Research Interests
    The regulation of apical membrane traffic in polarized epithelial cells; the mechanisms by which proteins are selected for apical delivery, incorporated into vesicular carriers, and targeted to the appropriate membrane.

    Dr. Weisz’s laboratory studies are directed towards identifying cytoplasmic proteins that facilitate the formation and budding of apically-destined transport carriers, and determining whether different classes of apical proteins utilize common sorting and transport machineries to reach the cell surface. Polarized epithelial cells have the remarkable capacity to generate and maintain differentiated apical and basolateral plasma membrane domains with distinct protein and lipid compositions. This is accomplished in part by the vectorial delivery of newly synthesized membrane proteins to these domains. In cells of renal origin, these proteins traffic together through the Golgi, and emerge from the trans-Golgi network (TGN) in distinct populations of carriers. Using the combined approaches of in vitro reconstitution assays with live-cell imaging, Dr. Weisz hopes to generate a more comprehensive view of how apical protein export from the TGN is regulated.


 
Selected Publications
  1. Weixel KM, Edinger RS, Kester L, Guerriero CJ, Wang H, Fang L, Kleyman TR, Welling PA, Weisz OA, Johnson JP. Phosphatidylinositol 4-phosphate 5-kinase reduces cell surface expression of the epithelial sodium channel (ENaC) in cultured collecting duct cells. J Biol Chem. 2007 Dec 14;282(50):36534-42. Epub 2007 Oct 16.
  2. Oztan A, Silvis M, Weisz OA, Bradbury NA, Hsu SC, Goldenring JR, Yeaman C, Apodaca G. Exocyst Requirement for Endocytic Traffic Directed Toward the Apical and Basolateral Poles of Polarized MDCK Cells. Mol Biol Cell. 2007 Oct;18(10):3978-92.
  3. Jin J, Sturgeon T, Chen C, Watkins SC, Weisz OA, Montelaro RC. Distinct intracellular trafficking of EIAV and HIV-1 gag during viral assembly and budding revealed by bimolecular fluorescence complementation assays. J Virol. 2007 Oct;81(20):11226-35.
  4. Cresawn KO, Potter BA, Oztan A, Guerriero CJ, Ihrke G, Goldenring JR, Apodaca G, Weisz OA. Differential involvement of endocytic compartments in the biosynthetic traffic of apical proteins. EMBO J. 2007 Aug 22;26(16):3737-48.
  5. Chen C, Jin J, Rubin M, Huang L, Sturgeon T, Weixel KM, Stolz DB, Watkins SC, Bamburg JR, Weisz OA, Montelaro RC. Association of gag multimers with filamentous actin during equine infectious anemia virus assembly. Curr HIV Res. 2007 May;5(3):315-23.

    Complete Publication Listing
 
Grant Support
  1. NIH 1R01DK064613
    Regulation of polarized traffic by PI-metabolizing enzymes.
    Principal Investigator
  2. Commonwealth of PA
    Polarized membrane traffic in kidney cells.
    Principal Investigator
  3. NIH 5R01 DK057718
    Trafficking and regulation of the epithelial Na+ channel.
    Co-Investigator
 
Other Links
Personal web site
Dept. of Medicine-Renal Electrolyte Division
University of Pittsburgh
 
   
     
  Ora A. Weisz, Ph.D., Associate Professor
Office:  978.1 Scaife Hall
Lab:978 Scaife Hall
Phone:412-383-8891
Fax: 412-383-8956
weisz@pitt.edu
 
Academic Affiliations
  • Department of Medicine (Renal-Electrolyte Division)

  • Cell Biology and Physiology Department

  • University of Pittsburgh Cancer Institute

  • McGowan Institute for Regenerative Medicine (affiliate member)

 
Education
  • 1984 B.S. Mol. Biophys. Biochem History
    Yale University
    New Haven, CT

  • 1990 Ph.D. Biochem., Cell and Mol. Biology
    Johns Hopkins School of Medicine
    Baltimore, MD

  • 1990-1995 Postdoctoral
    Johns Hopkins School of Medicine
    Baltimore, MD

 
Lab Personnel

Postdoctoral Fellow:
Polly Mattila, Ph.D.

Research Specialist:
Jennifer Bruns

Graduate Students:
Shanshan Cui, Chris J. Guerriero, Mark Miedel, Di Mo