Zhen Huang

Position title: Associate Professor Associate Professor, Neurology Ph.D., Harvard University

Email: z.huang@neurology.wisc.edu

Phone: Phone: (608) 263-2469 | Lab: (608) 262-2469 | Fax: (608) 265-5512

RESEARCH INTERESTS - Molecular mechanisms that regulate neuronal migration, laminar assembly, and vascular patterning in the cerebral cortex

Zhen Huang

Cortical neuron migration and laminar assembly

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Figure 1

My lab is interested in several aspects of the development of the cerebral cortex. We are interested in how the different levels of organization in the cortex, from global to cellular and synaptic organization and from neural to vascular patterning, arise during normal development and how they may be affected in and contribute to brain neural and vascular diseases. To investigate how the exquisite layer organization of the cortex arises, we focus on the question of how the generation and migration of neurons and glia are regulated. We employ mouse genetics approaches and use tissue specific gene knockout technology to answer this question. Among the genes of interest to us is a gene involved in G protein coupled receptor (GPCR) signaling. We have found that mutation in this gene, ric-8a, which encodes a guanine nucleotide exchange factor (GEF) for heterotrimeric G proteins, results in cobblestone lissencephaly-like malformation in the cerebral cortex as well as lobule formation defects in the cerebellum. One of our goals is to use this mutation as an entry point to gain new insights into mechanisms by which cell-cell communication coordinates the complex process of brain development.

The normal embryonic (E16.5) cortex contains a densely packed cortical plate underneath a cell-sparse marginal zone (Nuclear staining in green). A pial basement membrane (Laminin staining in red) enwraps the cortex on the surface. In ric-8a mutants, ectopic neurons are found at the pial surface, in association with breaks in the basement membrane, similar to phenotypes in type II (cobblestone) lissencephaly in humans.

Blood vessel development in the brain

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Figure 2

To understand how blood vessel development in the brain is regulated, we focus on interactions between neural and vascular cells. Specifically, we have found that radial glia, neural progenitor cells in the developing brain, play an unexpected in regulating the stabilization of nascent blood vessels. In the absence of radial glia, newly formed blood vessels in the cortex become destabilized and eventually undergo regression. This provides a unique model to determine how new blood vessels in the brain are stabilized. One of our goals is to determine the identity of the signal(s) involved as well as the vascular genes regulated by radial glia. We are also interested in whether and how these genes may be involved in and contribute to brain neurovascular diseases.

Blood vessels (outlined in green) form a stereotypic network in the neonatal mouse cortex in normal control animals. In mutants where radial glial neural progenitors are ablated, many vessels undergo regression and are lost (see details in Ma et al. 2012 PLoS Biology).

Career Opportunities

Postdoctoral position: Highly motivated applicants, preferably with a strong background in mouse development and/or transcriptional profiling, are encouraged to apply. Please send 1) curriculum vitae (CV), 2) a brief description of research plan, and 3) contact information for references to z.huang@neurology.wisc.edu.

Selected Publications

  • Ma, S., Kwon, H. J., Johng, H, Zang, K, and, Huang, Z. (2012). Radial glia neural progenitors regulate nascent brain vascular network stabilization via inhibition of Wnt signaling. (in press at PLoS Biology).
  • Ma, S., Kwon, H.J., Huang, Z. (2012). A functional requirement for astroglia in promoting blood vessel development in the early postnatal brain. PLoS One 7(10): e48001. doi:10.1371/journal.pone.0048001
  • Ma, S., Kwon, H.J., Huang, Z. (2012). Ric-8a, a guanine nucleotide exchange factor in GPCR signaling, regulates Bergmann glia-basement membrane adhesion during cerebellar foliation. The Journal of Neuroscience 32 (43): 14979 �14993
  • Kwon, H.J., Ma, S., and Huang, Z. (2011) Radial glia regulate Cajla-Retzius cell positioning in the early embryonic cerebral cortex. Developmental Biology 351: 25-34. [Epub ahead of print] 2010 Dec 23
  • Huang, Z. (2009) Molecular regulation of neuronal migration during neocortical development. Molecular Cellular Neuroscience42(1):11-22. Epub 2009 Jun 10
  • Huang, Z, Shimazu, K., Woo, N.H., Zang, K., Muller, U., Lu, B., and Reichardt, L.F. (2006). Distinct roles of the b1-class integrins at the developing and the mature hippocampal excitatory synapse. The Journal of Neuroscience 26 (43): 11208-11219
  • Huang, Z., Zang, K., and Reichardt, L.F. (2005). The origin recognition core complex regulates dendrite and dendritic spine development in postmitotic neurons. The Journal of Cell Biology 170 (4): 527-535.
  • Graus-Porta, D., Blaess, S., Senften, M., Littlewood-Evans, A., Damsky, C., Huang, Z., Orban, P., Klein, R., Schittny, J.C., and Muller, U. (2001). &Mac178;1-class integrins regulate the development of laminae and folia in the cerebral and cerebellar cortex. Neuron 31(3): 367-79.
  • Huang, Z., Shilo, B-Z., and Kunes, S. (1998). A retinal axon fascicle uses Spitz, an EGF receptor ligand, to construct a synaptic cartridge in the brain of Drosophila. Cell 95 (5): 693-703
  • Huang, Z. and Kunes, S. (1998). Signals transmitted along retinal axons in Drosophila: Hedgehog signal reception and the cell circuitry of lamina cartridge assembly. Development 125 (19), 3753-3764
  • Huang, Z. and Kunes, S. (1996). Hedgehog, transmitted along retinal axons, triggers neurogenesis in the developing visual centers of the Drosophila brain. Cell 86 (3): 411-422.