Cellular and ultra structural evidence for cytoskeletal localization of prolyl endopeptidase-like protein in neurons

Neuroscience. 2013 Jul 9:242:128-39. doi: 10.1016/j.neuroscience.2013.02.038. Epub 2013 Feb 26.

Abstract

The biochemical properties and subcellular localization of prolyl endopeptidase (PREP) in brain are well characterized and its implications in the realization of cognitive processes and in the pathogenesis of neurodegenerative disorders are a matter of intensive investigation. In contrast, very little is known about its homolog, the PREP-like protein (PREPL). In order to obtain initial hints about the involvement of PREPL in physiological processes, a differential proteomic screen was performed with human skin fibroblasts from controls and patients with PREPL deficiency (hypotonia-cystinuria syndrome). The majority of affected proteins represented cytoskeletal proteins, including caldesmon, tropomyosin α3 chain, lamin A, β-actin, γ-actin, vimentin and zyxin. Therefore, the analysis of PREPL subcellular localization by confocal laser scanning and electron microscopy in mouse neurons was focused on the cytoskeleton. The co-localization of PREPL with cytoskeletal marker proteins such as β-actin and microtubulin-associated protein-2 was observed, in addition to the presence of PREPL within Golgi apparatus and growth cones. In the mouse brain, PREPL is neuronally expressed and highly abundant in neocortex, substantia nigra and locus coeruleus. This mirrors to some extent the distribution pattern of PREP and points toward redundant functions of both proteins. In the human neocortex, PREPL immunostaining was found in the cytoplasm and in neuropil, in particular of layer V pyramidal neurons. This staining was reduced in the neocortex of Alzheimer's disease (AD) patients. Moreover, in AD brains, PREPL immunoreactivity was observed in the nucleus and in varicose neuritic processes. Our data indicate physiological functions of PREPL associated with the cytoskeleton, which may be affected under conditions of cytoskeletal degeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / metabolism
  • Animals
  • Case-Control Studies
  • Chromosome Deletion
  • Chromosomes, Human, Pair 21 / metabolism
  • Craniofacial Abnormalities / metabolism
  • Cystinuria / metabolism
  • Cytoskeletal Proteins / metabolism*
  • Cytoskeleton / metabolism*
  • Female
  • Fibroblasts / metabolism
  • Fibroblasts / ultrastructure
  • Humans
  • Intellectual Disability / metabolism
  • Locus Coeruleus / metabolism
  • Male
  • Mice
  • Mitochondrial Diseases / metabolism
  • Muscle Hypotonia / metabolism
  • Neocortex / metabolism
  • Neurons / metabolism*
  • Neurons / ultrastructure
  • Primary Cell Culture
  • Prolyl Oligopeptidases
  • Proteomics
  • Pyramidal Cells / metabolism
  • Serine Endopeptidases / metabolism*
  • Substantia Nigra / metabolism

Substances

  • Cytoskeletal Proteins
  • Serine Endopeptidases
  • PREPL protein, human
  • Prolyl Oligopeptidases

Supplementary concepts

  • Hypotonia-Cystinuria Syndrome