<?xml version="1.0" encoding="UTF-8"?><profile href="/about_us/FacultyDirectory/Neurobiology/PeterMacLeish/index.php">
   <image>
      <img src="/_resources/MSMimages/FacultyDirectoryImages/Neurobiology/MacLeish.jpg" alt="Peter R. MacLeish, Ph.D."></img>
   </image>
   <name>Peter R. MacLeish, Ph.D.</name>
   <title>Professor  </title>
   <department>Neurobiology</department>
   <title2></title2>
   <department2></department2>
   <email>pmacleish@msm.edu</email>
   <phone>404-756-5786 </phone>
   <location>Multidisciplinary Research Center F-22614</location>
   <education>
      <strong>POSTGRADUATE:
         <br></br>
      </strong>
      <span>Harvard Medical School</span>
      <br></br>
      <strong>Postdoctoral Training: </strong>
      <span>Neurobiology
         <br></br>
      </span>
      <br></br>
      <strong>
         <strong>GRADUATE:</strong>
         <br></br>
      </strong>
      <span>Harvard University</span>
      <br></br>
      <strong>Degree: </strong>
      <span>
         <span>Doctor of Philosophy 
            <br></br>
            <br></br>
            <strong>UNDERGRADUATE:</strong>
            <br></br>
         </span>
      </span>University of Western Ontario
      <br></br>
      <span>
         <strong>Degree:</strong> Bachelor of Engineering Science (Electrical)
         <br></br>
      </span>
   </education>
   <research>
      <p>One component of my work focuses on the functional properties of mature neurons from
         the salamander and primate retina. These are neurons that have completed their neuroanatomical
         differentiation in the animal. The general approach is to isolate cells following
         enzymatic treatment of tissue and to use the characteristic morphology of cells to
         identify them. Our main experimental approaches are electrophysiology and optical
         imaging. We have studied phototransduction, synapse formation among the classes of
         retinal cells and the ionic conductances and their compartmentalization in identified
         cells. To improve the poor adhesion of mature neurons to conventional substrates,
         we have immobilized select antibodies that target cell surface antigens to coverslips
         to promote cell adhesion.
         <br></br>
         <br></br>A second component focuses on the ability of adult newts to regenerate a new retina
         from retinal pigment epithelial (RPE) cells. Enucleation of an eye followed by re-implantation
         leads to retinal degeneration and to the generation of a new retina through a series
         of steps involving RPE cells. The steps include the depigmentation of the RPE cells
         followed by proliferation and differentiation of RPE-derived cells into an intact
         and functional retina. Our aim is to determine the conditions that support retinal
         regeneration in vitro to help identify the cellular and molecular events that control
         the retinal regenerative process.
      </p>
   </research>
   <boardcerts></boardcerts>
   <publications>
      <ul>
         <li>Klein L.R., 
            <strong>MacLeish P.R.</strong> and Wiesel, T.N. Immunolabelling by a newt retinal pigment epithelium antibody during
            retinal development and regeneration. J. Comp. Neurol. 293: 331-339, 1990.
         </li>
         <li>Yagi T. and 
            <strong>MacLeish, P. R</strong>. Ionic conductances of monkey solitary cone inner segments. J. Neurophysiol., 71:
            656-665, 1994.
         </li>
         <li>
            <strong>MacLeish, P.R.</strong> and Nurse, C.A. Ion channel compartments in photoreceptors: Evidence from salamander
            rods with intact and ablated terminals. J. Neurophysiology 98: 86-95, 2007.
         </li>
         <li>O’Brien, J.J., Chen, X., 
            <strong>MacLeish, P.R</strong>., O’Brien, J. and Massey, S.C.  Photoreceptor Coupling Mediated by Connexin 36 in
            the Primate Retina. J. Neuroscience 32:4675-4687, 2012.
         </li>
         <li>Jorgenson, L.A., Newsome, W.T., Anderson, D.J., Bargmann, C.I., Brown, E.N., Deisseroth,
            K., Donoghue, J.P., Hudson, K.L., Ling, G.S.F., 
            <strong>MacLeish, P.R.</strong>, Marder, E., Normann, R.A., Sanes, J.R., Schnitzer, M.J., Sejnowski, T.J., Tank,
            D.W., Tsien, R.Y., Ugurbil, K., Wingfield, J.C. The BRAIN Initiative: developing technology
            to catalyse neuroscience research. Phil. Trans.  R. Soc. B 370: 20140164, 2015.
         </li>
      </ul>
   </publications>
   <awards>
      <ul>
         <li>Member, Dana Alliance for Brain Initiatives</li>
         <li>Member, Institute of Medicine of the National Academies</li>
         <li>Member, NIH BRAIN Working Group</li>
      </ul>
   </awards>
</profile>