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. 1977 Oct 1;75(1):67–73. doi: 10.1083/jcb.75.1.67

Ultrastructural localization of glial fibrillary acidic protein in mouse cerebellum by immunoperoxidase labeling

PMCID: PMC2111556  PMID: 334780

Abstract

Glial fibrillary acidic protein was localized at the electron microscope level in the cerebellum of adult mice by indirect immunoperoxidase histology. In confirmation of previous studies at the light microscope level, the antigen was detectable in astrocytes and their processes, but not in neurons or their processes, or in oligodendroglia. Astrocytic processes were stained in white matter, in the granular layet surrounding synaptic glomerular complexes, and in the molecular layer in the form of radially oriented fibers and of sheaths surrounding Purkinje cell dendrites. Astrocytic endfeet impinging on meninges and perivascular membranes were also antigen positive. In astrocytic perikarya and processes, the immunohistochemical reaction product appears both as a diffuse cytoplasmic label and as elongated strands, which by their distribution and frequency could be considered glial filaments.

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Selected References

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  1. Bignami A., Dahl D. Astrocyte-specific protein and neuroglial differentiation. An immunofluorescence study with antibodies to the glial fibrillary acidic protein. J Comp Neurol. 1974 Jan 1;153(1):27–38. doi: 10.1002/cne.901530104. [DOI] [PubMed] [Google Scholar]
  2. Dahl D., Bignami A. Glial fibrillary acidic protein from normal human brain. Purification and properties. Brain Res. 1973 Jul 27;57(2):343–360. doi: 10.1016/0006-8993(73)90141-8. [DOI] [PubMed] [Google Scholar]
  3. Dahl D., Bignami A. Immunogenic properties of the glial fibrillary acidic protein. Brain Res. 1976 Oct 29;116(1):150–157. doi: 10.1016/0006-8993(76)90257-2. [DOI] [PubMed] [Google Scholar]
  4. Dahl D., Bignami A. Isolation from peripheral nerve of a protein similar to the glial fibrillary acidic protein. FEBS Lett. 1976 Jul 15;66(2):281–284. doi: 10.1016/0014-5793(76)80522-4. [DOI] [PubMed] [Google Scholar]
  5. Eng L. F., Vanderhaeghen J. J., Bignami A., Gerstl B. An acidic protein isolated from fibrous astrocytes. Brain Res. 1971 May 7;28(2):351–354. doi: 10.1016/0006-8993(71)90668-8. [DOI] [PubMed] [Google Scholar]
  6. GREY H. M., KUNKEL H. G. H CHAIN SUBGROUPS OF MYELOMA PROTEINS AND NORMAL 7S GAMMA-GLOBULIN. J Exp Med. 1964 Aug 1;120:253–266. doi: 10.1084/jem.120.2.253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Graham R. C., Jr, Karnovsky M. J. The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem. 1966 Apr;14(4):291–302. doi: 10.1177/14.4.291. [DOI] [PubMed] [Google Scholar]
  8. Ludwin S. K., Kosek J. C., Eng L. F. The topographical distribution of S-100 and GFA proteins in the adult rat brain: an immunohistochemical study using horseradish peroxidase-labelled antibodies. J Comp Neurol. 1976 Jan 15;165(2):197–207. doi: 10.1002/cne.901650206. [DOI] [PubMed] [Google Scholar]
  9. Nakane P. K., Kawaoi A. Peroxidase-labeled antibody. A new method of conjugation. J Histochem Cytochem. 1974 Dec;22(12):1084–1091. doi: 10.1177/22.12.1084. [DOI] [PubMed] [Google Scholar]
  10. Novikoff A. B., Novikoff P. M., Quintana N., Davis C. Diffusion artificats in 3,3'-diaminobenzidine cytochemistry. J Histochem Cytochem. 1972 Sep;20(9):745–749. doi: 10.1177/20.9.745. [DOI] [PubMed] [Google Scholar]
  11. REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]

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