Evidence that the central canal lining of the spinal cord contributes to oligodendrogenesis during postnatal development and adulthood in intact rats

J Comp Neurol. 2014 Oct 1;522(14):3194-207. doi: 10.1002/cne.23590. Epub 2014 Apr 12.

Abstract

Two waves of oligodendrogenesis in the ventricular zone of the spinal cord (SC-VZ) during rat development, which take place between embryonic days 14 and 18 (E14-E18) and E20-E21, have been described. In the VZ of the brain, unlike the SC-VZ, a third wave of oligodendrogenesis occurs during the first weeks of postnatal development. Using immunofluorescence staining of intact rat SC tissue, we noticed the presence of small numbers of Olig2(+) /Sox-10(+) cells inside the lining of the central canal (CC) during postnatal development and adulthood. Olig2(+) /Sox-10(+) cells appeared inside the lining of the CC shortly after birth, and their number reached a maximum of approximately 0.65 ± 0.14 cell/40-μm section during the second postnatal week. After the latter development, the number of Olig2(+) /Sox-10(+) cells decreased to 0.21 ± 0.07 (P36) and 0.18 ± 0.1 cell/section (P120). At P21, Olig2(+) /Sox-10(+) cells inside the CC lining started to express other oligodendroglial markers such as CNPase, RIP, and APC. Olig2(+) /Sox-10(+) cells usually did not proliferate inside the CC lining and were only rarely found to be immunoreactive against oligodendrocyte progenitor markers such as NG2 or PDGFRα. Using 5-bromo-2-deoxyuridine administration at P2, P11, P22, or P120-P125, we revealed that these cells arose in the CC lining during postnatal development and adulthood. Our findings confirmed that the CC lining is the source of a small number of cells with an oligodendroglial phenotype during postnatal development and adulthood in the SC of intact rats.

Keywords: ependyma; gliogenesis; oligodendrocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Animals, Newborn
  • Antigens / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Bromodeoxyuridine / metabolism
  • Cell Count
  • Cell Differentiation / physiology*
  • Cell Proliferation / physiology*
  • Embryo, Mammalian
  • Gene Expression Regulation, Developmental / physiology
  • Ki-67 Antigen / metabolism
  • Myelin Basic Protein / metabolism
  • Nerve Tissue Proteins / metabolism
  • Oligodendrocyte Transcription Factor 2
  • Oligodendroglia / physiology*
  • Proteoglycans / metabolism
  • Rats
  • Rats, Wistar
  • SOXB1 Transcription Factors / metabolism
  • Spinal Cord / cytology
  • Spinal Cord / embryology
  • Spinal Cord / growth & development*
  • Time Factors

Substances

  • Antigens
  • Basic Helix-Loop-Helix Transcription Factors
  • Ki-67 Antigen
  • Mbp protein, rat
  • Myelin Basic Protein
  • Nerve Tissue Proteins
  • Olig2 protein, rat
  • Oligodendrocyte Transcription Factor 2
  • Proteoglycans
  • SOXB1 Transcription Factors
  • Sox2 protein, rat
  • chondroitin sulfate proteoglycan 4
  • Bromodeoxyuridine