the nervous system, but also provide insights into regenerating adult neurons after injury.



10 Selected Publications:
Click here to view all the publications for this faculty

Chen Z,Gore BB,Long H,Ma L,Tessier-Lavigne M - Alternative splicing of the Robo3 axon guidance receptor governs the midline switch from attraction to repulsion. - Neuron [2008] May 8;58(3):325-32 PubMed

Ma L,Tessier-Lavigne M - Dual branch-promoting and branch-repelling actions of Slit/Robo signaling on peripheral and central branches of developing sensory axons. - J Neurosci [2007] Jun 20;27(25):6843-51 PubMed

López-Bendito G,Flames N,Ma L,Fouquet C,Di Meglio T,Chedotal A,Tessier-Lavigne M,Marín O - Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain. - J Neurosci [2007] Mar 28;27(13):3395-407 PubMed

Fouquet C,Di Meglio T,Ma L,Kawasaki T,Long H,Hirata T,Tessier-Lavigne M,Chédotal A,Nguyen-Ba-Charvet KT - Robo1 and robo2 control the development of the lateral olfactory tract. - J Neurosci [2007] Mar 14;27(11):3037-45 PubMed

Lebensohn AM,Ma L,Ho HY,Kirschner MW - Cdc42 and PI(4,5)P2-induced actin assembly in Xenopus egg extracts. - Methods Enzymol [2006] ;406():156-73 PubMed

Ho HY,Rohatgi R,Lebensohn AM,Le Ma,Li J,Gygi SP,Kirschner MW - Toca-1 mediates Cdc42-dependent actin nucleation by activating the N-WASP-WIP complex. - Cell [2004] Jul 23;118(2):203-16 PubMed

Grieshammer U,Le Ma,Plump AS,Wang F,Tessier-Lavigne M,Martin GR - SLIT2-mediated ROBO2 signaling restricts kidney induction to a single site. - Dev Cell [2004] May;6(5):709-17 PubMed

Long H,Sabatier C,Ma L,Plump A,Yuan W,Ornitz DM,Tamada A,Murakami F,Goodman CS,Tessier-Lavigne M - Conserved roles for Slit and Robo proteins in midline commissural axon guidance. - Neuron [2004] Apr 22;42(2):213-23 PubMed

Sabatier C,Plump AS,Le Ma,Brose K,Tamada A,Murakami F,Lee EY,Tessier-Lavigne M - The divergent Robo family protein rig-1/Robo3 is a negative regulator of slit responsiveness required for midline crossing by commissural axons. - Cell [2004] Apr 16;117(2):157-69 PubMed

Nguyen Ba-Charvet KT,Brose K,Ma L,Wang KH,Marillat V,Sotelo C,Tessier-Lavigne M,Chédotal A - Diversity and specificity of actions of Slit2 proteolytic fragments in axon guidance. - J Neurosci [2001] Jun 15;21(12):4281-9 PubMed


NCBI Disclaimers and copyright notice
Last updated: Monday August 10th 10:10am 2009

Return to   PIBBS home page  |  Research Topics page
  For more information contact the PIBBS Program

University of Southern California
1975 Zonal Avenue KAM-B16
Los Angeles, California 90089-9031
323-442-1609 (voice) / 323-442-1199 (fax)
E-mail: pibbs@usc.edu
 
 
© 1998-2008 The University of Southern California