Human retinal microglia: expression of immune markers and relationship to the glia limitans

• Published in: Glia Vol. 14; no. 4; p. 243
• Main Authors: Provis, J M, Penfold, P L, Edwards, A J, van Driel, D
• Format: Journal Article
• Language: English
• Published: United States 01-08-1995
• Subjects: Adolescent; Adult; Aged; Antibodies - immunology; Biomarkers; Child; Humans; Immunohistochemistry; Microglia - immunology; Microscopy, Electron; Middle Aged; Neuroglia - immunology; Neuroglia - ultrastructure; Retina - immunology; Retina - ultrastructure
• ISSN: 0894-1491
• DOI: 10.1002/glia.440140402

The immunoreactivity, morphology and relationship to the glia limitans of microglia were investigated in flatmounts and sections of normal human retina, using immunogold histochemistry, electron microscopy (EM), and antibodies directed against CD45, major histocompatability complex class I (MHC-I), MHC-II, and human macrophage antigens. Immunoreactivity was evident for all antibodies tested, including MHC-I, which labeled both microglia and retinal vascular endothelium. Most consistent labeling was obtained using antibodies to CD45, MHC-II, and anti-human macrophage (S22) antigen. Immunoreactive cells were seen in the perivascular space (perivascular cells), where they were closely adherent to the vessel profile, and in the retinal parenchyma (microglia). Some parenchymal microglia were also vessel associated and by EM were seen to be closely related to the glia limitans (paravascular microglia). Paravascular microglia were shown by optical densitometry, to express higher levels of MHC antigens than neighboring, non-vessel associated, parenchymal microglia. In addition, paravascular microglia were macrophage (S22) antigen positive, while other parenchymal microglia did not express macrophage antigens. Quantitative data indicate that similar populations of microglia are immunoreactive to CD45, MHC-I, and MHC-II, while relatively few microglia (approximately 10%) are immunoreactive for human macrophage (S22) antigens, supporting previous suggestions that microglia are a heterogeneous population.