Ling-Gang
Wu M.D., Ph.D., Senior InvestigatorDr. Wu received his M.D. in 1985 from Second Military Medical College, Shanghai, and his Ph.D. in neuroscience in 1994 from
Baylor College of Medicine, where he worked with Peter Saggau studying the role of presynaptic voltage-dependent calcium channels
in controlling transmitter release. From 1994 to 1996 he did postdoctoral training with William J. Betz at the University
of Colorado Medical School, where he studied the kinetic regulation of endocytosis at frog neuromuscular junctions using FM
dye imaging. From 1996 to 1999 he a second postdoctoral fellowship with Bert Sakmann at the Max Planck Institute in Heidelberg,
Germany, where he identified calcium channel types and studied the presynaptic mechanisms underlying short-term synaptic depression
at a giant nerve terminal, the calyx of Held in rat brainstem. From 1999 to 2003 he was an assistant professor at Washington
University in St. Louis, where his laboratory applied capacitance recording techniques to study regulation of the kinetics
of endocytosis at the calyx of Held. Dr. Wu joined NINDS as an investigator in 2003 and was promoted to senior investigator
in 2007. His laboratory is using electrophysiological, imaging, as well as biochemical and molecular biological techniques,
to investigate the cellular and molecular mechanisms underlying generation and regulation of endocytosis and synaptic plasticity
at the calyx-type synapse.
Laboratory StaffLi Bai, M.S. Technician
301-451-
3332
Abdeladim Elhamdani, Ph.D. Research Fellow
301-451-
3356
Junmei Fan, Ph.D. Visiting Fellow
301-594-
1287
Liming He, Ph.D. Research Fellow
301-451-
3358
Benjamin McNeil, B.S. Graduate Student
301-451-
2284
Kenneth Paradiso, Ph.D. Research Fellow
301-451-
3341
Jiansong Sheng, Visiting Fellow
301-451-
3334
Wonchul Shin, Visiting Fellow
301-451-
3335
Tao Sun, Ph.D. Visiting Fellow
301-451-
3339
Xin-Sheng Wu, Ph.D. Research Fellow
301-451-
3345
Jianhua Xu, Ph.D. Research Fellow
301-451-
3340
Lei Xue, Ph.D. Postdoctoral Fellow
301-451-
3357
Research InterestsNeurons communicate with each other via chemical synaptic transmission. Regulation of the strength of synaptic transmission
plays essential roles in many physiological and pathological processes, such as control of neuronal network outputs, neuronal
development, learning and memory, and neurological diseases. It remains poorly understood how synaptic strength is controlled
at nerve terminals. Filling this gap of knowledge is the goal of the Synaptic Transmission Unit.
Selected Recent PublicationsXu J, McNeil B, Wu W, Nees D, Bai L, Wu LG.GTP-independent rapid and slow endocytosis at a central synapse - Nat Neurosci.
11(1) 45-53 2008
He L, Wu LG. The debate on the kiss-and-run fusion at synapses. - Trends in Neuroscience
30(9) 447-55 2007
Wu LG, Ryan TA, Lagnado L.Modes of vesicle retrieval at ribbon synapses, calyx-type synapses, and small central synapses - J Neurosci.
27(44) 11793-802 2007
Xu J, He L, Wu LG.Role of Ca(2+) channels in short-term synaptic plasticity. - Curr Opin Neurobiol.
17(3) 352-9 2007
He L, Wu XS, Mohan R, and Wu LG. Two modes of fusion pore openings revealed by cell-attached recordings at a synapse - Nature
444 102-105 2006
Xu J and Wu LGThe decrease in the presynaptic calcium current is a major cause of short-term depression at a calyx-type synapse. - Neuron
46 633-645 2005
Selected Earlier Publications
Contact InformationSynaptic Transmission Section, NINDS Porter Neuroscience Research Center
Building 35, Room 2B-1012
35 Convent Drive, MSC 3706 Bethesda MD
20892-3706
Telephone:
301-451-
3338 (office), 301-
451-3338 (laboratory),
301-480-
1466 (fax), Email:
wul@ninds.nih.gov