Faculty Directory

Mary Ann Stepp

Mary Ann Stepp

Professor of Anatomy and Cell Biology
Professor of Ophthalmology (Secondary)

Office Phone: 202-994-0557
Email: Email
Department: Anatomy and Cell Biology

Education

  • BS, Simmons College, 1980
  • PhD, Boston University, 1986

Biography

Teaching Interests

Cell Biology; Cellular Junctions (desmosomes, hemidesmosomes, tight junctions, adherens; gap); Histology of the eye, connective tissues, and muscles; Integrins and the Extracellular Matrix; Rat and mouse development and use of transgenic mice as models.

Lab Site

https://smhs.gwu.edu/stepp-lab/

Research

The structural properties of the cornea make it strong to best protect the retina from damage while at the same time maintaining clarity and its curved shape so it can focus light properly. The epithelial cells that cover the cornea are maintained by a population of stem cells located within a specialized stem cell niche at a site called the limbus. Because of its clarity and strength, the cornea and its stem cell niche can be viewed using state of the art imaging methods to give us insight into how it is arranged in health and disease. In our lab, we are studying the cornea and its niche to understand is how corneal epithelial stem cells are maintained within their niche in normal tissue homeostasis and in during wound healing.

In particular, we have focused on how epithelial cells adhere to the underlying extracellular matrix via proteins called integrins. We have shown that corneal epithelial stem cells express higher amounts of specific types of integrins. These integrins mediate attachment to and the organization of the underlying matrix by binding to matrix protein in the niche. We have also developed a mouse model that allows us to reproducibly induce corneal epithelial stem cell deficiency and recurrent epithelial erosions. This model will be useful in developing treatments to minimize both the development and the progression of stem cell deficiency and to allow us to begin to design treatments for patients suffering from this disease. Our next steps involve analysis of the timing of the changes that happen as stem cell deficiency develops and the stem cell niche becomes depleted of its stem cells. For in vitro experiments, we use primary cell cultures derived from wildtype mouse keratinocytes and keratinocytes derived from various transgenic and knockout mice. Techniques used in the lab include brightfield,and confocal microscopy, time lapse cell migration studies, analyses of protein expression and signal transduction pathways using immunoblotting, immunoprecipitation, reporter assays, and zymography as well as primary culture of mouse epithelial cells.

Our long term goals are to better our understanding of how the cells that make up the epithelial niche of the cornea are maintained and what happens to those cells and their niche when the tissue they serve is injured. To be able to prevent stem cell loss and recurrent corneal erosions, we need to understand how they happen and our animal models will allow us to do just that. This knowledge will lead to improved treatment of patients with corneal epithelial stem cell deficiency and recurrent corneal erosions. It will also enhance our knowledge of the factors that regulate proliferation of epithelial stem cells during tumor and pterygia development.

Current Members

Publications

View publications by this faculty member from January 1, 2013 - present

Stepp MA, Liu Y, Pal-Ghosh S, Jurjus RA, Tadvalkar G, Sekaran A, Losicco K, Jiang L, Larsen M, Li L, and Yuspa SH. 2007. Reduced migration, altered matrix and enhanced TGF?1 signaling are signatures of mouse keratinocytes lacking Sdc1. J. Cell Sci. 120, 2851-2863. PDF

Vanhoutte D, Schellings MW, Gotte M, Swinnen M, Herias V, Wild MK, Vestweber D, Chorianopoulos E, Cortes V, Rigotti A, Stepp MA, Van de Werf F, Carmeliet P, Pinto YM, and Heymans S. 2007. Increased expression of syndecan-1 protects against cardiac dilatation and dysfunction after myocardial infarction. Circulation. 115, 475-482.

Stepp MA. 2006. Corneal integrins and their functions. Exp. Eye Res. 83:3-15. PDF

Pajoohesh-Ganji A, Pal-Ghosh S, Simmons SJ, and Stepp MA, 2006. Integrins in slow cycling corneal epithelial cells in the mouse. Stem Cells 24:1075-1086. PDF

Stepp MA and Zieske JD. 2005. The corneal epithelial stem cell niche. Ocul. Surf. 3, 15-26. PDF

Pajoohesh-Ganji A. and Stepp MA. 2005. In search of markers for the stem cells of the corneal epithelium. Biol. Cell 97:265-276. PDF

Pajoohesh-Ganji A, Pal-Ghosh S, and Stepp MA. 2004. Regional distribution of ?9?1 integrin within the limbus of the mouse ocular surface. Dev. Dyn. 230:518-528. PDF

Pal-Ghosh S, Pajoohesh-Ganji A, and Stepp MA. 2004. A mouse model for the study of recurrent epithelial erosions demonstrates a role for a9b1 integrin in progression of disease. Invest. Ophthalmol.Vis. Sci. 45:1775-1785.PDF

Tomczuk M, Takahashi Y, Huang J, Murase S, Mistretta M, Klaffky E, Sutherland A, Bolling L, Conrod S, Marcinkiewicz C, Sheppard D, Stepp MA, and White JM. 2003. Role of Multiple b1 Integrins in Cell Adhesion to The Disintegrins Domains of Adams 2 and 3. Exp. Cell Res. 290, 68-81.

Stepp MA, Gibson HE, Gala PH, Sta.Iglesia DD, Pajoohesh-Ganji A, Pal-Ghosh S, Brown M, Aquino C, Schwartz AM, Goldberger O, Hinkes MT, and Bernfield M. 2002. Defects in keratinocyte activation during wound healing in the syndecan-1 deficient mouse. J.Cell Sci., 115, 4517-4531. PDF

Belkin AH and Stepp MA.  2000.  Integrins as Receptors for Laminins.  Microscopy Research Techniques 51, 280-301.

Sta. Iglesia DD and Stepp MA.  2000. Disruption of the Basement Membrane After Corneal Debridement.  Invest. Ophthal. Vis. Sci.:  41, 1045-1053.

Sta. Iglesia DD, Gala PH, Qiu T, and Stepp MA.  2000.  Integrin Expression During Epithelial Migration and Restratification in the Tenascin-C-deficient Mouse Cornea. J. Histochemistry and Cytochemistry, 48, 363-376.

Additional publications published before January 1, 2013 may be available within Himmelfarb Library's database.

Industry Relationships and Collaborations

This faculty member (or a member of their immediate family) has reported a financial interest with the healthcare related companies listed below. These relations have been reported to the University and, when appropriate, management plans are in place to address potential conflicts.

  • None