Miles Epstein

Professor Emeritus
Ph.D., 1972, University of California - Los Angeles

Contact Information
Email: mepstein@wisc.edu
(608) 263-5074 Phone
(608) 263-2311 Lab
(608) 265-5512 Fax

 
Research Interests
Regulation of Neuronal Differentiation and Neurotransmitter Phenotype

Miles Epstein

After entering the gut, neural crest cells migrate, proliferate, and differentiate to form the intrinsic neurons of the gut. These neurons are located in ganglia along the length of the gut. Within a single ganglion, neurons of different transmitter phenotypes are found. These neurons form a network that controls the motor behavior of the gut. Thus, enteric neuronal circuitry is generated that processes intrinsic sensory information and produces a motor output, independent of the CNS.

Our interest is in elucidating the arrangement of the neurons in the enteric neuronal circuitry and mechanisms involved in the formation of this circuitry. Formation of the circuitry involves understanding what triggers the differentiation of precursor cells into neurons, what determines the type of transmitter synthesized, and what controls the neuron's finding the correct postsynaptic target. Growth factors play a major role in these processes. We are interested in determining both the location in the gut and the transmitter phenotype of daughters of a single progenitor cell. Our in vitro studies involve culturing neural crest-derived precursors to determine the role of the microenvironment on transmitter differentiation.

Selected Publications

  • Zaitoun, I., C. S. Erickson, K. Schell, and M. L. Epstein. (2010) Use of RNAlater in fluorescence-activated cell sorting (FACS) reduces the fluorescence from GFP but not from DsRed. BMC Research Notes 3:328
     
  • Mavlyutov, T.A., M.L. Epstein, K.A. Andersen and A.E. Ruoho. (2010) The sigma-1 receptor is enriched in c-terminals in mouse motoneurons. an anatomical and behavioral study. Neuroscience 167: 247-255.
     
  • Druckenbrod, N.R. and M. L. Epstein (2009) Age-dependent changes in the gut environment restrict the invasion of the hindgut by enteric neural progenitors. Development 136:3195-3203
     
  • Druckenbrod, N.R, P A. Powers, C. R. Bartley , J. W. Walker, and M. L. Epstein. (2008) Targeting of Endothelin Receptor-B to the Neural Crest. Genesis 46:396-400
     
  • Druckenbrod NR, Epstein ML. (2007) Behavior of enteric neural crest-derived cells varies with respect to the migratory wavefront. Dev. Dyn. 236:84-92
     
  • Druckenbrod, N.R. and M.L.Epstein. (2005) The pattern of neural crest advance in the cecum and colon. Developmental Biology 287:125-133
     
  • Conner, P.J., P.J.Focke., D.M.Noden, and M.L. Epstein. (2003) Appearance of Neurona and Glia with respect to the wavefront during colonization of the avain gut by neural crest cells. Dev. Dynamics 226:91-98.
     
  • Focke, P.J., A.R Swetlik, J.L. Schiltz and M.L. Epstein, (2003) GDNF and insulin cooperate to enhance the proliferation and differentiation of enteric crest-derived cells. J.Neurobiology 55:151-164
     
  • Focke,P.J., C.A.Schiltz, S.E.Jones, J.J.Watters, and M.L.Epstein, (2001) Enteric neuroblasts require the phosphatidylinositol 3- kinase pathway for GDNF-stimulated proliferation. J. Neurobiology 47:306-317
     

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