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Research Interests
    Have you ever wondered why you look differently from others? The answer is your cells are organized differently. But how? Multicellular organisms arrange cells in special patterns to form distinct structures through a set of developmental instructions that we do not fully understand. In my laboratory, we use the zebrafish retina as a model system to study the molecular mechanisms underlying cellular pattern formation in the central nervous system.

    The vertebrate retina develops from a single sheet of neuroepithelial cells, which later differentiate and reorganize into layered structures during retinal neurogenesis. Each retinal layer is composed of specific neuronal classes and executes distinct functions. Although the cellular architecture and function in the retina are relatively well characterized, the molecular mechanisms that control retinal pattern formation remain largely unknown.

    To understand how retinal cells organize, my lab uses a variety of experimental approaches that involve Genetics, Molecular Biology, Cell Biology, Biochemistry, and Developmental Biology. Our research is currently focused on the following areas: study how retinal epithelial polarity contributes to the formation of the layered cellular structure of the mature retina; investigate how cell-cell adhesion molecules play a role in retinal pattern formation; identify novel mutations that affect retinal development through mutagenesis screens



 
Selected Publications
  1. X. Yang, J. Zou, D. Hyde, L. Davidson, and X. Wei (2009) Stepwise maturation of apicobasal polarity of the neuroepithelium is essential for vertebrate neurulation. Journal of Neuroscience. 29:11426-11440.

  2. J. Zou , K. Lathrop, M. Sun, X. Wei (2008) "Intact retinal pigment epithelium maintained by Nok is essential for retinal epithelial polarity and cellular patterning in zebrafish" J Neurosci. 28:13684-95. | Abstract

  3. A. Catalano, P. Raymond, D. Goldman, X. Wei (2007) "Zebrafish dou yan mutation causes patterning defects and extensive cell death in the retina" Dev Dyn. 236:1295-306. | Abstract

  4. J. Zou, F. Beermann, J. Wang, K. Kawakami, and X. Wei. (2006) The Fugu rubripes tyrp1 promoter directs specific GFP expression in zebrafish: tools to study the RPE and neural crest-derived melanophores. Pigment Cell Research. 19:615-627. | Abstract

  5. Wei X, Zou J, Takechi M, Kawamura S, Li L. (2006) "Nok plays an essential role in maintaining the integrity of the outer nuclear layer in the zebrafish retina" Exp Eye Res. 83:31-44. | Abstract

 
Grant Support
  1. NIH RO1 EY016099
    PI: Xiangyun Wei
    Sept 30, 2005 -- Aug 31, 2010
  2. Research to Prevent Blindness Career Development Award
    PI: Xiangyun Wei
    Dec 2004-Dec 2008
  3. University of Pittsburgh Health System Competitive Medical Research Fund (CMRF) grant
    PI: Xiangyun Wei
    July 1, 2004-June 30, 2006
  4. University of Pittsburgh Startup fund
    PI: Xiangyun Wei
    Sept 2003-August 2006
 
Other Links

University of Pittsburgh
 
   
     
  Xiangyun Wei, Ph.D. Assistant Professor
Office:  Room 5060, BST3
Lab:Room 5065, BST3
Phone:412-383-5845
Fax: 412-647-5880
weix@upmc.edu
 
Academic Affiliations
  • Member, Biochemistry and Molecular Genetics Graduate Program

  • Department of Ophthalmology
    University of Pittsburgh School of Medicine

  • Department of Molecular Genetics and Biochemistry
    University of Pittsburgh School of Medicine

 
Education
  • University of Notre Dame
    Postdoc
    2002-2003
    Developmental biology

  • Harvard Medical School/MEEI, Boston
    Postdoc
    1998-2002
    Developmental biology

  • State University of New York at Buffalo
    Ph.D.
    1993-1998
    Cell Biology

 
Lab Personnel

Dr. Jian Zou, Postdoc

Dr. Xiaojun Yang, Postdoc

 
 


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