Mesoderm-derived cells proliferate in the embryonic central nervous system: confocal microscopy and three-dimensional visualization

Histochem Cell Biol. 1997 Mar;107(3):205-13. doi: 10.1007/s004180050105.

Abstract

In the chick and quail embryo, two cell populations migrate into the neural tube from the surrounding mesodermal tissues during the fourth day of incubation: individual cells which represent macrophages, and endothelial cells which remain continuous with the extraneural vessels. We report here on the proliferative capacity of these mesoderm-derived cells. A double-immunofluorescence protocol for two monoclonal antibodies of subtype IgG1, the endothelial cell/macrophage marker QH1, and the S-phase marker bromodeoxyuridine, was developed. With confocal laser scanning microscopy of thick microtome sections, labeling indices of intraneural individual QH1-positive cells (12%) and of endothelial cells (10%) were determined. In contrast, the labeling index of extraneural endothelial cells was 25%. With three-dimensional visualization of confocal data, the variable morphology of macrophages was shown. Our results indicate that: (1) proliferative activity of intraneural capillary endothelial cells is less than expected and that it is absent from sprouts; (2) both spheroidal and ramified macrophages proliferate inside the neural tissues; and (3) ramified macrophages frequently make contact with capillary endothelial cells. We conclude that most embryonic microglia may be derived from the early invasive QH1+ macrophages.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Division
  • Cell Separation
  • Central Nervous System / cytology
  • Central Nervous System / embryology*
  • Chick Embryo
  • Coturnix
  • DNA Replication
  • Endothelium / cytology
  • Image Processing, Computer-Assisted
  • Mesoderm / cytology*
  • Microglia / cytology*
  • Microscopy, Confocal
  • Microscopy, Fluorescence
  • Surface Properties