A Novel Marker for Purkinje Cells, Ribosomal Protein MPS1/S27: Expression of MPS1 in Human Cerebellum

Cancer Genomics Proteomics. 2016 Jan-Feb;13(1):47-53.

Abstract

Background: The ribosomal protein metallopanstimulin-1 (MPS1/S27) serves critical survival purposes in cell division, in normal and cancerous cells; for this reason, selective pressures of evolution have conserved the DNA sequences encoding MPS1/S27 in Archaea and Eukariotic cells. The expression of MPS1/S27 protein in human adult cerebellum has not been established.

Material and methods: The presence of MPS1/S27, was screened in paraffin-embedded human adult brain specimens processed for tissue inmunohistochemistry. Affinity-purified specific antibodies were directed against the N-terminus of MPS1.

Results: The antibodies to MPS1 detected Purkinje cells (PC) and their dendrites. In PC, MPS1 antigen-positive staining was found in: the nucleolus, which was strongly stained; ribosomes attached to the external nuclear membrane; cytoplasm of PC, with strong staining in a punctuate fashion; the soma-attached large dendrite trunks of PC, which were MPS1 antigen-positive; and the granular cell layer, where cellular staining in a few cells that appeared to resemble smaller PC was observed.

Conclusion: Since MPS1 is involved in cell division, DNA repair, and ribosomal biogenesis, it may be a useful antigen for studying processes such as protein synthesis, oncogenesis, regeneration, aging, and perhaps diseases of the human cerebellum.

Keywords: DNA repair protein; Metallopanstimulin-1; Purkinje cells; RP; cerebellum; immunohistochemistry marker; p53; ribosomal protein; ribosomal protein MPS1/S27; zinc-finger proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Cerebellum / cytology
  • Cerebellum / metabolism*
  • Humans
  • Immunohistochemistry
  • Male
  • Metalloproteins / metabolism*
  • Middle Aged
  • Nuclear Proteins / metabolism*
  • Purkinje Cells / metabolism*
  • RNA-Binding Proteins / metabolism*
  • Ribosomal Proteins / metabolism*

Substances

  • Metalloproteins
  • Nuclear Proteins
  • RNA-Binding Proteins
  • RPS27 protein, human
  • Ribosomal Proteins