Faculty and Staff

  • Randal E. Morris, PhD
  • Research Professor Emeritus
  •  
  • Department of Medical Education, University of Cincinnati College of Medicine
  • (513) 558-6007
  • randal.morris@uc.edu

Interest:

  • My research interest over the past 20 years has focused on endocytosis, i.e. the binding, internalization, and intracellular routing of ligands by eucaryotic cells. To monitor these events my colleagues and I have employed a variety of techniques, both biochemical and morphological. My forte is electron microscopy; more specifically, I use immunohistochemical techniques at the ultrastructural level toanswer questions central to cell biology.One of the 2 systems in which I am interested is the interaction of bacterial toxins with mammalian cells. Although I have studied a variety of toxins (including diphtheria, cholera, and botulinum toxins), the greatest effort has focused on the interaction of Pseudomonas exotoxin A (PE) with a sensitive cell line, mouse LM fibroblasts. My colleagues and I have elucidated the binding, internalization, intracellular trafficking of PE by mouse LM cells. Currently we are attempting to determine where activation of the toxin occurs, and from which intracellular compartment the toxin gains entry into the cytosol. Based on kinetic studies and morphological data, my interpretation is that the Golgi is the site of escape. The site of activation is less clear but recent data suggest it is either the cell surface, endosomal compartment, or in the Golgi.The second system to which I devote my research effort is the interaction of the major surfactant protein (SP-A) with rat alveolar Type II epithelial cells. Pulmonary surfactant is a complex mixture of lipids and proteins, of which SP-A is the most abundant protein. Several pathological conditions are associated with surfactant, and these are of significant consequence. Included among these pathological conditions are respiratory disease syndrome of children (hyaline membrane disease), adult respiratory disease syndrome (ARDS), and alveolar proteinosis. The goal of this project is to characterize the autocrine function of SP-A.

    Education:

  • B.S.: Aurora College, 1969
  • M.S.: Northern Illinois University, 1971
  • Ph.D.: Emory University, 1974

Awards and Honors:

  • Most Outstanding Teaching Award-Medical Histology, 2001
  • Most Outstanding Teaching Award-Medical Histology, 1997
  • Most Outstanding Teaching Award-Medical Histology, 1993
  • Most Outstanding Teaching Award-Medical Histology, 1990